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非胰岛素依赖型糖尿病患者的非糖尿病一级亲属基础葡萄糖生成和利用增加。

Increased basal glucose production and utilization in nondiabetic first-degree relatives of patients with NIDDM.

作者信息

Osei K

机构信息

Department of Internal Medicine, Ohio State University Hospitals, Columbus.

出版信息

Diabetes. 1990 May;39(5):597-601. doi: 10.2337/diab.39.5.597.

Abstract

To characterize the abnormalities in basal glucose homeostasis in people who are at increased risk for non-insulin-dependent diabetes mellitus (NIDDM), we measured the rates of basal hepatic glucose output (HGO), glucose disappearance, and metabolic clearance of glucose (MCR) in 27 nondiabetic first-degree relatives of NIDDM patients and 16 age-, sex-, and weight-matched healthy control subjects with no family history of NIDDM. Mean fasting plasma glucose was significantly lower (P less than 0.05) in control subjects (mean +/- SE 77 +/- 2 mg/dl) than in relatives (84 +/- 2 mg/dl). Mean basal insulin levels were not significantly different between relatives and control subjects (10.0 +/- 1.5 vs. 7.7 +/- 1.0 microU/ml). Mean basal HGO was significantly lower in control subjects compared with relatives (1.83 +/- 0.07 vs. 2.20 +/- 0.10 mg.kg-1.min-1, P less than 0.05). Mean MCR was similar in relatives (2.58 +/- 0.12 mg.kg-1.min-1) and control subjects (2.35 +/- 0.09 mg.kg-1.min-1). In summary, this study demonstrates that basal hepatic glucose production and glucose utilization are increased in glucose-tolerant first-degree relatives compared with healthy control subjects. We conclude that impaired basal hepatic glucose regulation rather than glucose disposal is present as an early defect in glucose-tolerant first-degree relatives of NIDDM patients.

摘要

为了描述非胰岛素依赖型糖尿病(NIDDM)风险增加人群基础葡萄糖稳态的异常情况,我们测量了27名NIDDM患者的非糖尿病一级亲属以及16名年龄、性别和体重匹配且无NIDDM家族史的健康对照者的基础肝葡萄糖输出(HGO)率、葡萄糖消失率和葡萄糖代谢清除率(MCR)。对照者的平均空腹血糖(均值±标准误77±2mg/dl)显著低于亲属(84±2mg/dl,P<0.05)。亲属与对照者的平均基础胰岛素水平无显著差异(10.0±1.5对7.7±1.0μU/ml)。与亲属相比,对照者的平均基础HGO显著降低(1.83±0.07对2.20±0.10mg·kg-1·min-1,P<0.05)。亲属(2.58±0.12mg·kg-1·min-1)和对照者(2.35±0.09mg·kg-1·min-1)的平均MCR相似。总之,本研究表明,与健康对照者相比,糖耐量正常的一级亲属的基础肝葡萄糖生成和葡萄糖利用增加。我们得出结论,基础肝葡萄糖调节受损而非葡萄糖处置受损是NIDDM患者糖耐量正常的一级亲属中的早期缺陷。

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