{"title":"Clopidogrel-Induced Insulin Autoimmune Syndrome: Efficacy of Glucocorticoid Therapy and Continuous Glucose Monitoring.","authors":"Lihui Luo, Xiaoqing Xiong, Jianmin Ran","doi":"10.2174/0118715303394353250727192242","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Insulin autoimmune syndrome (IAS) is a rare cause of spontaneous hyperinsulinemic hypoglycemia characterized by elevated insulin autoantibody (IAA). Over half of IAS cases involve exposure to sulfhydryl group-containing medications or their active metabolites, with clopidogrel being an uncommon trigger. We report a case of clopidogrel-induced IAS (CIAS) treated with glucocorticoid and managed by continuous glucose monitoring (CGM) during follow-up.</p><p><strong>Case report: </strong>A 77-year-old man developed recurrent severe hypoglycemia events after receiving clopidogrel for six months. Laboratory investigations showed significantly elevated serum insulin levels (peak: 1,452.52 mIU/L; normal range: 1.9-23.0 mIU/L) and a high IAA titer of 37.0 COI (>1.1 COI, positive). Following the exclusion of other potential causes of hypoglycemia, IAS was diagnosed. Consequently, clopidogrel was discontinued, and combination therapy incorporating prednisolone was initiated. During the 10-month follow-up, insulin levels declined to 8.09 mIU/L with IAA titers decreasing to 1.35 COI. Analysis of CGM data demonstrated a transition from glycemic fluctuations to stabilization.</p><p><strong>Conclusion: </strong>This single-patient case report highlights the significance of identifying CIAS as a rare adverse effect of a drug, the effectiveness of glucocorticoid therapy, and the role of CGM in IAS management.</p>","PeriodicalId":94316,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrine, metabolic & immune disorders drug targets","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0118715303394353250727192242","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Insulin autoimmune syndrome (IAS) is a rare cause of spontaneous hyperinsulinemic hypoglycemia characterized by elevated insulin autoantibody (IAA). Over half of IAS cases involve exposure to sulfhydryl group-containing medications or their active metabolites, with clopidogrel being an uncommon trigger. We report a case of clopidogrel-induced IAS (CIAS) treated with glucocorticoid and managed by continuous glucose monitoring (CGM) during follow-up.
Case report: A 77-year-old man developed recurrent severe hypoglycemia events after receiving clopidogrel for six months. Laboratory investigations showed significantly elevated serum insulin levels (peak: 1,452.52 mIU/L; normal range: 1.9-23.0 mIU/L) and a high IAA titer of 37.0 COI (>1.1 COI, positive). Following the exclusion of other potential causes of hypoglycemia, IAS was diagnosed. Consequently, clopidogrel was discontinued, and combination therapy incorporating prednisolone was initiated. During the 10-month follow-up, insulin levels declined to 8.09 mIU/L with IAA titers decreasing to 1.35 COI. Analysis of CGM data demonstrated a transition from glycemic fluctuations to stabilization.
Conclusion: This single-patient case report highlights the significance of identifying CIAS as a rare adverse effect of a drug, the effectiveness of glucocorticoid therapy, and the role of CGM in IAS management.