Forrest R D, Jackson C A, Gould B J, Casburn-Budd M, Taylor J E, Yudkin J S
Academic Unit of Diabetes & Endocrinology, Whittington Hospital, London, U.K.
Clin Chem. 1988 Jan;34(1):145-8.
We assessed the utility of four methods of glycated hemoglobin assay (agar gel electrophoresis with Schiff base, agar gel electrophoresis with prior removal of Schiff base, boronate affinity chromatography, and isoelectric focusing) as screening tests for diabetes mellitus, studying 223 subjects undergoing an oral glucose-tolerance test after fasting and 2 h after ingestion of 75 g of glucose. Assessment of glucose tolerance status according to the 1980 World Health Organization diagnostic criteria indicated that 13 subjects (5.8%) had diabetes, 48 (21.5%) had impaired glucose tolerance, and nine (4.0%) could not be classified (six of these because of missing values). Use of receiver-operating characteristic curves to compare the assays as screening tests showed the affinity chromatography assay to be superior. Assays for glycated hemoglobin after fasting had better precision than post-glucose-load assays as screening tests, and test characteristics of glycated hemoglobin assays on fasting subjects were similar to those of the blood-glucose estimation after fasting. We conclude that measurement of glycated hemoglobin may be a useful screening test for diabetes, and that such measurement of stable glycated hemoglobin is as accurate as measurement of fasting blood-glucose in screening for diabetes. For this use, we found methods that measure stable glycated hemoglobin superior to that measuring both stable and labile Schiff-base fractions.
我们评估了四种糖化血红蛋白检测方法(席夫碱琼脂凝胶电泳法、去除席夫碱后的琼脂凝胶电泳法、硼酸亲和色谱法和等电聚焦法)作为糖尿病筛查试验的效用,研究对象为223名在禁食后以及摄入75克葡萄糖2小时后接受口服葡萄糖耐量试验的受试者。根据1980年世界卫生组织诊断标准评估葡萄糖耐量状态,结果显示13名受试者(5.8%)患有糖尿病,48名(21.5%)葡萄糖耐量受损,9名(4.0%)无法分类(其中6名是因为数据缺失)。使用受试者工作特征曲线比较这些检测方法作为筛查试验的结果,显示亲和色谱法检测效果更佳。作为筛查试验,禁食后糖化血红蛋白检测的精密度优于葡萄糖负荷后检测,且禁食受试者糖化血红蛋白检测的试验特征与禁食后血糖测定的特征相似。我们得出结论,糖化血红蛋白检测可能是一种有用的糖尿病筛查试验,并且这种稳定糖化血红蛋白的检测在糖尿病筛查中与空腹血糖检测一样准确。对于此用途,我们发现测量稳定糖化血红蛋白的方法优于测量稳定和不稳定席夫碱组分的方法。