Plasma glucose and prediction of microvascular disease and mortality - Evaluation of 1997 American Diabetes Association and 1999 World Health Organization criteria for diagnosis of diabetes
Mm. Gabir et al., Plasma glucose and prediction of microvascular disease and mortality - Evaluation of 1997 American Diabetes Association and 1999 World Health Organization criteria for diagnosis of diabetes, DIABET CARE, 23(8), 2000, pp. 1113-1118
OBJECTIVE - The 1997 American Diabetes Association (ADA) and 1999 World Hea
lth Organization (WHO) criteria for diabetes and hyperglycemia were evaluat
ed and compared with respect to prediction of microvascular and macrovascul
ar disease and mortality.
RESEARCH DESIGN AND METHODS - The prevalence of retinopathy and nephropathy
at baseline and during the subsequent 10 years and mortality rates were ex
amined in relation to baseline fasting plasma glucose (FPG) and 2-h postloa
d plasma glucose (2-h PG) among 5,023 Pima Indian adults and in relation to
the cut points defined by the ADA and WHO criteria.
RESULTS - The frequencies of retinopathy and nephropathy were directly rela
ted to baseline FPG and 2-h PG with approximate thresholds near or below th
e current diagnostic criteria for diabetes (FPG greater than or equal to 7.
0 and 2-h PG greater than or equal to 11.1 mmol/l). The rates of retinopath
y were 4.7% in impaired fasting glucose (IFG) and 20.9% in diabetes by ADA
criteria; 1.6% for impaired glucose tolerance (IGT) and 19.7% for diabetes
by 1985 WHO criteria; and 1.2% for IGT and 19.2% for diabetes by the 1999 W
HO criteria. Mortality rates from cardiovascular-renal-related diseases wer
e higher in diabetic individuals (FPG greater than or equal to 7.0 or 2-h P
G greater than or equal to 11.1 mmol/l) than in those with normal FPG and 2
-h PG but were not elevated in those with IFG or IGT.
CONCLUSIONS - Retinopathy and nephropathy were directly related to higher F
PG or 2-h PG. FPG, which identifies those at high risk of microvascular dis
ease and mortality, can be used to predict these outcomes and to diagnose d
iabetes when oral glucose tolerance testing is not practical.