TY - JOUR
T1 - Systematic screening identifies medication and disease factors associated with schizophrenia risk
AU - Israel, Ariel
AU - Weizman, Abraham
AU - Israel, Sarah
AU - Stokar, Joshua
AU - Ashkenazi, Shai
AU - Vinker, Shlomo
AU - Magen, Eli
AU - Merzon, Eugene
N1 - Publisher Copyright:
© 2025 The Author(s).
PY - 2026/1
Y1 - 2026/1
N2 - Schizophrenia (SCZ) is a severe psychiatric disorder with a complex and poorly understood etiology. Previous studies have linked Toxoplasma gondii infection to SCZ, though its clinical relevance remains uncertain. To identify factors associated with SCZ risk, we analyzed electronic health records from a national Israeli health provider, retrospectively comparing 3,273 individuals with SCZ to 32,730 matched controls. We systematically screened all medication purchases and medical diagnoses recorded from 10 years to 30 days before SCZ onset. Significant associations, adjusted for residual confounding, were further evaluated in the TriNetX network, where large propensity score–matched cohorts were compared for incident SCZ following medication exposure. Among all medication classes screened, strong protective associations were detected for specific antimicrobials, notably atovaquone/proguanil, clindamycin, and ophthalmic fluoroquinolones. Nonsteroidal anti-inflammatory drugs, particularly COX-2 inhibitors, were also linked to reduced SCZ risk, whereas neomycin, tramadol, and desmopressin were associated with increased risk. Key associations were confirmed within TriNetX with high statistical significance. These observational findings, reproduced across two national cohorts, are hypothesis-generating and may reflect multiple, non-exclusive mechanisms, including antimicrobial, anti-inflammatory, and microbiome-related pathways, with T. gondii elimination through antiprotozoal activity representing one compelling explanatory hypothesis that warrants further investigation.
AB - Schizophrenia (SCZ) is a severe psychiatric disorder with a complex and poorly understood etiology. Previous studies have linked Toxoplasma gondii infection to SCZ, though its clinical relevance remains uncertain. To identify factors associated with SCZ risk, we analyzed electronic health records from a national Israeli health provider, retrospectively comparing 3,273 individuals with SCZ to 32,730 matched controls. We systematically screened all medication purchases and medical diagnoses recorded from 10 years to 30 days before SCZ onset. Significant associations, adjusted for residual confounding, were further evaluated in the TriNetX network, where large propensity score–matched cohorts were compared for incident SCZ following medication exposure. Among all medication classes screened, strong protective associations were detected for specific antimicrobials, notably atovaquone/proguanil, clindamycin, and ophthalmic fluoroquinolones. Nonsteroidal anti-inflammatory drugs, particularly COX-2 inhibitors, were also linked to reduced SCZ risk, whereas neomycin, tramadol, and desmopressin were associated with increased risk. Key associations were confirmed within TriNetX with high statistical significance. These observational findings, reproduced across two national cohorts, are hypothesis-generating and may reflect multiple, non-exclusive mechanisms, including antimicrobial, anti-inflammatory, and microbiome-related pathways, with T. gondii elimination through antiprotozoal activity representing one compelling explanatory hypothesis that warrants further investigation.
KW - Anti-Inflammatory Agents
KW - Antimicrobials
KW - Case-Control Studies
KW - Infection
KW - Neuroinflammation
KW - Pharmacoepidemiology
KW - Propensity Score Matching
KW - Risk Factors
KW - Schizophrenia
KW - Toxoplasma Gondii
UR - https://www.scopus.com/pages/publications/105020579703
U2 - 10.1016/j.bbi.2025.106135
DO - 10.1016/j.bbi.2025.106135
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C2 - 41106616
AN - SCOPUS:105020579703
SN - 0889-1591
VL - 131
JO - Brain, Behavior, and Immunity
JF - Brain, Behavior, and Immunity
M1 - 106135
ER -