Sex-differences in reporting of statin-associated diabetes mellitus to the US Food and Drug Administration.

IF 3.7 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM BMJ Open Diabetes Research & Care Pub Date : 2024-12-05 DOI:10.1136/bmjdrc-2024-004343
David P Kao, James L Martin, Christina L Aquilante, Elise L Shalowitz, Katarina Leyba, Elizabeth Kudron, Jane E B Reusch, Judith G Regensteiner
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Abstract

Introduction: Diabetes mellitus (DM) is increasingly recognized as a possible consequence of statin therapy. Secondary analysis of randomized clinical trials and limited observational cohort analyses have suggested that women may be more likely than men to experience statin-associated DM. No analyses of real-world drug safety data addressing this question have been published.

Research design and methods: This was a retrospective pharmacovigilance analysis of spontaneously reported adverse drug events (ADEs) submitted to the Food and Drug Administration Adverse Event Reporting System between January 1997 through December 2023. We analyzed cases that mentioned atorvastatin, fluvastatin, lovastatin, pitavastatin, pravastatin, rosuvastatin, or simvastatin in aggregate as well as cases reporting atorvastatin, pravastatin, rosuvastatin, simvastatin individually. DM events were identified using the Medical Dictionary for Regulatory Activities. We used the proportional reporting ratio to identify increased rates of statin-associated DM events in women and men compared with all other medications, and the reporting OR to compare reporting rates in women versus men.

Results: A total of 18,294,814 ADEs were reported during the study period. Among statin-associated ADEs, 14,874/519,209 (2.9%) reports mentioned DM in women compared with 7,411/489,453 (1.5%) in men, which were both significantly higher than background (0.6%). Statins were the primary-suspected or secondary-suspected cause of the ADE significantly more often in women than men (60 vs 30%), and reporting rates were disproportionately higher in women than in men for all statins. (reporting OR 1.9 (95% CI 1.9 to 2.0)). The largest difference in reporting of statin-associated DM between women and women was observed with atorvastatin.

Conclusions: Analysis of post-marketing spontaneous ADE reports demonstrated a higher reporting rate of DM-associated with statin use compared with other medications with a significantly higher reporting rate in women compared with men. Future studies should consider mechanisms of statin-associated DM moderated by sex.

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向美国食品和药物管理局报告他汀类药物相关糖尿病的性别差异
糖尿病(DM)越来越被认为是他汀类药物治疗的可能后果。随机临床试验的二次分析和有限的观察性队列分析表明,女性可能比男性更容易出现他汀类药物相关的糖尿病。目前还没有针对这一问题的实际药物安全性数据的分析发表。研究设计和方法:本研究对1997年1月至2023年12月期间提交给美国食品药品监督管理局不良事件报告系统的自发报告药物不良事件(ADEs)进行回顾性药物警戒分析。我们分析了阿托伐他汀、氟伐他汀、洛伐他汀、匹伐他汀、普伐他汀、瑞舒伐他汀或辛伐他汀的总体病例,以及单独报道阿托伐他汀、普伐他汀、瑞舒伐他汀、辛伐他汀的病例。DM事件的识别使用医学词典的监管活动。我们使用比例报告比率来确定与所有其他药物相比,他汀类药物相关糖尿病事件在女性和男性中的发生率增加,并使用报告OR来比较女性和男性的发生率。结果:研究期间共报告ade 18,294,814例。在他汀类药物相关的不良事件中,14874 /519,209例(2.9%)的报告提到了女性糖尿病,而7411 /489,453例(1.5%)的报告提到了男性糖尿病,两者均显著高于背景(0.6%)。他汀类药物是ADE的主要怀疑或次要怀疑原因,女性比男性更常见(60% vs 30%),所有他汀类药物中女性的报告率都不成比例地高于男性。(报告OR 1.9 (95% CI 1.9 ~ 2.0))。阿托伐他汀组女性和女性报告他汀类相关糖尿病的差异最大。结论:对上市后自发性ADE报告的分析表明,与其他药物相比,他汀类药物与dm相关的报告率更高,女性报告率明显高于男性。未来的研究应考虑他汀类药物相关糖尿病的性别调节机制。
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来源期刊
BMJ Open Diabetes Research & Care
BMJ Open Diabetes Research & Care Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
9.30
自引率
2.40%
发文量
123
审稿时长
18 weeks
期刊介绍: BMJ Open Diabetes Research & Care is an open access journal committed to publishing high-quality, basic and clinical research articles regarding type 1 and type 2 diabetes, and associated complications. Only original content will be accepted, and submissions are subject to rigorous peer review to ensure the publication of high-quality — and evidence-based — original research articles.
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