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二甲双胍与胰岛素治疗 2 型糖尿病与重大先天畸形风险:一项基于北欧注册的队列研究。

Metformin Versus Insulin and Risk of Major Congenital Malformations in Pregnancies With Type 2 Diabetes: A Nordic Register-Based Cohort Study.

机构信息

Department of Chronic Diseases, Norwegian Institute of Public Health, Oslo, Norway.

Centre for Pharmacoepidemiology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Diabetes Care. 2023 Aug 1;46(8):1556-1564. doi: 10.2337/dc23-0256.

Abstract

OBJECTIVE

To assess the risk of major congenital malformations with metformin versus insulin in pregnancies with type 2 diabetes.

RESEARCH DESIGN AND METHODS

This cohort study used four Nordic countries' nationwide registers of live and stillborn infants exposed to metformin or insulin during first trimester organogenesis. Main exclusion criteria were type 1 diabetes, polycystic ovary syndrome, fertility treatment, and exposure to other diabetes drugs. Adjusted risk ratios (RRs) and 95% CIs were estimated for any and cardiac malformations.

RESULTS

Of 3,734,125 infants in the source population, 25,956 were exposed to metformin or insulin in the first trimester, and 4,023 singleton infants were included. A malformation was diagnosed in 147 (4.7%) of 3,145 infants with exposure to any metformin (alone or in addition to insulin) and 50 (5.7%) of 878 infants with exposure to insulin alone (RR 0.84, 95% CI 0.46-1.54). Among 2,852 infants exposed to metformin alone and 293 infants exposed to metformin in addition to insulin 127 (4.4%) and 20 (6.8%), respectively, had a malformation. The adjusted risk was not increased for either metformin alone (0.83, 0.44-1.58) or both metformin and insulin (0.98, 0.56-1.69) versus insulin alone. Corresponding RRs for cardiac malformations were 1.01 (0.55-1.84) for any metformin, 0.92 (0.47-1.81) for metformin alone, and 1.72 (0.76-3.91) for both metformin and insulin.

CONCLUSIONS

No evidence of an increased malformation risk with metformin versus insulin in the first trimester was found. Results should be interpreted with caution since information on glycemic control was missing.

摘要

目的

评估二甲双胍与胰岛素在治疗 2 型糖尿病孕妇中的先天重大畸形风险。

研究设计与方法

本队列研究使用了四个北欧国家的活产和死胎婴儿全国登记处的数据,这些婴儿在器官发生期的第一 trimester 暴露于二甲双胍或胰岛素。主要排除标准为 1 型糖尿病、多囊卵巢综合征、生育治疗和其他糖尿病药物暴露。估计了任何畸形和心脏畸形的调整后的风险比(RR)和 95%置信区间(CI)。

结果

在源人群的 3734125 名婴儿中,有 25956 名在第一 trimester 暴露于二甲双胍或胰岛素,有 4023 名单胎婴儿被纳入。在暴露于任何二甲双胍(单独或与胰岛素联合使用)的 3145 名婴儿中,有 147 名(4.7%)诊断出畸形,在单独暴露于胰岛素的 878 名婴儿中,有 50 名(5.7%)(RR 0.84,95%CI 0.46-1.54)。在暴露于二甲双胍单独的 2852 名婴儿和暴露于二甲双胍联合胰岛素的 293 名婴儿中,分别有 127 名(4.4%)和 20 名(6.8%)患有畸形。单独使用二甲双胍(0.83,0.44-1.58)或二甲双胍联合胰岛素(0.98,0.56-1.69)与单独使用胰岛素相比,风险没有增加。任何二甲双胍的心脏畸形的相应 RR 为 1.01(0.55-1.84),二甲双胍单独使用的 RR 为 0.92(0.47-1.81),二甲双胍联合胰岛素使用的 RR 为 1.72(0.76-3.91)。

结论

没有发现第一 trimester 中使用二甲双胍与胰岛素相比,畸形风险增加的证据。由于缺乏血糖控制信息,结果应谨慎解释。

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