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Conditional ETDT analysis of the human leukocyte antigen region in type 1 diabetes

Koeleman, Bobby P. C. and Herr, Mathias H. and Zavattari, Patrizia and Dudbridge, Frank and March, Ruth E. and Campbell, Duncan K. G. and Barnett, Anthony H. and Bain, Stephen Charles and Mulargia, Annapaola and Loddo, Miriam and Amos, William Brad and Cucca, Francesco and Todd, John A. (2000) Conditional ETDT analysis of the human leukocyte antigen region in type 1 diabetes. Annals of Human Genetics, Vol. 64 (3), p. 215-221. eISSN 1469-1809. Article.

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DOI: 10.1046/j.1469-1809.2000.6430215.x


Several studies have indicated that additional genes in the major histocompatibility complex (MHC) region, other than the class II genes HLADQB1- and -DRB1 (the IDDM1 locus), may contribute to susceptibility and resistance to type 1 diabetes. The relative magnitude of these non-DR/DQ effects is uncertain and their map location is unknown owing to the extraordinary linkage disequilibrium that extends over the 3.5 Mb of the MHC. The homozygous parent test has been proposed as a method for detection of additional risk factors conditional on HLA-DQB1 and -DRB1. However, this method is inefficient since it uses only parents homozygous for the primary disease locus, the DQB1-DRB1 haplotype. To overcome this limitation, Conditional ETDT was used in the present report to test for association conditional on the DQB1-DRB1 haplotype, thereby allowing all parents to be included in the analysis. First, we confirm in UK and Sardinian type 1 diabetic families that allelic variation at HLA-DRB1 has a very significant effect on the association of DQB1 and vice versa. The Conditional ETDT was then applied to the HLA TNF (tumour necrosis factor) region and microsatellite marker D6S273 region, both of which have been reported to contribute to IDDM1 independent of the HLA-DQB1-DRB1 genes. We found no evidence for a major role for either of these two regions in IDDM1.

Item Type:Article
ID Code:4232
Uncontrolled Keywords:Necrosis-factor-alpha, major histocompatibility complex, factor tnf, hla-dq, linkage disequilibrium, genetic-polymorphism, mellitus, susceptibility, haplotypes, alleles
Subjects:Area 06 - Scienze mediche > MED/03 Genetica medica
Divisions:001 Università di Sassari > 01 Dipartimenti > Scienze biomediche
Publisher:Blackwell / Wiley
Copyright Holders:Journal compilation © 2010 Blackwell Publishing Ltd/University College London
Deposited On:22 Jul 2010 11:35

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