Comparison of the relationship of age and beta cell function in three ethnic groups
Authors: Chiu, Ken C.1; Martinez, Dorothy S.2; Chu, Audrey1
Source: Clinical Endocrinology, Volume 62, Number 3, March 2005 , pp. 296-302(7)
Publisher: Blackwell Publishing
Abstract:
Summary Design Prevalence of type 2 diabetes and glucose intolerance increase with age. It has been demonstrated that beta cell function declines at about 1% per year in glucose tolerant Caucasians. However, this relationship is not known to exist in other ethnic groups. Subjects and Measurements We investigated the relationship of age to beta cell function (%B) and insulin sensitivity (%S), estimated by the homeostasis model assessment, in a nationally representative sample of healthy US adults who participated in a cross-sectional study, the third National Health and Nutrition Examination Survey. Only those subjects who had never been told to have diabetes by a physician, with HbA1C < 6% and fasting plasma glucose concentration < 5·56 mmol/l with proper fasting glucose and insulin concentration were included in this analysis (560 non-Hispanic whites, 231 non-Hispanic blacks and 298 Hispanics). Results Age was positively correlated to HbA1C and fasting glucose concentration, but it was negatively correlated to %B in all three ethnic groups. In contrast, ageing had no influence on %S in all three ethnic groups. Pair-wise comparison showed age had a similar influence among three ethnic groups on fasting glucose concentration, HbA1C and %B, respectively. Multivariate analysis confirmed an independent influence of age on fasting glucose concentration, HbA1C and %B among three ethnic groups. Conclusions We observed %B declines at about 1% per year among all three ethnic groups. The age-related rising fasting plasma glucose concentration and HbA1C is most likely a consequence of age-related decline in beta cell function.Document Type: Research article
DOI: 10.1111/j.1365-2265.2005.02213.x
Affiliations: 1: Division of Clinical Epidemiology and Preventive Medicine and 2: Division of Endocrinology, Diabetes, and Hypertension, Department of Medicine, University of California and David Geffen School of Medicine, Los Angeles, California, USA

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