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首页> 外文期刊>Diabetes care >Does insulin glargine increase the risk of cancer compared with other basal insulins? A French nationwide cohort study based on national administrative databases
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Does insulin glargine increase the risk of cancer compared with other basal insulins? A French nationwide cohort study based on national administrative databases

机译:与其他基础胰岛素相比,甘精胰岛素会增加患癌症的风险吗?基于国家行政数据库的法国全国队列研究

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OBJECTIVE-To explore in France the relationship between insulin glargine use and overall and specific cancer risks in type 2 diabetic patients compared with other basal insulins. RESEARCH DESIGN AND METHODS-Data were extracted from French health insurance information system (Système National d'Information Inter-Régimes de l'Assurance Maladie) linked with data from the French Hospital Discharge database (Programme de Médicalisation des Systèmes d'Information). Included were 70,027 patients aged 40-79 years who started a basal insulin in 2007-2009. Cox proportional hazards models with age as time-scale were used to calculate multivariate-adjusted hazard ratios for associations between type of basal insulin and risk of overall cancer, breast cancer, and seven other cancer sites. RESULTS-The median follow-up was 2.67 years in patients exposed to insulin glargine. Absolute event rates for all cancer in patients exposed to glargine versus other basal insulin users were 1,622 and 1,643 per 100,000 person-years, respectively. No significant association was observed between glargine exposure and overall cancer incidence after adjustment for sex, with a hazard ratio of 0.97 (95% CI 0.87-1.07), or after additional adjustment for any other hypogly-cemic agent use and duration of diabetes. No increased risk of breast cancer was observed for glargine users compared with other basal insulins users, with a fully adjusted hazard ratio of 1.08 (0.72-1.62). CONCLUSIONS-In a large cohort of patients newly treated by basal insulin, no increased risk of any cancer was observed in insulin glargine users compared with other basal insulin users. Because follow-up did not exceed 4 years, longer-term studies are needed.
机译:目的-在法国探索与其他基础胰岛素相比,使用甘精胰岛素与2型糖尿病患者的总体和特定癌症风险之间的关系。研究设计与方法-数据是从法国健康保险信息系统(国家医疗机构信息系统)中提取的,并与法国医院出院数据库(系统医疗信息系统)的数据相关联。其中包括2007-2009年开始使用基础胰岛素的70,027名年龄在40-79岁的患者。使用以年龄为时间尺度的Cox比例风险模型计算基础胰岛素类型与整体癌症,乳腺癌和其他七个癌症部位风险之间的关联的多元调整风险比。结果:接受甘精胰岛素治疗的患者中位随访时间为2.67年。甘精胰岛素与其他基础胰岛素使用者相比,所有癌症患者的全部癌症绝对事件发生率分别为每100,000人年1,622和1,643。在调整性别,风险比为0.97(95%CI 0.87-1.07)或对其他降血糖药的使用和糖尿病持续时间进行额外调整后,未发现甘精氨酸暴露与总体癌症发生率之间存在显着关联。与其他基础胰岛素使用者相比,甘精胰岛素使用者未观察到患乳腺癌的风险增加,完全调整后的危险比为1.08(0.72-1.62)。结论-在接受基础胰岛素治疗的一大批患者中,与其他基础胰岛素使用者相比,甘精胰岛素使用者中未发现任何癌症的风险增加。由于随访时间不超过4年,因此需要进行长期研究。

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