J Clin Med Res
Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
Journal website http://www.jocmr.org

Original Article

Volume 8, Number 7, July 2016, pages 519-523


Toxoplasma gondii Infection and Mixed Anxiety and Depressive Disorder: A Case-Control Seroprevalence Study in Durango, Mexico

Cosme Alvarado-Esquivela, h, Luis Francisco Sanchez-Anguianob, Jesus Hernandez-Tinocob, Luis Omar Berumen-Segoviaa, Yazmin Elizabeth Torres-Prietoc, Sergio Estrada-Martinezb, Alma Rosa Perez-Alamosb, Maria Nalleli Ortiz-Juradod, Gabriel Molotla-de-Leond, Isabel Beristain Garciac, Elizabeth Rabago-Sancheza, e, Oliver Liesenfeldf, g

aFaculty of Medicine and Nutrition, Juarez University of Durango State, Avenida Universidad S/N, 34000 Durango, Durango, Mexico
bInstitute for Scientific Research “Dr. Roberto Rivera Damm”, Juarez University of Durango State, Avenida Universidad S/N, 34000 Durango, Durango, Mexico
cFacultad de Enfermeria y Obstetricia, Juarez University of Durango State, Cuauhtemoc 223 Norte, 34000 Durango, Mexico
dHospital of Mental Health “Dr. Miguel Vallebueno”, Servicios de Salud de Durango, Durango, Mexico
eGeneral Hospital, Secretary of Health, Avenida 5 de febrero 220, 34000 Durango, Mexico
fInstitute for Microbiology and Hygiene, Campus Benjamin Franklin, Charite Medical School, Hindenburgdamm 27, D-12203 Berlin, Germany
gCurrent address: Roche Molecular Systems, Pleasanton, CA 94588, USA
hCorresponding Author: Cosme Alvarado-Esquivel, Laboratorio de Investigacion Biomedica, Facultad de Medicina y Nutricion, Avenida Universidad S/N, 34000 Durango, Dgo, Mexico

Manuscript accepted for publication May 03, 2016
Short title: Toxoplasma and Depression
doi: http://dx.doi.org/10.14740/jocmr2576w

Abstract▴Top 

Background: The parasite Toxoplasma gondii (T. gondii) may invade the brain and might induce behavioral changes. We sought to determine the association of T. gondii infection and mixed anxiety and depressive disorder.

Methods: Through an age- and gender-matched case-control seroprevalence study, we examined 65 patients suffering from mixed anxiety and depressive disorder (WHO ICD-10 code: F41.2) attending in a public hospital of mental health and 260 control subjects without this disorder from the general population. Sera of participants were analyzed for anti-Toxoplasma IgG and IgM antibodies using enzyme-linked immunoassays.

Results: Fifteen (23.1%) of the 65 patients and 18 (6.9%) of the 260 controls had anti-T. gondii IgG antibodies (odds ratio (OR): 4.03; 95% confidence interval (CI): 1.90 - 8.53; P < 0.001). The frequency of high (> 150 IU/mL) anti-T. gondii IgG levels was similar in cases and controls (OR: 0.25; 95% CI: 0.05 - 1.06; P = 0.05). Seroprevalence was similar in male cases and controls (P = 1.0); however, seroprevalence was significantly higher in female cases than in female controls (OR: 7.08; 95% CI: 2.83 - 17.67; P < 0.00001). Patients aged 31 - 50 years old had a significantly higher seroprevalence of T. gondii infection than controls of the same age group (OR: 21.04; 95% CI: 5.22 - 84.80; P < 0.00001). Anti-T. gondii IgM antibodies were found in four (26.7%) of the 15 anti-T. gondii IgG seropositive cases and in 10 (55.6%) of the 18 anti-T. gondii IgG seropositive controls (P = 0.15).

Conclusions: Results support for the first time an association between seropositivity to T. gondii and mixed anxiety and depressive disorder. Further research to confirm this association and to determine the seroepidemiology of T. gondii infection in patients with this disorder is needed.

Keywords: Toxoplasma gondii; Seroprevalence; Mixed anxiety and depressive; Psychiatric patients; Case-control

Introduction▴Top 

Toxoplasma gondii (T. gondii) is a coccidian parasite causing infections worldwide [1]. About 30% of humanity is currently infected with T. gondii [2]. Infection with this parasite is usually acquired by ingestion of raw or undercooked meat containing tissue cysts, and water or food contaminated with oocysts shed by cats [3]. Other routes of T. gondii infection include congenital transmission [4], organ transplantation [5], and blood transfusion [6]. Although infections with T. gondii are usually asymptomatic, some infected individuals develop a symptomatic disease known as toxoplasmosis with involvement of lymph nodes, central nervous system or eyes [2, 7, 8]. Some psychiatric disorders have been associated with infection with T. gondii, i.e. schizophrenia [9, 10], bipolar disorder [11], obsessive compulsive disorder [11, 12], depression [13], and generalized anxiety disorder [14]. However, to the best of our knowledge, the association of infection with T. gondii and mixed anxiety and depressive disorder has not been reported. In this disorder, with the code F41.2 according to the classification of mental and behavioral disorders of the ICD-10 (http://apps.who.int/classifications/icd10/browse/2016/en#/F40-F48), anxiety and depression are both present in an individual, but neither is predominant, and neither symptom is present to an extent that justifies a separated diagnosis. Given the lack of information about the link of infection with T. gondii and this specific diagnosis, we attempted to determine the association between T. gondii infection and mixed anxiety and depressive disorder in a sample of patients attending in a public hospital of mental health in the northern Mexican city of Durango.

Materials and Methods▴Top 

Study design and populations studied

We performed an age- and gender-matched case-control study of 65 psychiatric patients suffering from mixed anxiety and depressive disorder attending in a public hospital of mental health in Durango City, Mexico and 260 control subjects without mixed anxiety and depressive disorder from the general population of the same city. This case-control study was performed from August 2015 to February 2016. Inclusion criteria for cases were: 1) patients suffering from mixed anxiety and depressive disorder attending in the Hospital of Mental Health “Dr. Miguel Vallebueno” of the Secretary of Health in Durango City; 2) aged 18 years and older; and 3) who accepted to participate in the study. Diagnosis of mixed anxiety and depressive disorder was made by psychiatrists and was classified as ICD-10 code F41.2. Of the 65 cases, 42 (64.6%) were females and 22 (35.4%) were males. Mean age in cases was 39.43 ± 14.05 (range 18 - 77) years old. Control subjects were randomly selected from the general population of Durango City and matched with cases for age (± 3 years) and gender. Inclusion criteria for controls were: 1) subjects of the general population of Durango City without anxiety and depression; 2) aged 18 years and older; and 3) who accepted to participate in the study. Of the 260 controls, 168 (64.6%) were females and 92 (35.4%) were males. Mean age in controls was 39.45 ± 13.98 (range 18 - 78) years old. No statistically significant differences in age (P = 0.99) and gender (P = 1.0) between cases and controls were found.

Detection of anti-T. gondii IgG and IgM antibodies

A blood sample from each participant was collected. Blood samples were centrifuged and serum samples were obtained and stored at -20 °C until analyzed. Sera were analyzed for anti-T. gondii IgG antibodies with the commercially available enzyme immunoassay (EIA) kit “Toxoplasma IgG” (Diagnostic Automation/Cortez Diagnostics Inc., Woodland Hills, CA, USA). A cut-off of ≥ 8 International Units (IU)/mL of anti-T. gondii IgG antibody was used. Sera of patients seropositive for anti-T. gondii IgG antibodies were further analyzed for anti-T. gondii IgM antibodies by the commercially available EIA “Toxoplasma IgM” kit (Diagnostic Automation/Cortez Diagnostics Inc.). All IgG and IgM assays were performed following the manufacturer’s instructions.

Statistical analysis

We used the software Epi Info version 7 and the SPSS version 15.0 (SPSS Inc. Chicago, IL) to perform the statistical analysis. For calculation of the sample size, we used a 95% confidence interval (CI) level, a power of 80%, a 1:4 proportion of cases and controls, a reference seroprevalence of 6.1% [15] as the expected frequency of exposure in controls, and an odds ratio (OR) of 3.5. The result of the sample size calculation was 60 cases and 237 controls. We used the Student’s t-test to compare the age among cases and controls. The association of T. gondii infection and mixed anxiety and depressive disorder was assessed with the two-tailed Pearson’s Chi-squared test. OR and 95% CI were calculated, and a P value < 0.05 was considered as statistically significant.

Ethical aspects

The Ethics Committee of the General Hospital of the Secretary of Health in Durango City, Mexico approved this project. The purpose and procedures of this study were explained to all participants. In addition, a written informed consent was obtained from each participant.

Results▴Top 

Fifteen (23.1%) of the 65 patients with mixed anxiety and depressive disorder and 18 (6.9%) of the 260 controls had anti-T. gondii IgG antibodies. The difference in seroprevalence of T. gondii infection between cases and controls was statistically significant (OR: 4.03; 95% CI: 1.90 - 8.53; P < 0.001). Of the 15 anti-T. gondii IgG positive cases, five (33.3%) had IgG levels higher than 150 IU/mL, one (6.7%) between 100 and 150 IU/mL, and nine (60.0%) between 8 and 99 IU/mL. In contrast, of the 18 anti-T. gondii IgG positive controls, 12 (66.7%) had IgG levels higher than 150 IU/mL, one (5.5%) between 100 and 150 IU/mL, and five (27.8%) between 8 and 99 IU/mL. The frequency of high (> 150 IU/mL) anti-T. gondii IgG levels was similar in cases and controls (OR: 0.25; 95% CI: 0.05 - 1.06; P = 0.05).

Seroprevalence of T. gondii infection was stratified by sex and age (Table 1). We observed that seroprevalence was similar in male cases and male controls (P = 1.0); however, seroprevalence was significantly higher in female cases than in female controls (OR: 7.08; 95% CI: 2.83 - 17.67; P < 0.00001). Patients aged 31 - 50 years old had a significantly higher seroprevalence of T. gondii infection than controls of the same age group (OR: 21.04; 95% CI: 5.22 - 84.80; P < 0.00001). Seroprevalence did not vary between cases and controls in the age groups of 30 years and younger, and older than 50 years.

Table 1.
Click to view
Table 1. Comparison of Seropositivity Rate to T. gondii According to Sex and Age Between Cases (F41.2) and Controls
 

With respect to IgM seropositivity, anti-T. gondii IgM antibodies were found in four (26.7%) of the 15 anti-T. gondii IgG seropositive cases and in 10 (55.6%) of the 18 anti-T. gondii IgG seropositive controls. No statistically significant difference in the frequency of IgM seropositivity among cases and controls was found (P = 0.15).

Discussion▴Top 

The association of T. gondii infection and mixed anxiety and depressive disorder is largely unknown. This case-control seroprevalence study aimed to determine whether T. gondii seropositivity is associated with mixed anxiety and depressive disorder in Durango City, Mexico. Results of the present study show that psychiatric patients suffering from mixed anxiety and depressive disorder have a significantly higher frequency of anti-T. gondii IgG antibodies than age- and gender-matched control subjects without this disorder of the same city. Remarkably, the seroprevalences found in women (31.0%) and patients aged 31 - 50 years old (38.5%) suffering from mixed anxiety and depressive disorder in our study are very high in Durango City, compared with the 6.1% seroprevalence of T. gondii exposure reported in the general population in the same city [15]. To the best of our knowledge, this is the first report of an association of T. gondii infection and mixed anxiety and depressive disorder. There are some reports of the association of T. gondii infection with either anxiety or depression but not about the association of infection with the presence of both anxiety and depression in the same patients. In a recent study, generalized anxiety disorder was associated with both seroprevalence of T. gondii infection and high levels of anti-T. gondii IgG antibodies in subjects drawn from the Detroit Neighborhood Health Study in the USA [14]. In a study of pregnant women, those with serological evidence of T. gondii exposure showed positive correlations between IgG levels and the profile of mood scales depression and anxiety subscales [16]. In a study of male rats with experimental infection with T. gondii, researchers found that infected rats with T. gondii cysts in the forebrain showed an increased anxiety-related behavior [17]. There are conflicting results about the association of T. gondii infection and depression. Duffy and coworkers found a relationship between chronic T. gondii infection, depression and dysphoric mood in a military veteran women population [13]. On the other hand, in a study in mice, reactivation of chronic T. gondii infection by an immunosuppressive regimen caused induction of depressive-like behaviors [18]. In contrast, in a meta-analysis of 50 studies reporting seroprevalence of T. gondii infection in any psychiatric disorder compared with control subjects, researchers found no association of anti-T. gondii antibodies with major depression [11]. Differences in the finding of an association between T. gondii infection and depression could be due to differences in the severity of depression among the studies. Depression in mixed anxiety and depressive disorder is mild. Therefore, it is likely that T. gondii infection can be rather associated with mild depression than with severe depression. Further studies including patients suffering from minor and major depression to elucidate the link of T. gondii exposure and depression should be conducted. Very little is known about the mechanisms that T. gondii uses to cause anxiety and depression. It is well known that T. gondii invades the brain [12], and this invasion might result in behavioral changes. Mood disorders associated with T. gondii can be due to changes in the concentrations of some neurotransmitters in brain including dopamine and serotonin [19]. In the present study, the association of T. gondii infection with mixed anxiety and depressive disorder was related to IgG seropositivity but not to IgM seropositivity. This finding suggests that this disorder is associated with latent infection rather than with acute infection.

We observed that the association of infection with T. gondii and mixed anxiety and depressive disorder was influenced by gender and age. A strong association was found in females and in patients aged 31 - 50 years old. It is not clear why the association was influenced by these gender and age groups. Seroprevalence of T. gondii infection in Durango is similar in male and females, and increases with age [15]. On the other hand, women suffer from anxiety and depression more frequently than men. In a recent study in a treatment-seeking population, women had a higher prevalence of anxiety disorders than men [20]. Similarly, in the population-based Hispanic Community Health Study/Study of Latinos in the USA, the prevalences of depression and anxiety were higher in women than in men, and in the age group of 45 - 64 years than in the groups of 18 - 44 years and 65 - 74 years [21]. Therefore, the fact that the association of T. gondii infection and mixed anxiety and depressive disorder was stronger in women and in people of middle age than in men and in younger and older age groups in our study further supports a contributing role of T. gondii infection and this disorder. Our findings have also epidemiological importance; if this association is confirmed in other studies, the benefit of treatment against T. gondii infection should be evaluated in patients suffering from anxiety and depressive disorder. Patients with bipolar disorder seropositive to T. gondii showed more depressive episodes when treated by drugs without anti-T. gondii activity than patients who received drugs with anti-T. gondii activity [22].

A limitation of the present study was a small sample size of patients suffering from anxiety and depressive disorder. Further studies should have a larger sample size of patients.

Conclusions

Results support for the first time an association between seropositivity to T. gondii and mixed anxiety and depressive disorder. Further research to confirm this association and to determine the seroepidemiology of T. gondii infection in patients with this disorder is needed.

Conflicts of Interest

The authors declare that no conflict of interest exists.

Grant Support

This study was financially supported by Secretary of Public Education, Mexico (Grant No. DSA/103.5/14/11311).


References▴Top 
  1. Dubey JP. History of the discovery of the life cycle of Toxoplasma gondii. Int J Parasitol. 2009;39(8):877-882.
    doi pubmed
  2. Schluter D, Daubener W, Schares G, Gross U, Pleyer U, Luder C. Animals are key to human toxoplasmosis. Int J Med Microbiol. 2014;304(7):917-929.
    doi pubmed
  3. Montoya JG, Liesenfeld O. Toxoplasmosis. Lancet. 2004;363(9425):1965-1976.
    doi
  4. Hide G, Morley EK, Hughes JM, Gerwash O, Elmahaishi MS, Elmahaishi KH, Thomasson D, et al. Evidence for high levels of vertical transmission in Toxoplasma gondii. Parasitology. 2009;136(14):1877-1885.
    doi pubmed
  5. Derouin F, Pelloux H. Prevention of toxoplasmosis in transplant patients. Clin Microbiol Infect. 2008;14(12):1089-1101.
    doi pubmed
  6. Figueroa Damian R. [Risk of transmission of infectious diseases by transfusion]. Ginecol Obstet Mex. 1998;66:277-283.
    pubmed
  7. Maenz M, Schluter D, Liesenfeld O, Schares G, Gross U, Pleyer U. Ocular toxoplasmosis past, present and new aspects of an old disease. Prog Retin Eye Res. 2014;39:77-106.
    doi pubmed
  8. Machala L, Kodym P, Maly M, Geleneky M, Beran O, Jilich D. [Toxoplasmosis in immunocompromised patients]. Epidemiol Mikrobiol Imunol. 2015;64(2):59-65.
    pubmed
  9. Flegr J. Schizophrenia and Toxoplasma gondii: an undervalued association? Expert Rev Anti Infect Ther. 2015;13(7):817-820.
    doi pubmed
  10. Alvarado-Esquivel C, Urbina-Alvarez JD, Estrada-Martinez S, Torres-Castorena A, Molotla-de-Leon G, Liesenfeld O, Dubey JP. Toxoplasma gondii infection and schizophrenia: a case control study in a low Toxoplasma seroprevalence Mexican population. Parasitol Int. 2011;60(2):151-155.
    doi pubmed
  11. Sutterland AL, Fond G, Kuin A, Koeter MW, Lutter R, van Gool T, Yolken R, et al. Beyond the association. Toxoplasma gondii in schizophrenia, bipolar disorder, and addiction: systematic review and meta-analysis. Acta Psychiatr Scand. 2015;132(3):161-179.
    doi pubmed
  12. Fond G, Capdevielle D, Macgregor A, Attal J, Larue A, Brittner M, Ducasse D, et al. [Toxoplasma gondii: a potential role in the genesis of psychiatric disorders]. Encephale. 2013;39(1):38-43.
    doi pubmed
  13. Duffy AR, Beckie TM, Brenner LA, Beckstead JW, Seyfang A, Postolache TT, Groer MW. Relationship Between Toxoplasma gondii and Mood Disturbance in Women Veterans. Mil Med. 2015;180(6):621-625.
    doi pubmed
  14. Markovitz AA, Simanek AM, Yolken RH, Galea S, Koenen KC, Chen S, Aiello AE. Toxoplasma gondii and anxiety disorders in a community-based sample. Brain Behav Immun. 2015;43:192-197.
    doi pubmed
  15. Alvarado-Esquivel C, Estrada-Martinez S, Pizarro-Villalobos H, Arce-Quinones M, Liesenfeld O, Dubey JP. Seroepidemiology of Toxoplasma gondii infection in general population in a northern Mexican city. J Parasitol. 2011;97(1):40-43.
    doi pubmed
  16. Groer MW, Yolken RH, Xiao JC, Beckstead JW, Fuchs D, Mohapatra SS, Seyfang A, et al. Prenatal depression and anxiety in Toxoplasma gondii-positive women. Am J Obstet Gynecol. 2011;204(5):433 e431-437.
  17. Evans AK, Strassmann PS, Lee IP, Sapolsky RM. Patterns of Toxoplasma gondii cyst distribution in the forebrain associate with individual variation in predator odor avoidance and anxiety-related behavior in male Long-Evans rats. Brain Behav Immun. 2014;37:122-133.
  18. Mahmoud ME, Ihara F, Fereig RM, Nishimura M, Nishikawa Y. Induction of depression-related behaviors by reactivation of chronic Toxoplasma gondii infection in mice. Behav Brain Res. 2016;298(Pt B):125-133.
  19. Henriquez SA, Brett R, Alexander J, Pratt J, Roberts CW. Neuropsychiatric disease and Toxoplasma gondii infection. Neuroimmunomodulation. 2009;16(2):122-133.
    doi pubmed
  20. Pesce L, van Veen T, Carlier I, van Noorden MS, van der Wee NJ, van Hemert AM, Giltay EJ. Gender differences in outpatients with anxiety disorders: the Leiden Routine Outcome Monitoring Study. Epidemiol Psychiatr Sci. 2016;25(3):278-287.
    doi pubmed
  21. Wassertheil-Smoller S, Arredondo EM, Cai J, Castaneda SF, Choca JP, Gallo LC, Jung M, et al. Depression, anxiety, antidepressant use, and cardiovascular disease among Hispanic men and women of different national backgrounds: results from the Hispanic Community Health Study/Study of Latinos. Ann Epidemiol. 2014;24(11):822-830.
    doi pubmed
  22. Fond G, Boyer L, Gaman A, Laouamri H, Attiba D, Richard JR, Delavest M, et al. Treatment with anti-toxoplasmic activity (TATA) for toxoplasma positive patients with bipolar disorders or schizophrenia: a cross-sectional study. J Psychiatr Res. 2015;63:58-64.
    doi pubmed


This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Journal of Clinical Medicine Research is published by Elmer Press Inc.

 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Journal of Clinical Medicine Research, monthly, ISSN 1918-3003 (print), 1918-3011 (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.jocmr.org   editorial contact: editor@jocmr.org     elmer.editorial2@hotmail.com
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.