Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: Evidence for genetic heterogeneity
| Autor: | Céline Pierlot, Elisabeth Petit, José Osorio, Olivier Alibert, Thomas Bardin, Sandra Lasbleiz, Claudia de Toma, Bernard Prum, Sabine Fauré, Maria Martinez, François Cornelis, Philippe Dieudé, Séverine Cailleau-Moindrault |
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| Rok vydání: | 2002 |
| Předmět: |
030203 arthritis & rheumatology
Genetics 0303 health sciences Linkage disequilibrium business.industry Genetic heterogeneity Immunology Haplotype Odds ratio Transmission disequilibrium test Genetic determinism 3. Good health 03 medical and health sciences 0302 clinical medicine Rheumatology Genetic linkage Genotype Immunology and Allergy Medicine Pharmacology (medical) business 030304 developmental biology |
| Zdroj: | Arthritis & Rheumatism. 46:2039-2044 |
| ISSN: | 0004-3591 |
| Popis: | Objective Tumor necrosis factor α (TNFα) binds the receptors TNFRI and TNFRII. Results of genome scans have suggested that TNFR2 is a candidate rheumatoid arthritis (RA) locus. A case–control study in a UK Caucasian population has shown an association between a TNFR2 genotype (196R/R in exon 6) and familial, but not sporadic, RA. The present study was undertaken to test this association in the French Caucasian population. Methods To test for an association in sporadic RA, 100 families were genotyped for the 196M/R polymorphism and analyzed using the transmission disequilibrium test and haplotype relative risk. To test for an association in familial RA, RA index cases from 100 affected sibpair (ASP) families were genotyped for 196M/R. Linkage analysis was performed with 3 TNFR2 microsatellite markers. Results The TNFR2 196R/R genotype was not associated with sporadic RA (odds ratio [OR] 0.59, P = 0.72), but was associated with familial RA (OR 4.0, P = 0.026). The association was most marked in the context of TNFR2 “twin-like” RA sibs (affected sibs sharing both TNFR2 haplotypes) (OR 9.2, P = 0.0017). Linkage analysis results were consistent with the association; most of the TNFR2 linkage evidence was found in the subgroup of families with 196R/R ASP index cases. Conclusion This study is the first to replicate evidence of the involvement of TNFR2 in RA genetic heterogeneity. Our data refine the initial hypothesis, to suggest that a TNFR2 recessive factor, in linkage disequilibrium with the 196R allele, plays a major role in a subset of families with multiple cases of RA. |
| Databáze: | OpenAIRE |
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