OBJECTIVE - To examine the influence of glycemic and nonglycemic parameters on HbA 1c concentrations in young adults, the majority of whom had normal glucose tolerance. RESEARCH DESIGN AND METHODS - We compared the diagnosis of normal glucose tolerance, prediabetes, and diabetes between a standard oral glucose tolerance test (OGTT; World Health Organization 2006 criteria) and HbA 1c concentrations (American Diabetes Association [ADA] 2009 criteria) in 116 young adults (average age 21.6 years) from the Pune Children's Study. We also studied the contribution of glycemic and nonglycemic determinants to HbA 1c concentrations. RESULTS - The OGTT showed that 7.8% of participants were prediabetic and 2.6% were diabetic. By ADA HbA 1c criteria, 23.3% were prediabetic and 2.6% were diabetic. The negative predictive value of HbA 1c was 93% and the positive predictive value was 20% (only 20% had prediabetes or diabetes according to the OGTT; this figure was 7% in anemic participants). Of participants, 34% were anemic, 37% were iron deficient (ferritin < 15 ng/mL), 40% were vitamin B 12 deficient (<150 pmol/L), and 22% were folate deficient (<7 nmol/L). On multiple linear regression analysis, HbA 1c was predicted by higher 2-h glucose (R 2 = 25.6%) and lower hemoglobin (R 2 = 7.7%). When hematological parameters were replaced by ferritin, vitamin B 12, and folate, HbA 1c was predicted by higher glycemia (R 2 = 25.6%) and lower ferritin (R 2 = 4.3%). CONCLUSIONS - The use of HbA 1c to diagnose prediabetes and diabetes in iron-deficient populations may lead to a spuriously exaggerated prevalence. Further investigation is required before using HbA 1c as a screening tool in nutritionally compromised populations. © 2012 by the American Diabetes Association.
CITATION STYLE
Hardikar, P. S., Joshi, S. M., Bhat, D. S., Raut, D. A., Katre, P. A., Lubree, H. G., … Yajnik, C. S. (2012). Spuriously high prevalence of prediabetes diagnosed by HbA 1c in young Indians partly explained by hematological factors and iron deficiency anemia. Diabetes Care, 35(4), 797–802. https://doi.org/10.2337/dc11-1321
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