Complementation of HLA-DQA and DQB genes confers susceptibility and protection to insulin-dependent diabetes mellitus.

Henry Heimberg, Peter Nagy, Guido Somers, I. De Leeuw, Franciscus Schuit

Research output: Contribution to journalArticlepeer-review

52 Citations (Scopus)

Abstract

Lack of an aspartic acid 57 in the HLA-DQ-beta-chain was introduced as a genetic marker of insulin-dependent diabetes mellitus (IDDM). Because 25% of the control population carries the same marker, we analyzed the DQ locus for the presence of more specific disease susceptibility markers, taking into account a possible role for the polymorphic DQA gene. We thereby identified the DQA3-DQB3.2/DQA4.1-DQB2 (DQA1*0301-DQB1*0302/DQA1*0501-DQB1*0201) genotype which was detected in 30% of the 268 typed IDDM patients and only in 1% of the 331 typed healthy controls, resulting in a relative risk of 35. This genetic marker was more frequent in patients with clinical onset before age 18 years (36%) than in patients diagnosed between age 18 and 40 years (22%) and was not observed in patients with non-IDDM. The new susceptibility genotype DQA3-DQB3.2/DQA4.1-DQB2 (DQA1*0301-DQB1*0302/DQA1*0501-DQB1*0201) may explain the well-known excess of DR3/DR4 heterozygous IDDM patients and is expected to help identify individuals at risk for developing the disease.
Original languageEnglish
Pages (from-to)10-17
Number of pages8
JournalHum Immunol
Volume33
Issue number1
Publication statusPublished - 1992

Bibliographical note

Human Immunol. 33: 10-17, 1992.

Fingerprint

Dive into the research topics of 'Complementation of HLA-DQA and DQB genes confers susceptibility and protection to insulin-dependent diabetes mellitus.'. Together they form a unique fingerprint.

Cite this