Skip to main content

Prevalence and risk factors for Giardia duodenalis infection among children: A case study in Portugal



Giardia duodenalis is a widespread parasite of mammalian species, including humans. The prevalence of this parasite in children residing in Portugal is currently unknown. This study intended to estimate G. duodenalis infection prevalence and identify possible associated risk factors in a healthy paediatric population living in the District of the Portuguese capital, Lisbon.


Between February 2002 and October 2008, 844 children were randomly selected at healthcare centres while attending the national vaccination program. A stool sample and a questionnaire with socio-demographic data were collected from each child. Giardia infection was diagnosed by direct examination of stools and antigen detection by ELISA.


The population studied revealed a gender distribution of 52.8% male and 47.2% female. Age distribution was 47.4% between 0-5 years and 52.6% between 6-15 years.

The prevalence of Giardia infection was 1.9% (16/844) when estimated by direct examination and increased to 6.8% (57/844) when ELISA results were added. The prevalence was higher among children aged 0-5 years (7.8%), than among older children (5.8%), and was similar among genders (6.9% in boys and 6.5% in girls). The following population-variables were shown to be associated risk factors for G. duodenalis infection: mother's educational level (odds ratio (OR)= 4.49; confidence interval (CI): 1.20-16.84), father's educational level (OR = 12.26; CI: 4.08-36.82), presence of Helicobacter pylori infection (OR = 1.82; CI: 1.05-3.15), living in houses with own drainage system (OR = 0.10; CI: 0.02-0.64) and reported household pet contact, especially with dogs (OR = 0.53; CI: 0.31-0.93).


The prevalence of giardiasis in asymptomatic children residing in the region of Lisbon is high. Several risk factors were associated with Giardia prevalence and highlight the importance of parents' education and sanitation conditions in the children's well being. The association between G. duodenalis and H. pylori seems an important issue deserving further investigation in order to promote prevention or treatment strategies.


The intestinal protozoan Giardia duodenalis (synonym of Giardia intestinalis and Giardia lamblia) is a cosmopolitan parasite frequently found in diarrhoeal disease throughout the world [1]. It is one of the most common causes of waterborne disease outbreaks associated with drinking water [2, 3]. The prevalence of giardiasis is 2 to 5% in developed countries and 20 to 30% in developing countries [4]. The high prevalence in these countries has been suggested to be associated with long-term growth retardation in children [5]. In the United States of America and United Kingdom, G. duodenalis is the most commonly reported intestinal protozoan in humans [6], mainly affecting children. The pathogenesis is not clearly understood and symptoms, including acute or chronic diarrhoea, dehydration or abdominal pain, are highly variable [3, 7], and may even not be evident in a significant proportion of infected patients [8]. In children less than five years old, Giardia infection may produce severe acute diarrhoea. On the other hand, chronic infection may result in weight loss and growth retardation [9].

The cysts are the environmentally stable stage and are resistant to inactivation by drinking water disinfectants, remaining viable for up to two months [10]. The relative contribution of person-to-person, animal-to-person, foodborne and waterborne transmission to sporadic human giardiasis remains unclear [3, 11].

The diagnosis is initially based on clinical signs and symptoms and confirmed by the presence of cysts and trophozoites in stool samples. There is no gold standard for the diagnosis of giardiasis [12]. Historically, trophozoites or cysts of G. duodenalis were detected in stool samples by microscopic examination (direct examination), whereas antigen detection of stools by enzyme immunoassay (ELISA) is a more sensitive method, recently developed [13]. A definitive diagnosis may require repeated stool examinations, stool immunoassays, or even sampling of the upper intestinal contents [14].

Although G. duodenalis is recognized as a common parasite in humans in Portugal (Antunes, personal communications), the actual prevalence of this infection in children residing in Portugal remains unknown.

The goal of the present work is to estimate the G. duodenalis infection prevalence and identify possible associated-risk factors in a healthy paediatric population living in the Lisbon area. This is the first comprehensive study in children residing in Portugal, analysing a group of infants and children attending the national vaccination programme in the District of Lisbon, in order to assess factors predisposing to Giardia infection as well as co-infection with potential enhancing microorganisms.


Stool samples

Between February 2002 and October 2008, 844 healthy children were randomly selected at 15 health care centres from the urban and rural areas of the District of Lisbon, while attending the national vaccination program. In order to participate in the study, parents gave written informed consent, following an explanation of the study aims and procedures. For each participating child, one stool specimen was collected. At the time of specimen collection, parents completed a written questionnaire with information regarding demographic data, personal details of housing and living conditions, contact with pets, child and parents' level of education and any recent illness of children was also obtained. A stool sample was collected from each child, transferred into a sterile universal plastic container, and sent to the Infectious Diseases Department of the National Institute of Health (INSA), in Lisbon, within 24 h of specimen collection. Specimens were aliquoted and conserved at -80'C until tested, and the remaining sample was used for direct examination.

Ethical Approval

This study received the approval of INSA's Ethics Committee.

Determination of Giardia prevalence

Fresh stool samples were used to prepare a wet mount and analysed for the presence of G. duodenalis cysts by direct microscopic examination (direct examination). All detected cysts were identified according to morphological characteristics under light microscopy using 400 × magnification. Stool antigen detection was performed with Ridascreen Giardia enzyme immunoassay (ELISA) test (R-Biopharm AG, Landwehrstr, Darmstadt) according to the manufacturer's instructions [15, 16]. One positive and two negative controls were used at each run. Optical density (OD) was measured with an automatic microplate spectrophotometer (Spectramax, Molecular Devices, USA). A positive result was defined as an OD reading 10% over the cut-off value (negative control OD + 0.15), according to the manufacturer's instructions.

Statistical analysis

The variables analysed potentially associated with G. duodenalis infection were: gender, age, the number of adults and children in the family, birth order of the child, mother's and father's educational level, attendance of a day care institution/kindergarten, the child medical status, residence (rural versus urban), housing, and contact with pets. All statistical analysis was performed with SPSS software for Windows 18.01 (2009). Results were analysed by the Fisher Exact test, and differences between two proportions were compared. A probability under 0.05 was considered significant. The variables were calculated with their adjusted odds ratios (OR), 95% confidence intervals and significance levels. A multiple logistic regression analysis was performed to study the independence of the association of the variables with a significant p value. The level of significance of p < 0.05 was set for multivariable analysis; the model was interpreted using adjusted ORs and 95% CIs.


The study included 844 children, comprising 446 (52.8%) boys and 398 (47.2%) girls. Children were stratified in two age groups: 403 (47.7%) children age 0 (1 month) -5 years, 441 (52.3%) children age 6-15 years (Table 1).

Table 1 Distribution of children according to gender and age.

A stool sample was considered positive for G. duodenalis if at least one test was positive. Results showed that 16 out of 844 (1.9%) stool samples were positive by direct examination. Using the monoclonal ELISA method, 54 out of 807 (6.7%) were positive. The small size of sample in 37 samples prevented the use of the ELISA method. Three samples revealed as positive by microscopy were negative using ELISA; on the other hand 42 samples were negative by microscopy but positive using ELISA. Overall, 57 out of 844 samples (6.8%) were positive for G. duodenalis infection. When age and gender were considered, the prevalence was: 7.8% (31/396) among children aged 0-5 years and 5.8% (25/439) in the oldest ones (6-15); 6.9% (31/447) for males and 6.5% (26/397) for females.

Parents' educational level was found to be highly associated with the prevalence of giardiasis among children. Actually, children with mothers without any education were more likely to be infected with G. duodenalis than those with educated mothers (p = 0.047; OR = 4.49; 95% CI: 1.20-16.84). Similarly, children living with fathers with no education had a 12.26 times higher risk (p < 0.001; 95%CI: 4.08-36.82) of being infected with Giardia than those with educated fathers (Table 2). On the other hand, children living in houses with their own drainage system were more protected from this infection (p = 0.038; OR = 0.10; 95%CI: 0.02-0.64). Children were also tested for H. pylori infection by antigen stool detection [17], and co-infection was detected in 25 children (p < 0.037; OR = 1.82; 95%CI: 1.05-3.15). A sub-set of children negative for H. pylori infection were monitored every 6 months, during 36 months, in order to evaluate the incidence of H. pylori infection [16]. This group of children was also tested for Giardia infection, using the same methods described above. Results showed that 11 children were infected with both Giardia and H. pylori, with two of these cases positive for both agents in the 18-months sample. Also, 8 of those children were first infected with Giardia and then with H. pylori, with a time-frame of 6 months (n = 5), 18 months (n = 1) and 30 months (n = 2); one child was first infected with H. pylori and then with Giardia 6 months later.

Table 2 Prevalence of Giardia duodenalis infection according to demographic data and family characteristics.

Children with pets were also more likely to be infected with G. duodenalis (p = 0.026; OR = 0.53; 95%CI: 0.31-0.93), with a borderline statistical association found for dogs (p = 0.050; OR = 0.50; 95%CI: 0.23-1.00) (Table 3). No association was found between giardiasis prevalence and some variables, such as gender, age, family structure (adults and children members in the family, children birth order), attendance of day care institution/kindergarten, children, medical status (chronic disease), housing characteristics (rural or urban, house/apartment, existence of current water, electricity, full bathroom, garden or terrace) (Tables 2 and 3).

Table 3 Prevalence of Giardia duodenalis infection according to housing characteristics.

When a multiple logistic regression analysis was applied, using the five variables detected as significantly associated with G. duodenalis infection in the univariate analysis (p < 0.05), no additional support was found for this statistical significance (data not shown).


This study evaluated the prevalence of G. duodenalis infections in asymptomatic children in the District of Lisbon as well as potential risk factors for infection. Most epidemiological studies on G. duodenalis infection use microscopic detection, mainly due to its low cost, however, the low sensitivity of this test may result in the underestimation of the true prevalence of the parasite. In our study, we used both direct microscope detection and ELISA and the overall prevalence of G. duodenalis infection was 6.8%, with the ELISA presenting a much higher sensitivity, as expected [1821]. Nevertheless, it should be stressed that the use of a single stool sample for diagnosis of this infection, as it was the case of our study, might underestimate the parasite prevalence, due to the intermittent excretion of cysts in stools.

Giardiasis is linked to the socioeconomic level of a country, with prevalence ranging between 2 and 7% in most industrialized regions and reaching 40% in developing countries [22]. Actually, in the American continent, with countries showing highly different levels of development, G. duodenalis prevalence ranges between 1.4% in the North and 24% in Latin America being the latest considered a high-risk area for the general population [23]. Recent studies in asymptomatic children reported Giardia prevalence ranging from 0.8% in Italy (0-14 years, direct microscope detection) [24], 1.3% in the UK (0-5 years, immunomagnetic and immunofluorescence microscopy) [25], 1.5% in Berlin (0-6 years, immunofluorescence microscopy) [26] to 31.9% in Russia (0-5 years, direct microscope detection) [27].

The prevalence of 6.8% found in our study, although not as high as the Russian value, is considerably higher than other European countries showing similar levels of welfare (i.e. Italy, UK, Germany op. cit.). On the other hand, considering the prevalence obtained using the direct exam only (1.9%), results are similar to the values reported in those countries. This discrepancy among methods may however, at least partly, be a consequence of the tendency of ELISA to overestimate positive results. Nevertheless, considering that Portugal reveals a prevalence of other gastrointestinal agents, such as H. pylori, much higher than that observed in other European countries, it is likely that G. duodenalis infection is higher as well [17].

In Portugal, Almeida et al [28] studying a group of 177 asymptomatic children from the north region of Portugal reported a prevalence of 4% using the direct examination with sample concentration. Considering that socioeconomic conditions are relatively similar in both regions, the differences found in both studies, also reinforces the idea that results are influenced by the different accuracy of ELISA when compared with direct methods. The prevalence of intestinal parasites is a direct consequence of a set of constant factors, particularly climate, food and water supplies, personal and community hygiene, sanitation, proximity to both domestic and wild animals, and socioeconomic condition, all play a role regarding the risk of exposure to intestinal parasites [23]. The present study showed similar results regarding the factors enhancing the risk of giardiasis, revealing that the higher risk for G. duodenalis infection was related to the lower parents' educational level. Results match previous studies [2931], which indicated that maternal educational level was inversely correlated with the risk of children infection. Similar studies in Uganda showed that the mother's educational level was the best predictor of health and nutrition inequalities among children in rural communities [31]. Furthermore, Nematian et al [29] highlighted that the higher the educational level of the mothers, the lower the parasitic infection rate in children in Iran. Interestingly our study revealed that an illiterate father represented a risk for G. duodenalis infection almost three times higher when compared with an illiterate mother. This result may suggest that father's educational level reflects more clearly the family socio-economic level, corroborating the known association of Giardia infection with a low social status and consequently poorer sanitary conditions.

Another association found was between H. pylori infection and Giardia infection, which may indicate that they both share the same route of transmission. Actually, the fecal-oral transmission route has been proposed for the two microorganisms [32] and the prevalence of H. pylori in Portuguese children has been reported to reach 50% [17, 33]. The co-infection with these two agents has been previously reported among Brazilian healthy children, in a population with high levels of H. pylori infection [32]. Other authors showed the existence of H. pylori infection in 37 of 41 (90.2%) patients with gastric giardiasis [34], suggesting that this condition increases the susceptibility to H. pylori infection. Other authors sustain that H. pylori-induced chronic gastritis may increase the susceptibility to G. duodenalis infection [32]. Present results showed that 8 in 11 children acquired H. pylori infection after giardiasis, supporting the first hypothesis. On the other hand, the reciprocal antagonism of T-helper-1 (Th-1) and Th-2 type immune responses suggests that parasitic infection may ameliorate disease where a Th-1 type response dominates, such as H. pylori-induced gastritis and gastric carcinoma [35]. Thus, the association between G. duodenalis and H. pylori and its benefits or injuries is a promising line of research.

The zoonotic transmission of G. duodenalis cysts from animals to humans has been raised, although many questions still remain. Among animals, dogs are the most studied species for giardiasis. Evidence of zoonotic transmission among humans and dogs has been reported by Traub et al [36] based on epidemiological data combined with molecular techniques. In many countries the role of dogs as a definitive G. duodenalis host has been widely recognized as a public health problem. The present study also shows a positive association regarding the prevalence of this parasite and the contact with pets, especially dogs. Nevertheless, the multiple logistic regression did not confirm the univariate significant associations, likely due to the fact that a reduced number of individuals for which an association was found, thus hindering the disclosure of significant associations. Moreover, the likelihood that the results are the outcome of interactions and confounding effects that are not evident in a simple comparison of two treatment groups may also explain the absence of significant associations.

The literature shows no agreement on paediatric age and gender as associated factors. Nevertheless, some studies referred to a positive association [29, 37, 38] with female gender in adulthood, mostly due to the nursing activity in communities with a high infection prevalence among children [38]. On the other hand several authors considered age an important risk factor for this infection, finding higher prevalence in young adults and children [16, 29, 3844]. The present study showed no association either for gender or age regarding the prevalence of Giardia infection. Longitudinal and case-control studies carried out in Israel, Brazil and Kenya reported a higher risk of G. duodenalis infection for children after the first year of life [16]. The reasons for this age-associated risk are not well understood, although the lack of acquired immunity, more adventurous travel styles, or different diet regimes have been implicated [31, 40]. Although our study did not reveal a significant association with Giardia prevalence and age, the prevalence was slightly higher in younger children (0 - 5 years).


The present study revealed the high prevalence of G. duodenalis infection in asymptomatic children residing in the District of Lisbon. The factor more directly associated with the risk of giardiasis infection was shown to be the parents' educational level, suggesting that an increment in parents' education is likely to have a positive influence on the well being of Portuguese children. Co-infection with G. duodenalis and H. pylori was detected and seems an important issue deserving further investigation.

Studies regarding giardiasis prevalence show worldwide, a clear gap from developed to developing countries, mainly reflecting socioeconomic level. Nevertheless, this approach is somehow limited as even in developed countries the trilogy of socioeconomic-educational level/sanitation/veterinary care with pets, was shown to be an association to follow in order to prevent giardiasis.


The authors are grateful to Assunção António for laboratory assistance. We like to thank Professor José Guerreiro for the manuscript revision. Very special thanks to all the dedicated staff of the health care centres and to all the children and their parents for participating in this study.


  1. 1.

    Flanagan PA: Giardia - diagnosis, clinical course and epidemiology. A review. Epidemiol Infect. 1992, 109: 1-22.

    PubMed Central  CAS  PubMed  Google Scholar 

  2. 2.

    Bertrand I, Gantzer C, Chesnot T, Schwartzbrod J: Improved specificity for Giardia lamblia cyst quantification in wastewater by development of a real-time PCR method. J Microbiol Met. 2004, 57: 41-53.

    CAS  Article  Google Scholar 

  3. 3.

    Yoder J, Beach M: Giardiasis Surveillance - United States, 2003-2005. Surveill Summ. 2007, 56 (SS07): 11-18.

    Google Scholar 

  4. 4.

    Oberhuber G, Kastner N, Stolte M: Giardiasis: A histologic analysis of 567 cases. Scand J Gastroenrol. 1997, 32 (1): 48-51. 10.3109/00365529709025062.

    CAS  Article  Google Scholar 

  5. 5.

    Adam RD: Biology of Giardia lamblia. Clin Microbiol Rev. 2001, 14 (3): 447-475. 10.1128/CMR.14.3.447-475.2001.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  6. 6.

    Noor AMY, San YM, Gan CC, Yusri MY, Nurulsyamzawaty Y, Zuhaizam AH, Maslawaty MN, Norpartina I, Vythilingam I: Prevalence of intestinal protozoa in an aborigine community in Pahang, Malaysia. Trop Biomed. 2007, 24 (1): 55-62.

    Google Scholar 

  7. 7.

    Thompson RC: The zoonotic significance and molecular epidemiology of Giardia and giardiasis. Vet Parasitol. 2004, 126: 15-35. 10.1016/j.vetpar.2004.09.008.

    Article  PubMed  Google Scholar 

  8. 8.

    Doğruman A, Kustimur S, Özekinci T, Balaban N, Ilhan M: The use of Enzyme Linked Immunosorbent Assay (ELISA) and Direct Fluorescent Antibody (DFA) Methods for Diagnosis of Giardia intestinalis. Türkiye Parazitoloji Derneği. 2006, 30 (4): 275-278.

    Google Scholar 

  9. 9.

    Teixeira J, Heller L, Barreto M: Giardia duodenalis infection: risk factors for children living in sub-standard settlements in Brazil. Cad Saúde Pública. 2007, 23 (6): 1489-1493.

    Article  PubMed  Google Scholar 

  10. 10.

    Vernile A, Nabi AQ, Bonadonna L, Briancesco Massa S: Occurrence of Giardia and Cryptosporidium in Italian water supplies. Environ Monit Assess. 2009, 152: 203-207. 10.1007/s10661-008-0308-4.

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Cacciò SM, Thompson RC, McLauchlin J, Smith HV: Unravelling Cryptosporidium and Giardia epidemiology. Trends Parasitol. 2005, 21 (9): 430-437. 10.1016/

    Article  PubMed  Google Scholar 

  12. 12.

    Yakoob J, Jafri W, Abib S, Jafri N, Hamid S, Shah HA, Rizvi L, Islam M, Shaikh H: Giardiasis in patients with dyspeptic symptoms. World J Gastroenterol. 2005, 11 (2): 6667-6670.

    PubMed Central  PubMed  Google Scholar 

  13. 13.

    Al-Saeed AT, Issa SH: Detection of Giardia lamblia antigen in stool specimens using enzyme-linked immunosorbent assay. East Mediterr Health J. 2010, 16 (4): 362-364.

    CAS  PubMed  Google Scholar 

  14. 14.

    Savioli L, Smith H, Thompson A: Giardia and Cryptosporidium join the "Neglected Diseases Initiative". Trends Parasitol. 2006, 22 (5): 203-208. 10.1016/

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Schunk M, Jelinek T, Wetzel K, Nothdurft H: Detection of Giardia lamblia and Entamoeba histolytica in stool samples by two enzyme immunoassays. Eur J Clin Microbiol Infect Dis. 2001, 20 (6): 389-391.

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Pereira M, Atwill E, Barbosa A: Prevalence and associated risk factors for Giardia lamblia infection among children hospitalized for diarrhea in Goiânia, Goiás State, Brazil. Rev Inst Med Trop S Paulo. 2007, 49 (3): 139-145. 10.1590/S0036-46652007000300002.

    Article  PubMed  Google Scholar 

  17. 17.

    Oleastro M, Pelerito A, Nogueira P, Benoliel J, Santos A, Cabral J, Lopes AI, Ramalho PM, Monteiro L: Prevalence and incidence of Helicobacter pylori infection in a healthy pediatric population in the Lisbon area. Helicobacter. 2011, 16 (5): 363-372. 10.1111/j.1523-5378.2011.00858.x.

    Article  PubMed  Google Scholar 

  18. 18.

    Smith HV, Robertson LJ, Campbell AT, Gidwood RWA: Giardia and giardiasis: what's in a name?. Microbiol Eur. 1995, 3 (1): 22-29.

    Google Scholar 

  19. 19.

    Thompson RCA, Reynoldson JA: Giardia and Giardiasis. Adv Parasitol. 1993, 32: 71-160.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Xiao L: Giardia infection in farm animals. Parasitol Today. 1994, 10 (11): 436-438. 10.1016/0169-4758(94)90178-3.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Schunk M, Jelinek T, Wetzel K, Nothdurft HD: Detection of Giardia lamblia and Entamoeba histolytica in stool samples by two enzyme immunoassays. Eur J Clin Microbiol Infect Dis. 2001, 20: 389-391.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Upcroft P: Meeting report: Anaerobic Protozoan Parasites, Prague, Czech Republic, July 15-19, 2001. Protist. 2001, 152 (4): 241-242. 10.1078/1434-4610-00000.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Reinthaler F, Feierl G, Stünzner D, Marth E: Diarrhea in returning Austrian Tourists: Epidemiology, Etiology, and Cost-Analyses. J Travel Med. 1998, 5: 65-72. 10.1111/j.1708-8305.1998.tb00466.x.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Guidetti C, Ricci L, Vecchi L: Prevalenza delle parassitosi intestinali a Reggio Emilia e Provincia nel corso del 2009. Infez Med. 2010, 3: 154-161.

    Google Scholar 

  25. 25.

    Davies AP, Campbell B, Evans MR, Bone A, Roche A, Chalmers RM: Asymptomatic carriage of protozoan parasites in children in day care centers in the United kingdom. Pediatr Infect Dis J. 2009, 28 (9): 838-840. 10.1097/INF.0b013e31819d646d.

    Article  PubMed  Google Scholar 

  26. 26.

    Sagebiel D, Weitzel T, Stark K, Leitmeyer K: Giardiasis in kindergartens: prevalence study in Berlin, Germany, 2006. Parasitol Res. 2009, 105 (3): 681-687. 10.1007/s00436-009-1438-5.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    Kramar' LV, Reznikov EV, Kramar' OG: Prevalence if giardiasis in Volgograd city population. Med Parazitol (Mosk). 2003, 4: 38-39.

    Google Scholar 

  28. 28.

    Almeida AA, Delgado ML, Soares SC, Castro AO, Moreira MJ, Mendonça CM, Canada NB, Da Costa JM: Genotype analysis of Giardia isolated from asymptomatic children in northern Portugal. Eukaryot Microbiol. 2006, 53 (1): S177-178. 10.1111/j.1550-7408.2006.00222.x.

    CAS  Article  Google Scholar 

  29. 29.

    Nematian J, Nematian E, Gholamrezanezhad A, Asgari A: Prevalence of intestinal parasitic infections and their relation with socio-economic factors and hygienic habits in Tehran primary school students. Acta Trop. 2004, 92: 179-186. 10.1016/j.actatropica.2004.06.010.

    Article  PubMed  Google Scholar 

  30. 30.

    Quihui L, Valencia M, Crompton D, Phillips S, Hagan P, Morales G, Díaz-Camacho SP: Role of the employment status and educational of mothers in the prevalence of intestinal parasitic infections in Mexican rural. BMC Public Health. 2006, 6: 225-233. 10.1186/1471-2458-6-225.

    PubMed Central  Article  PubMed  Google Scholar 

  31. 31.

    Wamanin H, Tylleskär T, Åstrøm A, Tumwine J, Peterson S: Mother's educational but not father's educational, household assets or land ownership is the best predictor of child health inequalities in rural Uganda. Int J Equity Health. 2004, 3 (1): 9-10.1186/1475-9276-3-9.

    Article  Google Scholar 

  32. 32.

    Moreira ED, Nassri VB, Santos RS, Matos JF, Carvalho WA, Silvani CS, Sant Ána CS: Association of Helicobacter pylori infection and giardiasis: Results from a study of surrogate markers for fecal exposure among children. World J Gastroenterol. 2005, 11 (18): 2759-2763.

    Article  PubMed  Google Scholar 

  33. 33.

    Quina M: Helicobacter pylori: the Portuguese scene. Grupo de Estudo Português do Helicobacter pylori (GEPHP). Eur J Cancer Prev. 1994, 3: 65-67.

    Article  PubMed  Google Scholar 

  34. 34.

    Doglioni C, De Boni M, Cielo R, Laurino L, Pelosio P, Braidotti P, Viale G: Gastric giardiasis. Clin Pathol. 1992, 45 (11): 964-967. 10.1136/jcp.45.11.964.

    CAS  Article  Google Scholar 

  35. 35.

    Sagar M, Padol I, Khan WI, Bonin RP, Blennerhassett PA, Hunt RH: Establishment of T-Helper-2 immune response based gerbil model of enteric infection. Scand J Gastroenterol. 2004, 39 (7): 668-673. 10.1080/00365520410005315.

    CAS  Article  PubMed  Google Scholar 

  36. 36.

    Traub R, Monis P, Robertson I, Irwin P, Mencke N, Thompson R: Epidemiological and molecular evidence supports the zoonotic transmission of Giardia among humans and dogs living in the same community. Parasitol. 2004, 128: 253-262. 10.1017/S0031182003004505.

    CAS  Article  Google Scholar 

  37. 37.

    Siwila J, Phiri I, Enemark H, Nchito M, Olsen A: Intestinal helminths and protozoan in children in pre-schools in Kafue district, Zambia. Trans R Soc Trop Med Hyg. 2010, 104 (2): 122-128. 10.1016/j.trstmh.2009.07.024.

    Article  PubMed  Google Scholar 

  38. 38.

    Mahdy A, Surin J, Wan K, Mohd-Adnan A, Al-Mekhlafi M, Lim Y: Giardia intestinalis genotypes: Risk factors and correlation with clinical symptoms. Acta Tropica. 2009, 112: 67-70. 10.1016/j.actatropica.2009.06.012.

    Article  Google Scholar 

  39. 39.

    Spinelli R, Brandonisio O, Serio G, Trerotoli P, Ghezzani F, Carito V, Dajçi N, Doçi A, Picaku F, Dentico P: Intestinal parasites in healthy subjects in Albania. Eur J Epidemiol. 2006, 21: 161-166. 10.1007/s10654-005-5926-3.

    CAS  Article  PubMed  Google Scholar 

  40. 40.

    Wongstitwilairoong B, Srijan A, Serichantalergs O, Fukuda CD, McDaniel P, Bodhidatta L, Mason CJ: Intestinal parasitic infection among pre-school children in Sangkhlaburi, Thailand. Am J Trop Med Hyg. 2007, 76 (2): 345-350.

    PubMed  Google Scholar 

  41. 41.

    Raso G, Luginbühl A, Adjoua C, Tian-Bi NT, Silué KD, Matthys B, Vounatsou P, Wang Y, Dumas ME, Holmes E, Singer BH: Multiple parasite infections and their relationship to self-reported morbidity in a community of rural Côte d'Ivoire. Int J Epidemiol. 2004, 33: 1092-1102. 10.1093/ije/dyh241.

    Article  PubMed  Google Scholar 

  42. 42.

    Mehraj V, Hatcher J, Akhtar S, Rafique G, Beg M: Prevalence and Factors Associated with Intestinal Parasitic Infection among Children in an Urban Slum of Karachi. Plos One. 2008, 3 (11): e3680-10.1371/journal.pone.0003680.

    PubMed Central  Article  PubMed  Google Scholar 

  43. 43.

    Londoño A, Mejía S, Gómez-Marín J: Prevalencia y factores de Riesgo Asociados a Parasitismo Intestinal en Preescolares de Zona Urbana en Calarcá, Colombia. Rev Salud Pública. 2009, 11 (1): 72-81.

    Article  PubMed  Google Scholar 

  44. 44.

    Nkrumah B, Nguah SB: Giardia lamblia: a major parasitic cause of childhood diarrhoea in patients attending a district hospital in Ghana. Parasite Vectors. 2011, 4: 163-10.1186/1756-3305-4-163.

    Article  Google Scholar 

Download references

Author information



Corresponding author

Correspondence to Cláudia Júlio.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MO and LM conceived the study and collected all samples. CJ, AV, IF, SG performed all the experiments, analyses and wrote the paper with RT and HA. BN was involved in the statistical analysis. All authors read and approved the final manuscript.

Anabela Vilares, Mónica Oleastro, Idalina Ferreira, Salomé Gomes, Lurdes Monteiro, Baltazar Nunes, Rogério Tenreiro and Helena Ângelo contributed equally to this work.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and Permissions

About this article

Cite this article

Júlio, C., Vilares, A., Oleastro, M. et al. Prevalence and risk factors for Giardia duodenalis infection among children: A case study in Portugal. Parasites Vectors 5, 22 (2012).

Download citation


  • Giardia duodenalis
  • prevalence
  • risk factors
  • children
  • Portugal