Postprandial Insulin Response and Clearance Among Black and White Women: The Federal Women's Study.
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ABSTRACT: Context:Postprandial hyperinsulinemia might be an important cardiometabolic risk determinant in black compared with white women. However, the contributions of insulin clearance and ?-cell function to racial differences in postprandial insulin response are unknown. Objective:To compare, by race and menopause, early insulin response to oral and intravenous glucose and to measure postprandial intact glucagon-like peptide 1 (GLP-1) concentrations, insulin clearance, and ?-cell function. Design and Participants:119 federally employed women without diabetes [87 premenopausal (52 black, 35 white) and 32 postmenopausal (19 black, 13 white)] underwent an oral glucose tolerance test, insulin-modified frequently sampled intravenous glucose test (IM-FSIGT), and mixed meal tolerance test (MMTT). Outcome Measures:Early insulin response was measured as follows: (i) insulinogenic index (oral glucose tolerance test); (ii) acute insulin response to glucose (IM-FSIGT); and (iii) ratio of incremental insulin/glucose area under the curve in the first 30 minutes of the MMTT. Insulin clearance was assessed during the IM-FSIGT and MMTT. During the MMTT, intact GLP-1 was measured and ?-cell function assessed using the insulin secretion rate and ?-cell responsivity indexes. Results:Black pre-menopausal and postmenopausal women had a greater insulin response and lower insulin clearance and greater dynamic ?-cell responsivity (P ? 0.05 for all). No differences were found in the total insulin secretion rates or intact GLP-1 concentrations. Conclusions:Greater postprandial hyperinsulinemia in black pre-menopausal and postmenopausal women was associated with lower hepatic insulin clearance and heightened ?-cell capacity to rapid changes in glucose, but not to higher insulin secretion. The relationship of increased ?-cell secretory capacity, reduced insulin clearance, and ambient hyperinsulinemia to the development of cardiometabolic disease requires further investigation.
SUBMITTER: Chung ST
PROVIDER: S-EPMC6286409 | biostudies-literature | 2019 Jan
REPOSITORIES: biostudies-literature
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