Toxoplasma gondii infection as a risk factor for osteoporosis: a case–control study

Background More than one-third of the total world population is infected by Toxoplasma gondii (T. gondii). T. gondii has been linked to various diseases, such as cancer, mental disorders, type 2 diabetes mellitus (T2DM), etc. However, the effects of T. gondii infection on the risk of osteoporosis are unclear. Our study aimed to uncover evidence to determine whether patients exposed to T. gondii have an increased or decreased risk of osteoporosis in people with abnormal bone mineral density (BMD) by using case–control study. Methods A total of 729 patients, including 316 osteopenia and 413 osteoporosis patients of Han Chinese ancestry were selected in the study. Their blood samples were collected and the levels of specific IgG antibodies against T. gondii were measured using ELISA assay. We obtained some information about the patients from the medical record that included demographic indexes and clinical data. A logistic regression analysis was used to evaluate the effects of T. gondii infection on femur osteoporosis, lumbar osteoporosis and compound osteoporosis. Potential interaction was analyzed using multifactor dimensionality reduction software 1.0.0 (MDR 1.0.0). Results 113 positive patients with T. gondii infections have been detected, including 80 cases of osteoporosis and 33 cases of osteopenia, the infection rates of T. gondii were 19.37% (80/413) and 10.44% (33/316), respectively. The patients with T.gondii infections were at a 2.60 times higher risk of suffering from compound osteoporosis than those without T. gondii infections (OR = 2.60, 95% CI 1.54–4.39, P < 0.001), but not associated with femur osteoporosis (OR = 1.01, 95% CI 0.43–2.34, P = 0.989) and lumbar osteoporosis (OR = 0.84, 95% CI 0.34–2.07, P = 0.705) after adjusting for the covariates. Moreover, a significantly higher risk of compound osteoporosis in the individuals with all two factors (T. gondii infection, Female) was observed compared with reference group (without T. gondii infection, male) under the interaction model (OR = 11.44, 95%CI = 5.44–24.05, P < 0.001). And the individuals with all two factors (T. gondii infection, over 70 years) exhibited a 8.14-fold higher possibility of developing compound osteoporosis compared with reference group (without T. gondii infection, under 70 years) (OR = 8.14, 95% CI 3.91–16.93, P < 0.001). We further stratified by age and sex, and found that women with T. gondii infection was more likely to develop compound osteoporosis than those without infection(OR = 3.12, 95% CI  1.67–5.81, P < 0.001), but we not found the association between T. gondii infection and compound osteoporosis in males (OR = 1.36, 95% CI 0.37–4.94, P = 0.645). Conclusions T. gondii infection is a risk factor for osteoporosis, especially compound osteoporosis. Meanwhile, it is very necessary for patients with osteoporosis to further diagnose and treat T. gondii infection, especially women. Graphical Abstract Supplementary Information The online version contains supplementary material available at 10.1186/s13071-022-05257-z.


Background
Osteoporosis, characterized by the degeneration the microstructure of bone tissue and the decrease of bone mass, has become a public health problem affecting more than 200 million people worldwide [1,2]. Clinically, osteoporosis will increase the fragility and susceptibility to fracture and osteoporosis-related fractures are common causes of morbidity and death in older adults [2][3][4]. Among the Chinese population aged 50 years or older, 65 million people are diagnosed with osteoporosis, while an additional 213 million were estimated to have osteopenia [5]. Zhang et al. reported that the prevalence of osteoporosis in Chinese women after menopause reach up more than 60% [6]. It brings great health and economic burden to old women [7].
Osteopenia refers to the bone mineral density (BMD) lower than the normal population but higher than the bone density of the osteoporotic population. Although the people with osteopenia had an increased fracture risk compared with the healthy, it was not severe enough to be considered a diseased state in the absence of a fragility fracture, if left untreated, they can eventually lead to osteoporosis and future fractures [6,8,9]. Most osteoporosis are asymptomatic, which makes epidemiological research especially difficult [10].
Gender, age, history of fractures, drinking, smoking, bone diseases and lack of physical activity are wellknown risk factors for osteoporosis, particularly calcium deficiency, inadequate Vitamin D intake, and deficiencies in certain hormones, such as estrogen [11][12][13][14]. Furthermore, genetic polymorphisms also play a role in the development of osteoporosis [15]. Interestingly, it has been found that schistosome infection promotes osteoclast-mediated bone loss in mice [16]. However, the relationship between Toxoplasma gondii infection and osteoporosis is still unclear.
Toxoplasma gondii (T. gondii) belongs to apical complex protozoa, an important opportunistic pathogenic protozoan that infects almost all endotherms, including mammals, birds, and humans [17]. T. gondii can replicate and invade almost any nucleated cell in humans [18][19][20]. As an obligate intracellular parasite, It forms vacuoles in cells during infection, parasitizes in vacuoles and secretes effector molecules to regulate host cell biological processes such as energy metabolism, immune response, cell signaling, and lead to cell lysis to death along with the reproduction of T. gondii [21]. About 2 billion people worldwide are chronically infected with T. gondii, affecting approximately 30-50% of the world's population [22][23][24]. In a total of 49,784 Chinese blood donors from 1986 to 2017, the infection rate of T. gondii was detected at 6.26% [25]. Clinically, most infections are asymptomatic or taken in a mild, self-limiting form characterized by fever, malaise and lymphadenopathy [26]. T. gondii can lead to serious illnesses and even death of immunodeficiency patients [27]. Primary infection in pregnant women is a matter of great concern, the women in the first and second trimesters, infection with T. gondii may cause severe congenital toxoplasmosis, and can result in intrauterine fetal death and spontaneous abortion [28].
T. gondii has been linked to a various diseases.T. gondii infection is a serious problem in cancer patients in a case-control study [29]. And some studies have found that T. gondii might be a factor associated with hypertension in type 2 diabetes mellitus (T2DM) patients [30]. Moreover, T. gondii has been linked to a variety of mental disorders, such as schizophrenia, Alzheimer diseases, obsessive-compulsive disorder, recurrent migraines and even suicidal behavior [31][32][33][34][35]. Furthermore, T. gondii infection leads to deficits in goal-directed behavior in healthy elderly by altering dopaminergic neural transmission [36]. However, the chronic long-term damage to human health caused by latent T. gondii infection is not entirely clear, especially osteoporosis.
Until now, there is a lack of research supporting the relationship between T. gondii infections and osteoporosis in human. Therefore, our study aimed to uncover evidence to determine whether patients exposed to T. gondii have an increased or decreased risk of osteoporosis in people with abnormal bone mineral density (BMD) by using case-control study.

Patients
A total of 729 osteopenia and osteoporosis patients of Chinese ancestry were included in our study, there were 316 osteopenia and 413 osteoporosis cases. All of these were inpatients at the Guangzhou Overseas Chinese Hospital from 2015 to 2019. And 5 ml peripheral venous blood sample from each patient was collected with the EDTA vacuum blood collection tubes and saved at 4℃, then transported to laboratory. Our study was approved by the Ethics Committee of the School of Medicine of Jinan University, Guangzhou, China, and performed strictly in accordance with the Declaration of Helsinki.

Data collection
We obtained some information about the patients from the medical record that included demographic indexes (age, gender, marriage, education, job, smoking, drinking), clinical data including, bone mineral density (BMD) of whole-body, lumbar and femur, diabetes, hypertension and cardiovascular disease (CVD), and current osteoporosis treatment. This information and dual-energy densitometry (DXA) report were led together by date.

The diagnosis of osteopenia and osteoporosis
Clinically, osteoporosis can be screened by physical examination. However, BMD measured by DXA is needed to confirm such a diagnosis, DXA is the gold standard for diagnosing osteoporosis [37]. Before DXA inspection, patients were instructed to rest at least 8 h during the previous night and to avoid strenuous exercise and alcohol consumption for 24 h, and during the measurement, subjects were in light clothing. The radiologist asked the patient to lie flat on the machine bed, the legs were fully extended, and the lower extremities were internally rotated (45 degrees), and if necessary, the lower limbs were fixed to expose the femoral neck as much as possible. When testing the whole body and lumbar spine, the patient just needs to lie down. In general, the entire inspection is maintained for 15 to 20 min.
The BMD value of an individual patient is expressed in terms of the number of standard deviations (SD) from the mean BMD of a healthy young-adult reference population, commonly referred to as the T-score [38]. Patients whose DXA showed low BMD by World Health Organization (WHO) guidelines were identified: individuals were considered to be osteoporosis when the T-score was below − 2.5 (T-score ≤ − 2.5) and were considered to be normal when the T-score was above − 1.0 (T-score > − 1.0), the BMD value of osteopenia is less than − 1.0 but above − 2.5 (T-score ≤ − 1.0 and > − 2.5) [39][40][41][42][43].

Serological analysis
Approximately 5 ml of venous blood was drawn from each patient and then centrifuged at 1000 ×g for 10 min. Serums were separated from the blood sample and stored at -80 ℃. Seroprevalence of T. gondii infection was assessed by enzyme-linked immunosorbent assay (ELISA) Kit by Haitai Biological Pharmaceuticals (registration number: 20153400072). Positive, negative serum controls, and three critical control were included in each plate. The results (A value) were read by a microplate reader (TZCAN-SAFIRZ-Z) and Magellan software at the dual wavelength of 450/630 nm. Follow the manufacturer instructions, each experiment needed to fulfill the following three conditions: (1) the mean value of A in the positive control was ≥ 0.50; (2) the mean value of A in the negative control was ≤ 0.10; (3) the A values in the critical control range from 0.12 to 0.35. When A value of the sample is greater than the average value of the critical control group, it is judged as positive, otherwise negative.

Statistical analysis
Statistical analysis was performed using the statistical software SPSS (version 13.0). For the continuous variables were compared using Student's t test. For categorical variables, the Chi-square test was used to determine associations between osteoporosis and potential risk factors, the strength of the associations was assessed by odds ratios (OR) and 95% confidence intervals (CI) were calculated. The continuous variables were reported as the means ± standard deviation. The frequency and proportion were reported for the categorical variables. Multivariate logistic regression models were used to adjust for potential confounders. Additionally, potential interaction was analyzed using multifactor dimensionality reduction software 1.0.0 (MDR 1.0.0). Results were considered significant at P < 0.05.

Demographic characteristics
A total of 729 patients with abnormal BMD of Chinese ancestry were included in our study, 56.65% with osteopenia and 43.35% with osteoporosis. The mean ages of people with osteopenia, and osteoporosis were 67.28 ± 9.64 years, and 71.89 ± 9.60 years, and there was significant difference in age (t = − 6.41, df = 727, P < 0.001). The proportion of female in the osteoporosis group (83.05%) was higher than that in the osteopenia group (65.51%) (χ 2 = 29.75, df = 1, P < 0.001). The proportion of high triglyceride (TG > 1.5 mmol/L) in the osteopenia group (42.46%) was higher than that in the osteoporosis group (31.69%) (χ 2 = 8.22, df = 1, P = 0.004). In this study, 113 cases of T. gondii infections have been detected, and the T. gondii infection rates of osteoporosis and osteopenia were 19.37% and 10.44%, respectively, and there was significant difference (χ 2 = 10.89, df = 1, P = 0.001). No differences were observed between the groups in smoking, drinking, hormone taking, job, total cholesterol level (TC), and the number of comorbidities including hypertension, diabetes and cardiovascular disease (CVD) ( Table 1).

Risk of osteoporosis associated with T. gondii infection
Among the 413 patients with osteoporosis, according to the different sites of osteoporosis, we divided them into three groups: femur osteoporosis, lumbar osteoporosis and compound osteoporosis (including both femoral and lumbar osteoporosis or whole-body osteoporosis), and the osteopenia was regarded as the control group. A logistic regression analysis showed that patients with T.gondii infections were at a 2.60 times higher risk of suffering from compound osteoporosis than those without T. gondii infections (OR = 2.60, 95% CI 1.54-4.39, P < 0.001) ( Table 2) after adjusting age, sex, job, smoking, drinking, hormone taking, TG, TC, number of comorbidities. There were no statistically significant differences among the femur osteoporosis and lumbar osteoporosis (Fig. 1).

The interaction models of compound osteoporosis
We summarized the best interaction models for different types of osteoporosis by MDR, the best model was determined by the testing balanced accuracy (TBA) and crossvalidation consistency (CVC) indices. P values obtained from the MDR analysis among three groups. Our results revealed that age and sex have an interactive effect on compound osteoporosis (P = 0.039) ( Table 3).
We further analyzed the interactive effects of T. gondii infection with age or sex on compound osteoporosis. In comparison with the reference group (without T. gondii infection, male), the individuals with all two factors (T. gondii infection, Female) exhibited a 11.44-fold higher possibility of developing compound osteoporosis (OR = 11.44, 95% CI 5.44-24.05, P < 0.001) ( Table 4). In the interaction of T. gondii infection and age, the individuals with all two factors (T. gondii infection, over 70 years) were 8.14 times more likely to suffer from compound osteoporosis when compared with reference group (without T. gondii infection, under 70 years) (OR = 8.14, 95% CI 3.91-16.93, P < 0.001) ( Table 5). We further stratified the population by age and sex, and found that women with T. gondii infection was more likely to develop compound osteoporosis than those without infection (OR = 3.12, 95% CI 1.67-5.81, P < 0.001), but we not found the association between T. gondii infection and compound osteoporosis in males (OR = 1.36, 95% CI 0.37-4.94, P = 0.645) (Additional file 1: Table S1). Furthermore, T. gondii infection was associated with compound osteoporosis in women under 70 years (OR = 4.35, 95%CI = 1.79-10.57, P = 0.001) and over 70 years (OR = 2.48, 95% CI 1.03-6.01, P = 0.044) (Additional file 2: Table S2).

Discussion
In order to find out whether T. gondii infection is related to the occurrence of osteoporosis in patients with abnormal BMD, we collected a total of 729 blood samples with osteoporosis and osteopenia between 2015 and 2019, and collected corresponding demographic and clinical information. The IgG antibody against T. gondii was measured by ELISA, and 113 (113/729, 15.50%) cases of T. gondii infection were Table 1 Characteristics among the population with abnormal BMD (% within group) BMD bone mineral density, TG triglyceride, TC total cholesterol, CVD comorbidities including hypertension, diabetes and cardiovascular disease, SD standard deviation * P < 0.05; **P < 0.01; ***P < 0.001;

Variables
Overall (N = 729) found, is obviously higher than the average level in China (10%) [44]. In this study, women account for a much larger proportion in osteoporosis (83.05%) than the group of osteopenia (65.51%). This is consistent with the results of other studies that women are more likely to suffer from osteoporosis, especially postmenopausal women [45,46]. This is because estrogen deficiency in postmenopausal women leads to reduce bone mass by approximately 10%, and it can be as high as 20% in those 5-6 years around menopause [47]. We found that the osteopenia group had more people with high TG (> 1.5 mmol/L) and our results was consistent with Dennison et al. research in which a significant   positive correlation between fasting TG levels and lumbar spine BMD by cohort study was observed [48]. Osteopenia is the disease progression process of osteoporosis, in other words, osteopenia is a necessary condition for osteoporosis [49]. Interestingly, we found that patients with osteoporosis have a higher proportion of T. gondii infection (19.37%) than osteopenia group (10.44%). T. gondii can infect all nucleated cells (including bone marrow cells), in animal studies, Brazilian T. gondii Laboratory (LabTXOP) extracts high concentrations of T. gondii DNA from the bones sample (vertebrae and ribs) of mice [50], and some studies have shown that T. gondii may present serious effects on bone marrow cells in human bone marrow transplantation [51,52]. At the cellular level, osteoblast and osteoclast are two main types of cells that maintain bone mass [53]. In normal circumstances, osteoblasts and osteoclasts maintain a certain number and constrain each other, the bone formation and bone resorption mediated by them are in balance [14]. However, the decreased bone marrow cells and decreased osteogenesis are important factors leading to osteoporosis, and it has been proved that chronic inflammatory response or inflammation caused by acute infection will increase the activity of osteoclasts, osteocytes are decomposed and absorbed, and eventually lead to the loss of bone mass [54]. And many inflammatory mediators have been implicated in driving osteoclastmediated bone destruction [55,56]. Indeed, TNF is a potent osteoclastogenic agent [57]. IL-12, TNF-α and IFN-γ are important cytokines produced after T. gondii infection [58]. Therefore, we propose that T. gondii infection may be a risk factor for osteoporosis. The possible mechanism is that the immune response to T. gondii infection activates osteoclasts, resulting in bone resorption over bone formation, which needs to be proved by further experiments.
In order to further analyze the type of bone that T. gondii affects osteoporosis, we divided osteoporosis into three different types of osteoporosis (femur, lumbar and compound), logistic regression showed that T. gondii infections were at a 2.60 times higher risk of compound osteoporosis than those without T. gondii infections (OR = 2.60, 95% CI 1.54-4.39, P < 0.001), but there is no significant difference from other types of osteoporosis (femur and lumbar). Obviously, T. gondii infection is a risk factor for osteoporosis, especially compound osteoporosis. On the one hand, the BMD in this study was measured by iDAX, and the precision of the BMD of the compound (0.7%) is higher than lumbar and femur (0.8%) measured by iDAX [59]. This may make compound osteoporosis caused by T. gondii easier to detected. On the other hand, compound osteoporosis includes osteoporosis of lumbar, femur, skull, ribs, etc. This may be that T. gondii is more likely to affect more active, rich blood vessels, and more vulnerable bone parts, such as skull, ribs, etc. But it needs to be confirmed by more detailed epidemiological data.
Some studies have shown that age and gender have an interactive effect on bone microstructure [60]. We also considered whether the T. gondii infection has an interaction effect with age and sex on compound osteoporosis, and found that women infected with T. gondii and people over 70 years infected with T. gondii have a higher risk of compound osteoporosis than other people. The results of the stratified analysis suggest that T. gondii infection needs to be monitored in women to prevent compound osteoporosis.
Our research has a potential limitation. Worldwide genotypic analysis of T. gondii isolates has identified a population structure consisting of three widespread clonal lineages, termed type I, II, and III [61], and each displays are distinct biological traits, such as virulence. In the existing article shows that the genotype Chinese 1 (ToxoDB#9) type II strain is very popular in southern China [62]. Therefore, the type II strain may be the main type affecting whole-body bone mineral density values in patients with osteoporosis. Selection bias from one hospital cannot be avoided completely and this is one limitation. In the future research, a large  sample size from multiple hospitals is needed to confirm the relationship between T. gondii infection and osteoporosis risk. In addition, this was a hospital-based case-control study and we want to explore the relationship between T. gondii infection and osteoporosis progression. Since the blood samples are collected in the orthopedics department in the hospital, it is difficult for us to obtain blood sample with normal BMD. Obviously, using osteopenia as a control group would greatly underestimate the risk of T. gondii on osteoporosis. Although the use of osteopenia as a control might underestimate the risk, the results will provide the important clues for the future research. Next we will conduct community-based case-control study using a health control. In this study, we found positive association between T. gondii infection and osteoporosis..
In conclusion, our study shows that T. gondii infection is a risk factor for osteoporosis, especially compound osteoporosis. Meanwhile, it is very necessary for patients with osteoporosis to further diagnose and treat T. gondii infection, especially women.