Candida Albicans Exposures, Sex Specificity and Cognitive Deficits in Schizophrenia and Bipolar Disorder
Overview
Authors
Affiliations
Immune aberrations in schizophrenia and bipolar disorder have led to the hypotheses that infectious agents or corresponding immune responses might contribute to psychiatric etiopathogeneses. We investigated case-control differences in exposure to the opportunistic fungal pathogen, Candida albicans, and examined associations with cognition, medication, lifestyle, and somatic conditions. We quantified C. albicans IgG antibodies in two cohorts totaling 947 individuals and evaluated odds ratios (OR) of exposure with psychiatric disorder using multivariate regressions. The case-control cohort included 261 with schizophrenia, 270 with bipolar disorder, and 277 non-psychiatric controls; the second included 139 with first-episode schizophrenia, 78 of whom were antipsychotic naive. No differences in C. albicans exposures were found until diagnostic groups were stratified by sex. In males, C. albicans seropositivity conferred increased odds for a schizophrenia diagnosis (OR 2.04-9.53, P⩽0.0001). In females, C. albicans seropositivity conferred increased odds for lower cognitive scores on Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) in schizophrenia (OR 1.12, P⩽0.004), with significant decreases on memory modules for both disorders (P⩽0.0007-0.03). C. albicans IgG levels were not impacted by antipsychotic medications. Gastrointestinal (GI) disturbances were associated with elevated C. albicans in males with schizophrenia and females with bipolar disorder (P⩽0.009-0.02). C. albicans exposure was associated with homelessness in bipolar males (P⩽0.0015). In conclusion, sex-specific C. albicans immune responses were evident in psychiatric disorder subsets. Inquiry regarding C. albicans infection or symptoms may expedite amelioration of this treatable comorbid condition. Yeast exposure as a risk factor for schizophrenia and its associated cognitive and GI effects require further investigation including the possible contribution of gut-brain mechanisms.
Sexual dimorphism in immunity and longevity among the oldest old.
Arakelyan N, Kupriyanova D, Vasilevska J, Rogaev E Front Immunol. 2025; 16:1525948.
PMID: 40034689 PMC: 11872714. DOI: 10.3389/fimmu.2025.1525948.
Singh D, Roberts A, Wang X, Li G, Quesada Moraga E, Alliband D PLoS Biol. 2025; 23(2):e3003020.
PMID: 39946503 PMC: 11825051. DOI: 10.1371/journal.pbio.3003020.
Oral fungal dysbiosis and systemic immune dysfunction in Chinese patients with schizophrenia.
Liu X, Ling Z, Cheng Y, Wu L, Shao L, Gao J Transl Psychiatry. 2024; 14(1):475.
PMID: 39572530 PMC: 11582559. DOI: 10.1038/s41398-024-03183-5.
Toxoplasma-induced behavior changes - is microbial dysbiosis the missing link?.
Prandovszky E, Severance E, Splan V, Liu H, Xiao J, Yolken R Front Cell Infect Microbiol. 2024; 14:1415079.
PMID: 39403206 PMC: 11471644. DOI: 10.3389/fcimb.2024.1415079.
Dopaminergic Perturbation in the Aetiology of Neurodevelopmental Disorders.
Ijomone O, Oria R, Ijomone O, Aschner M, Bornhorst J Mol Neurobiol. 2024; 62(2):2420-2434.
PMID: 39110391 PMC: 11772124. DOI: 10.1007/s12035-024-04418-8.