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血红蛋白A与空腹及餐后2小时血糖检测在高危南印度人群中诊断糖尿病及糖尿病前期的比较

Comparison of Hemoglobin A with Fasting and 2-h Plasma Glucose Tests for Diagnosis of Diabetes and Prediabetes among High-risk South Indians.

作者信息

Radhakrishna Pedapati, Vinod Kolar Vishwanath, Sujiv Akkilagunta, Swaminathan Rathinam Palamalai

机构信息

Department of General Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.

Department of Preventive and Social Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.

出版信息

Indian J Endocrinol Metab. 2018 Jan-Feb;22(1):50-56. doi: 10.4103/ijem.IJEM_254_17.

Abstract

BACKGROUND

Glycosylated hemoglobin (HbA1c) has not been evaluated extensively for diabetes and prediabetes diagnosis and short-term variability of fasting plasma glucose (FPG), 2-h PG post-75 g glucose load (2 hPG) and HbA1c has not been studied among Indians.

OBJECTIVES

The study aimed to compare the sensitivity of HbA1c, FPG and 2 hPG for diabetes and prediabetes diagnosis as per the American Diabetes Association criteria, assess short-term variability of three tests and determine optimal HbA1c cutoffs for diabetes and prediabetes diagnosis among high-risk south Indians.

METHODS

This diagnostic accuracy study, conducted at a tertiary care teaching hospital located in South India, enrolled 332 adults at high risk for diabetes and subjected them to testing (FPG, 2 hPG, and HbA1c) twice at 2-3 weeks interval. Sensitivity of three tests for diagnosing diabetes and prediabetes was determined based on the final diagnosis of normoglycemia/prediabetes/diabetes made with six test results for each participant. Optimal HbA1c cutoffs for diabetes and prediabetes were determined based on the final diagnosis of glycemic status made with four test results of FPG and 2 hPG.

RESULTS

FPG, 2 hPG, and HbA1c, at American Diabetes Association recommended values, had sensitivity of 84.4%, 97%, and 93.8% respectively for diabetes diagnosis. HbA1c had lowest short-term variability (CVw = 1.6%). Receiver operating characteristic curve plotted with mean (of two values) HbA1c for each participant showed optimal HbA1c cutoffs of 6.5% for diabetes (area under curve [AUC] =0.990, sensitivity = 95.8%, specificity = 96.2%, accuracy = 95.2%) and 5.9% for prediabetes (AUC = 0.893, sensitivity = 84.3%, specificity = 80%, accuracy = 75.6%) diagnosis respectively. HbA1c <5.6% had 100% negative predictive value to exclude prediabetes/diabetes.

CONCLUSIONS

HbA1c ≥6.5% is a convenient and reliable alternative to plasma glucose tests to diagnose diabetes among high-risk South Indians. HbA1c ≥5.9% is optimal for prediabetes diagnosis and value <5.6% excludes prediabetes/diabetes.: ADA: American Diabetes Association, AUC: Area under curve, CVw: Within-person coefficient of variation, FPG: Fasting plasma glucose, 2 hPG: Two-hour plasma glucose post-75 g oral glucose load, HbA1c: Glycosylated haemoglobin, IFG: Impaired fasting glucose, IGT: Impaired glucose tolerance, NPV: Negative predictive value, PPV: Positive predictive value; PG: Plasma glucose, ROC: Receiver operating characteristic.

摘要

背景

糖化血红蛋白(HbA1c)尚未被广泛用于糖尿病和糖尿病前期的诊断,且印度人群中空腹血糖(FPG)、75克葡萄糖负荷后2小时血糖(2hPG)和HbA1c的短期变异性尚未得到研究。

目的

本研究旨在根据美国糖尿病协会标准比较HbA1c、FPG和2hPG对糖尿病和糖尿病前期诊断的敏感性,评估这三项检测的短期变异性,并确定高危南印度人群中糖尿病和糖尿病前期诊断的最佳HbA1c临界值。

方法

这项诊断准确性研究在印度南部的一家三级护理教学医院进行,招募了332名糖尿病高危成年人,并让他们每隔2 - 3周接受两次检测(FPG、2hPG和HbA1c)。根据每位参与者的六项检测结果做出的正常血糖/糖尿病前期/糖尿病的最终诊断,确定这三项检测对糖尿病和糖尿病前期诊断的敏感性。基于FPG和2hPG的四项检测结果做出的血糖状态最终诊断,确定糖尿病和糖尿病前期的最佳HbA1c临界值。

结果

按照美国糖尿病协会推荐值,FPG、2hPG和HbA1c对糖尿病诊断的敏感性分别为84.4%、97%和93.8%。HbA1c的短期变异性最低(个体内变异系数[CVw]=1.6%)。用每位参与者的平均(两个值)HbA1c绘制的受试者工作特征曲线显示,糖尿病的最佳HbA1c临界值为6.5%(曲线下面积[AUC]=0.990,敏感性=95.8%,特异性=96.2%,准确性=95.2%),糖尿病前期的最佳HbA1c临界值为5.9%(AUC = 0.893,敏感性=84.3%,特异性=80%,准确性=75.6%)。HbA1c<5.6%对排除糖尿病前期/糖尿病具有100%的阴性预测值。

结论

对于高危南印度人群中的糖尿病诊断,HbA1c≥6.5%是一种方便且可靠的替代血浆葡萄糖检测的方法。HbA1c≥5.9%对糖尿病前期诊断最佳,<5.6%的值可排除糖尿病前期/糖尿病。:ADA:美国糖尿病协会,AUC:曲线下面积,CVw:个体内变异系数,FPG:空腹血糖,2hPG:75克口服葡萄糖负荷后两小时血浆葡萄糖,HbA1c:糖化血红蛋白,IFG:空腹血糖受损,IGT:糖耐量受损,NPV:阴性预测值,PPV:阳性预测值;PG:血浆葡萄糖,ROC:受试者工作特征

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94ab/5838911/b65b6f432aa0/IJEM-22-50-g002.jpg

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