A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetes.

49Citations
Citations of this article
27Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Mutations in CD36 / fatty acid translocase (FAT) gene are responsible for insulin resistance in the rat but contribution to human Type 2 diabetes is unknown. A nominal evidence for linkage of familial T2D at the CD36 locus led us to identify a rare nonsense mutation c.1079T>G (p.L360X) in one Caucasian pedigree presenting with autosomal dominant diabetes. Adiponectin levels, as marker of insulin sensitivity, were found to be significantly lower in the p.L360X variant carriers compared to homozygous for wild type CD36. Furthermore, expression studies of the truncated protein showed a defective binding of acetylated-LDL. Thus, our findings suggest a possible role for CD36 in the pathogenesis of T2D associated with reduced insulin sensitivity. Copyright 2004 Wiley-Liss, Inc.

Cite

CITATION STYLE

APA

Leprêtre, F., Vasseur, F., Vaxillaire, M., Scherer, P. E., Ali, S., Linton, K., … Froguel, P. (2004). A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetes. Human Mutation, 24(1), 104. https://doi.org/10.1002/humu.9256

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free