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Diabetes, Vol 46, Issue 1 63-69, Copyright © 1997 by American Diabetes Association
Insulin sensitivity and acute insulin response in African-Americans, non-Hispanic whites, and Hispanics with NIDDM: the Insulin Resistance Atherosclerosis Study
SM Haffner, G Howard, E Mayer, RN Bergman, PJ Savage, M Rewers, L Mykkanen, AJ Karter, R Hamman and MF Saad
Department of Medicine, University of Texas Health Science Center, San Antonio 78284-7873, USA.
NIDDM is usually characterized by beta-cell failure and decreased insulin
sensitivity. It has been reported that a high proportion of
African-American NIDDM subjects are insulin sensitive. To examine this
issue, we determined insulin sensitivity (S(I)) in 479 NIDDM subjects by
minimal model analyses of frequently sampled intravenous glucose tolerance
(FSIGT) from the Insulin Resistance Atherosclerosis Study (IRAS), a large
multicenter study of insulin sensitivity and cardiovascular risk in
African-Americans, Hispanics, and non-Hispanic whites. The
African-Americans and non-Hispanic whites were sampled in Los Angeles and
Oakland, California. The non-Hispanic whites and Hispanics were sampled in
San Antonio, Texas, and San Luis Valley, Colorado. We defined the
proportion of insulin-sensitive (S(I)) subjects as > or =1.61 min-1 x
microU-1 x ml-1, which is above the median for nondiabetic subjects of all
ethnic groups in the IRAS. Using this definition, the proportion of
insulin-sensitive diabetic subjects was very low in all ethnic groups
(non-Hispanic whites [14.3%] vs. African-Americans [6.5%], P = 0.039 in Los
Angeles and Oakland; non-Hispanic whites [6.8%] vs. Hispanics [4.9%], P =
0.737 in San Luis Valley and San Antonio). These results were also similar
in newly diagnosed mildly hyperglycemic diabetic subjects. In addition,
these results were not affected by the adjustment for differences in
obesity, body fat distribution, and severity of hyperglycemia. Even in
nonobese subjects (with BMI <30 kg/m2), the proportion of
insulin-sensitive subjects (S(I) > or =1.61 min-1 x microU-1 x ml-1) was
low (3.6-9.7%). The acute insulin response (AIR) was significantly higher
in African-Americans than in non-Hispanic whites; there were no ethnic
differences in AIR between Hispanics and non-Hispanic whites. There were no
significant ethnic differences for non-insulin-mediated glucose disposal
(S(G)). We conclude that the number of insulin-sensitive NIDDM subjects is
low and similar among non-Hispanic whites, Hispanics, and African-Americans
in the U.S.

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Copyright © 1997 by the American Diabetes Association.
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