DETERMINING DIABETES PREVALENCE - A RATIONAL BASIS FOR THE USE OF FASTING PLASMA-GLUCOSE CONCENTRATIONS

被引:70
作者
FINCH, CF
ZIMMET, PZ
ALBERTI, KGMM
机构
[1] Lions-International Diabetes Institute, Melbourne
[2] Department of Medicine, University of Newcastle Upon Tyne
关键词
Diabetes mellitus; Diagnostic cut‐off; Fasting plasma glucose; Prevalence estimate;
D O I
10.1111/j.1464-5491.1990.tb01457.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The World Health Organization and the National Diabetes Data Group each recommend a diagnostic cut‐off point for diabetes of 7.8 mmol l−1 for fasting plasma glucose concentrations as part of the diagnostic criteria for epidemiological studies. However, this cut‐off has been shown to be insensitive compared with a screening test based on 2‐h plasma glucose levels. In thirteen Pacific populations, from four ethnic groups (Asian Indian, Melanesian, Micronesian, and Polynesian), we have examined whether a different cut‐off point for fasting plasma glucose would be more accurate for obtaining an estimate of the prevalence of diabetes when compared with 2‐h levels. A fasting plasma glucose diagnostic cut‐off of 7.0 mmol l−1 gave an estimate of prevalence not significantly different from that based on the 2‐h plasma glucose in 12 of the 13 populations (mean difference 0.27, range −1.51 to +2.44,%). On the other hand, when a cut‐off of 7.8 mmol l−1 for fasting plasma glucose was used, the resulting prevalence over‐estimated the 2‐h glucose prevalence in all populations (mean difference 1.91, range 0.14–5.80,%). Thus for Pacific populations, a fasting plasma glucose cut‐off of 7.0 mmol l−1 provides estimates of prevalence that are equivalent to those based on 2‐h plasma glucose levels. In epidemiological studies designed to estimate diabetes prevalence, we recommend use of a fasting plasma glucose cut‐off of 7.0 mmol l−1 in preference to a detection level of 7.8 mmol l−1, if glucose loading is not possible. The low sensitivity associated with the 7.0 mmol l−1 cut‐off however, precludes its use as a definitive screening test for diabetes, particularly in the clinical setting. 1990 Diabetes UK
引用
收藏
页码:603 / 610
页数:8
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