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Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program
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2007 (English)In: Diabetologia, ISSN 0012-186X, E-ISSN 1432-0428, Vol. 51, no 3, 451-457 p.Article in journal (Refereed) Published
Abstract [en]

Aims/hypothesis: Wolfram syndrome (diabetes insipidus, diabetes mellitus, optic atrophy and deafness) is caused by mutations in the WFS1 gene. Recently, single nucleotide polymorphisms (SNPs) in WFS1 have been reproducibly associated with type 2 diabetes. We therefore examined the effects of these variants on diabetes incidence and response to interventions in the Diabetes Prevention Program (DPP), in which a lifestyle intervention or metformin treatment was compared with placebo.

Methods: We genotyped the WFS1 SNPs rs10010131, rs752854 and rs734312 (H611R) in 3,548 DPP participants and performed Cox regression analysis using genotype, intervention and their interactions as predictors of diabetes incidence. We also evaluated the effect of these SNPs on insulin resistance and beta cell function at 1 year.

Results: Although none of the three SNPs was associated with diabetes incidence in the overall cohort, white homozygotes for the previously reported protective alleles appeared less likely to develop diabetes in the lifestyle arm. Examination of the publicly available Diabetes Genetics Initiative genome-wide association dataset revealed that rs10012946, which is in strong linkage disequilibrium with the three WFS1 SNPs (r 2 = 0.88–1.0), was associated with type 2 diabetes (allelic odds ratio 0.85, 95% CI 0.75–0.97, p = 0.026). In the DPP, we noted a trend towards increased insulin secretion in carriers of the protective variants, although for most SNPs this was seen as compensatory for the diminished insulin sensitivity.

Conclusions/interpretation: The previously reported protective effect of select WFS1 alleles may be magnified by a lifestyle intervention. These variants appear to confer an improvement in beta cell function.

Place, publisher, year, edition, pages
Berlin: Springer-Verlag , 2007. Vol. 51, no 3, 451-457 p.
Keyword [en]
Beta cell function, diabetes prevention, genetic association study, single nucleotide polymorphism, type 2 diabetes, wolfram syndrome
URN: urn:nbn:se:umu:diva-6555DOI: doi:10.1007/s00125-007-0891-xPubMedID: 18060660OAI: diva2:146224
Available from: 2007-12-14 Created: 2007-12-14 Last updated: 2011-04-12Bibliographically approved

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Franks, Paul
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Department of Public Health and Clinical Medicine
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