Genome-Wide and Fine-Mapping Linkage Studies of Type 2 Diabetes and Glucose Traits in the Old Order Amish

Author:

Hsueh Wen-Chi1,St. Jean Pamela L.2,Mitchell Braxton D.3,Pollin Toni I.3,Knowler William C.4,Ehm Margaret G.2,Bell Callum J.5,Sakul Hakan5,Wagner Michael J.2,Burns Daniel K.2,Shuldiner Alan R.36

Affiliation:

1. Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas

2. GlaxoSmithKline, Research Triangle Park, North Carolina

3. Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland

4. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Phoenix, Arizona

5. Axys Pharmaceuticals, La Jolla, California

6. Geriatrics Research and Education Clinical Center, Baltimore Veterans Administration Medical Center, Baltimore, Maryland

Abstract

We conducted a genome scan using a 10-cM map to search for genes linked to type 2 diabetes in 691 individuals from a founder population, the Old Order Amish. We then saturated two regions on chromosomes 1 and 14 showing promising linkage signals with additional markers to produce a ∼2-cM map for fine mapping. Analyses of both discrete traits (type 2 diabetes and the composite trait of type 2 diabetes and/or impaired glucose homeostasis [IGH]), and quantitative traits (glucose levels during a 75-g oral glucose challenge, designated glucose 0–180 and HbA1c) were performed. We obtained significant evidence for linkage to type 2 diabetes in a novel region on chromosome 14q11 (logarithm of odds [LOD] for diabetes = 3.48, P = 0.00005). Furthermore, we observed evidence for the existence of a diabetes-related locus on chromosome 1q21-q24 (LOD for type 2 diabetes/IGH = 2.35, P = 0.0008), a region shown to be linked to diabetes in several other studies. Suggestive evidence for linkage to glucose traits was observed on three other regions: 14q11-q13 (telomeric to that above with LOD = 1.82–1.85 for glucose 150 and 180), 1p31 (LOD = 1.28–2.30 for type 2 diabetes and glucose 120–180), and 18p (LOD = 3.07, P = 0.000085 for HbA1c and LOD = 1.50 for glucose 0). In conclusion, our findings provide evidence that type 2 diabetes susceptibility genes reside on chromosomes 1, 14, and 18.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference51 articles.

1. Elston RC, Namboodiri KK, Nino HV, Pollitzer WS: Studies on blood and urine glucose in Seminole Indians: indications for segregation of a major gene. Am J Hum Genet 26:13–34,1974

2. Rich SS: Mapping genes in diabetes: genetic epidemiological perspective. Diabetes 39:1315–1319,1990

3. Hanson RL, Elston RC, Pettitt DJ, Bennett PH, Knowler WC: Segregation analysis of non-insulin-dependent diabetes mellitus in Pima Indians: evidence for a major-gene effect. Am J Hum Genet 57:160–170,1995

4. Stern MP, Mitchell BD, Blangero J, Reinhart L, Krammerer CM, Harrison CR, Shipman PA, O’Connell P, Frazier ML, MacCluer JW: Evidence for a major gene for type II diabetes and linkage analyses with selected candidate genes in Mexican-Americans. Diabetes 45:563–568,1996

5. Silver K, Shuldiner AR: Candidate genes for type II diabetes mellitus. In Diabetes Mellitus: A Fundamental and Clinical Text. LeRoith D, Taylor SI, Eds. Philadelphia, Lippincott,2000, p.709–719

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