Linkage analysis of chromosome 2q in osteoarthritis

被引:58
作者
Loughlin, J [1 ]
Mustafa, Z
Smith, A
Irven, C
Carr, AJ
Clipsham, K
Chitnavis, J
Bloomfield, VA
McCartney, M
Cox, O
Sinsheimer, JS
Sykes, B
Chapman, KE
机构
[1] Univ Oxford, Inst Mol Med, Oxford, England
[2] Nuffield Orthopaed Ctr, Oxford OX3 7LD, England
[3] Musgrave Pk Hosp, Belfast, Antrim, North Ireland
[4] Univ Calif Los Angeles, Dept Biostat & Biomath, Los Angeles, CA 90024 USA
关键词
osteoarthritis; linkage; affected sibling pairs; chromosome; 2q; susceptibility loci;
D O I
10.1093/rheumatology/39.4.377
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. In independent linkage studies chromosome 2q11-q24 and chromosome 2q23-35 have previously been implicated as regions potentially harbouring susceptibility loci for osteoarthritis (OA), Objective. To test chromosome 2q for linkage to idiopathic osteoarthritis. Methods. Using a cohort of 481 OA families that each contained at least one affected sibling pair with severe end-stage disease (ascertained by hip or knee joint replacement surgery), we conducted a linkage analysis of chromosome 2q using 16 polymorphic microsatellite markers at an average spacing of one marker every 8.5 cM. Results. Our results provide suggestive evidence for a locus at 2q31 with a maximum multipoint logarithm of the odds score (MLS) of 1.22 which increased to 2.19 in those families concordant for hip-only disease (n = 311). This suggestive linkage was greater in male-hip families (MLS = 1.57, n = 71) than in female-hip families (MLS = 0.71, n = 132). Conclusions. Chromosome 2q is likely to contain at least one susceptibility locus for OA.
引用
收藏
页码:377 / 381
页数:5
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