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从新出现的空腹血糖受损进展为2型糖尿病。

Progression from newly acquired impaired fasting glusose to type 2 diabetes.

作者信息

Nichols Gregory A, Hillier Teresa A, Brown Jonathan B

机构信息

Center for Health Research, 3800 N. Interstate Avenue, Portland, OR 97227-1098, USA.

出版信息

Diabetes Care. 2007 Feb;30(2):228-33. doi: 10.2337/dc06-1392.

Abstract

OBJECTIVE

We sought to estimate the rate of progression from newly acquired (incident) impaired fasting glucose (IFG) to diabetes under the old and new IFG criteria and to identify predictors of progression to diabetes.

RESEARCH DESIGN AND METHODS

We identified 5,452 members of an HMO with no prior history of diabetes, with at least two elevated fasting glucose tests (100-125 mg/dl) measured between 1 January 1994 and 31 December 2003, and with a normal fasting glucose test before the two elevated tests. All data were obtained from electronic records of routine clinical care. Subjects were followed until they developed diabetes, died, left the health plan, or until 31 December 2005.

RESULTS

Overall, 8.1% of subjects whose initial abnormal fasting glucose was 100-109 mg/dl (added IFG subjects) and 24.3% of subjects whose initial abnormal fasting glucose was 110-125 mg/dl (original IFG subjects) developed diabetes (P < 0.0001). Added IFG subjects who progressed to diabetes did so within a mean of 41.4 months, a rate of 1.34% per year. Original IFG subjects converted at a rate of 5.56% per year after an average of 29.0 months. A steeper rate of increasing fasting glucose; higher BMI, blood pressure, and triglycerides; and lower HDL cholesterol predicted diabetes development.

CONCLUSIONS

To our knowledge, these are the first estimates of diabetes incidence from a clinical care setting when the date of IFG onset is approximately known under the new criterion for IFG. The older criterion was more predictive of diabetes development. Many newly identified IFG patients progress to diabetes in <3 years, which is the currently recommended screening interval.

摘要

目的

我们试图根据旧的和新的空腹血糖受损(IFG)标准,估算新获得(新发)的IFG进展为糖尿病的发生率,并确定进展为糖尿病的预测因素。

研究设计与方法

我们在一个健康维护组织(HMO)中识别出5452名无糖尿病既往史的成员,他们在1994年1月1日至2003年12月31日期间至少有两次空腹血糖检测值升高(100 - 125mg/dl),且在两次升高检测之前空腹血糖检测正常。所有数据均从常规临床护理的电子记录中获取。对受试者进行随访,直至其患糖尿病、死亡、退出健康计划或至2005年12月31日。

结果

总体而言,初始空腹血糖异常为100 - 109mg/dl的受试者(新增IFG受试者)中有8.1%发展为糖尿病,初始空腹血糖异常为110 - 125mg/dl的受试者(原IFG受试者)中有24.3%发展为糖尿病(P < 0.0001)。进展为糖尿病的新增IFG受试者平均在41.4个月内发生,年发生率为1.34%。原IFG受试者平均在29.0个月后年转化率为5.56%。空腹血糖上升速度更快、体重指数(BMI)、血压和甘油三酯更高以及高密度脂蛋白胆固醇更低可预测糖尿病的发生。

结论

据我们所知,这是在IFG新诊断标准下大致已知IFG发病日期时,首次从临床护理环境中对糖尿病发病率进行的估算。旧标准对糖尿病发展的预测性更强。许多新诊断的IFG患者在不到3年的时间里进展为糖尿病,而3年正是目前推荐的筛查间隔时间。

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