Department of Endocrinology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, J&K, India.
Department of Endocrinology, Metabolism and Diabetes, All India Institute of Medical Sciences, New Delhi, India.
Gynecol Endocrinol. 2020 Apr;36(4):308-312. doi: 10.1080/09513590.2019.1675044. Epub 2019 Nov 8.
The aim of this study was to compare the efficacy and safety of adding metformin or spironolactone to rosiglitazone in women with polycystic ovary syndrome (PCOS). This is a prospective non-randomized study in a tertiary care with at in a tertiary care endocrine clinic. Women ( = 138) diagnosed with PCOS on the basis of Rotterdam criteria 2003 were categorized into three groups on the basis of drug intake as - rosiglitazone (R), rosiglitazone with spironolactone (R + S), and rosiglitazone with metformin (R + M). Clinical, biochemical, hormonal, and insulin sensitivity parameters were assessed at baseline and after six months of follow up. There was a significant improvement in number of menstrual cycles per year and Ferriman Gallwey (FG) score in all three groups after 6 months. Plasma insulin (0, 2 h), HOMA-IR and serum total testosterone levels decreased after six months in all the three groups. The inter group comparison showed higher efficacy of R + S in improving hyperandrogenism whereas R + M was most effective in decreasing body weight and plasma insulin levels compared to R and R + S (<.05). Treatment of women with PCOS using rosiglitazone alone and in combination with spironolactone or metformin is safe and efficacious with limited adverse events however randomized trials with longer duration of follow up are warranted.
本研究旨在比较在多囊卵巢综合征(PCOS)妇女中添加二甲双胍或螺内酯与罗格列酮的疗效和安全性。这是一项在三级保健内分泌诊所进行的前瞻性非随机研究。根据 2003 年鹿特丹标准诊断为 PCOS 的妇女(n=138),根据药物摄入分为三组:罗格列酮(R)、罗格列酮加螺内酯(R+S)和罗格列酮加二甲双胍(R+M)。基线和随访 6 个月时评估临床、生化、激素和胰岛素敏感性参数。所有三组在 6 个月后,月经周期数和 Ferriman-Gallwey(FG)评分均显著改善。所有三组的血浆胰岛素(0、2 h)、HOMA-IR 和血清总睾酮水平在 6 个月后均降低。组间比较显示,R+S 组在改善高雄激素血症方面更有效,而与 R 和 R+S 相比,R+M 更有效地降低体重和血浆胰岛素水平(<.05)。单独使用罗格列酮以及与螺内酯或二甲双胍联合治疗 PCOS 妇女是安全有效的,不良反应有限,但需要进行随访时间更长的随机试验。