Yuk Jin-Sung, Kim Jung Min
From the Department of Obstetrics and Gynecology, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Republic of Korea.
Department of Internal Medicine, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Republic of Korea.
Menopause. 2023 May 1;30(5):497-505. doi: 10.1097/GME.0000000000002170. Epub 2023 Mar 12.
Menopausal hormone therapy (MHT) is known to reduce the incidence of type 2 diabetes mellitus (T2DM); however, since the Women's Health Initiative study, the types and doses of female hormones used for MHT have changed considerably. Therefore, this study was conducted to determine whether MHT, which is currently widely prescribed, increases the risk of T2DM.
We performed a retrospective cohort study based on national health insurance data and cancer screening data from 2002 to 2019. We included the MHT group as postmenopausal women older than 40 years who used at least one MHT for at least 6 months between 2003 and 2011. We subclassified the MHT group into five categories; tibolone, combined estrogen plus progestin by the manufacturer (CEPM), oral estrogen, combined estrogen plus progestin by the physician (CEPP), and transdermal estrogen. We selected the non-MHT group as postmenopausal women who had never been prescribed MHT from 2002 to 2019. We compared the incidence of T2DM between the MHT group and the non-MHT group.
We enrolled 330,771 women in the MHT group and 798,550 women in the control group. T2DM was diagnosed in 15.2% of the non-MHT group, 16.6% of the tibolone group, 12.1% of the CEPM group, 16.6% of the oral estrogen group, 15.4% of the CEPP group, and 17% of the transdermal estrogen group. In Cox proportional hazard analysis adjusted for variable factors, tibolone, oral estrogen, CEPP, and transdermal estrogen increased the incidence of T2DM. In contrast, there was no change in the risk of T2DM in the CEPM group.
MHT, including tibolone, which is currently the most prescribed agent, increased the risk of T2DM; however, CEPM did not increase the risk of T2DM. Only tibolone increased the risk of T2DM in participants older than 70 years.
已知绝经激素治疗(MHT)可降低2型糖尿病(T2DM)的发病率;然而,自妇女健康倡议研究以来,用于MHT的女性激素类型和剂量发生了很大变化。因此,本研究旨在确定目前广泛应用的MHT是否会增加T2DM的风险。
我们基于2002年至2019年的国民健康保险数据和癌症筛查数据进行了一项回顾性队列研究。MHT组纳入2003年至2011年期间年龄超过40岁且使用至少一种MHT至少6个月的绝经后女性。我们将MHT组细分为五类;替勃龙、制造商提供的雌激素加孕激素联合制剂(CEPM)、口服雌激素、医生处方的雌激素加孕激素联合制剂(CEPP)以及经皮雌激素。我们选择非MHT组为2002年至2019年期间从未接受过MHT处方的绝经后女性。我们比较了MHT组和非MHT组中T2DM的发病率。
我们在MHT组纳入了330771名女性,在对照组纳入了798550名女性。非MHT组中15.2%被诊断为T2DM,替勃龙组为16.6%,CEPM组为12.1%,口服雌激素组为16.6%,CEPP组为15.4%,经皮雌激素组为17%。在对可变因素进行调整的Cox比例风险分析中,替勃龙、口服雌激素、CEPP和经皮雌激素增加了T2DM的发病率。相比之下,CEPM组中T2DM的风险没有变化。
包括目前处方最多的替勃龙在内的MHT增加了T2DM的风险;然而,CEPM并未增加T2DM的风险。只有替勃龙在70岁以上参与者中增加了T2DM的风险。