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Exposure to topiramate may not increase the risk of urolithiasis: A nationwide cohort study
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Chang, Kimoon | - |
| dc.contributor.author | Ha, Woo-Seok | - |
| dc.date.accessioned | 2026-04-29T07:39:43Z | - |
| dc.date.available | 2026-04-29T07:39:43Z | - |
| dc.date.created | 2026-04-28 | - |
| dc.date.issued | 2026-06 | - |
| dc.identifier.issn | 2589-9864 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/211944 | - |
| dc.description.abstract | Background and purpose: Although topiramate is mechanistically linked to an increased risk of urolithiasis, real-world evidence remains conflicting. This study aimed to evaluate the risk of a first-time episode of urolithiasis associated with topiramate exposure in the Korean population. Methods: Using the Korean National Health Insurance Service-National Sample Cohort, we identified participants from the 2015 national health screening. After excluding individuals with a prior diagnosis of urolithiasis, we performed 1:4 propensity score matching between patients with and without topiramate exposure. Matching variables included age, sex, body mass index, comorbidities, and a history of gout. Participants were followed longitudinally, and the risk of urolithiasis was assessed using Kaplan-Meier analysis and Cox proportional hazards regression. Results: The final cohort included 1,560 patients exposed to topiramate and 6,240 matched controls who were followed for five years. During the follow-up period, urolithiasis was diagnosed in 47 patients (3.0%) in the topiramate group and 170 patients (2.7%) in the control group. The risk of developing urolithiasis was not significantly different between the two groups (p = 0.545). Furthermore, subgroup analyses stratified by current use or the cumulative duration of topiramate exposure also showed no significant associations. Conclusions: In this large, nationwide cohort, topiramate exposure was not associated with an increased risk of urolithiasis. Our findings suggest that in a real-world setting, the risk may not be as significant as suggested by its pharmacological mechanism. | - |
| dc.language | 영어 | - |
| dc.publisher | ELSEVIER SCIENCE INC | - |
| dc.relation.isPartOf | EPILEPSY & BEHAVIOR REPORTS | - |
| dc.title | Exposure to topiramate may not increase the risk of urolithiasis: A nationwide cohort study | - |
| dc.type | Article | - |
| dc.contributor.googleauthor | Chang, Kimoon | - |
| dc.contributor.googleauthor | Ha, Woo-Seok | - |
| dc.identifier.doi | 10.1016/j.ebr.2026.100864 | - |
| dc.identifier.pmid | 42004439 | - |
| dc.subject.keyword | Urolithiasis | - |
| dc.subject.keyword | Carbonic anhydrase inhibitors | - |
| dc.subject.keyword | Topiramate | - |
| dc.subject.keyword | Epilepsy | - |
| dc.subject.keyword | Migraine disorders | - |
| dc.contributor.affiliatedAuthor | Ha, Woo-Seok | - |
| dc.identifier.scopusid | 2-s2.0-105034556669 | - |
| dc.identifier.wosid | 001740197600001 | - |
| dc.citation.volume | 34 | - |
| dc.identifier.bibliographicCitation | EPILEPSY & BEHAVIOR REPORTS, Vol.34, 2026-06 | - |
| dc.identifier.rimsid | 92564 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | Urolithiasis | - |
| dc.subject.keywordAuthor | Carbonic anhydrase inhibitors | - |
| dc.subject.keywordAuthor | Topiramate | - |
| dc.subject.keywordAuthor | Epilepsy | - |
| dc.subject.keywordAuthor | Migraine disorders | - |
| dc.subject.keywordPlus | KIDNEY-STONES | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Clinical Neurology | - |
| dc.relation.journalResearchArea | Neurosciences & Neurology | - |
| dc.identifier.articleno | 100864 | - |
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