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利用糖化血红蛋白(HbA1c)提高美国糖尿病协会空腹血糖标准对美国印第安人2型糖尿病的筛查效能:强心研究

Using HbA(1c) to improve efficacy of the american diabetes association fasting plasma glucose criterion in screening for new type 2 diabetes in American Indians: the strong heart study.

作者信息

Wang Wenyu, Lee Elisa T, Fabsitz Richard, Welty Thomas K, Howard Barbara V

机构信息

College of Public Health, University of Oklahoma, Health Sciences Center, Oklahoma City, Oklahoma 73190, USA.

出版信息

Diabetes Care. 2002 Aug;25(8):1365-70. doi: 10.2337/diacare.25.8.1365.

DOI:10.2337/diacare.25.8.1365
PMID:12145236
Abstract

OBJECTIVE

To find an optimal critical line in the fasting plasma glucose (FPG)-HbA(1c) plane for identifying diabetes in participants with impaired fasting glucose (IFG) and thereby improve the efficacy of using FPG alone in diabetes screening among American Indians.

RESEARCH DESIGN AND METHODS

We used FPG, 2-h postload glucose (2hPG), and HbA(1c) measured in the 2,389 American Indians (aged 45-74 years, without diabetes treatment or prior history of diabetes) in the Strong Heart Study (SHS) baseline (second) examination. Participants were classified as having diabetes if they had either FPG > or =126 mg/dl or 2hPG > or =200 mg/dl, as having IFG if they had 110 < or = FPG < 126 mg/dl, and as having normal fasting glucose (NFG) if they had FPG <110, according to the American Diabetes Association (ADA) definition. Logistic regression models were used for identifying diabetes (2hPG > or =200 mg/dl) in IFG participants. The areas under the receiver operating characteristic (ROC) curves generated by different logistic regression models were evaluated and compared to select the best model. A utility function based on the best model and the cost-to-benefit ratio was used to find the optimal critical line. The data from the second examination were used to study the effect of the time interval between the successive diabetes screenings on both the FPG criterion and the optimal critical line.

RESULTS

A total of 37% of all subjects with new diabetes at baseline and 55.2% of those in the second exam had 2hPG > or =200 but FPG <126. There was a very large portion of IFG participants with diabetes (19.3 and 22.9% in the baseline and second exam, respectively). Among the areas under the ROC curves, the area generated by the logistic regression model on FPG plus HbA(1c) is the largest and is significantly larger than that based on FPG (P = 0.0008). For a cost-to-benefit ratio of 0.23888, the optimal critical line that has the highest utility is: 0.89 x HbA(1c) + 0.11 x FPG = 17.92. Those IFG participants whose FPG and HbA(1c) were above or on the line were referred to take an oral glucose tolerance test (OGTT) to diagnose diabetes. The optimal critical line is lower if a successive diabetes screening will be conducted 4 years after the previous screening.

CONCLUSIONS

FPG > or =126 and 2hPG > or =200, as suggested by the ADA, are used independently to define diabetes. The FPG level is easy to obtain, and using FPG alone is suggested for diabetes screening. It is difficult to get physicians and patients to perform an OGTT to get a 2hPG level because of the many drawbacks of the OGTT, especially in those patients who already have FPG <126. It is also impractical to conduct an OGTT for everyone in a diabetes screening. Our data show that 37% of all subjects with new diabetes in the SHS baseline exam and 55.2% of those in the second exam have 2hPG > or =200 but FPG <126. These cases of diabetes cannot be detected if FPG is used alone in a diabetes screening. Therefore, although the small portion of diabetes in the NFG group (4.7% in the baseline and 6.9% in the second exam) may be ignored, those cases of diabetes among IFG participants ( approximately 20% in our data) need further consideration in a diabetes screening. It may be worthwhile for those IFG participants identified by the optimal critical line to take an OGTT. The optimal critical line and time interval between successive diabetes screenings need further study.

摘要

目的

在空腹血糖(FPG)-糖化血红蛋白(HbA₁c)平面中找到一条最佳临界线,用于识别空腹血糖受损(IFG)参与者中的糖尿病患者,从而提高仅使用FPG在美国印第安人糖尿病筛查中的效果。

研究设计与方法

我们采用了在强心研究(SHS)基线(第二次)检查中对2389名美国印第安人(年龄45 - 74岁,未接受糖尿病治疗且无糖尿病病史)测量的FPG、服糖后2小时血糖(2hPG)和HbA₁c。根据美国糖尿病协会(ADA)的定义,如果参与者的FPG≥126mg/dl或2hPG≥200mg/dl,则被分类为患有糖尿病;如果110≤FPG<126mg/dl,则被分类为患有IFG;如果FPG<110,则被分类为空腹血糖正常(NFG)。使用逻辑回归模型识别IFG参与者中的糖尿病(2hPG≥200mg/dl)。评估并比较不同逻辑回归模型生成的受试者工作特征(ROC)曲线下的面积,以选择最佳模型。基于最佳模型和成本效益比的效用函数用于找到最佳临界线。第二次检查的数据用于研究连续糖尿病筛查之间的时间间隔对FPG标准和最佳临界线的影响。

结果

在基线时所有新诊断糖尿病的受试者中,共有37%以及在第二次检查中55.2%的受试者2hPG≥200但FPG<126。IFG参与者中糖尿病患者的比例非常高(基线和第二次检查中分别为19.3%和22.9%)。在ROC曲线下的面积中,基于FPG加HbA₁c的逻辑回归模型生成的面积最大,且显著大于基于FPG的面积(P = 0.0008)。对于成本效益比为0.23888,效用最高的最佳临界线为:0.89×HbA₁c + 0.11×FPG = 17.92。那些FPG和HbA₁c高于或在该线之上的IFG参与者被建议进行口服葡萄糖耐量试验(OGTT)以诊断糖尿病。如果在前一次筛查后4年进行连续糖尿病筛查,最佳临界线会更低。

结论

ADA建议的FPG≥126和2hPG≥200被独立用于定义糖尿病。FPG水平易于获得,建议仅使用FPG进行糖尿病筛查。由于OGTT存在诸多缺点,尤其是在那些FPG<126的患者中,很难让医生和患者进行OGTT以获得2hPG水平。在糖尿病筛查中对每个人都进行OGTT也是不切实际的。我们的数据显示,在SHS基线检查中所有新诊断糖尿病的受试者中,37%以及在第二次检查中55.2%的受试者2hPG≥200但FPG<126。如果在糖尿病筛查中仅使用FPG,则这些糖尿病病例无法被检测到。因此,尽管NFG组中糖尿病的小部分(基线时为4.7%,第二次检查时为6.9%)可能被忽略,但IFG参与者中的那些糖尿病病例(我们数据中约为20%)在糖尿病筛查中需要进一步考虑。对于由最佳临界线识别出的那些IFG参与者进行OGTT可能是值得的。最佳临界线和连续糖尿病筛查之间的时间间隔需要进一步研究。

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