Investigating the potential effect of topiramate on anorexia nervosa and binge eating behaviour using drug-target Mendelian randomization
- 1Institute for Molecular Bioscience, The University of Queensland
Abstract
Topiramate is an antiseizure medication used to treat epilepsy and migraine and is commonly prescribed for appetite suppression and weight loss. However, whether its pharmacological actions influence eating disorder risk remains unclear. We applied drug-target Mendelian randomization (MR) to investigate potential causal effects of topiramate on the risk of anorexia nervosa (AN; 24,223 cases and 1,243,971 controls) and binge-eating behaviour (BE; 39,279 cases and 1,227,436 controls) and, exploratorily, eight other psychiatric disorders: attention-deficit/hyperactivity disorder, anxiety disorders, alcohol use disorder, bipolar disorder, major depressive disorder, panic disorder, post-traumatic stress disorder, and schizophrenia. We used summary-data-based Mendelian randomization (SMR) to investigate genetically predicted pharmacological actions of topiramate using brain- and blood-derived cis-expression quantitative trait loci for genes encoding its molecular targets. Five genetic instruments consistent with topiramate's antiepileptic action were validated: CA4 and CACNB3 expression in the brain and CA4, GRIK1, and GRIK3 expression in the blood. Robustness of the findings was assessed using SMR-multi, HEIDI, and colocalization analyses. After multiple-testing correction, genetically predicted inhibition of CA4 expression in blood was associated with decreased BE risk (OR = 0.867, 95% CI = 0.792 - 0.950, p = 0.002) and remained significant in SMR-multi (p = 0.0049). Colocalization provided moderate support for a shared causal variant underlying CA4 expression and BE (PPH4 = 0.58). No robust evidence was identified for AN or the eight exploratory psychiatric outcomes. Overall, our findings warrant further clinical and functional investigations into mechanisms underlying topiramate-associated appetite suppression and weight loss and their relevance to eating-disorder risk.
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BibTeX
@misc{nguyen2026investigating,
title = {{Investigating the potential effect of topiramate on anorexia nervosa and binge eating behaviour using drug-target Mendelian randomization}},
author = {K.-M. Nguyen and E. Y.-H. Chang and B. Kim and P. Ebert and J.-C. Chiang and L.-D. Hwang},
howpublished = {medRxiv},
year = {2026},
month = nov,
doi = {10.64898/2026.11.05.26367397},
url = {https://www.medrxiv.org/content/10.64898/2026.11.05.26367397v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - Investigating the potential effect of topiramate on anorexia nervosa and binge eating behaviour using drug-target Mendelian randomization
AU - K.-M. Nguyen
AU - E. Y.-H. Chang
AU - B. Kim
AU - P. Ebert
AU - J.-C. Chiang
AU - L.-D. Hwang
PY - 2026
DA - 2026/11/05
PB - medRxiv
DO - 10.64898/2026.11.05.26367397
UR - https://www.medrxiv.org/content/10.64898/2026.11.05.26367397v1
AB - Topiramate is an antiseizure medication used to treat epilepsy and migraine and is commonly prescribed for appetite suppression and weight loss. However, whether its pharmacological actions influence eating disorder risk remains unclear. We applied drug-target Mendelian randomization (MR) to investigate potential causal effects of topiramate on the risk of anorexia nervosa (AN; 24,223 cases and 1,243,971 controls) and binge-eating behaviour (BE; 39,279 cases and 1,227,436 controls) and, exploratorily, eight other psychiatric disorders: attention-deficit/hyperactivity disorder, anxiety disorders, alcohol use disorder, bipolar disorder, major depressive disorder, panic disorder, post-traumatic stress disorder, and schizophrenia. We used summary-data-based Mendelian randomization (SMR) to investigate genetically predicted pharmacological actions of topiramate using brain- and blood-derived cis-expression quantitative trait loci for genes encoding its molecular targets. Five genetic instruments consistent with topiramate's antiepileptic action were validated: CA4 and CACNB3 expression in the brain and CA4, GRIK1, and GRIK3 expression in the blood. Robustness of the findings was assessed using SMR-multi, HEIDI, and colocalization analyses. After multiple-testing correction, genetically predicted inhibition of CA4 expression in blood was associated with decreased BE risk (OR = 0.867, 95% CI = 0.792 - 0.950, p = 0.002) and remained significant in SMR-multi (p = 0.0049). Colocalization provided moderate support for a shared causal variant underlying CA4 expression and BE (PPH4 = 0.58). No robust evidence was identified for AN or the eight exploratory psychiatric outcomes. Overall, our findings warrant further clinical and functional investigations into mechanisms underlying topiramate-associated appetite suppression and weight loss and their relevance to eating-disorder risk.
ER -