A Genome-Wide Search for Genes Involved in Type 2 Diabetes in a Recently Genetically Isolated Population From the Netherlands
- Yurii S. Aulchenko12,
- Norbert Vaessen1,
- Peter Heutink3,
- Jan Pullen4,
- Pieter J.L.M. Snijders1,
- Albert Hofman1,
- Lodewijk A. Sandkuijl5,6†,
- Jeanine J. Houwing-Duistermaat1,
- Mark Edwards4,
- Simon Bennett4,
- Ben A. Oostra3 and
- Cornelia M. van Duijn1
- 1Genetic Epidemiology Unit, Department of Epidemiology & Biostatistics, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands
- 2Institute of Cytology and Genetics SD RAS, Novosibirsk, Russia
- 3Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, the Netherlands
- 4Oxagen Limited, Abingdon, U.K
- 5Leiden University Medical Center, Leiden, the Netherlands
- Address correspondence and reprint requests to Cornelia M. van Duijn, Genetic Epidemiology Unit, Department of EpidemiologyBiostatistics, Erasmus Medical Center Rotterdam, P.O. Box 1738, 3000 DR Rotterdam, Netherlands. E-mail: c.vanduijn{at}erasmusmc.nl
Abstract
Multiple genes, interacting with the environment, contribute to the susceptibility to type 2 diabetes. We performed a genome-wide search to localize type 2 diabetes susceptibility genes in a recently genetically isolated population in the Netherlands. We identified 79 nuclear families with type 2 diabetes who were related within 13 generations and performed a 770-marker genome-wide scan search for shared founder alleles. Twenty-six markers yielded a logarithm of odds (LOD) score >0.59 (nominal P < 0.05), of which 7 reached LOD scores >1.17 (nominal P < 0.01). The strongest evidence for a type 2 diabetes locus was at marker D18S63 on chromosome 18p (LOD 2.3, P = 0.0006). This region was investigated further using additional markers. For one of these markers (D18S1105), we found a significant association with type 2 diabetes (odds ratio 6.7 [95% CI 1.5–30.7], P = 0.005 for the 97-bp allele, assuming a dominant model), which increased when limiting the analysis to patients with high BMI (12.25 [2.1–71], P = 0.003). A locus on chromosome 18p in patients with high BMI was suggested earlier by Parker et al. Our study is the first to confirm this locus.
Footnotes
- †
† Deceased. This study is dedicated to the memory of Lodewijk A. Sandkuijl.
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- Accepted September 2, 2003.
- Received March 20, 2003.
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