首页> 外文期刊>Experimental and clinical endocrinology and diabetes: Official journal, German Society of Endocrinology [and] German Diabetes Association >A pilot study to examine the feasibility of insulin glargine in subjects with impaired fasting glucose, impaired glucose tolerance or new-onset type 2 diabetes.
【24h】

A pilot study to examine the feasibility of insulin glargine in subjects with impaired fasting glucose, impaired glucose tolerance or new-onset type 2 diabetes.

机译:空腹血糖受损,葡萄糖耐量受损或新发2型糖尿病患者中进行甘精胰岛素胰岛素可行性研究的初步研究。

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVE: People with early type 2 diabetes and pre-diabetes (impaired glucose tolerance [IGT] and/or impaired fasting glucose [IFG]) are at risk of hyperglycaemia-related complications, including cardiovascular disease. Insulin, traditionally reserved as late treatment in type 2 diabetes, may also be a useful therapy in this population. We examined the short-term efficacy and tolerability of insulin glargine (glargine) in individuals with early or pre-type 2 diabetes. RESEARCH DESIGN AND METHODS: In this multicentre, double-blind, placebo-controlled, randomized, parallel group, 12-day study, subjects with IGT/IFG (n=9), newly diagnosed type 2 diabetes (n=9) or normal glucose tolerance (n=3) (confined to a clinical research unit taking a prescribed diet) were randomized to once-daily glargine (n=16) or placebo (saline; n=5) at bedtime. Dose was titrated to achieve target fasting blood glucose (FBG) 80-95 mg/dL. RESULTS: Over the treatment period, mean FBG decreased in glargine-treated subjects (from 100.0+/-18.8 to 85.6+/-18.4 mg/dL), but was unchanged in placebo-treated subjects (from 112.5+/-10.6 to 111.3+/-17.5 mg/dL). Mean eight-point blood glucose value decreased by 9.7 mg/dL in the glargine group, but increased by 8.1 mg/dL in the placebo group. Mean post-exercise blood glucose was similar before and after glargine treatment, but increased after placebo treatment. Five subjects receiving glargine experienced 16 mild symptomatic hypoglycaemia episodes; however, no hypoglycaemia occurred during exercise. Mean body weight decreased in both the glargine (-0.44 kg) and placebo (-0.25 kg) groups, in line with dietary restrictions. CONCLUSIONS: The results of this pilot study suggest that glargine can be used by people with IFG, IGT or new-onset type 2 diabetes for management of hyperglycaemia with low risk of hypoglycaemia. However titration of insulin in people on dietary restrictions should be more cautious as they may be more prone to hypoglycaemia. Further studies are warranted to determine the clinical benefits of this approach.
机译:目的:患有早期2型糖尿病和糖尿病前期(糖耐量[IGT]受损和/或空腹血糖[IFG]受损)的人有发生高血糖相关并发症的风险,包括心血管疾病。在2型糖尿病中,传统上被保留为晚期治疗的胰岛素在该人群中也可能是有用的治疗方法。我们研究了甘精胰岛素(甘精胰岛素)对早期或2型糖尿病早期患者的短期疗效和耐受性。研究设计和方法:在这个多中心,双盲,安慰剂对照,随机,平行组,为期12天的研究中,患有IGT / IFG(n = 9),新诊断为2型糖尿病(n = 9)或正常的受试者睡前将葡萄糖耐量(n = 3)(仅限于服用规定饮食的临床研究单位)随机分配到每天一次的甘精胰岛素(n = 16)或安慰剂(盐水; n = 5)。滴定剂量以达到目标空腹血糖(FBG)80-95 mg / dL。结果:在整个治疗期间,甘精胰岛素治疗的受试者的平均FBG降低(从100.0 +/- 18.8降至85.6 +/- 18.4 mg / dL),而安慰剂治疗的受试者的平均FBG则没有变化(从112.5 +/- 10.6降至111.3) +/- 17.5 mg / dL)。甘精胰岛素组的八点平均血糖值下降了9.7 mg / dL,而安慰剂组则上升了8.1 mg / dL。甘精胰岛素治疗前后的平均运动后血糖相似,但安慰剂治疗后平均血糖升高。接受甘精氨酸治疗的五名受试者经历了16次轻度症状性低血糖发作。但是,运动期间没有发生低血糖症。甘精胰岛素(-0.44 kg)和安慰剂(-0.25 kg)组的平均体重均下降,符合饮食限制。结论:这项初步研究的结果表明,IFG,IGT或新发2型糖尿病患者可以使用甘精胰岛素治疗低血糖风险较低的高血糖症。但是,在饮食限制的人中滴定胰岛素应该更加谨慎,因为他们可能更容易发生低血糖症。必须进行进一步的研究以确定这种方法的临床益处。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号