Action Mechanisms of Metformin Combined with Exenatide and Metformin Only in the Treatment of PCOS in Obese Patients

IF 2.3 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Jingwen Gan, Jie Chen, Rui-lin Ma, Yan Deng, Xue-song Ding, Shi-yang Zhu, Ai-jun Sun
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Abstract

Background. Polycystic ovary syndrome (PCOS) is the most common endocrine disease in women of reproductive age, whose clinical characteristics are hyperandrogenism (HA), ovulatory dysfunction, and polycystic ovary, often accompanied by insulin resistance (IR) and metabolic abnormalities. Glucagon-like peptide (GLP)-1 receptor agonists (GLP-1Ra), such as exenatide, can bind to specific receptors on tissues such as the ovaries to improve the clinical phenotype of PCOS, while insulin-sensitizing agents, such as metformin, can also benefit to metabolic abnormalities in PCOS. Liquid chromatography-mass spectrometry (LC/MS) metabolomics revealed differences between the mechanisms of exenatide and metformin treatment of PCOS to some extent. Methods. In this study, 50 obese subjects with PCOS were randomly divided into the exenatide combined with metformin group (COM group, n = 28) and the metformin group (MF group, n = 22) for 12-week treatment. Before and after, serum samples were subjected to LC/MS analysis. Results. After treatment, there were 153 named differential metabolites in the COM group and 99 in the MF group. Most phosphatidylcholines (PC) and deoxycholic acid 3-glucuronide (DA3G) were significantly upregulated, while most glycerophosphoethanolamine (PE-NMe2), glycerophosphocholine (GPC), and threonine were downregulated in both groups. Only the decrease of neuromedin B, glutamate, and glutamyl groups and the increase of chenodeoxycholic acid sulfate docosadienoate (22: 2n6), and prostaglandin E2 have been observed in the COM group. In addition, salicylic acid and spisulosine increased and decanoylcarnitine decreased in the MF group. Both groups were enriched in glycerophospholipid, choline, and sphingolipid metabolism, while the COM group was especially superior in the glutamine and glutamate, bile secretion, and amino acid metabolism. Conclusion. Compared with metformin alone in the treatment of PCOS, the differential metabolites of the exenatide combined with metformin group are more extensive. The COM group may act on the hypothalamic-pituitary-gonadal axis (HPO) and its bypass, regulate multiple metabolism pathways such as phospholipids, amino acids, fatty acids, carnitine, bile acids, and glucose directly or indirectly in obese PCOS patients.
二甲双胍联合艾塞那肽与仅使用二甲双胍治疗肥胖患者多囊卵巢综合征的作用机制
背景。多囊卵巢综合征(Polycystic ovarian syndrome, PCOS)是育龄妇女最常见的内分泌疾病,其临床特征为雄激素分泌过多(hyperandrogenism, HA)、排卵功能障碍、多囊卵巢,常伴有胰岛素抵抗(insulin resistance, IR)和代谢异常。胰高血糖素样肽(GLP)-1受体激动剂(GLP- 1ra)如艾塞那肽可与卵巢等组织上的特异性受体结合,改善PCOS的临床表型,而胰岛素增敏剂如二甲双胍也可有益于PCOS的代谢异常。液相色谱-质谱(LC/MS)代谢组学分析显示艾塞那肽与二甲双胍治疗PCOS的作用机制存在一定差异。方法。本研究将50例肥胖多囊卵巢综合征患者随机分为艾塞那肽联合二甲双胍组(COM组,n = 28)和二甲双胍组(MF组,n = 22),治疗12周。前后血清样品进行LC/MS分析。结果。治疗后,COM组有153个命名的差异代谢物,MF组有99个。两组中大部分磷脂酰胆碱(PC)和脱氧胆酸3-葡糖苷(DA3G)均显著上调,而大部分甘油磷酸乙醇胺(PE-NMe2)、甘油磷酸胆碱(GPC)和苏氨酸均下调。COM组仅神经素B、谷氨酸、谷氨酰基降低,硫酸鹅去氧胆酸(22:22 . 6)、前列腺素E2升高。此外,MF组水杨酸和葡聚糖含量升高,十二烷基肉碱含量降低。两组的甘油磷脂、胆碱和鞘脂代谢均丰富,而COM组在谷氨酰胺和谷氨酸、胆汁分泌和氨基酸代谢方面尤为突出。结论。与单用二甲双胍治疗PCOS相比,艾塞那肽联合二甲双胍组差异代谢物更广泛。COM组可能作用于下丘脑-垂体-性腺轴(HPO)及其旁路,直接或间接调节肥胖PCOS患者的磷脂、氨基酸、脂肪酸、肉碱、胆汁酸、葡萄糖等多种代谢途径。
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来源期刊
International Journal of Endocrinology
International Journal of Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
5.20
自引率
0.00%
发文量
147
审稿时长
1 months
期刊介绍: International Journal of Endocrinology is a peer-reviewed, Open Access journal that provides a forum for scientists and clinicians working in basic and translational research. The journal publishes original research articles, review articles, and clinical studies that provide insights into the endocrine system and its associated diseases at a genomic, molecular, biochemical and cellular level.
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