MINIMAL MODEL ANALYSES OF INSULIN SENSITIVITY AND GLUCOSE-DEPENDENT GLUCOSE DISPOSAL IN BLACK-AND-WHITE AMERICANS - A STUDY OF PERSONS AT RISK FOR TYPE-2 DIABETES

Citation
K. Osei et Da. Cottrell, MINIMAL MODEL ANALYSES OF INSULIN SENSITIVITY AND GLUCOSE-DEPENDENT GLUCOSE DISPOSAL IN BLACK-AND-WHITE AMERICANS - A STUDY OF PERSONS AT RISK FOR TYPE-2 DIABETES, European journal of clinical investigation, 24(12), 1994, pp. 843-850
Citations number
43
Categorie Soggetti
Medicine, Research & Experimental
ISSN journal
00142972
Volume
24
Issue
12
Year of publication
1994
Pages
843 - 850
Database
ISI
SICI code
0014-2972(1994)24:12<843:MMAOIS>2.0.ZU;2-T
Abstract
We have examined the impact of race and positive family history of typ e 2 diabetes on glucose/insulin dynamics and the two components of glu cose disposal in healthy, first-degree relatives of black and white Am erican patients with type 2 diabetes mellitus who are at a greater ris k from the disease and their healthy control subjects. Seventeen black and 15 white relatives were studied. Twenty-two black people and 24 w hite people, without family history of type 2 diabetes, served as heal thy control subjects. Standard oral glucose tolerance test (OGTT) and tolbutamide-modified frequent sampling intravenous glucose tolerance ( FSIGT) tests were performed in each subject. Insulin sensitivity index (S-I) and glucose effectiveness (S-G) were calculated using the MINI- MOD method described by Bergman et al. Mean fasting and post-stimulati on serum glucose levels were not significantly different in the black and white relatives. However, mean serum insulin responses to oral and /or intravenous stimulation were significantly greater in the blacks t han whites, irrespective of positive family history of diabetes. The m ean S-I was significantly (P < 0.02) lower (52%) in the black (3.67 +/ - 0.56) than the white [7.50 +/- 1.93 x 10(-4) min(-1) (mU 1)(-1)] rel atives. Comparing the healthy controls, the mean S-I was significantly (P < 0.02) lower (51%) in black than white controls (4.84 +/- 0.78 vs . 9.71 +/- 1.27 x 10 min(-1) (mU 1)(-1)]. Mean S-G and K-G were greate r (P < 0.05) in the blacks than whites, irrespective of family history of diabetes. In summary, the present study demonstrates that non-diab etic black people manifest insulin resistant and hyperinsulinaemia, ir respective of family history of diabetes, when compared to white peopl e. We speculate that these metabolic changes could play a potential ro le in the higher prevalence of type 2 diabetes in the black Americans.