Singh Surjit, Bhansali Anil
Department of Pharmacology, All India Institute of Medical Sciences (AIIMS), Jodhpur, 342005, India.
Department of Endocrinology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, 160012, India.
BMC Dermatol. 2016 Aug 17;16(1):12. doi: 10.1186/s12895-016-0049-y.
Increased prevalence of metabolic syndrome (MS) is observed in psoriasis. Metformin has shown improvement in cardiovascular risk factors while pioglitazone demonstrated anti proliferative, anti-inflammatory and anti angiogenic effects. Study objective is to evaluate the efficacy and safety of Insulin sensitizers (metformin and pioglitazone) in psoriasis patients with metabolic syndrome (MS).
Single centre, parallel group, randomized, study of metformin, pioglitazone and placebo in psoriasis patients with MS.
Statistically significant improvement was observed in Psoriasis Area and Severity Index (PASI), Erythema, Scaling and Induration (ESI) and Physician global assessment (PGA) scores in pioglitazone (p values - PASI = 0.001, ESI = 0.002, PGA = 0.008) and metformin groups (p values - PASI = 0.001, ESI = 0.016, PGA = 0.012) as compared to placebo. There was statistically significant difference in percentage of patients achieving 75 % reduction in PASI and ESI scores in metformin (p value - PASI = 0.001, ESI = 0.001) and pioglitazone groups (p vaue - PASI = 0.001, ESI = 0.001). Significant improvement was observed in fasting plasma glucose (FPG) and triglycerides levels in metformin and pioglitazone arms. Significant improvement was noted in weight, BMI, waist circumference, FPG, triglycerides and total cholesterol after 12 weeks of treatment with metformin while pioglitazone showed improvement in FPG, triglyceride levels, systolic blood pressure (SBP), diastolic blood pressure (DBP), total cholesterol and LDL cholesterol levels. There was no difference in pattern of adverse drug reaction in three groups.
Insulin sensitizers have shown improvement in the parameters of MS as well as disease severity in psoriasis patients.
CTRI Registration Number: CTRI/2011/12/002252 . Registered on 19/12/2011.
银屑病患者中代谢综合征(MS)的患病率有所增加。二甲双胍已显示出对心血管危险因素有改善作用,而吡格列酮则具有抗增殖、抗炎和抗血管生成作用。本研究的目的是评估胰岛素增敏剂(二甲双胍和吡格列酮)对患有代谢综合征(MS)的银屑病患者的疗效和安全性。
在患有MS的银屑病患者中进行单中心、平行组、随机的二甲双胍、吡格列酮和安慰剂研究。
与安慰剂相比,吡格列酮组(p值 - PASI = 0.001,ESI = 0.002,PGA = 0.008)和二甲双胍组(p值 - PASI = 0.001,ESI = 0.016,PGA = 0.012)的银屑病面积和严重程度指数(PASI)、红斑、鳞屑和硬结(ESI)以及医生整体评估(PGA)评分有统计学意义的改善。在二甲双胍组(p值 - PASI = 0.001,ESI = 0.001)和吡格列酮组(p值 - PASI = 0.001,ESI = 0.001)中,达到PASI和ESI评分降低75%的患者百分比有统计学意义的差异。二甲双胍和吡格列酮组的空腹血糖(FPG)和甘油三酯水平有显著改善。二甲双胍治疗12周后,体重、BMI、腰围、FPG、甘油三酯和总胆固醇有显著改善,而吡格列酮则使FPG、甘油三酯水平、收缩压(SBP)、舒张压(DBP)、总胆固醇和低密度脂蛋白胆固醇水平有所改善。三组的药物不良反应模式没有差异。
胰岛素增敏剂已显示出对MS参数以及银屑病患者疾病严重程度有改善作用。
CTRI注册号:CTRI/2011/12/002252。于2011年12月19日注册。