Familial NIDDM probably results from combined inherited defects of insulin secretion and action. Members of the facilitative glucose transporter family are strong candidates for both defects, and RFLPs for both GLUT1 (erythrocyte) and GLUT2 (liver/islet) genes have been associated with NIDDM in some populations. To test the hypothesis that GLUT1 and GLUT2 mutations contribute to the inherited predisposition to NIDDM, we examined linkage of these loci with NIDDM in 18 large Utah white pedigrees (two and three generation) ascertained for >2 NIDDM siblings. We used two RFLPs detected with Xba1 and Stu1 for the GLUT1 transporter. For the GLUT2 (liver/β-cell) transporter gene, we used an RFLP detected with EcoR1 and a highly polymorphic (6-allele) dinucleotide (microsatellite) repeat. Analysis was performed with the MLINK program of the LINKAGE package. We tested four models for each locus: dominant and recessive, with IGT alternately considered as unknown affection status, or affected if IGT was diagnosed <45 yr of age and unknown if >45 yr. Disease gene frequencies were chosen to give approximate disease prevalence in American whites (q = 0.03, dominant; q = 0.25, recessive). Linkage of GLUT1 and NIDDM was strongly and significantly rejected under all models, with total (pooled) LOD scores of −5.7 to −8.9, indicating >500,000:1 odds against linkage. Pooled LOD scores were significantly negative (<−2.0, or 100:1 odds against linkage) to a recombination fraction of >5%. No heterogeneity was apparent. Analysis of GLUT2 gave similar results, with LOD scores of <−4.0 under each model, indicating at least 10,000:1 odds against linkage. Again, linkage was excluded within a 5% recombination fraction. Two pedigrees had individual LOD scores of >0.8 under some models, which may have suggested heterogeneity. Formal testing did not support the presence of a linked subgroup for either gene, however. These data fail to support a role for either GLUT1 or GLUT2 genes in the genetic predisposition to NIDDM. However, mutations of either or both genes may be present in rare pedigrees, in other racial groups, or as minor contributors in a polygenic disease.
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Original Articles|
December 01 1992
Linkage Analysis of GLUT1 (HepG2) and GLUT2 (Liver/Islet) Genes in Familial NIDDM
Steven C Elbein;
Steven C Elbein
Division of Endocrinology and Metabolism, Department of Internal Medicine, Veterans Affairs Medical Center and University of Utah School of Medicine
Salt Lake City, Utah
Metabolism Division, Department of Internal Medicine, Washington University School of Medicine
St. Louis, Missouri
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Michael D Hoffman;
Michael D Hoffman
Division of Endocrinology and Metabolism, Department of Internal Medicine, Veterans Affairs Medical Center and University of Utah School of Medicine
Salt Lake City, Utah
Metabolism Division, Department of Internal Medicine, Washington University School of Medicine
St. Louis, Missouri
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Akira Matsutani;
Akira Matsutani
Division of Endocrinology and Metabolism, Department of Internal Medicine, Veterans Affairs Medical Center and University of Utah School of Medicine
Salt Lake City, Utah
Metabolism Division, Department of Internal Medicine, Washington University School of Medicine
St. Louis, Missouri
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M Alan Permutt
M Alan Permutt
Division of Endocrinology and Metabolism, Department of Internal Medicine, Veterans Affairs Medical Center and University of Utah School of Medicine
Salt Lake City, Utah
Metabolism Division, Department of Internal Medicine, Washington University School of Medicine
St. Louis, Missouri
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Address correspondence and reprint requests to Steven C. Elbein, MD, Endocrinology 111E, Veterans Affairs Medical Center, 500 Foothill Blvd., Salt Lake City, UT 84148.
Citation
Steven C Elbein, Michael D Hoffman, Akira Matsutani, M Alan Permutt; Linkage Analysis of GLUT1 (HepG2) and GLUT2 (Liver/Islet) Genes in Familial NIDDM. Diabetes 1 December 1992; 41 (12): 1660–1667. https://doi.org/10.2337/diab.41.12.1660
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