The effect of the new ADA and WHO guidelines on the number of diagnosed cases of diabetes mellitus

被引:13
作者
Jorgensen, LGM [1 ]
Brandslund, I
Petersen, PH
Olivarius, ND
Stahl, M
机构
[1] Vejle Cty Hosp, Lab Ctr, Dept Clin Biochem, DK-7100 Vejle, Denmark
[2] Odense Univ Hosp, Dept Clin Biochem, DK-5000 Odense, Denmark
[3] Univ Copenhagen, Panum Inst, Cent Res Unit Gen Practice, DK-2200 Copenhagen, Denmark
关键词
diabetes mellitus; plasma glucose; capillary blood glucose;
D O I
10.1515/CCLM.2003.191
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
In the new lowered diagnostic discriminator for diabetes mellitus (DM) from the American Diabetes Association (ADA), fasting peripheral venous plasma glucose (fvPG) of 7.0 mmol/l is identical to the 99.9 centile of fvPG (7.05 mmol/l, 95%CI: 6.917.20 mmol/l) in a lowrisk reference population. We investigated its diagnostic concordance with other diagnostic discriminators. As no index test is available for DM we used the ADA discriminator as gold standard. We isolated a lowrisk reference population (n = 424) from a randomised general population (n = 726) by ruling out of all cases with clinical and biochemical risk indicators for DM. We based our analysis on measurements traceable to primary standard concentration, a bias of <1.5% and CV% < 2.5. The distribution of the fasting capillary whole blood glucose (fCBG; mmol/l) in the reference population was ln Gaussian with the 99.9 centile of 6.62 mmol/l (95% CI 6.476.77 mmol/l) and the 97.5 centile of 5.92 mmol/l (5.826.02 mmol/l). The 6.1 mmol/l fCBG WHO limit corresponds approximately to the 97.6 centile, and this limit is thus not traceable to the ADA discriminator, which corresponds to fCBG of 6.4 mmol/l. This is the case in groups only, as recalculation will introduce unpredictable errors. Thus, in our general population a varying number of subjects will be at risk of DM as a mere consequence of different limits. The fCBG limit of 6.1 mmol/l will thus lead to 2.4% falsepositive diagnoses or, in EU, to around 44 x 10(6) adults being diagnosed. The number of cases at risk of DM vary from 5.4 x 10(6) to 44 x 10(6) in EU. We conclude that application of different diagnostic limits results in highly variable number of diagnosed DM cases, and therefore one diagnostic discriminator is needed to provide reproducible diagnoses.
引用
收藏
页码:1246 / 1250
页数:5
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