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Ann Intern Med. 2011 Mar 1;154(5):303-9. doi: 10.7326/0003-4819-154-5-201103010-00004.

Racial differences in glycemic markers: a cross-sectional analysis of community-based data.

Author information

  • 1Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland, USA. lselvin@jhsph.edu

Abstract

BACKGROUND:

Although differences between black and white persons in hemoglobin A(1c) (HbA(1c)) values are well established, recent studies suggest that this might not reflect differences in glycemia.

OBJECTIVE:

To investigate racial disparities in glycemic markers, including those that reflect biological processes independent of hemoglobin glycation and erythrocyte turnover.

DESIGN:

Cross-sectional.

SETTING:

Community-based.

PARTICIPANTS:

1376 nondiabetic and 343 diabetic adults in a substudy of the Atherosclerosis Risk in Communities Study.

MEASUREMENTS:

Hemoglobin A(1c), fasting glucose, glycated albumin, fructosamine, and 1,5-anhydroglucitol levels.

RESULTS:

Among persons with and without diabetes, black persons had significantly higher HbA(1c), glycated albumin, and fructosamine levels than white persons before and after adjustment for covariates and fasting glucose concentration. Serum 1,5-anhydroglucitol levels, which are reduced in the setting of hyperglycemia-induced glycosuria, were lower in black persons than in white persons, although this difference was statistically significant only in nondiabetic adults.

LIMITATION:

The design was cross-sectional, a limited number of participants with a history of diabetes was included, and the study did not include integrated measures of circulating nonfasting glycemia.

CONCLUSION:

Differences between black and white persons in glycated albumin, fructosamine, and 1,5-anhydroglucitol levels parallel differences between these groups in HbA(1c) values. Racial differences in hemoglobin glycation and erythrocyte turnover cannot explain racial disparities in these serum markers. The possibility that black persons have systematically higher levels of nonfasting glycemia warrants further study.

PRIMARY FUNDING SOURCE:

National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases.

PMID:
21357907
[PubMed - indexed for MEDLINE]
PMCID:
PMC3131743
Free PMC Article

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