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Article

Association between Suicide and Toxoplasma gondii Seropositivity

by
Laura Alejandra Mendoza-Larios
1,
Fernando García-Dolores
1,
Luis Francisco Sánchez-Anguiano
2,
Jesús Hernández-Tinoco
2 and
Cosme Alvarado-Esquivel
2,*
1
Amphitheater and Department of Education, Institute of Forensic Sciences, Mexico City 06720, Mexico
2
Biomedical Research Laboratory, Faculty of Medicine and Nutrition, Juárez University of Durango State, Durango 34000, Mexico
*
Author to whom correspondence should be addressed.
Pathogens 2021, 10(9), 1094; https://doi.org/10.3390/pathogens10091094
Submission received: 4 August 2021 / Revised: 19 August 2021 / Accepted: 25 August 2021 / Published: 27 August 2021
(This article belongs to the Special Issue Effects of Toxoplasma gondii Infection on Human Behaviour)

Abstract

:
This study aimed to determine the association between suicide and Toxoplasma gondii (T. gondii) seropositivity. Serum samples of 89 decedents who committed suicide (cases) and 58 decedents who did not commit suicide (controls) were tested for anti-T. gondii IgG and IgM antibodies using enzyme-linked immunosorbent assays. Anti-T. gondii IgM antibodies were further detected by enzyme-linked fluorescence assay (ELFA). A total of 8 (9.0%) of the 89 cases and 6 (10.3%) of the 58 controls were positive for anti-T. gondii IgG antibodies (OR: 0.85; 95% CI: 0.28–2.60; p = 0.78). Anti-T. gondii IgG levels were higher than 150 IU/mL in two (2.2%) cases and in five (8.6%) controls (OR: 0.24; 95% CI: 0.04–1.30; p = 0.11). Anti-T. gondii IgM antibodies were not found in any case or control using the enzyme immunoassay and were found in only one (1.7%) control using ELFA (p = 0.39). Rates of IgG seropositivity and high levels of anti-T. gondii antibodies were similar in cases and in controls regardless of their sex or age groups. The results do not support an association between T. gondii seropositivity and suicide. However, the statistical power of the test was low. Further research is necessary to confirm this lack of association.

1. Introduction

The apicomplexan protozoan Toxoplasma gondii (T. gondii) can infect any nucleated cell in any warm-blooded animal and causes a disease called toxoplasmosis [1]. The disease is an important zoonosis with medical and veterinary importance worldwide [2]. The main routes of T. gondii transmission are by ingestion of tissue cysts in raw or undercooked meat of infected animals, ingestion of water of raw vegetables contaminated with T. gondii oocysts from cat feces, and transplacental transmission [3]. Toxoplasmosis is one of the most common infections in the world due to the lifelong persistence of T. gondii in a latent stage [4]. Primary infection is usually subclinical, but some patients may develop cervical lymphadenopathy or ocular disease [5]. Acute infection with T. gondii during pregnancy is detrimental to the developing fetus [6]. In immunocompromised patients, reactivation of the latent disease can cause life-threatening encephalitis [5]. T. gondii can persist in the central nervous system leading to behavioral changes of the host [7]. Subacute and chronic infections with T. gondii are associated with an increased risk of psychiatric diseases such as schizophrenia [8]. Seroprevalence of infection with T. gondii has been associated with bipolar disorder [9], mixed anxiety and depressive disorder [10], aggression and impulsivity [11], obsessive–compulsive disorder, addiction [12], mental retardation [13], and generalized anxiety disorder [14]. In addition, infection with T. gondii has been linked to suicide attempts. Seroprevalence of T. gondii infection was higher in suicide attempters than in healthy controls in studies in Korea [15] and Turkey [16]. High levels of anti-T. gondii IgG antibodies were associated with suicide attempts in psychiatric outpatients in Mexico [17]. There is scarce information about the link between T. gondii seropositivity and suicide. Therefore, this study aimed to determine the association between T. gondii seropositivity and suicide in decedents in a forensic setting in Mexico City.

2. Results

A total of 8 (9.0%) of the 89 cases and 6 (10.3%) of the 58 controls were positive for anti-T. gondii IgG antibodies. The frequency of anti-T. gondii IgG antibodies in cases was similar to that found in controls (OR: 0.85; 95% CI: 0.28–2.60; p = 0.78). Anti-T. gondii IgG levels were higher than 150 IU/mL in two (2.2%) cases and in five (8.6%) controls. The frequency of high (>150 IU/mL) anti-T. gondii IgG antibody levels in cases was similar to that found in controls (OR: 0.24; 95% CI: 0.04–1.30; p = 0.11). Anti-T. gondii IgM antibodies were not found in any case or control using the enzyme immunoassay, whereas anti-T. gondii IgM antibodies were found in only one (1.7%) control using ELFA (p = 0.39). Stratification by age and sex of seroprevalence of T. gondii infection in cases and controls is shown in Table 1.
IgG seropositivity rates were similar in cases and controls regardless of their sex or age groups. Stratification by age and sex of the frequency of high (>150 IU/mL) anti-T. gondii IgG antibody levels in cases and controls is shown in Table 2. No association between the rates of high levels of anti-T. gondii antibodies and suicide among sex or age groups was found.

3. Discussion

Seropositivity to T. gondii or high anti-T. gondii IgG antibody levels have been associated with suicide attempts in several studies [15,16,17]; however, the link between suicide and T. gondii seroprevalence and serointensity has been poorly studied. Therefore, in this case–control study, we sought to determine the association between T. gondii seropositivity and serointensity and suicide in a forensic setting in Mexico City. We found a comparable seroprevalence of T. gondii infection in decedents who died by suicide and in decedents who did not die by suicide. In addition, we found a similar frequency of high levels of anti-T. gondii IgG antibodies in cases and in controls. Furthermore, the frequency of anti-T. gondii IgM antibodies in cases was similar to that found in controls. Thus, the results suggest that seropositivity and serointensity of T. gondii was not associated with suicide in the decedents studied in Mexico City. Our results conflict with those found in a study of women in 20 European countries where researchers identified statistically significant relationships between T. gondii seropositivity and suicide rates in women of postmenopausal age [18]. Our results also conflict with those found in a study of decedents in Poland where investigators observed a significantly higher seroprevalence (71.4%) of T. gondii infection in decedents 38–58 years old whose deaths resulted from suicide compared to the seroprevalence (44.4%) found in control groups [19]. Differences in the findings between the studies might be due to differences in the design of the studies and the study populations. In the current study, male and female decedents were included in the study, whereas only women were included in the study of 20 European countries [18]. Our study was performed in a low-T. gondii-seroprevalence population, whereas the study in Poland was performed in a high-T. gondii-seroprevalence population [19]. Mexico City (formerly called the Federal District) has an intermediate (31.0%) seroprevalence of T. gondii infection compared to other Mexican states, where the lowest (17.1%) seroprevalence is in the state of Baja California Sur and the highest (67.5%) seroprevalence is in the state of Tabasco using the indirect immunofluorescence assay [20]. It is unclear why the population of Mexico City has a relatively low seroprevalence of T. gondii infection. Studies are necessary to determine the risk factors associated with T. gondii infection in population groups in Mexico City. On the other hand, our results conflict with those reported in some studies of living populations where suicide attempts have been associated with T. gondii seropositivity or serointensity. For instance, T. gondii seropositivity was associated with suicide attempts in psychiatric patients in Korea [15], and T. gondii serointensity was associated with suicide attempts in patients with recurrent mood disorders in the USA [21], and psychiatric patients in Mexico [17]. In contrast, our results agree with a lack of association between T. gondii exposure and suicidal ideation found in a study of patients suffering from mental and behavioral disorders due to psychoactive substance use in Mexico [22], and a lack of association between T. gondii seropositivity and suicide attempts in adolescents in Turkey [23]. In addition, in a longitudinal general population study in Finland, suicidal outcomes were not associated with T. gondii seropositivity [24]. The negative result found in the present study does not indicate that there is not any association between T. gondii infection and completed suicide. Firstly, seropositivity does not indicate that T. gondii has infected the brain and has led to behavioral changes including suicidal behavior. Secondly, toxoplasmosis has been involved not only in suicidal behavior, but also in a number of diseases that could be present in cases as well as in controls; for instance, T. gondii infection has been linked to heart disease [25], and heart disease was present in some controls. In addition, the real statistical power of the test was low. The low sample size, and low statistical power of the test, increased the likelihood of a type II error. Therefore, our study may not be able to detect a true effect. Stratification by sex and age groups did not show a difference in T. gondii seropositivity or serointensity between cases and controls. It raises the question of whether factors other than sex and age might be involved in a link between suicide and T. gondii infection. It is unknown whether decedents included in the control group had had suicidal behavior in life. Recent studies in Mexico have shown an association between T. gondii seropositivity and suicidal behavior in several population groups including patients attending primary health care clinics [26] and people with alcohol consumption [27]. Further studies including a wide range of sociodemographic, clinical, and behavioral variables to determine the association between T. gondii infection and suicide should be conducted.
In the present study, the number of controls was smaller than the number of cases. Decedents who died by traffic accidents were not enrolled as controls in the study because this factor has been linked to T. gondii exposure [28]. The establishment of an exclusion criterion in controls but not in cases reduced the availability of controls. Results found in the 58 controls made us understand that even increasing the number of controls to 89 (the same as the number of cases) would not have changed the lack of a positive association between T. gondii seropositivity and suicide.

4. Materials and Methods

Through a case–control study design, we studied decedents who died because of suicide (cases) and decedents who died by causes other than suicide (controls). Cases and controls were studied at a forensic setting (Instituto de Ciencias Forenses) in Mexico City, Mexico, from November 2015 to December 2016. Inclusion criteria for cases were decedents who died by suicide, male or female, and of any age. Inclusion criteria for controls were decedents who died by causes other than suicide, male or female, and of comparable age to cases. In total, 89 cases and 58 controls were included in the study. Of the cases, 68 were men and 21 were women, and their mean age was 35.21 ± 17.48 (range 10–90) years. Of the controls, 48 were men and 10 were women, and their mean age was 31.82 ± 15.01 (range 8–75) years. There was no difference in age (p = 0.24) or gender (p = 0.35) between cases and controls. Data about age, sex, and cause of death of decedents were obtained from records. Causes of death in control decedents included alcohol poisoning, asphyxia, burns, carbon monoxide poisoning, electrocution, gas embolism, generalized visceral congestion, gunshot wounds, heart infarction, hypoglycemia, injuries, knife wounds, meningitis, pneumonia, pulmonary edema, strangulation, suffocation, and traumatic brain injury. The exclusion criterion for controls was decedents who died by traffic accidents.
Blood samples of decedents were collected more than 12 h after death. After blood centrifugation, serum was obtained and frozen down at −20 °C, then analyzed. All serum samples were analyzed for anti-T. gondii IgG and IgM antibodies using the commercially available enzyme immunoassays “Toxoplasma gondii IgG” kit (Diagnostic Automation/Cortez Diagnostics, Inc., Woodland Hills, CA. USA) and “Toxoplasma gondii IgM” kit (Diagnostic Automation/Cortez Diagnostics, Inc.), respectively. Anti-T. gondii IgG antibody levels were expressed as International Units (IU)/mL, and a value of 8 IU/mL was used as a cut-off for seropositivity. Anti-T. gondii IgG antibody levels were arbitrarily considered as “high” when found at >150 IU/mL. We selected this high antibody level because the highest calibrator provided in the commercially available enzyme immunoassay used was 150 IU/mL and for comparison purposes with other studies in the region that have used this high antibody level. In addition, anti-T. gondii IgM antibodies were further detected using the commercially available enzyme-linked fluorescent assay (ELFA) kit “VIDAS Toxo IgM” (BioMérieux, Marcy-l’Etoile, France). All assays were performed according to the instructions of the manufacturers.
Statistical analysis was performed with the aid of the software Epi Info version 7 and Microsoft Excel. We calculated the sample size using the following parameters: a two-sided confidence level of 95%, a power of 80%, a 0.65 ratio of controls to cases, a reference seroprevalence of 27.97% [29] as the percentage outcome of exposure in controls, and an odds ratio of 2.7. The result of the sample size calculation with the Fleiss method was 88 cases and 57 controls. The Student’s t-test was used to compare the age of cases and controls. The seropositivity rates between the groups were compared with the Pearson’s Chi-square test or the Fisher exact test (when a value was ≤5). We calculated the odd ratios (OR) and 95% confidence intervals (CI), and a p value less than 0.05 was considered statistically significant. An additional statistical analysis to determine the statistical power of the test was performed. For this purpose, we used the following data: a sample size of 89 cases and 58 controls, a 10.3% seroprevalence of T. gondii infection, an OR of 2.7, and a significance level of 0.05. The actual power of the test was 53.5%.

5. Conclusions

The results of this study of decedents in Mexico City do not support an association between T. gondii seropositivity and suicide. Further research is necessary to confirm this lack of association.

Author Contributions

Conceptualization, C.A.-E.; methodology, L.A.M.-L., F.G.-D., L.F.S.-A. and J.H.-T.; formal analysis, C.A.-E.; data curation, C.A.-E. and L.A.M.-L.; writing—original draft preparation, C.A.-E.; writing—review and editing, C.A.-E.; funding acquisition, J.H.-T. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Juárez University of Durango State, Mexico.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethical Committee of the “Instituto de Ciencias Forenses” in Mexico City (protocol code CEI-014-2016).

Informed Consent Statement

Informed consent was obtained from relatives of decedents.

Data Availability Statement

Data are provided within the article.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Smith, N.C.; Goulart, C.; Hayward, J.A.; Kupz, A.; Miller, C.M.; van Dooren, G.G. Control of human toxoplasmosis. Int. J. Parasitol. 2021, 51, 95–121. [Google Scholar] [CrossRef]
  2. Liu, Q.; Wang, Z.D.; Huang, S.Y.; Zhu, X.Q. Diagnosis of toxoplasmosis and typing of Toxoplasma gondii. Parasites Vectors 2015, 8, 292. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Almeria, S.; Dubey, J.P. Foodborne transmission of Toxoplasma gondii infection in the last decade: An overview. Res. Vet. Sci. 2021, 135, 371–385. [Google Scholar] [CrossRef]
  4. Sabou, M.; Doderer-Lang, C.; Leyer, C.; Konjic, A.; Kubina, S.; Lennon, S.; Rohr, O.; Viville, S.; Cianférani, S.; Candolfi, E.; et al. Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways. Cell. Mol. Life Sci. 2020, 77, 2141–2156. [Google Scholar] [CrossRef] [Green Version]
  5. Montoya, J.G.; Liesenfeld, O. Toxoplasmosis. Lancet 2004, 363, 1965–1976. [Google Scholar] [CrossRef]
  6. Hampton, M.M. Congenital Toxoplasmosis: A Review. Neonatal Netw. 2015, 34, 274–278. [Google Scholar] [CrossRef]
  7. Parlog, A.; Schlüter, D.; Dunay, I.R. Toxoplasma gondii-induced neuronal alterations. Parasite Immunol. 2015, 37, 159–170. [Google Scholar] [CrossRef] [PubMed]
  8. Ihara, F.; Tanaka, S.; Fereig, R.M.; Nishimura, M.; Nishikawa, Y. Involvement of Toll-like receptor 2 in the cerebral immune response and behavioral changes caused by latent Toxoplasma infection in mice. PLoS ONE 2019, 14, e0220560. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Chen, X.; Chen, B.; Hou, X.; Zheng, C.; Yang, X.; Ke, J.; Hu, X.; Tan, F. Association between Toxoplasma gondii infection and psychiatric disorders in Zhejiang, Southeastern China. Acta Trop. 2019, 192, 82–86. [Google Scholar] [CrossRef] [PubMed]
  10. Alvarado-Esquivel, C.; Sanchez-Anguiano, L.F.; Hernandez-Tinoco, J.; Berumen-Segovia, L.O.; Torres-Prieto, Y.E.; Estrada-Martinez, S.; Perez-Alamos, A.R.; Ortiz-Jurado, M.N.; Molotla-de-Leon, G.; Beristain Garcia, I.; et al. Toxoplasma gondii Infection and Mixed Anxiety and Depressive Disorder: A Case-Control Seroprevalence Study in Durango, Mexico. J. Clin. Med. Res. 2016, 8, 519–523. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Coccaro, E.F.; Lee, R.; Groer, M.W.; Can, A.; Coussons-Read, M.; Postolache, T.T. Toxoplasma gondii infection: Relationship with aggression in psychiatric subjects. J. Clin. Psychiatry 2016, 77, 334–341. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Sutterland, A.L.; Fond, G.; Kuin, A.; Koeter, M.W.; Lutter, R.; van Gool, T.; Yolken, R.; Szoke, A.; Leboyer, M.; de Haan, L. Beyond the association. Toxoplasma gondii in schizophrenia, bipolar disorder, and addiction: Systematic review and meta-analysis. Acta Psychiatr. Scand. 2015, 132, 161–179. [Google Scholar] [CrossRef]
  13. Zhu, S.; Guo, M.F.; Feng, Q.C.; Fan, J.M.; Zhang, L.X. Epidemiological evidences from China assume that psychiatric-related diseases may be associated with Toxoplasma gondii infection. Neuro. Endocrinol. Lett. 2007, 28, 115–120. [Google Scholar] [PubMed]
  14. Akaltun, İ.; Kara, S.S.; Kara, T. The relationship between Toxoplasma gondii IgG antibodies and generalized anxiety disorder and obsessive-compulsive disorder in children and adolescents: A new approach. Nord. J. Psychiatry 2018, 72, 57–62. [Google Scholar] [CrossRef]
  15. Bak, J.; Shim, S.H.; Kwon, Y.J.; Lee, H.Y.; Kim, J.S.; Yoon, H.; Lee, Y.J. The Association between Suicide Attempts and Toxoplasma gondii Infection. Clin. Psychopharmacol. Neurosci. 2018, 16, 95–102. [Google Scholar] [CrossRef] [Green Version]
  16. Yagmur, F.; Yazar, S.; Temel, H.O.; Cavusoglu, M. May Toxoplasma gondii increase suicide attempt-preliminary results in Turkish subjects? Forensic. Sci. Int. 2010, 199, 15–17. [Google Scholar] [CrossRef]
  17. Alvarado-Esquivel, C.; Sánchez-Anguiano, L.F.; Arnaud-Gil, C.A.; López-Longoria, J.C.; Molina-Espinoza, L.F.; Estrada-Martínez, S.; Liesenfeld, O.; Hernández-Tinoco, J.; Sifuentes-Álvarez, A.; Salas-Martínez, C. Toxoplasma gondii infection and suicide attempts: A case-control study in psychiatric outpatients. J. Nerv. Ment. Dis. 2013, 201, 948–952. [Google Scholar] [CrossRef]
  18. Ling, V.J.; Lester, D.; Mortensen, P.B.; Langenberg, P.W.; Postolache, T.T. Toxoplasma gondii seropositivity and suicide rates in women. J. Nerv. Ment. Dis. 2011, 199, 440–444. [Google Scholar] [CrossRef] [Green Version]
  19. Samojłowicz, D.; Borowska-Solonynko, A.; Gołab, E. Prevalence of Toxoplasma gondii parasite infection among people who died due to sudden death in the capital city of Warsaw and its vicinity. Przegl. Epidemiol. 2013, 67, 29–33. [Google Scholar] [PubMed]
  20. Velasco-Castrejón, O.; Salvatierra-Izaba, B.; Valdespino, J.L.; Sedano-Laram, A.M.; Galindo-Virgen, S.; Magos, C.; Llausás, A.; Tapia-Conyer, R.; Gutiérrez, G.; Sepúlveda, J. Seroepidemiología de la toxoplasmosis en México [Seroepidemiology of toxoplasmosis in Mexico]. Salud Publica Mex. 1992, 34, 222–229. [Google Scholar]
  21. Arling, T.A.; Yolken, R.H.; Lapidus, M.; Langenberg, P.; Dickerson, F.B.; Zimmerman, S.A.; Balis, T.; Cabassa, J.A.; Scrandis, D.A.; Tonelli, L.H.; et al. Toxoplasma gondii antibody titers and history of suicide attempts in patients with recurrent mood disorders. J. Nerv. Ment. Dis. 2009, 197, 905–908. [Google Scholar] [CrossRef]
  22. Alvarado-Esquivel, C.; Carrillo-Oropeza, D.; Pacheco-Vega, S.J.; Hernández-Tinoco, J.; Salcedo-Jaquez, M.; Sánchez-Anguiano, L.F.; Ortiz-Jurado, M.N.; Alarcón-Alvarado, Y.; Liesenfeld, O.; Beristain-García, I. Toxoplasma gondii exposure in patients suffering from mental and behavioral disorders due to psychoactive substance use. BMC Infect. Dis. 2015, 15, 172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Sari, S.A.; Kara, A. Association of suicide attempt with seroprevalence of Toxoplasma gondii in adolescents. J. Nerv. Ment. Dis. 2019, 207, 1025–1030. [Google Scholar] [CrossRef] [PubMed]
  24. Lindgren, M.; Holm, M.; Markkula, N.; Härkänen, T.; Dickerson, F.; Yolken, R.H.; Suvisaari, J. Exposure to common infections and risk of suicide and self-harm: A longitudinal general population study. Eur. Arch. Psychiatry Clin. Neurosci. 2020, 270, 829–839. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Alvarado-Esquivel, C.; Salcedo-Jaquez, M.; Sanchez-Anguiano, L.F.; Hernandez-Tinoco, J.; Rabago-Sanchez, E.; Beristain-Garcia, I.; Liesenfeld, O.; Estrada-Martinez, S.; Perez-Alamos, A.R.; Alvarado-Soto, E. Association between Toxoplasma gondii exposure and heart disease: A case-control study. J. Clin. Med. Res. 2016, 8, 402–409. [Google Scholar] [CrossRef] [Green Version]
  26. Alvarado-Esquivel, C.; Estrada-Martínez, S.; Ramos-Nevárez, A.; Pérez-Álamos, A.R.; Beristain-García, I.; Alvarado-Félix, Á.O.; Cerrillo-Soto, S.M.; Sifuentes-Álvarez, A.; Alvarado-Félix, G.A.; Guido-Arreola, C.A.; et al. Association between Toxoplasma gondii exposure and suicidal behavior in patients attending primary health care clinics. Pathogens 2021, 10, 677. [Google Scholar] [CrossRef]
  27. Alvarado-Esquivel, C.; Estrada-Martínez, S.; Pérez-Álamos, A.R.; Beristain-García, I.; Alvarado-Félix, Á.O.; Alvarado-Félix, G.A.; Sifuentes-Álvarez, A. Toxoplasma gondii Infection and suicidal behavior in people with alcohol consumption. Pathogens 2021, 10, 734. [Google Scholar] [CrossRef]
  28. Flegr, J.; Havlícek, J.; Kodym, P.; Malý, M.; Smahel, Z. Increased risk of traffic accidents in subjects with latent toxoplasmosis: A retrospective case-control study. BMC Infect. Dis. 2002, 2, 11. [Google Scholar] [CrossRef] [Green Version]
  29. Galvan-Ramirez Mde, L.; Troyo, R.; Roman, S.; Calvillo-Sanchez, C.; Bernal-Redondo, R. A systematic review and meta-analysis of Toxoplasma gondii infection among the Mexican population. Parasites Vectors 2012, 5, 271. [Google Scholar] [CrossRef] [Green Version]
Table 1. Association between suicide and T. gondii seropositivity: stratification by sex and age groups.
Table 1. Association between suicide and T. gondii seropositivity: stratification by sex and age groups.
CasesControls
Seropositivity Seropositivity 95%
No.To T. gondii No.To T. gondii Confidencep
CharacteristicTestedNo.%TestedNo.%ORIntervalValue
Sex
Male6868.848612.50.670.20–2.240.52
Female2129.51000.0--1.00
Age (years)
≤30 43614.03538.61.720.39–7.480.50
31–503013.31516.70.480.02–8.291.00
>501616.38225.00.200.01–2.640.24
All8989.058610.30.850.28–2.600.78
Table 2. Association between suicide and high (>150 IU/mL) levels of anti-T. gondii IgG: stratification by sex and age.
Table 2. Association between suicide and high (>150 IU/mL) levels of anti-T. gondii IgG: stratification by sex and age.
CasesControls
>150 IU/mL >150 IU/mL 95%
No.Of IgGNo.Of IgG Confidencep
CharacteristicTestedNo.%TestedNo.%ORIntervalValue
Sex
Male6811.548510.40.120.01–1.130.08
Female2114.81000.0--1.00
Age (years)
≤30 4324.73525.70.800.10–6.021.00
31–503000.01516.7--0.33
>501600.08225.0--0.10
All8922.25858.60.240.04–1.300.11
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Mendoza-Larios, L.A.; García-Dolores, F.; Sánchez-Anguiano, L.F.; Hernández-Tinoco, J.; Alvarado-Esquivel, C. Association between Suicide and Toxoplasma gondii Seropositivity. Pathogens 2021, 10, 1094. https://doi.org/10.3390/pathogens10091094

AMA Style

Mendoza-Larios LA, García-Dolores F, Sánchez-Anguiano LF, Hernández-Tinoco J, Alvarado-Esquivel C. Association between Suicide and Toxoplasma gondii Seropositivity. Pathogens. 2021; 10(9):1094. https://doi.org/10.3390/pathogens10091094

Chicago/Turabian Style

Mendoza-Larios, Laura Alejandra, Fernando García-Dolores, Luis Francisco Sánchez-Anguiano, Jesús Hernández-Tinoco, and Cosme Alvarado-Esquivel. 2021. "Association between Suicide and Toxoplasma gondii Seropositivity" Pathogens 10, no. 9: 1094. https://doi.org/10.3390/pathogens10091094

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