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Restriction-fragment-length polymorphism in insulin-receptor gene and insulin resistance in NIDDM.

作者信息

McClain D A, Henry R R, Ullrich A, Olefsky J M

机构信息

Department of Medicine, Veterans Administration Medical Center, San Diego, CA 92161.

出版信息

Diabetes. 1988 Aug;37(8):1071-5. doi: 10.2337/diab.37.8.1071.

Abstract

Restriction-enzyme analysis of genomic DNA from 52 White and Hispanic nondiabetic subjects and 51 subjects with non-insulin-dependent diabetes (NIDDM) was carried out with insulin-receptor cDNA probes. A polymorphic 5.8-kilobase SstI fragment was found in 12 (23.5%) of 51 NIDDM subjects but only in 4 (7.7%) of 52 nondiabetic control subjects. This association is significant by chi 2-analysis (P less than .05). Furthermore, the nondiabetic subjects with the polymorphism were found to have hyperinsulinemia and/or nondiagnostic glucose tolerance. The polymorphism is a genetic marker for a phenotype that is neither necessary nor, by itself, sufficient for NIDDM. Nevertheless, it may indicate that insulin resistance functionally related to an insulin-receptor gene polymorphism is the proximal cause of NIDDM in at least one subset of the population.

摘要

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