Javed Zeeshan, Papageorgiou Maria, Madden Leigh A, Rigby Alan S, Kilpatrick Eric S, Atkin Stephen L, Sathyapalan Thozhukat
Department of Academic Diabetes, Endocrinology and Metabolism, Hull York Medical School, University of Hull, Hull, UK.
Department of Endocrinology and Diabetes, Pakistan Kidney and Liver Institute and Research Centre, Knowledge City, Lahore, Pakistan.
Endocr Connect. 2020 Jun;9(6):563-569. doi: 10.1530/EC-20-0173.
Endothelial microparticles (EMPs) are novel, surrogate biomarkers of endothelial function and have been shown to be elevated in women with polycystic ovary syndrome (PCOS). It remains poorly understood how pharmacological options for managing PCOS affect EMP levels.
To characterise and compare the effects of empagliflozin vs metformin on the circulating levels of EMPs in overweight/obese women with PCOS.
This was a randomised, comparative, 12-week single-centre trial conducted at the Academic Diabetes, Endocrinology and Metabolism Research Centre, Hull, UK. This analysis includes data from 39 overweight/obese women with PCOS who completed the study and were randomised to empagliflozin (15 mg/day) (n = 19) or metformin (1500 mg/day) (n = 20). Blood samples were collected at baseline and 12 weeks after treatment and analysed for specific surface proteins (ICAM-1, VCAM-1, PECAM-1, E-selectin and endoglin) expressed by circulating EMPs using flow cytometry.
In the empagliflozin group, ICAM-1 (P = 0.006), E-selectin (P = 0.016) and VCAM-1 (P = 0.001) EMPs increased significantly following 12 weeks of treatment, but no changes were seen in PECAM-1 (P = 0.93) or endoglin (P = 0.13) EMPs. In the metformin group, VCAM-1 EMPs (P < 0.001) increased significantly after 12 weeks of treatment, whereas all other EMPs remained unchanged. When data were expressed as percentage change from baseline in each group, no significant differences were seen between groups for any biomarker (P-values from 0.22 to 0.80).
Short-term administration of empagliflozin and metformin in overweight/obese women with PCOS appear to increase EMPs expressed by endothelial cells during their activation.
内皮微粒(EMPs)是内皮功能的新型替代生物标志物,已证明在多囊卵巢综合征(PCOS)女性中水平升高。目前对于治疗PCOS的药物选择如何影响EMPs水平仍知之甚少。
表征并比较恩格列净与二甲双胍对超重/肥胖PCOS女性循环中EMPs水平的影响。
这是一项在英国赫尔学术糖尿病、内分泌与代谢研究中心进行的为期12周的随机、对照、单中心试验。该分析纳入了39名完成研究并被随机分配至恩格列净组(15毫克/天)(n = 19)或二甲双胍组(1500毫克/天)(n = 20)的超重/肥胖PCOS女性的数据。在基线和治疗12周后采集血样,使用流式细胞术分析循环EMPs表达的特定表面蛋白(ICAM-1、VCAM-1、PECAM-1、E-选择素和内皮糖蛋白)。
在恩格列净组,治疗12周后ICAM-1(P = 0.006)、E-选择素(P = 0.016)和VCAM-1(P = 0.001)EMPs显著增加,但PECAM-1(P = 0.93)或内皮糖蛋白(P = 0.13)EMPs未见变化。在二甲双胍组,治疗12周后VCAM-1 EMPs(P < 0.001)显著增加,而所有其他EMPs保持不变。当数据表示为每组相对于基线的百分比变化时,各生物标志物在组间均无显著差异(P值范围为0.22至0.80)。
在超重/肥胖PCOS女性中短期给予恩格列净和二甲双胍似乎会增加内皮细胞激活时表达的EMPs。