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Systematic review to evaluate a potential association between helminth infection and physical stunting in children



Despite considerable public health efforts over the past 20 years, childhood stunting (physical and/or cognitive) levels globally remain unacceptably high—at 22% amongst children under 5 years old in 2020. The aetiology of stunting is complex and still largely unknown. Helminths can cause significant mortality and morbidity and have often been cited as major causative agents for stunting, although their actual role in childhood stunting remains unclear. Our aim was to systematically review the current evidence to help support or refute the hypothesis that helminths cause physical stunting in children.


Inclusion criteria were as follows: infected with (and/or exposed to) helminths (soil-transmitted helminths, schistosomes or food-borne trematodes), children, pregnant or breastfeeding women as study participants (children included infants 0–1 year old, preschool-age children 1–5 years and school-age children > 5 years old), anthelmintic treatment intervention, stunting-related variables reported (e.g. height, height-for-age z-score, birth weight), helminth infection reported in relation to stunting, any geographic location, any date, peer-reviewed literature only. Exclusion criteria were: non-primary research, study protocols, studies with no new data, non-English language papers and animal (non-human) helminth studies. Seven databases were searched on 28 May 2021. Risk of bias was assessed for included studies and GRADE was used for studies included in RCT subgroup meta-analyses (in preschool-age children and pregnant women). This systematic review was registered with PROSPERO (CRD42021256201).


Eighty studies were included in the analyses. No significant overall evidence was found in support of the hypothesis that helminths cause physical stunting in children, although there was some association with wasting.


Whilst analyses of the available literature to date failed to support a direct association between helminth infection and childhood stunting, there was significant heterogeneity between studies, and many had follow-up periods which may have been too short to detect impacts on growth. Most apparent was a lack of available data from key demographic groups wherein one may predict the greatest association of helminth infection with stunting—notably that of infants, preschool-age children, and pregnant or nursing women. Thus this review highlights the urgent need for further targeted empirical research amongst these potentially most vulnerable demographic groups.

Graphical Abstract


Childhood stunting is a major public health issue leading to lifelong adverse health, education and economic outcomes [1, 2]. While public health efforts have led to a considerable reduction in the global number of stunted children over the past 20 years, from 203 to 149 million [3], stunting levels remain unacceptably high. Indeed, the absolute figure for stunted children in Central and West Africa has risen during this time, partly due to the speed of population growth [3]. Data show that 22% of all children under 5 years old were stunted in 2020 [3], despite specific targets such as those by the World Health Organization (WHO) to reduce stunting by 40% in children under 5 by 2025 [4].

Stunting refers to both reduced physical growth and cognitive impairment, although the WHO definition focuses on the anthropometric aspect, where stunted children have a height for age that is “more than 2 standard deviations below the WHO child growth standards median” [5]. However, children who are not stunted according to this definition can still be short for their age and suffer from growth faltering [2]. Stunting reflects chronic undernutrition [6] and is the most common form of malnutrition in children under 5 [1,2,3]. Other forms of undernutrition include wasting (low weight for height), underweight (low weight for age) and micronutrient deficiency [6].

Stunted children have higher morbidity and mortality risks compared with non-stunted children [7]. Cognitive stunting leads to poorer school performance and an inability to reach their full potential [7]. This has adverse economic consequences for future productivity and earnings [8]. Stunted children also suffer a double burden of malnutrition, as evidence shows they have an increased risk of non-communicable diseases in later life [9, 10]. The importance of childhood stunting globally is emphasised by its inclusion in the calculation of the Global Hunger Index [11], as well as the Global Nutrition Targets 2025 [4].

Multiple factors are thought to contribute to stunting, including, but not exclusive to, nutrition, infections, the environment and maternal health [7]. Stunting also has an intergenerational aspect, where women with short maternal stature are more likely to have stunted children [2, 12]. It can therefore be challenging to disentangle which aspects have the greatest effects and, hence, which elements should be prioritised for interventions and integrated into public health programmes. Stunting and helminthiasis are also strongly associated with poverty and affect the most vulnerable populations [7, 13,14,15]. Helminth infections (i.e. parasitic worms) have been proposed as a major cause of stunting [16]. Helminthiasis caused by soil-transmitted helminths (STHs), Schistosoma spp. and food-borne trematodes (FBTs) can lead to significant morbidity [17,18,19], ranging from anaemia, haematuria, hepatomegaly and portal hypertension to intestinal obstruction, rectal prolapse and cancer in severe cases. Most people in endemic regions suffer from multiple helminth species infections concurrently [20, 21]. Children are especially vulnerable to infection due to their hygiene and play habits [22]. A recent study [23] showed that preschool-age children (PSAC) with schistosomiasis had significantly poorer early childhood development scores, but that these improved to the same levels as un-infected children with anthelmintic treatment. Along with children, pregnant and breastfeeding women have also been suspected as potential high-risk groups for helminth infections [16], due to hormonal changes and possible immunosuppression [24]. WHO classifies stunting as a subtle morbidity of helminthiasis [16], yet the short-term and long-term adverse health and economic consequences of stunting are significant for affected individuals and wider communities [2].

The first 1000 days of a child’s life, from conception to their second birthday, are recognised as the most critical time for growth and development [1, 2]. Yet helminth-infected PSAC and pregnant and nursing women have only more recently been included, and indeed actively promoted as regards the latter, in treatment programmes [25]. For infants and PSAC with schistosomiasis, this can partly be explained by the lack of a suitable licensed praziquantel formulation [26], although a paediatric praziquantel is currently in phase III clinical trials [27]. For pregnant and nursing women, their initial exclusion was due to, now alleviated, lack of safety data regarding anthelmintic use in these groups [28,29,30].

Evidence relating to the often-cited association between helminth infections in children and physical stunting [7, 31,32,33] is, however, often conflicting. Some studies propose no association [34, 35], several report a positive association [36, 37], whilst others propose associations for specific helminth species only (such as Ascaris lumbricoides only) [38]. Intensity of infection is acknowledged to be a potential key factor, with associations sometimes only found for moderate or high-intensity infections [39], although others suggest a different dynamic, where stunting is a predictor of STH infection [40]. An updated Cochrane review concluded that deworming did “not appear to improve height, haemoglobin, cognition, school performance, or mortality” [41]. However, the Cochrane review focused on STHs only and randomised controlled trials (RCTs) or quasi-RCTs. Whilst Cochrane systematic reviews are considered the gold standard in human medicine, their rigid protocols may not always allow the necessary scope to explore multifactorial and complex concepts such as stunting. Other systematic reviews on the topic of helminths and stunting in children are also already available, although to date these have either examined different aspects—notably that of cognitive rather than physical stunting [42], a range of outcomes based on secondary data from demographic and health surveys [43], or sanitation [44], and/or were restricted to STHs only [45, 46].

Bearing in mind the current knowledge gaps, our study therefore aimed to systematically review the available literature and synthesise the evidence to evaluate the potential association between helminth infection and physical stunting in children, notably with an aim to uniquely include infants and PSAC in particular, as well as pregnant and nursing women. Furthermore, whilst most studies to date have focused on STHs or schistosomiasis, few have examined both, and to our knowledge, no systematic reviews on this topic to date have aimed to include Strongyloides stercoralis or the FBTs. Finally, our review aimed to cast a wider net than the Cochrane systematic review [41] as it incorporated a range of study designs, including case reports and case series, rather than only RCTs.


This review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [47, 48] and was registered with the International Prospective Register of Systematic Reviews (PROSPERO) on 28 June 2021. Registration number; CRD42021256201.

A search strategy was developed using the PICO approach, by breaking down the research question:

  • Population and problem—infants and children, pregnant and breastfeeding women infected with (and/or exposed to) helminths

  • Intervention—treatment with an anthelmintic

  • Comparison—treated vs controls, infected vs un-infected or pre- and post-treatment

  • Outcome—physical stunting in children (a sub-set of the population of interest).

The search strategy comprised terms representing four concepts: helminths, stunting-related variables, the relevant populations (children, pregnant and breastfeeding women) and treatment. Relevant medical subject headings were also used as part of the search strategy for Medline, Embase and Global Health. Cognitive stunting terms were not included in the search strategy as this review focused on physical stunting. Since the term “children” covers a wide range of ages, for clarity, this review, and the search strategy therein, was selected from the age thresholds provided in WHO’s STH preventive chemotherapy guidelines as shown in Table 1 [16].

Table 1 Age group category thresholds for children (as defined by WHO [16])

Infants, young children and PSAC were grouped together here as “PSAC” (due to the age ranges covered by included studies), and our SAC grouping included a wider age range to accommodate the available studies. (Please see Supplementary information for study protocol [Additional file 1], search concepts [Additional file 2] and search strategies [Additional file 3]).

A total of seven databases were searched to identify studies. These were chosen based on the topics and regions covered. The databases searched were MEDLINE, Embase, Global Health, Africa-Wide Information, Latin American and Caribbean Health Sciences Literature (LILACS), Scopus and Web of Science.

Searches were carried out on 28 May 2021. No language, date limits or other filters were used at the search stage. Searches sought published peer-reviewed literature only. Search results from all seven databases were exported to EndNote reference manager (Clarivate Analytics) [49], de-duplicated and screened.

Titles and abstracts of search result records were initially screened using the inclusion and exclusion criteria shown in Table 2.

Table 2 Inclusion and exclusion criteria

Data were collected in Excel [50] by one main reviewer, with another working independently to double-check that appropriate and correct data were extracted for potential meta-analysis.

Data were sought relating to prevalence of helminth infection (for example, infected vs un-infected), intensity of infection if present (such as low, moderate or heavy), diagnostics used (for example, Kato-Katz or urine filtration) and time until follow-up. Data were obtained from studies regarding stunting-related variables in children, in particular measurements of height, height/length-for-age z-scores (HAZ/LAZ), supine length, proportion stunted, low birth weight (LBW, < 2500 g) and very low birth weight (VLBW, < 1500 g). Information was also sought relating to the age of children, location, year of study and treatment intervention.

Studies were assessed for risk of bias by checking for randomisation, comparator groups, adequate blinding (multi-arm studies only), sensitivity and appropriateness of diagnostic tests and potential confounding. The Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework [51] was used to assess the risk of bias at the outcome level for RCT studies included in subgroup meta-analyses. It was not possible to use GRADE to assess the quality and certainty of evidence for all included studies, since it relies on comparison groups (e.g. treatment and control groups) [52].

For height and birth weight, mean difference and standard deviation (SD) of the mean difference were used in the synthesis and presentation of results. For HAZ/LAZ, the mean difference and SD of the mean difference were used for synthesis of results, and for LBW and VLBW, odds ratios were used.

A total of 80 studies were included in this review, and results were initially synthesised narratively, grouped by study design.


Meta-analyses were performed in R [53] using the “meta” package for two key subgroups: PSAC and pregnant women. Odds ratios were obtained for binary outcomes (e.g. LBW) and mean differences were calculated for continuous outcomes (e.g. height). Fixed and random-effects were employed for pooling the results of the individual analyses. The Mantel–Haenszel (MH) method was used for pooling the odds ratios (i.e. calculating weights), and the inverse variance method was employed in the case of continuous variables. The between-study variance τ2 in the random-effects model was estimated with the DerSimonian and Laird method. The I2 statistic was used to check for the presence and extent of heterogeneity [54]. A meta-analysis using data from all the included studies was not feasible for several reasons including methodological diversity, clinical diversity (e.g. heterogeneity in study participants' age, geographic location, urban or rural settings) and statistical heterogeneity [54]. Performing a meta-analysis in such cases can lead to misleading results [55]. Considering these issues, meta-analyses were only performed for PSAC and pregnant women subgroups. Although the main body of literature identified related to SAC, trying to evaluate a possible association between helminth infection and stunting in this demographic group was complicated by growth changes due to puberty. Most studies in SAC did not take puberty into account, meaning relationships for this group could not be clearly explored.


Study selection is shown in Fig. 1; a final total of 80 studies were included. The number of studies listed in the “records excluded” box in Fig. 1 does not add up to 669 because the subgroups (e.g. non-English language) underneath represent just a few of the reasons reports were excluded. The 131 non-intervention studies (*) identified at the title and abstract screening stage were excluded because one of the inclusion criteria for this review was anthelmintic treatment, due to the causal nature of the systematic review hypothesis. The discrepancy between the number of reports (n = 82) and studies (n = 80) is because three reports were on studies already included in the review (n = 79), and one additional study was identified from a systematic review reference giving a total of 80 studies. A narrative synthesis was carried out for all included studies and meta-analyses were carried out on RCT studies for two subgroups of PSAC (n = 5) and pregnant women (n = 3).

Fig. 1
figure 1

PRISMA flow diagram [48]

A range of different study designs were included in this review, as shown in Table 3, the majority of which were either RCTs (43) or pre-post studies (21).

Table 3 Range of study designs included in systematic review

(For a table of all included studies sorted by risk of bias, please see Additional file 4.)

Included studies covered several different demographic groups among the population of interest as shown in Table 4. The great majority were on SAC (42), followed by PSAC and SAC (17), infants and PSAC (12), pregnant women (8) and breastfeeding women (1).

Table 4 Demographic groups as participants in included studies

A range of different helminths were covered, as shown in Table 5; however, most included studies were interested in STHs only (61), and none were identified for FBTs in relation to stunting. Participants in some studies were infected with multiple helminths. However, Table 5 is based on the helminths that were of interest to the researchers and therefore the focus of their studies. For example, for studies listed as STHs only, these may have included participants who were also infected with other helminths such as Taenia spp., but the emphasis of the investigations was on STHs only.

Table 5 Helminths investigated in included studies

Case reports and case series

One study [56] included some of the same participants as two other studies [57, 58]. Therefore, to avoid any duplication, the latter two case series were excluded from data synthesis.

Seven eligible case reports and case series were identified in the search results (see Table 6). Although based on a relatively small sample of 10 women, a retrospective case series on pregnant travellers with Schistosoma spp. [59] suggested that infected and untreated women can suffer adverse effects such as lower birth weight babies, even many years after exposure. This is noteworthy because women living in endemic areas experience constant helminth exposure. Meanwhile, another case series [56] suggested significant catch-up growth in children following treatment for Trichuris dysentery syndrome (TDS), a severe form of helminthiasis. This report emphasised that children could recover height, even after the first 1000 days of life. In another report [60], a 9-month-old baby girl was diagnosed with hookworm infection after concerns were raised regarding growth retardation. Another series [61] reported that all included children were stunted and anaemic; however, they were all hospitalised with TDS. Weight loss was reported in another case report [62], and although poor growth was discussed in relation to TDS, there was no mention of whether the patient was stunted.

Table 6 Case reports and case series included in systematic review

Pre-post studies and non-RCTs

Table 7 shows the pre-post and non-RCT studies included in this review. There were 21 pre-post studies, covering both PSAC and SAC, and nine non-RCT studies. Within this group there was significant heterogeneity in terms of sample size, number of faecal and/or urine samples obtained per participant for diagnosis, urban or rural settings, whether treatment was observed and whether an association between helminth infection and stunting was found. Only three studies [63,64,65] from this group found a significant association between helminth infection and stunting, one of which was in PSAC [65] and another which only found an association for urban children [64]. Out of the remaining nine non-RCT studies, three were in pregnant women [66,67,68] and two of these found an association between deworming during pregnancy and reduced risk of having a LBW baby [67, 68]. However, none of these studies made use of diagnostic tests to confirm actual helminth infection status and one study [66] used the WHO VLBW threshold to classify babies as LBW, instead of the WHO LBW threshold.

Table 7 Pre-post and non-randomised controlled trial studies included in systematic review


There were 43 RCTs included in this review (see Table 8), covering PSAC, SAC, and pregnant and breastfeeding women. Within this group there was also significant heterogeneity in sample size, blinding (not blinded, single-blind or double-blind), baseline helminth prevalence and anthelmintic treatment. Most studies in this group measured the intensity of helminth infection, and many had follow-up periods of 12 months or more. Only four studies [69,70,71,72] from this group found an association between helminth infection and stunting, all of which were in SAC, and three were conducted in sub-Saharan Africa [69, 70, 72]. Although the study in breastfeeding women [73] found no significant difference in infant growth between treatment and placebo groups at 6 months, further analysis of STH-infected mothers revealed significant improvements in infant length gain and length-for-age z-scores (LAZ).

Table 8 Randomised controlled trial studies included in systematic review


Subgroup meta-analyses were carried out for five RCT studies in PSAC and three RCT studies in pregnant women (two different anthelmintic treatment arms were included for one study). Several RCT studies for PSAC were not included in meta-analyses because of statistically significant differences between treatment and control groups at baseline [74] or data reported were not amenable to meta-analyses [75,76,77]. One RCT study for pregnant women [78] could not be included in the meta-analysis because the relevant data were not provided separately for treated and control groups.

Preschool-age children

As the meta-analysis in Fig. 2 shows, no significant difference (p = 0.40) was found between anthelmintic treatment or placebo on height using either the fixed- or random-effects model. The I2 statistic detected 45% heterogeneity, indicating moderate but not necessarily important heterogeneity [54]. The meta-analysis results presented in Fig. 3 also showed no significant difference (p = 0.63) between anthelmintic treatment or placebo on height-for-age/length-for-age z-scores (HAZ/LAZ) using either the fixed- or random-effects model. The I2 statistic detected no heterogeneity.

Fig. 2
figure 2

Preschool-age children (PSAC)—effect of anthelmintic treatment on height (cm)

Fig. 3
figure 3

Preschool-age children (PSAC)—effect of anthelmintic treatment on height-for-age/length-for-age z-score

Pregnant women

As Fig. 4 shows, meta-analysis for the pregnant women subgroup found no significant difference (p = 0.23) between anthelmintic treatment or placebo on the likelihood of a LBW (< 2500 g) baby using either the fixed- (MH) or random-effects model. The I2 statistic detected no heterogeneity.

Fig. 4
figure 4

Pregnant women—effect of anthelmintic treatment on low birth weight (< 2500 g)

The meta-analysis results shown in Fig. 5 for pregnant women also found no significant difference (p = 0.26) between anthelmintic treatment or placebo on the likelihood of a VLBW (< 1500 g) baby using either the fixed- (MH) or random-effects model. The I2 statistic detected 35% heterogeneity, representing moderate but not necessarily important heterogeneity [54].

Fig. 5
figure 5

Pregnant women—effect of anthelmintic treatment on very low birth weight (< 1500 g)

As Fig. 6 shows, meta-analysis similarly found no significant difference (p = 0.74) between anthelmintic treatment or placebo on mean birth weight using either the fixed- or random-effects model. The I2 statistic detected no heterogeneity.

Fig. 6
figure 6

Pregnant women—effect of anthelmintic treatment on mean birth weight (kg)

Certainty of evidence

Two GRADE summary of findings tables were produced based on the meta-analyses presented; one for PSAC and one for pregnant women [79]. The certainty of the evidence in the PSAC meta-analysis for height was high (Table 9); however, there were serious concerns about risk of bias and possible confounding (see explanations). Similarly, for height-for-age/length-for-age z-scores (HAZ/LAZ), the certainty of the evidence was moderate and there were serious concerns about risk of bias. Table 10 shows the certainty of the evidence in pregnant women was moderate for LBW and mean birth weight, again due to concerns regarding risk of bias (see explanations). The certainty was high for VLBW; however, very few studies were included in that meta-analysis due to limited available data.

Table 9 GRADE summary of findings table for preschool-age children (PSAC) [79]
Table 10 GRADE summary of findings table for pregnant women [79]


The findings of this systematic review indicate, based on the age groups studied to date, there is currently no significant overall evidence that helminths cause physical stunting in children. This is important considering this concept is so frequently cited in the literature and is shown as a cause of stunting in WHO’s stunting conceptual framework [7]. Our findings agree with the most recent Cochrane systematic review on deworming effects in children [41], but contrast with a previous systematic review looking at effects of STHs on child growth and nutrition in settings with > 50% STH prevalence [45] and an empirical analysis of deworming in PSAC based on demographic and health surveys [43]. Notably, however, the present systematic review highlighted the limited available data in the crucial demographic age group of infants and PSAC, as well as pregnant and breastfeeding women. The results also suggested that helminth infection in children may have a greater effect on wasting and/or underweight than on stunting [77, 80,81,82,83,84].

Subgroup meta-analyses for PSAC showed that anthelmintic treatment was not associated with significant improvements in height or HAZ/LAZ (Figs. 2 and 3). However, these meta-analyses were only able to include RCT study designs (to compare treatment with placebo groups); therefore, one non-RCT study in PSAC that did find an association between helminth infection and stunting [65] was not considered. The results of such meta-analyses should therefore be interpreted with caution. Equally, such clear-cut benefit or harm thinking in relation to meta-analyses and GRADE summary of findings tables can lead to more nuanced results being overlooked. For example, one of the included studies in the PSAC meta-analyses [85] did not find an association between helminth infection and stunting but did report a better response in growth when infants were treated at the age of 12 months rather than 18 months. Evidence such as this has the potential to be very useful for clinicians and policymakers, although further similar studies are needed to corroborate such findings. Another study in PSAC [77] reported that although no association was found between helminth infection and stunting, treatment did reduce wasting in children < 30 months old. Again, such information has implications for future research and public health policy, although it would also need verification by other studies.

Importantly, neither the Cochrane Systematic Review nor Hall et al. [41, 45] included, or even considered, the impact of helminthiasis on pregnant women and/or the possible role of stunting beginning in utero. In our study, subgroup meta-analyses showed that deworming during pregnancy did not reduce the risk of having a LBW or VLBW baby, although the evidence base was small and therefore the results must be interpreted with caution. However, as with PSAC, the meta-analyses were only able to include RCT study designs; therefore, non-RCT studies that did find an association between helminth infection and LBW [67, 68] were not considered as part of the analysis. Although not obvious from Fig. 4, one RCT study included in the pregnant women meta-analysis [86] did report a “suggestion of benefit of albendazole among women with moderate to heavy hookworm infection”. Interestingly, the small case series in pregnant travellers [59] found that pregnant women infected with Schistosoma spp. who did not receive treatment had babies with lower birth weight compared to those who were treated. Considering that those women were not living in endemic settings and therefore not being constantly re-exposed to helminths, the results are quite remarkable. Given that past reviews [87,88,89] found no benefit of deworming pregnant women on the outcome of LBW, more, ideally carefully-controlled and multidisciplinary studies are needed to explore this relationship further. One potential mechanism of benefit for pregnant women with helminthiasis who receive anthelmintics is a possible [89] or significant reduction in maternal anaemia [88]. Network meta-analyses [87] that consider anthelmintic treatment for pregnant women in the context of other interventions to improve maternal health may prove more fruitful than evaluating a single intervention at a time.

Pre-post treatment study designs were integral to this review, yet such non-RCT studies tend to be routinely excluded from Cochrane systematic reviews, although the nutritional interventions review is a notable exception [90]. However, for some field intervention studies, a control group is not ethical [63, 91, 92] such as in high helminth prevalence settings or areas where public health programmes are already in place; hence, pre-post treatment study designs are the next best alternative.

When interpreting the results of this review, it is possible that a lack of effect may not necessarily equate to a genuine lack of association between helminth infection and physical stunting in children. This may be because (i) children in the available studies were generally older than the ideal demographic group (infants and PSAC); (ii) follow-up periods may have been too short to see an effect on height (for example, [45] suggests longitudinal studies on growth in children should last 1–2 years); and/or (iii) there may have been low anthelmintic efficacy [93, 94]. For example, as regards the latter point, benzimidazoles such as albendazole and mebendazole, two of the most widely used drugs in STH mass drug administration (MDA) programmes and recommended by WHO [17], have been shown to exhibit reduced efficacy against Trichuris trichiura and hookworms [93]. Furthermore, for S. mansoni, a study showed potential reduced efficacy of praziquantel in SAC amongst populations that had undergone multiple rounds of MDA [94].

Other factors may also have influenced the findings of studies included in this review. These include differences in available nutrition, helminth prevalence and intensity of infection, helminth species and confounding due to concurrent infections. For example, several studies in children [95, 96] also investigated intestinal protozoa such as Giardia, which is known to cause weight loss [97] and has been implicated as a cause of stunting [98, 99]. Other studies [100,101,102] took place in malaria-endemic regions, which may also have caused confounding, since malaria has been identified as a risk factor for stunting and wasting [103]. Reasons such as these may partly explain the conflicting results of studies that have tried to evaluate whether a potential association exists between helminths and stunting.

This review has demonstrated that significant evidence gaps remain regarding helminths and stunting in children. In summary, we do not yet know whether there is truly no association between helminth infection and physical stunting in children, or whether this is simply due to a scarcity of currently available data for infants and PSAC in their first 1000 days of life. In many cases, we do not know whether a lack of effect on growth is due to reduced anthelmintic efficacy, as this tends not to be routinely monitored [94]. Perhaps most importantly for infants and PSAC, the widely used diagnostic tests such as Kato-Katz and urine filtration are not sufficiently sensitive to detect light infections, which have been shown to be common in this demographic group [104]. This makes it challenging to assess the true disease burden in this important demographic group, and consequently whether any potential association with stunting exists.

As the results highlight, there were few intervention studies that focused on schistosomiasis and stunting (only six, compared with 61 for STHs). This was disappointing, because one of the aims of this review was to evaluate the evidence base for a wide range of helminths in relation to childhood stunting, including schistosomes. Perhaps this demonstrates that stunting is not yet considered a significant indicator of morbidity for schistosomiasis. No intervention studies were found relating to FBTs and potential effects on child growth. This evidence gap should also be urgently addressed, especially as these helminths are now included in the Neglected Tropical Diseases (NTD) 2030 roadmap [105]. Perhaps most starkly of all, despite a comprehensive search strategy, only one intervention study [73] was identified evaluating breastfeeding women with helminthiasis and potential effects on their infant’s growth. This therefore highlights a potentially critical evidence gap.

Some studies included measured the intensity of helminth infection whereas others recorded a binary infected or un-infected result. Assessing the intensity of helminth infections is important because intensity usually correlates with severity of morbidity [16]. It is also possible that potential associations between helminthiasis and stunting only become apparent with higher-intensity infections or in higher-prevalence settings. This too might help explain why one systematic review [45] found an association between helminth infection and stunting, since it only included studies in high-prevalence settings. However, another recent study [106] concluded that treatment to reduce helminth burden might “not improve growth in high S. mansoni transmission settings”.

One robust longitudinal cohort study (not eligible for inclusion in this review) found that maternal and child factors were most important for growth during the first two  years, but that environmental factors become more influential in later life [107]. This complements the concept of the nurturing care framework [108], which emphasises the many aspects and layers influencing healthy growth and development of children as they progress through life stages.

It is also important to recognise the limits of stunting as an outcome measure, and to see the condition in the wider context of the social determinants of health, especially in relation to poverty [7, 109, 110]. Researchers, clinicians and policymakers should remain mindful that children can still be short for their age or experiencing growth faltering without necessarily being stunted according to the WHO definition [2]. Undernutrition encompasses stunting, underweight and wasting, yet these are not mutually exclusive conditions, and children may fall into all these categories [6, 111]. Several authors have emphasised the need to address stunting and wasting concurrently rather than treating them as separate issues from a research and policy perspective, since they may share similar risk factors [112, 113]. Some have proposed that physical stunting may partly be the result of previous wasting episodes [113]. Some studies included in our review suggested a possible association of helminthiasis with wasting rather than stunting in children; however, this too needs further exploration since wasting was not the focus of the present study. Considering that helminth infection reduces appetite [114, 115], it might be logical for an association to exist with wasting and/or being underweight. However, this review has also highlighted that much is still unknown, and the evidence base for infants, PSAC, and pregnant and breastfeeding women with helminthiasis is small.


This systematic review had several limitations, the first being that the inclusion and exclusion criteria inevitably led to a degree of publication and language bias. Perhaps the most important limitation was that most of the included studies—by necessity, as that was largely all that was available—focused on SAC. This made evaluating a potential association between helminth infections in children and physical stunting quite challenging, since the first 1000 days are known to be critical for child growth and development [1, 2, 116]. Few of the SAC studies included in our review considered the effect of puberty, which is important because participants in many studies were approaching or in adolescence, and children experience a “pre-adolescent dip” followed by a “pubertal growth spurt” during this time [117]. Evidence suggests that puberty can be delayed by stunting [118], but also that some children who are stunted at preschool-age can experience catch-up growth and recovery from stunting during adolescence [119]. There were relatively few studies on pregnant women (eight) and only one on breastfeeding women, so this is an evidence gap that still needs to be addressed in future research. Some studies also had a relatively short time interval following treatment before anthropometric measurements and faecal and/or urine testing were repeated [120, 121], making changes in height or HAZ more difficult to detect. Many studies used the coprological Kato-Katz diagnostic test, yet more sensitive diagnostic tests, notably those now of multi-parallel quantitative polymerase chain reaction (qPCR), are vital for lower-prevalence settings and lighter-intensity infections [122]. The requirement for RCT study designs for meta-analyses also restricted the number of studies that could be included within them.

Implications for future research

Studies that combine elements of several of the studies in this review [73, 86] are likely to be most useful for future research, for example deworming during the second or third trimester and then monitoring not only the birth weight of babies, but also their subsequent growth over the first 12 months. Such studies could potentially capture whether helminthiasis leads to intrauterine growth restriction (IUGR) and/or postnatal growth stunting. The benefits of anthelmintic treatment for pregnant women themselves should also not be overlooked. Many women in endemic countries experience several pregnancies during their reproductive lives [32]; therefore, improving their overall health status is likely to have profound repercussions on childhood health. Encouraging countries to record their birth weight data is also essential, as the lack of data currently holds back monitoring and evaluation efforts [123].

The scarcity of available data relating to helminth infections and stunting in the key demographic groups of infants, PSAC, and pregnant and breastfeeding women needs to be urgently addressed. This problem was also clearly highlighted in a recent update of a Cochrane systematic review [89], in which the authors report they were unable to perform planned subgroup analyses due to too few studies. A very recent study [23] looking at early childhood development, stunting and schistosomiasis in Zimbabwe has already begun to address this evidence gap.

Case series such as the study of pregnant travellers infected with schistosomiasis [59] can be very useful. By focusing on travellers from non-endemic regions, that study significantly reduced the chances of confounding, from co-infections for example, which are almost impossible to avoid in endemic areas. Although prone to a high risk of bias, this review shows that case reports and case series can still provide helpful information, and perhaps could be utilised more widely in the scientific literature.


This systematic review found no overall significant evidence that helminths cause physical stunting in children, albeit some association with wasting and/or undernutrition. However, the main finding was the limited available data for the key demographic groups of infants and PSAC, as well as pregnant and nursing women. Considering the importance of the first 1000 days of life for child growth and development, this evidence gap needs to be urgently addressed in future research. Some of the included studies also suggest there may be a possible relationship between helminth infection and wasting and/or being underweight, indicating that a broader perspective may be needed to evaluate potential relationships between helminth infection and malnutrition in future research.

Availability of data and materials

PROSPERO record (CRD42021256201) and full data can be made available upon request to the corresponding authors.



Food-borne trematodes


Low birth weight


Mass drug administration


Neglected tropical diseases


Preschool-age children


School-age children


Soil-transmitted helminths


Very low birth weight


World Health Organization


  1. Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382:427–51.

    Article  PubMed  Google Scholar 

  2. de Onis M, Branca F. Childhood stunting: a global perspective. Matern Child Nutr. 2016;12:12–26.

    Article  PubMed  PubMed Central  Google Scholar 

  3. UNICEF Malnutrition. 2021.*%2C%2022%20per%20cent,203.6%20million%20to%20149.2%20million. Accessed 2 May 2021.

  4. World Health Organization. Global Nutrition Targets 2025: Stunting Policy Brief, Geneva: World Health Organization, 2014. Accessed 2 May 2021.

  5. World Health Organization. Stunting in a Nutshell. Geneva: World Health Organization, 2015.,WHO%20Child%20Growth%20Standards%20median. Accessed 2 May 2021.

  6. World Health Organization. Malnutrition. Geneva: World Health Organization, 2020. Accessed 2 May 2021.

  7. World Health Organization. Childhood Stunting Conceptual Framework. Geneva: World Health Organization, 2013. Accessed 2 May 2021.

  8. McGovern ME, Krishna A, Aguayo VM, Subramanian S. A review of the evidence linking child stunting to economic outcomes. Int J Epidemiol. 2017;46:1171–91.

    Article  PubMed  PubMed Central  Google Scholar 

  9. De Lucia RE, de França GVA, Vianna CA, Gigante DP, Miranda JJ, Yudkin JS, et al. Associations of stunting in early childhood with cardiometabolic risk factors in adulthood. PLoS ONE. 2018;13:e0192196.

    Article  CAS  Google Scholar 

  10. Grey K, Gonzales GB, Abera M, Lelijveld N, Thompson D, Berhane M, et al. Severe malnutrition or famine exposure in childhood and cardiometabolic non-communicable disease later in life: a systematic review. BMJ Glob Health. 2021;6:e003161.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Von Grebmer, K., J. Bernstein, R. Alders, O. Dar, R. Kock, F. Rampa, et al. 2020 Global Hunger Index: One Decade to Zero Hunger: Linking Health and Sustainable Food Systems. 2020. Bonn: Welthungerhilfe; and Dublin: Concern Worldwide

  12. Khatun W, Alam A, Rasheed S, Huda TM, Dibley MJ. Exploring the intergenerational effects of undernutrition: association of maternal height with neonatal, infant and under-five mortality in Bangladesh. BMJ Glob Health. 2018;3:e000881.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Wakelin D. Helminths: Pathogenesis and Defenses. In: Baron S, editor. Medical Microbiology. 4th edition. Galveston (TX): University of Texas Medical Branch at Galveston. Chapter 87, 1996.

  14. Hotez, PJ., Bundy, DAP., Beegle, K., Brooker, S., Drake, L., de Silva, N., et al. Helminth Infections: Soil-transmitted Helminth Infections and Schistosomiasis. In: Jamison DT, Breman JG, Measham AR, et al., editors. Disease Control Priorities in Developing Countries. 2nd edition. Washington (DC): The International Bank for Reconstruction and Development / The World Bank. Chapter 24, 2006. Oxford University Press, New York.

  15. Keiser J, Utzinger J. Food-Borne Trematodiases. Clin Microbiol Rev. 2009;22:466–83.

    Article  PubMed  PubMed Central  Google Scholar 

  16. World Health Organization. Guideline: Preventive Chemotherapy to control soil-transmitted helminth infections in at-risk population groups. Geneva: World Health Organization, 2017.;jsessionid=76AA1C10D1F20A59F0CBB8FA5ABE041B?sequence=1. Accessed 2 May 2021.

  17. World Health Organization. Soil-transmitted helminth infections. Geneva: World Health Organization, 2020. Accessed 2 May 2021.

  18. World Health Organization. Schistosomiasis. Geneva: World Health Organization, 2021. Accessed 2 May 2021.

  19. World Health Organization. Foodborne trematode infections. Geneva: World Health Organization, 2021. Accessed 2 May 2021.

  20. Tchuem Tchuenté L-A, Behnke JM, Gilbert FS, Southgate VR, Vercruysse J. Polyparasitism with Schistosoma haematobium and soil-transmitted helminth infections among school children in Loum. Cameroon Trop Med Int Health. 2003;8:975–86.

    Article  PubMed  Google Scholar 

  21. Mupfasoni D, Karibushi B, Koukounari A, Ruberanziza E, Kaberuka T, Kramer MH, et al. Polyparasite Helminth Infections and Their Association to Anaemia and Undernutrition in Northern Rwanda. PLoS Negl Trop Dis. 2009;3:e517.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Pasaribu AP, Alam A, Sembiring K, Pasaribu S, Setiabudi D. Prevalence and risk factors of soil-transmitted helminthiasis among school children living in an agricultural area of North Sumatera, Indonesia. BMC Public Health. 2019;19:1066.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Mutapi F, Pfavayi L, Osakunor D, Lim R, Kasambala M, Mutemeri A, et al. Assessing early child development and its association with stunting and schistosome infections in rural Zimbabwean children using the Griffiths Scales of Child Development. PLoS Negl Trop Dis. 2021;15:e0009660.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Mpairwe H, Tweyongyere R, Elliott A. Pregnancy and helminth infections. Parasite Immunol. 2014;36:328–37.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. Bustinduy AL, Stothard JR, Friedman JF. Paediatric and maternal schistosomiasis: shifting the paradigms. Br Med Bull. 2017;123:115–25.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Reinhard-Rupp J, Klohe K. Developing a comprehensive response for treatment of children under 6 years of age with schistosomiasis: research and development of a pediatric formulation of praziquantel. Infect Dis Poverty. 2017;6:122.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Pediatric Praziquantel Consortium. The Pediatric Formulation, 2021. Accessed 2 May 2021.

  28. Friedman JF, Olveda RM, Mirochnick MH, Bustinduy AL, Elliott AM. Praziquantel for the treatment of schistosomiasis during human pregnancy. Bull World Health Organ. 2018;96:59–65.

    Article  PubMed  Google Scholar 

  29. Gyorkos TW, St-Denis K. Systematic review of exposure to albendazole or mebendazole during pregnancy and effects on maternal and child outcomes, with particular reference to exposure in the first trimester. Int J Parasitol. 2019;49:541–54.

    CAS  Article  PubMed  Google Scholar 

  30. Nicolas P, Maia MF, Bassat Q, Kobylinski KC, Monteiro W, Rabinovich NR, et al. Safety of oral ivermectin during pregnancy: a systematic review and meta-analysis. Lancet Glob Health. 2020;8:e92–100.

    Article  PubMed  Google Scholar 

  31. Stephenson LS. Helminth parasites, a major factor in malnutrition. World Health Forum. 1994;15:169–72.

    CAS  PubMed  Google Scholar 

  32. Crompton DW, Nesheim MC. Nutritional impact of intestinal helminthiasis during the human life cycle. Annu Rev Nutr. 2002;22:35–59.

    CAS  Article  PubMed  Google Scholar 

  33. Forrer A, Khieu V, Schär F, Hattendorf J, Marti H, Neumayr A, et al. Strongyloides stercoralis is associated with significant morbidity in rural Cambodia, including stunting in children. PLoS Negl Trop Dis. 2017;11:e0005685.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Campbell SJ, Nery SV, D’Este CA, Gray DJ, McCarthy JS, Traub RJ, et al. Investigations into the association between soil-transmitted helminth infections, haemoglobin and child development indices in Manufahi District, Timor-Leste. Parasit Vectors. 2017;10:192.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Farrant O, Marlais T, Houghton J, Goncalves A, Cassama E, Cabral MG, et al. Prevalence, risk factors and health consequences of soil-transmitted helminth infection on the Bijagos Islands, Guinea Bissau: A community-wide cross-sectional study. PLoS Negl Trop Dis. 2020;14:e0008938.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Shang Y, Tang LH, Zhou SS, Chen YD, Yang YC, Lin SX. Stunting and soil-transmitted-helminth infections among school-age pupils in rural areas of southern China. Parasit Vectors. 2010;3:97.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Blouin B, Casapia M, Joseph L, Gyorkos TW. A longitudinal cohort study of soil-transmitted helminth infections during the second year of life and associations with reduced long-term cognitive and verbal abilities. PLoS Negl Trop Dis. 2018;12:e0006688.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Moncayo AL, Lovato R, Cooper PJ. Soil-transmitted helminth infections and nutritional status in Ecuador: findings from a national survey and implications for control strategies. BMJ Open. 2018;8:e021319.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Sanchez AL, Gabrie JA, Usuanlele M-T, Rueda MM, Canales M, Gyorkos TW. Soil-Transmitted Helminth Infections and Nutritional Status in School-age Children from Rural Communities in Honduras. PLoS Negl Trop Dis. 2013;7:e2378.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Kabatende J, Mugisha M, Ntirenganya L, Barry A, Ruberanziza E, Mbonigaba JB, et al. Prevalence, Intensity, and Correlates of Soil-Transmitted Helminth Infections among School Children after a Decade of Preventive Chemotherapy in Western Rwanda. Pathogens. 2020;9:1076.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Taylor-Robinson DC, Maayan N, Donegan S, Chaplin M, Garner P. Public health deworming programmes for soil-transmitted helminths in children living in endemic areas. Cochrane Database Syst Rev. 2019;9:18.

    Google Scholar 

  42. Pabalan N, Singian E, Tabangay L, Jarjanazi H, Boivin MJ, Ezeamama AE. Soil-transmitted helminth infection, loss of education and cognitive impairment in school-aged children: A systematic review and meta-analysis. PLoS Negl Trop Dis. 2018;12:e0005523.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Lo NC, Snyder J, Addiss DG, Heft-Neal S, Andrews JR, Bendavid E. Deworming in pre-school age children: A global empirical analysis of health outcomes. PLoS Negl Trop Dis. 2018;12:e0006500.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Rakotomanana H, Komakech JJ, Walters CN, Stoecker BJ. The WHO and UNICEF Joint Monitoring Programme (JMP) Indicators for Water Supply, Sanitation and Hygiene and Their Association with Linear Growth in Children 6 to 23 Months in East Africa. Int J Environ Res Public Health. 2020;17 17.

  45. Hall A, Hewitt G, Tuffrey V, De Silva N. A review and meta-analysis of the impact of intestinal worms on child growth and nutrition. Matern Child Nutr. 2008;4:118–236.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Thayer WM, Clermont A, Walker N. Effects of deworming on child and maternal health: a literature review and meta-analysis. BMC Public Health. 2017;17:830.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Beller EM, Glasziou PP, Altman DG, Hopewell S, Bastian H, Chalmers I, et al. PRISMA for Abstracts: Reporting Systematic Reviews in Journal and Conference Abstracts. PLoS Med. 2013;10:e1001419.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:71.

    Article  Google Scholar 

  49. EndNote, 2020, The EndNote Team, EndNote X9, Clarivate, Philadelphia, PA.

  50. Excel, Microsoft Excel 2016. Redmond, WA: Microsoft Corporation; 2016.

    Google Scholar 

  51. Guyatt GH, Oxman AD, Vist GE, Kunz R, Falck-Ytter Y, Alonso-Coello P, et al. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ. 2008;336:924.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Guyatt G, Oxman AD, Akl EA, Kunz R, Vist G, Brozek J, et al. GRADE guidelines: 1 Introduction—GRADE evidence profiles and summary of findings tables. J Clin Epidemiol. 2011;64:383–94.

    Article  PubMed  Google Scholar 

  53. R Core Team, 2021. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.

  54. Altman, D., Ashby, D., Birks, J., Borenstein, M., Campbell, M., Deeks, J., et al. Chapter 10: Analysing Data and undertaking meta-analyses. In: Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA (editors). 2021. Cochrane Handbook for Systematic Reviews of Interventions version 6.2 (updated February 2021). Cochrane. Accessed 25 June 2021.

  55. McKenzie, JE., Brennan, SE. Chapter 12: Synthesizing and presenting findings using other methods. In: Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA (editors). 2021. Cochrane Handbook for Systematic Reviews of Interventions version 6.2 (updated February 2021). Cochrane. Accessed 25 June 2021.

  56. Cooper ES, Duff EM, Howell S, Bundy DA. “Catch-up” growth velocities after treatment for Trichuris dysentery syndrome. Trans R Soc Trop Med Hyg. 1995;89:653.

    CAS  Article  PubMed  Google Scholar 

  57. Cooper ES, Bundy DA, MacDonald TT, Golden MH. Growth suppression in the Trichuris dysentery syndrome. Eur J Clin Nutr. 1990;44:285–91.

    CAS  PubMed  Google Scholar 

  58. Callender JE, Grantham-McGregor SM, Walker SP, Cooper ES. Treatment effects in Trichuris dysentery syndrome. Acta Paediatr. 1994;83:1182–7.

    CAS  Article  PubMed  Google Scholar 

  59. Ben-Chetrit E, Lachish T, Morch K, Atias D, Maguire C, Schwartz E. Schistosomiasis in pregnant travelers: a case series. J Travel Med. 2015;22:94–8.

    Article  PubMed  Google Scholar 

  60. Intra J, Sarto C, Manuli E, Vannini PM, Brambilla P. Multiple parasitic infestation in a nine-month-old patient: a case report. Helminthologia. 2019;56:53–6.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  61. Kaminsky RG, Castillo RV, Flores CA. Growth retardation and severe anemia in children with Trichuris dysenteric syndrome. Asian Pac J Trop Biomed. 2015;5:591–7.

    Article  Google Scholar 

  62. Zanwar VG, Pawar SV, Jain SS, Rathi SP, Contractor QQ, Rathi PM. An unusual cause of overt gastrointestinal bleeding in a malnourished child. Trop Doct. 2016;46:100–2.

    Article  PubMed  Google Scholar 

  63. Ahmed A, Al-Mekhlafi HM, Al-Adhroey AH, Ithoi I, Abdulsalam AM, Surin J. The nutritional impacts of soil-transmitted helminths infections among Orang Asli schoolchildren in rural Malaysia. Parasit Vectors. 2012;5:119.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Staudacher O, Heimer J, Steiner F, Kayonga Y, Havugimana JM, Ignatius R, et al. Soil-transmitted helminths in southern highland Rwanda: associated factors and effectiveness of school-based preventive chemotherapy. Trop Med Int Health. 2014;19:812–24.

    CAS  Article  PubMed  Google Scholar 

  65. Osakunor DNM, Mduluza T, Midzi N, Chase-Topping M, Mutsaka-Makuvaza MJ, Chimponda T, et al. Dynamics of paediatric urogenital schistosome infection, morbidity and treatment: a longitudinal study among preschool children in Zimbabwe. BMJ glob. 2018;3:e000661.

    Article  Google Scholar 

  66. de Silva NR, Sirisena JL, Gunasekera DP, Ismail MM, de Silva HJ. Effect of mebendazole therapy during pregnancy on birth outcome. Lancet. 1999;353:1145–9.

    Article  PubMed  Google Scholar 

  67. Passerini L, Casey GJ, Biggs BA, Cong DT, Phu LB, Phuc TQ, et al. Increased birth weight associated with regular pre-pregnancy deworming and weekly iron-folic acid supplementation for Vietnamese women. PLoS Negl Trop Dis. 2012;6:e1608.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  68. Walia B, Kmush BL, Lane SD, Endy T, Montresor A, Larsen DA. Routine deworming during antenatal care decreases risk of neonatal mortality and low birthweight: A retrospective cohort of survey data. PLoS Negl Trop Dis. 2021;15:e0009282.

    Article  PubMed  PubMed Central  Google Scholar 

  69. Stephenson LS, Latham MC, Kurz KM, Kinoti SN, Brigham H. Treatment with a single dose of albendazole improves growth of Kenyan schoolchildren with hookworm, Trichuris trichiura, and Ascaris lumbricoides infections. Am J Trop Med Hyg. 1989;41:78–87.

    CAS  Article  PubMed  Google Scholar 

  70. Stephenson LS, Latham MC, Adams EJ, Kinoti SN, Pertet A. Physical fitness, growth and appetite of Kenyan school boys with hookworm, Trichuris trichiura and Ascaris lumbricoides infections are improved four months after a single dose of albendazole. J Nutr. 1993;123:1036–46.

    CAS  Article  PubMed  Google Scholar 

  71. Hadju V, Satriono S, Abadi K, Stephenson LS. Relationships between soil-transmitted helminthiases and growth in urban slum schoolchildren in Ujung Pandang. Indonesia Int J Food Sci Nutr. 1997;48:85–93.

    CAS  Article  PubMed  Google Scholar 

  72. Stoltzfus RJ, Albonico M, Tielsch JM, Chwaya HM, Savioli L. School-based deworming program yields small improvement in growth of Zanzibari school children after one year. J Nutr. 1997;127:2187–93.

    CAS  Article  PubMed  Google Scholar 

  73. Mofid LS, Casapia M, Aguilar E, Silva H, Montresor A, Rahme E, et al. A Double-Blind Randomized Controlled Trial of Maternal Postpartum Deworming to Improve Infant Weight Gain in the Peruvian Amazon. PLoS Negl Trop Dis. 2017;11:e0005098.

    Article  PubMed  PubMed Central  Google Scholar 

  74. Garg R, Lee LA, Beach MJ, Wamae CN, Ramakrishnan U, Deming MS. Evaluation of the Integrated Management of Childhood Illness guidelines for treatment of intestinal helminth infections among sick children aged 2–4 years in western Kenya. Trans R Soc Trop Med Hyg. 2002;96:543–8.

    Article  PubMed  Google Scholar 

  75. Rousham EK, Mascie-Taylor CG. An 18-month study of the effect of periodic anthelminthic treatment on the growth and nutritional status of pre-school children in Bangladesh. Ann Hum Biol. 1994;21:315–24.

    CAS  Article  PubMed  Google Scholar 

  76. Northrop-Clewes CA, Rousham EK, Mascie-Taylor CN, Lunn PG. Anthelmintic treatment of rural Bangladeshi children: effect on host physiology, growth, and biochemical status. Am J Clin Nutr. 2001;73:53–60.

    CAS  Article  PubMed  Google Scholar 

  77. Stoltzfus RJ, Chway HM, Montresor A, Tielsch JM, Jape JK, Albonico M, et al. Low dose daily iron supplementation improves iron status and appetite but not anemia, whereas quarterly anthelminthic treatment improves growth, appetite and anemia in Zanzibari preschool children. J Nutr. 2004;134:348–56.

    CAS  Article  PubMed  Google Scholar 

  78. Satya Deepti S, Nandini L. Effects of deworming during pregnancy on maternal and perinatal outcomes: A randomized controlled trial. Res J Pharm, Biol Chem Sci. 2015;6:1521–6.

    Google Scholar 

  79. GRADEpro GDT: GRADEpro Guideline Development Tool [Software]. McMaster University, 2020 (developed by Evidence Prime, Inc.). Accessed 29 July 2021.

  80. Stephenson LS, Latham MC, Kurz KM, Kinoti SN. Single dose metrifonate or praziquantel treatment in Kenyan children. II. Effects on growth in relation to Schistosoma haematobium and hookworm egg counts. Am J Trop Med Hyg. 1989;41:445–53.

    CAS  Article  PubMed  Google Scholar 

  81. Watkins WE, Pollitt E. Effect of removing Ascaris on the growth of Guatemalan schoolchildren. Pediatrics. 1996;97:871–6.

    CAS  PubMed  Google Scholar 

  82. Hagel I, Lynch NR, Di Prisco MC, Perez M, Sanchez JE, Pereyra BN, et al. Helminthic infection and anthropometric indicators in children from a tropical slum: Ascaris reinfection after anthelmintic treatment. J Trop Pediatr. 1999;45:215–20.

    CAS  Article  PubMed  Google Scholar 

  83. Sarkar NR, Anwar KS, Biswas KB, Mannan MA. Effect of deworming on nutritional status of Ascaris infested slum children of Dhaka. Bangladesh Indian Pediatrics. 2002;39:1021–6.

    PubMed  Google Scholar 

  84. Zhou H, He Y, Ohtsuka R. Sex differences in the malnourished status of Chinese children due to schistosomiasis infections and inadequate dietary intake. Environ. 2005;12:145–53.

    Google Scholar 

  85. Joseph SA, Casapia M, Montresor A, Rahme E, Ward BJ, Marquis GS, et al. The Effect of Deworming on Growth in One-Year-Old Children Living in a Soil-Transmitted Helminth-Endemic Area of Peru: A Randomized Controlled Trial. PLoS Negl Trop Dis. 2015;9:e0004020.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  86. Ndibazza J, Muhangi L, Akishule D, Kiggundu M, Ameke C, Oweka J, et al. Effects of deworming during pregnancy on maternal and perinatal outcomes in Entebbe, Uganda: a randomized controlled trial. Clin Infect Dis. 2010;50:531–40.

    CAS  Article  PubMed  Google Scholar 

  87. Park JJH, Harari O, Siden E, Zoratti M, Dron L, Zannat NE, et al. Interventions to improve birth outcomes of pregnant women living in low- and middle-income countries: a systematic review and network meta-analysis. Gates Open Res. 2019;3:1657.

    Article  PubMed  Google Scholar 

  88. Salam RA, Cousens S, Welch V, Gaffey M, Middleton P, Makrides M, et al. Mass deworming for soil-transmitted helminths and schistosomiasis among pregnant women: A systematic review and individual participant data meta-analysis. Campbell Syst Rev. 2019;15:e1052.

    Google Scholar 

  89. Salam RA, Das JK, Bhutta ZA. Effect of mass deworming with antihelminthics for soil-transmitted helminths during pregnancy. Cochrane Database Syst Rev. 2021;5:798.

    Google Scholar 

  90. Goudet SM, Bogin BA, Madise NJ, Griffiths PL. Nutritional interventions for preventing stunting in children (birth to 59 months) living in urban slums in low‐ and middle‐income countries (LMIC). Cochrane Database of Systematic Reviews. 2019; 6.

  91. Forrester JE, Bailar IJC, Esrey SA, Jose MV, Castillejos BT, Ocampo G. Randomised trial of albendazole and pyrantel in symptomless trichuriasis in children. Lancet. 1998;352:1103–8.

    CAS  Article  PubMed  Google Scholar 

  92. Crellen T, Sithithaworn P, Pitaksakulrat O, Khuntikeo N, Medley GF, Hollingsworth TD. Towards Evidence-based Control of Opisthorchis viverrini. Trends Parasitol. 2021;37:370–80.

    CAS  Article  PubMed  Google Scholar 

  93. Moser W, Schindler C, Keiser J. Efficacy of recommended drugs against soil transmitted helminths: systematic review and network meta-analysis. BMJ. 2017;358:4307.

    Article  Google Scholar 

  94. Crellen T, Walker M, Lamberton PHL, Kabatereine NB, Tukahebwa EM, Cotton JA, et al. Reduced Efficacy of Praziquantel Against Schistosoma mansoni Is Associated With Multiple Rounds of Mass Drug Administration. Clin Infect Dis. 2016;63:1151–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  95. Best JC, Welch JS, Filippich C, McPhee L. Treatment of intestinal parasites in Australian aboriginal children. Med J Aust. 1976;1:14–20.

    CAS  Article  PubMed  Google Scholar 

  96. Gupta MC, Urrutia JJ. Effect of periodic antiascaris and antigiardia treatment on nutritional status of preschool children. Am J Clin Nutr. 1982;36:79–86.

    CAS  Article  PubMed  Google Scholar 

  97. Centers for Disease Control and Prevention (CDC). Giardia: Illness and Symptoms, 2021. Accessed 14 July 2021.

  98. Fraser D, Bilenko N, Deckelbaum RJ, Dagan R, El-On J, Naggan L. Giardia lamblia Carriage in Israeli Bedouin Infants: Risk Factors and Consequences. Clin Infect Dis. 2000;30:419–24.

    CAS  Article  PubMed  Google Scholar 

  99. Botero-Garces JH, Garcia-Montoya GM, Grisales-Patino D, Aguirre-Acevedo DC, Alvarez-Uribe MC. Giardia intestinalis and nutritional status in children participating in the complementary nutrition program, Antioquia, Colombia, May to October 2006. Rev Inst Med Trop Sao Paulo. 2009;51:155–62.

    Article  PubMed  Google Scholar 

  100. Befidi-Mengue RN, Ratard RC, D’Alessandro A, Rice J, Befidi-Mengue R, Kouemeni LE, et al. The impact of Schistosoma haematobium infection and of praziquantel treatment on the growth of primary school children in Bertoua. Cameroon J Trop Med Hyg. 1992;95:404–9.

    CAS  PubMed  Google Scholar 

  101. Hurlimann E, Houngbedji CA, N’Dri PB, Banninger D, Coulibaly JT, Yap P, et al. Effect of deworming on school-aged children’s physical fitness, cognition and clinical parameters in a malaria-helminth co-endemic area of Cote d’Ivoire. BMC Infect Dis. 2014;14:411.

    Article  PubMed  PubMed Central  Google Scholar 

  102. Abudho BO, Guyah B, Ondigo BN, Ndombi EM, Ireri E, Carter JM, et al. Evaluation of morbidity in Schistosoma mansoni-positive primary and secondary school children after four years of mass drug administration of praziquantel in western Kenya. Infect. 2020;9:67.

    Google Scholar 

  103. Gari T, Loha E, Deressa W, Solomon T, Lindtjørn B. Malaria increased the risk of stunting and wasting among young children in Ethiopia: Results of a cohort study. PLoS ONE. 2018;13:e0190983.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  104. Ojja S, Kisaka S, Ediau M, Tuhebwe D, Kisakye AN, Halage AA, et al. Prevalence, intensity and factors associated with soil-transmitted helminths infections among preschool-age children in Hoima district, rural western Uganda. BMC Infect Dis. 2018;18:408.

    Article  PubMed  PubMed Central  Google Scholar 

  105. World Health Organization. Ending the Neglect to attain the Sustainable Development Goals: A road map for neglected tropical diseases 2021–2030. Geneva: World Health Organization, 2020. Accessed 2 May 2021.

  106. Nampijja M, Lubyayi L, Tumusiime J, Nabulime J, Kizindo R, Kabuubi P, et al. Effect of intensive versus standard anthelminthic treatment on growth and cognition among children living in a high Schistosoma mansoni transmission setting: a study nested within a cluster-randomised trial [version 1; peer review: 1 approved with reservations]. Wellcome Open Research. 2020;5 258.

  107. Investigators M-EN. Childhood stunting in relation to the pre- and postnatal environment during the first 2 years of life: The MAL-ED longitudinal birth cohort study. PLOS Medicine. 2017;14 10:e1002408.

  108. Black MM, Behrman JR, Daelmans B, Prado EL, Richter L, Tomlinson M, et al. The principles of Nurturing Care promote human capital and mitigate adversities from preconception through adolescence. BMJ Glob Health. 2021;6:e004436.

    Article  PubMed  PubMed Central  Google Scholar 

  109. Bommer C, Vollmer S, Subramanian SV. How socioeconomic status moderates the stunting-age relationship in low-income and middle-income countries. BMJ Glob Health. 2019;4:e001175.

    Article  PubMed  PubMed Central  Google Scholar 

  110. Hesham Al-Mekhlafi M, Surin J, Atiya AS, Ariffin WA, Mohammed Mahdy AK, Che Abdullah H. Pattern and predictors of soil-transmitted helminth reinfection among aboriginal schoolchildren in rural Peninsula Garenne M, Myatt M, Khara T, Dolan C, Briend A. Concurrent wasting and stunting among under-five children in Niakhar, Senegal. Maternal & Child Nutrition. 2019;15 2:e12736;r Malaysia. Acta Trop. 2008;107 2:200–4.

  111. Garenne M, Myatt M, Khara T, Dolan C, Briend A. Concurrent wasting and stunting among under-five children in Niakhar, Senegal. Matern Child Nutr. 2019;15:e12736.

    Article  PubMed  Google Scholar 

  112. Angood C, Khara T, Dolan C, Berkley JA, WaSt Technical Interest G. Research Priorities on the Relationship between Wasting and Stunting. PLOS ONE. 2016;11 5:e0153221.

  113. Schoenbuchner SM, Dolan C, Mwangome M, Hall A, Richard SA, Wells JC, et al. The relationship between wasting and stunting: a retrospective cohort analysis of longitudinal data in Gambian children from 1976 to 2016. Am J Clin Nutr. 2019;110:498–507.

    Article  PubMed  PubMed Central  Google Scholar 

  114. Stephenson LS. Optimising the Benefits of Anthelmintic Treatment in Children. Paediatr Drugs. 2001;3:495–508.

    CAS  Article  PubMed  Google Scholar 

  115. Else KJ, Keiser J, Holland CV, Grencis RK, Sattelle DB, Fujiwara RT, et al. Whipworm and roundworm infections. Nat Rev Dis Primers. 2020;6:44.

    Article  PubMed  Google Scholar 

  116. Victora CG, de Onis M, Hallal PC, Blössner M, Shrimpton R. Worldwide Timing of Growth Faltering: Revisiting Implications for Interventions. Pediatrics. 2010;125:e473.

    Article  PubMed  Google Scholar 

  117. Yap F, Lee YS, Aw MMH. Growth Assessment and Monitoring during Childhood. Ann Acad Med Singap. 2018;47:149–55.

    PubMed  Google Scholar 

  118. Svefors P, Pervin J, Islam Khan A, Rahman A, Ekström E-C, El Arifeen S, et al. Stunting, recovery from stunting and puberty development in the MINIMat cohort. Bangladesh Acta Paediatrica. 2020;109:122–33.

    Article  PubMed  Google Scholar 

  119. Gausman J, Kim R, Subramanian SV. Stunting trajectories from post-infancy to adolescence in Ethiopia, India, Peru, and Vietnam. Matern Child Nutr. 2019;15:e12835.

    Article  PubMed  PubMed Central  Google Scholar 

  120. Nokes C, McGarvey ST, Shiue L, Wu G, Wu H, Bundy DA, et al. Evidence for an improvement in cognitive function following treatment of Schistosoma japonicum infection in Chinese primary schoolchildren. Am J Trop Med Hyg. 1999;60:556–65.

    CAS  Article  PubMed  Google Scholar 

  121. Degarege A, Erko B. Association between intestinal helminth infections and underweight among school children in Tikur Wuha Elementary School. Northwestern Ethiopia J Infect Public Health. 2013;6:125–33.

    Article  PubMed  Google Scholar 

  122. Easton AV, Oliveira RG, O’Connell EM, Kepha S, Mwandawiro CS, Njenga SM, et al. Multi-parallel qPCR provides increased sensitivity and diagnostic breadth for gastrointestinal parasites of humans: field-based inferences on the impact of mass deworming. Parasit Vectors. 2016;9:38.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  123. UNICEF Low birthweight. 2021. Accessed 2 May 2021.

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We are extremely grateful to librarians Russell Burke and Kate Perris at the London School of Hygiene and Tropical Medicine for valuable support with literature searching and search terms. We thank Sarah Dolman, study skills tutor at The Royal Veterinary College, for helpful advice on research writing. We also appreciate the constructive discussions provided through the Stunting Hub Gut Health group. Our Graphical Abstract was produced in


This work was funded by the Royal Veterinary College (ER) and the Global Challenges Research Fund: Action against Stunting Hub (Ref MR/S01313X/1) (BC-U; CH; JPW).

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Conceptualisation: JPW; PICO search strategy design: JH, ER, JPW: Literature Research: ER, JH, BC-U, JPW; Meta-analyses: BC-U, ER; Manuscript preparation ER with input from BC-U, JPW, JH; Graphical Abstract JPW. This paper was based on an MSc thesis by ER under the co-supervision of JPW, JH and BC-U. All authors read and approved the final manuscript.

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Correspondence to E. Raj or J. P. Webster.

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Supplementary Information

Additional file 1.

Study protocol.

Additional file 2.

Search concepts.

Additional file 3.

Search Strategies for individual databases.

Additional file 4.

Table of all included studies.

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Raj, E., Calvo-Urbano, B., Heffernan, C. et al. Systematic review to evaluate a potential association between helminth infection and physical stunting in children. Parasites Vectors 15, 135 (2022).

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  • Soil-transmitted helminths
  • Schistosomes
  • Stunting
  • Children
  • Infants
  • Pregnant women
  • Systematic review
  • Meta-analyses
  • z-scores