Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), 7491 Trondheim, Norway.
Centre of Molecular Inflammation Research (CEMIR), Norwegian University of Science and Technology, 7491 Trondheim, Norway.
J Clin Endocrinol Metab. 2023 Aug 18;108(9):e743-e753. doi: 10.1210/clinem/dgad145.
Polycystic ovary syndrome (PCOS) is a common endocrine disorder associated with low-grade systemic inflammation and increased risk of pregnancy complications. Metformin treatment reduces the risk of late miscarriage and preterm birth in pregnant women with PCOS. Whether the protective effect of metformin involves immunological changes has not been determined.
To investigate the effect of metformin on the maternal immunological status in women with PCOS.
A post-hoc analysis was performed of two randomized controlled trials, PregMet and PregMet2, including longitudinal maternal serum samples from 615 women with PCOS. Women were randomized to metformin or placebo from first trimester to delivery. Twenty-two cytokines and C-reactive protein were measured in serum sampled at gestational weeks 5 to 12, 19, 32, and 36.
Metformin treatment was associated with higher serum levels of several multifunctional cytokines throughout pregnancy, with the strongest effect on eotaxin (P < .001), interleukin-17 (P = .03), and basic fibroblast growth factor (P = .04). Assessment of the combined cytokine development confirmed the impact of metformin on half of the 22 cytokines. The immunomodulating effect of metformin was more potent in normal weight and overweight women than in obese women. Moreover, normoandrogenic women had the strongest effect of metformin in early pregnancy, whereas hyperandrogenic women presented increasing effect throughout pregnancy.
It appears that metformin has immunomodulating rather than anti-inflammatory properties in pregnancy. Its effect on the serum levels of many multifunctional cytokines demonstrates robust, persisting, and body mass-dependent immune mobilization in pregnant women with PCOS.
多囊卵巢综合征(PCOS)是一种常见的内分泌疾病,与低水平的全身炎症和妊娠并发症风险增加有关。二甲双胍治疗可降低多囊卵巢综合征孕妇晚期流产和早产的风险。二甲双胍的保护作用是否涉及免疫变化尚未确定。
研究二甲双胍对多囊卵巢综合征妇女母体免疫状态的影响。
对两项随机对照试验(PregMet 和 PregMet2)进行了事后分析,共纳入 615 例多囊卵巢综合征妇女的纵向血清样本。从孕早期到分娩,妇女被随机分配至二甲双胍或安慰剂组。在妊娠 5-12 周、19 周、32 周和 36 周时采集血清,检测 22 种细胞因子和 C 反应蛋白。
二甲双胍治疗与整个孕期多种多功能细胞因子的血清水平升高有关,其中以嗜酸粒细胞趋化因子(eotaxin)(P <.001)、白细胞介素-17(IL-17)(P =.03)和碱性成纤维细胞生长因子(basic fibroblast growth factor,bFGF)(P =.04)的作用最强。对联合细胞因子的评估证实了二甲双胍对 22 种细胞因子中的一半的影响。二甲双胍的免疫调节作用在正常体重和超重妇女中比肥胖妇女更强。此外,正常雄激素妇女在孕早期的二甲双胍作用最强,而高雄激素妇女在整个孕期的作用呈递增趋势。
二甲双胍在妊娠期间似乎具有免疫调节而非抗炎特性。它对多种多功能细胞因子血清水平的影响表明,多囊卵巢综合征孕妇存在强大、持续且依赖于体重的免疫动员。