Salvina Maria de Campos-Carli1, Érica Leandro Marciano Vieira1, Natalia Pessoa Rocha1,2, Keliane de Oliveira3, Fernanda Carneiro Guimarães3, Izabela Guimarães Barbosa1, João Luís Vieira Monteiro de Barros1, Olaoluwa Okusaga2, Olindo Assis Martins-Filho4, João Vinícius Salgado1,3, Antônio Lúcio Teixeira1,2
1 Interdisciplinary Laboratory of Medical Research, Faculty of Medicine, Federal University of Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
2 Neuropsychiatry Program, Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
3 Instituto Raul Soares, Hospital Foundation of the State of Minas Gerais (FHEMIG), Belo Horizonte, MG, Brazil.
4 Laboratory of Diagnostic and Monitoring Biomarkers, René Rachou Research Center, Oswaldo Cruz Foundation (Fiocruz), Belo Horizonte, MG, Brazil.
Received: 03/07/2017 – Accepted: 10/14/2017
Address for correspondence: Antônio Lúcio Teixeira. Department of Psychiatry and Behavioral Sciences. The University of Texas Health Science Center at Houston 1941 East Road, Houston, TX 77054, USA. BBSB 3140. Telephone: +1 71 486-2555. Email: [email protected]
Background: Toxoplasma gondii (T. gondii) infection has been identified as a risk factor for schizophrenia. Objectives: Herein, we sought to evaluate the association between T. gondii infection and clinical symptoms and quality of life in patients with schizophrenia. Methods: We conducted a cross-sectional study with 48 patients with chronic schizophrenia and 40 controls. Peripheral blood was drawn, and IgM and IgG anti-T. gondii antibodies were evaluated by Enzyme-Linked Immunosorbent Assay (ELISA). Depressive, positive and negative symptoms were assessed, respectively, by the Calgary Depression Scale (CDS) and the Positive and Negative Syndrome Scale (PANSS). Cognitive performance was assessed in patients by the Brazilian version of the Schizophrenia Cognition Rating Scale (SCoRS-BR). Quality of life was assessed by the Brazilian version of the Quality of Life in Schizophrenia scale (QLS-BR). Results: The prevalence and titers of T. gondii IgM and IgG antibodies did not differ between patients and controls. The positive serology for T. gondii IgG antibodies was not associated with illness symptoms, cognitive performance, depressive symptoms or quality of life. Discussion: Our findings suggest that toxoplasmosis infection is not associated with severity of symptoms, quality of life, cognitive or depressive symptoms in schizophrenia patients.
Campos-Carli SM et al. / Arch Clin Psychiatry. 2017;44(6):145-8
Keywords: Toxoplasma gondii, schizophrenia, cognition, depression, quality of life.
Schizophrenia is a pervasive psychiatry disease whose etiopathogenesis results from complex gene-environmental interactions. Accumulating evidence suggests that infection is an important environmental factor implicated in schizophrenia pathogenesis1. Epidemiological and meta-analytic studies have shown an association between infections and increased risk of schizophrenia2.
Toxoplasma gondii is a protozoan with a worldwide distribution3. It has been estimated that up to one third of the world population has been exposed to the parasite4. The exposure rate and the prevalence of T. gondii infection varies according to geographic region, population habits as well as socioeconomic conditions5. For instance, in Brazil the rate of T. gondii infection in humans is high: up to 50% of elementary school children and 50-80% of women of child-bearing age have antibodies to T. gondii6.
In healthy adults, infection with T. gondii generally results in a latent infection that persists for life. This chronic infection was largely regarded as asymptomatic, but this assumption has changed lately. Latent toxoplasmosis has been linked to changes in cognitive function in both children7 and elderly individuals8. T. gondii infection has also been regarded as a risk factor for schizophrenia. A recent meta-analysis showed that T. gondii infection is associated with several psychiatric disorders including schizophrenia, bipolar disorder (BD) and obsessive-compulsive disorder9. Noteworthy, the reactivation of latent T. gondii infection may occur in patients with schizophrenia9. Moreover, T. gondii infection was associated with an increased risk for mortality in patients with schizophrenia10.
Although the association between T. gondii infection and schizophrenia has already been investigated, the results are still controversial and only few studies have focused on whether the infection is associated with clinical outcomes. Therefore, this study was carried out to investigate differences in T. gondii seroprevalence in patients with schizophrenia and controls, as well as to evaluate whether seroprevalence and anti-T. gondii antibody titers are associated with clinical parameters.
This is a cross-sectional study in which 48 patients with chronic schizophrenia and 40 controls were evaluated. Schizophrenia diagnosis was confirmed by the structured psychiatric interview MINI-Plus11 using the DSM-IV-TR criteria12.
Inclusion criteria for patients were: (a) age between 18-60 years; (b) diagnosis of schizophrenia; c) patients who were clinically stable as assessed by scores on the PANSS (see below). Controls were recruited from the local community using the following inclusion criteria (a) age between 18-60 years; (b) no current or past history of psychiatric disorder; (c) no family history of major psychiatry disorder. Exclusion criteria for both groups were: (a) history of epilepsy, dementia, brain trauma, tumor or other primary neurological diseases; (b) current dependence/use of drugs (alcohol, cannabis, cocaine, opioid); (c) current or recent (past four weeks) infections; (d) autoimmune or severe clinical diseases; (e) current or recent (past four weeks) use of corticosteroid or anti-inflammatory drugs. The study conformed to the declaration of Helsinki, with its protocol approved by the local Ethics Research Committee. Both patients and controls provided written informed consent.
Clinical, cognitive and quality of life assessments
Positive and negative symptoms were assessed by the Positive and Negative Syndrome Scale, PANSS13. Clinical stability was defined as a PANSS positive score of 19 or less, and less than 4 in any individual item of the positive scale for at least four weeks. The clinical stability criterion was based on positive symptoms due to their high impact on cognitive functioning assessment. The validity and applicability of SCoRS has been demonstrated in patients with clinical stable schizophrenia, but not in patients with a recent exacerbation of the illness and/or with significant positive symptomatology14. The Calgary Depression Scale (CDS) was used to assess depressive symptoms15.
Cognitive performance was assessed by the Brazilian version of the Schizophrenia Cognition Rating Scale (SCoRS-BR)16. This is an interview-based scale that includes information provided by both the patient and an informant. It generates three different ratings: from the patient, from the informant and from the interviewer. The interview is composed of 18 items covering several cognitive domains, including memory, attention, reasoning and problem solving, working memory, motor skills and language. The total score is the sum of scores on the 18 SCoRS items with a higher the score indicating greater degree of cognitive impairment. A global rating is also generated17.
Quality of life was assessed by the Quality of Life in Schizophrenia Scale (QLS) validated for use in Brazil (QLS-BR)18. This scale has a total of 21 items distributed among three factors: i) instrumental domain, ii) intrapsychic foundations and iii) interpersonal relations domain. Items include information on patient functioning during the three weeks preceding the interview. The sum of the values obtained in the 21 items of the scale is used to assess the overall quality of life. Higher scores denote better quality of life.
Peripheral blood was drawn from each subject by venipuncture into a vacuum tube without anticoagulant. Blood was immediately centrifuged at 3,000 rpm for 10 minutes, serum was collected and kept frozen at -80°C until assayed. IgM and IgG anti-T. gondii antibodies were determined by Enzyme-Linked Immunosorbent Assay (ELISA), using kits SERION – ELISA classic test by VIRION (Würzburg, Germany), following the manufacturer’s guidelines. The test sensitivity were 10 IU/mL and 5 IU/mL to IgM and IgG, respectively.
All variables were tested for Gaussian distribution by the Kolmogorov-Smirnov normality test. Association between dichotomous variables was assessed with the Fisher’s exact test. Two groups were compared by Mann-Whitney or Student’s t tests when non-normally or normally distributed, respectively. Spearman’s correlation analyses were performed for correlation analyses. All statistical tests were two-tailed and were performed using a significance level of α = 0.05. Statistical analyses were performed using SPSS software version 22.0 (SPSS Inc., Chicago, IL, USA), as well as GraphPad Prism 5.0 (GraphPad Software, Inc., La Jolla, California, EUA).
Demographic and clinical data
Demographic and clinical data are shown in Table 1. Patients and controls did not differ regarding age and gender. Patients with schizophrenia had less years of formal education than controls. The mean (± SD) length of illness was 15.20 (± 10.50) years. The mean (± SD) scores in the positive and negative subscales of the PANSS were, respectively, 10.28 (± 2.78) and 19.67 (± 7.73), indicating a chronic condition with predominance of negative symptoms.
T. gondii seroprevalence and association with clinical parameters
Patients with schizophrenia and controls presented similar seroprevalence and titers for both IgG and IgM anti-T. gondii antibodies (Table 1).
Patients with schizophrenia were then categorized into two groups: anti-T gondii IgG positive (Toxoplasma-seropositive, N = 27) and anti-T gondii IgG negative (Toxoplasma-seronegative, N = 21). We did not find any difference between Toxoplasma-seronegative and Toxoplasma-seropositive patients regarding age, gender, educational level, age of onset, length of illness, chlorpromazine equivalent level and PANSS subsets (Table 2). Toxoplasma-seropositive and Toxoplasma-seronegative patients presented similar scores in the scales that evaluated depressive symptoms, cognitive performance and quality of life (Table 2).
We did not find any significant correlation between anti-T. gondii IgM and IgG levels and age, age at onset, duration of illness, chlorpromazine equivalent level, positive PANSS, negative PANSS, total PANSS, patient SCoRS, informant SCoRS, interviewer SCoRS, global SCoRS, CDS or QLS scores. No difference was found when comparing male and female participants.
The current study was conducted in order to compare the prevalence of T. gondii infection between patients with schizophrenia and controls, as well as to evaluate the potential association between T. gondii infection and clinical symptoms in Brazilian patients with schizophrenia. We found similar rates of positive serological reaction to T. gondii in controls and patients with schizophrenia. In addition, we did not find any association between T. gondii seroprevalence and demographic data, positive, negative and depressive symptoms, cognitive performance and quality of life in patients with schizophrenia.
Previous studies found higher rates of T. gondii infection in patients with schizophrenia in comparison with controls19-23. In contrast, some authors have questioned this association24,25. A recent meta-analysis reported a significant association between T. gondii infection as estimated by IgG antibodies and schizophrenia (odds ratio 1.81, P < 0.0001). A very high heterogeneity was observed among studies, and the amplitude of the odds ratio was influenced by region and general seroprevalence9. Accordingly, the possibility of finding association between toxoplasmosis and schizophrenia is lower in regions with high seroprevalence rates when compared with regions with low rates. Brazil has a high prevalence of T. gondii infection which could be an explanation for the current findings. Moreover, our sample was composed by chronic patients under high dose of antipsychotics that may affect anti-T. gondii IgG titers26.
T. gondii infection has been associated with symptom severity in schizophrenia23,27,28. In addition, latent toxoplasmosis may have a negative impact on the disease course and treatment response in patients with schizophrenia29. Corroborating these clinical data, patients with schizophrenia T. gondii-seropositive presented more significant morphological changes in the caudate, cingulate, thalamus and occipital cortex in comparison with seronegative patients30. In the current study, we did not find significant differences between seropositive and seronegative patients regarding the clinical symptoms of schizophrenia as assessed by PANSS. The fact that the enrolled patients were clinically stable comprising a relatively homogenous sample may partially explain this result.
Data on whether T. gondii infection is associated with cognitive aspects in schizophrenia are still controversial. For instance, one study showed that people diagnosed with schizophrenia who were exposed in utero to T. gondii presented impaired performance in two executive function tests: the Wisconsin Card Sorting Test (WCST) and the Trail Making Test (TMT) part B31. These patients also exhibited deficits on figural fluency, letter-number sequencing and backward digit span31. Conversely, other studies failed to show any association between latent toxoplasmosis and cognitive function in schizophrenia32,33. According to our results, T. gondii infection is not associated with self-reported cognitive performance as evaluated by the SCoRS. Discrepancies among studies can also be explained, at least in part, by strain related specific effects of T. gondii on human brain9. Indeed, regional differences in strain distribution have been reported, and T. gondii strain-specific effects in depression have already been demonstrated9.
It is worth mentioning that the use of antipsychotic and/or mood stabilizers presenting in vitro anti-toxoplasmic activity was associated with a better clinical outcome in a population of BD patients. Patients with BD seropositive for T. gondii presented more lifetime depressive episodes when treated by drugs having no anti-toxoplasmic activity (e.g. aripiprazole, carbamazepine, clozapine, lamotrigine, lithium, olanzapine, quetiapine) compared to patients who received drugs with anti-toxoplasmic activity (e.g. fluphenazine, haloperidol, levomepromazine, paliperidone, risperidone, thioridazine, valproate)34. It remains to be determined whether the treatment with drugs with anti-toxoplasmic activity is also associated with better clinical outcomes of the patients with schizophrenia.
We are aware of the limitations of our study. First the sample size is small and consists of chronic patients using antipsychotics. It is uncertain whether our results can be applied to patients with prodromal or early schizophrenia. Cohort studies involving a larger sample of drug naïve patients are critical to confirm the specificity to clarify the pathogenic role of T. gondii in schizophrenia and its symptoms. Cognitive assessment of patients was based on self-reported measures. Although SCoRS is highly correlated to cognitive performance and functioning, a comprehensive neuropsychological evaluation in both patients and controls could add more specific information, including the domains potentially affected by toxoplasmosis.
In conclusion, our data showed that T. gondii infection is not associated with schizophrenia. In addition, T. gondii seroprevalence and levels of IgG antibodies were not associated with demographic data, disease severity, depressive and cognitive symptoms and quality of life. Our results might be influenced by strain-specific brain effects and high prevalence of T. gondii infection in our sample. Further studies are needed in order to elucidate the role of T. gondii in schizophrenia pathophysiology.
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