Singh Surjit, Bhansali Anil
Department of Pharmacology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
Department of Endocrinology, Postgraduate Institute of Medical Education and Research, Chandigarh, Punjab, India.
Indian J Endocrinol Metab. 2017 Jul-Aug;21(4):581-587. doi: 10.4103/ijem.IJEM_46_17.
Psoriasis has been found to be associated with obesity, metabolic syndrome (MS), diabetes, and cardiovascular risk factors. Metformin treatment showed improvement in cardiovascular risk factors and hyperinsulinemia.
To evaluate the efficacy and safety of metformin in psoriasis patients with MS.
This was a single-center, parallel-group, randomized, open-label study with blinded end point assessment of metformin (1000 mg once daily for 12 weeks; = 20) and placebo ( = 18) in psoriasis patients with MS. Total sample size was 38 participants.
Statistically significant improvement was observed in mean percentage change in erythema, scaling, and induration (ESI) ( = 0.048) in metformin as compared to placebo while mean percentage change in psoriasis area and severity index (PASI) and physician global assessment (PGA) scores was not significant (PASI - = 0.215, PGA - = 0.070). There was a statistically significant difference in percentage of parameters of MS improved following 12 weeks of treatment in metformin (19%) as compared to placebo (8.9%) group ( = 0.046). Statistically significant difference in percentage of patients achieving 75% reduction in ESI scores ( = 0.024). Significant improvement was observed in mean weight, body mass index (BMI), total cholesterol, and low-density lipoprotein (LDL) cholesterol in metformin group as compared to placebo. Improvement in BMI, fasting plasma glucose, serum triglycerides, high-density lipoprotein, LDL, systolic blood pressure, diastolic blood pressure, and total cholesterol was statistically significant in metformin group over the period of 12 weeks. There was no significant difference in adverse events in two groups except weight gain.
Metformin has shown improvement in psoriasis and parameters of MS, hence can be used for the benefit of psoriasis patients having MS. Large, controlled studies are needed to confirm.
已发现银屑病与肥胖、代谢综合征(MS)、糖尿病及心血管危险因素相关。二甲双胍治疗可改善心血管危险因素及高胰岛素血症。
评估二甲双胍对合并MS的银屑病患者的疗效及安全性。
这是一项单中心、平行组、随机、开放标签研究,对合并MS的银屑病患者采用二甲双胍(每日1000 mg,共12周;n = 20)和安慰剂(n = 18)进行治疗,并对终点进行盲法评估。总样本量为38名参与者。
与安慰剂相比,二甲双胍治疗后红斑、鳞屑和硬结(ESI)的平均百分比变化有统计学显著改善(P = 0.048),而银屑病面积和严重程度指数(PASI)及医生整体评估(PGA)评分的平均百分比变化无显著差异(PASI - P = 0.215,PGA - P = 0.070)。治疗12周后,二甲双胍组(19%)MS参数改善的百分比与安慰剂组(8.9%)相比有统计学显著差异(P = 0.046)。达到ESI评分降低75%的患者百分比有统计学显著差异(P = 0.024)。与安慰剂相比,二甲双胍组的平均体重、体重指数(BMI)、总胆固醇和低密度脂蛋白(LDL)胆固醇有显著改善。在12周期间,二甲双胍组的BMI、空腹血糖、血清甘油三酯、高密度脂蛋白、LDL、收缩压、舒张压和总胆固醇的改善有统计学显著意义。除体重增加外,两组不良事件无显著差异。
二甲双胍已显示出对银屑病及MS参数有改善作用,因此可用于合并MS的银屑病患者。需要大型对照研究来证实。