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ANALYSIS OF HLA HAPLOTYPES IN FAMILIES WITH TYPE 1 DIABETES MELLITUS IN LA RÉUNION ISLAND
Author(s) -
Feugeas J. P.,
Tortosa P.,
Dulay S.,
AugustinPascalis I.,
Charron D.,
Krishnamoorthy R.,
Caillens H.,
MontchampMoreau C.
Publication year - 1996
Publication title -
international journal of immunogenetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.41
H-Index - 47
eISSN - 1744-313X
pISSN - 1744-3121
DOI - 10.1111/j.1744-313x.1996.tb00136.x
Subject(s) - haplotype , human leukocyte antigen , allele , genetics , hla dq , population , restriction fragment length polymorphism , type 1 diabetes , polymerase chain reaction , biology , typing , immunogenetics , genetic predisposition , diabetes mellitus , immunology , medicine , antibody , gene , antigen , endocrinology , environmental health
SUMMARY To analyse HLA and insulin‐dependent diabetes mellitus (IDDM) association in the ethnically mixed population of La Réunion island, we carried out a family study on 70 diabetic subjects. HLA‐DQA1, ‐DQB1 and ‐DRB1 typing was performed by polymerase chain reaction‐restriction fragment length polymorphism (PCR‐RFLP), completed by PCR‐sequence‐specific oligonucleotide (SSO) and PCR‐sequence‐specific priming (SSP). Haplotype‐relative risks (HRR) were determined with the non‐transmitted parental haplotypes as controls, and relative risks (RR) were calculated with a classical case‐control study. The most significant risks were found for the cis and trans combinations between DQA1*03 or *0501 (Arg52 + ) and DQB1*02 or *0302 (Asp57 − ) alleles, suggesting a direct role for the HLA‐DQ heterodimer in IDDM susceptibility. Interestingly, due to the mixed origin of the population, the trans ‐encoded DQ molecules in the (DR3)‐DQA1*0501‐DQB1*02/(DR4)‐DQA1*03‐DQB 1*0302 subjects were also found cis ‐encoded in patients with the (DR7 or 9)‐DQA1*03‐DQB1*02 haplotype and in a patient with the rare (DR 11)‐DQA1*0501‐DQB 1*0302 haplotype. A relative predispositional effect (RPE) analysis gave significant haplotype‐IDDM + associations in the following order: (DR3)‐DQA1*0501‐DQB1*02>(DR4)‐DQA1*03‐DQB1*0302>(DR9)‐DQA1*03‐DQB*02>(DR7)‐DQA1*03‐DQB1*02>(DR2)‐DQA1*01‐DQB1*0502. No protective effect remained significant once the susceptible haplotypes were removed. A stratification study showed a stronger influence of the DQ genes than DRB1 alleles within the DR7 haplotypes. On the other hand, IDDM subjects with only one susceptible haplotype had inherited this haplotype more often from their father than from their mother. This paternal effect could be related to the greater risk of IDDM in offspring of diabetic fathers than the risk in offspring of diabetic mothers.