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首页> 外文期刊>Archives of dermatological research. >Effect of etanercept on insulin secretion and insulin sensitivity in a randomized trial with psoriatic patients at risk for developing type 2 diabetes mellitus.
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Effect of etanercept on insulin secretion and insulin sensitivity in a randomized trial with psoriatic patients at risk for developing type 2 diabetes mellitus.

机译:牛皮癣患者有发生2型糖尿病风险的一项随机试验中,依那西普对胰岛素分泌和胰岛素敏感性的影响。

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Tumor necrosis factor-alpha (TNF-alpha) inhibitors have been used in the treatment of psoriasis, which is associated with the insulin resistance syndrome. The purpose of this study was to determine the effect of etanercept, a TNF-alpha inhibitor, on insulin secretion and insulin sensitivity in psoriatic patients with high risk factors to develop type 2 diabetes mellitus. Randomized double blind clinical trial with 2 weeks of follow-up. The allocation was done by simple randomization. The investigation was performed in 12 psoriatic patients with indication of systemic treatment and 2 or more risk factors for type 2 diabetes mellitus. Patients with infections, topical corticosteroids or salicylic acid ointments for 6 weeks before the study, diabetes, acromegaly, cancer and other systemic diseases were excluded. All subjects gave written informed consent to participate in the study and the protocol was approved by the hospital-based Ethical Committee. Etanercept was injected in a subcutaneous dose of 25 mg in 1 ml twice by week for 2 weeks or 1 ml of saline solution as placebo. Insulin secretion was estimated with the formula for the homeostasis model analysis beta-cell function index and insulin sensitivity was assessed using the euglycemic-hyperinsulinemic clamp technique. There was no significant difference in insulin secretion and insulin sensitivity with etanercept. Fasting serum insulin levels were decreased in the etanercept group (146 +/- 117-111 +/- 87 pmol/l, P = 0.04). Etanercept did not modify insulin secretion and insulin sensitivity in psoriatic patients with risk factors for type 2 diabetes mellitus.
机译:肿瘤坏死因子-α(TNF-α)抑制剂已用于治疗牛皮癣,其与胰岛素抵抗综合征有关。这项研究的目的是确定etanercept(一种TNF-α抑制剂)对患有高危因素发展为2型糖尿病的银屑病患者的胰岛素分泌和胰岛素敏感性的影响。随机双盲临床试验,随访2周。通过简单的随机分配进行分配。该研究在12例银屑病患者中进行,这些患者有全身治疗的指征,并且有2个或更多2型糖尿病的危险因素。在研究前6周内有感染,外用皮质类固醇或水杨酸软膏,糖尿病,肢端肥大症,癌症和其他全身性疾病的患者被排除在外。所有受试者均签署了知情同意书以参加研究,并且该方案已由总部位于医院的伦理委员会批准。每周两次以1毫升的皮下剂量注射25毫克的Etanercept,持续2周,或以1毫升的盐溶液作为安慰剂注射。用体内稳态模型分析的公式估算β细胞的胰岛素分泌,用正常血糖-高胰岛素钳夹技术评估胰岛素敏感性。依那西普在胰岛素分泌和胰岛素敏感性方面无显着差异。依那西普组的空腹血清胰岛素水平降低(146 +/- 117-111 +/- 87 pmol / l,P = 0.04)。在具有2型糖尿病危险因素的银屑病患者中,Etanercept不会改变胰岛素分泌和胰岛素敏感性。

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