CARD15 gene polymorphisms in patients with spondyloarthropathies identify a specific phenotype previously related to Crohn's disease

被引:72
作者
Laukens, D
Peeters, H
Marichal, D
Vander Cruyssen, B
Mielants, H
Elewaut, D
Demetter, P
Cuvelier, C
Van Den Berghe, M
Rottiers, P
Veys, EM
Remaut, E
Steidler, L
De Keyser, F
De Vos, M
机构
[1] Ghent Univ Hosp, Dept Gastroenterol, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Mol Biomed Res, B-9000 Ghent, Belgium
[3] Flanders Interuniv Inst Biotechnol VIB, Ghent, Belgium
[4] Ghent Univ Hosp, Dept Rheumatol, B-9000 Ghent, Belgium
[5] Ghent Univ Hosp, Dept Pathol, B-9000 Ghent, Belgium
[6] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
关键词
D O I
10.1136/ard.2004.028837
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The association between spondyloarthropathy and Crohn's disease is well known. A risk for evolution to Crohn's disease has already been shown in the subgroup of patients with spondyloarthropathy associated with chronic gut inflammation. Objective: To investigate whether the reported polymorphisms in the CARD15 gene, a susceptibility gene for Crohn's disease, are associated with the presence of preclinical intestinal inflammation observed in spondyloarthropathies. Methods: 104 patients with spondyloarthropathies were studied. All underwent ileocolonoscopy with biopsies between 1983 and 2004. The prevalence of three single nucleotide polymorphisms in the CARD15 gene (R702W, G908R, and 1007fs) was assessed using restriction fragment length polymorphism - polymerase chain reaction (RFLP-PCR); the patients were compared with an ethnically matched Crohn's disease population and a control population. Results: The carrier frequency of R702W, G908R, or 1007fs variants in the spondyloarthropathy populations (20%) was similar to the control population (17%), but increased to 38% in the spondyloarthropathy subgroup with chronic gut inflammation. This frequency was significantly higher than in the other spondyloarthropathy subgroups ( p = 0.001) or the control group ( p = 0.006), but not different from the Crohn's disease group (49%) (NS). This indicates that CARD15 polymorphisms are associated with a higher risk for development of chronic gut inflammation. Conclusions: CARD15 gene polymorphisms clearly identify a subgroup of patients with spondyloarthropathies associated with chronic intestinal inflammation.
引用
收藏
页码:930 / 935
页数:6
相关论文
共 59 条
[1]   Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease [J].
Abreu, MT ;
Taylor, KD ;
Lin, YC ;
Hang, T ;
Gaiennie, J ;
Landers, CJ ;
Vasiliauskas, EA ;
Kam, LY ;
Rojany, M ;
Papadakis, KA ;
Rotter, JI ;
Targan, SR ;
Yang, HY .
GASTROENTEROLOGY, 2002, 123 (03) :679-688
[2]   The molecular classification of the clinical manifestations of Crohn's disease [J].
Ahmad, T ;
Armuzzi, A ;
Bunce, M ;
Mulcahy-Hawes, K ;
Marshall, SE ;
Orchard, TR ;
Crawshaw, J ;
Large, O ;
De Silva, A ;
Cook, JT ;
Barnardo, M ;
Cullen, S ;
Welsh, KI ;
Jewell, DP .
GASTROENTEROLOGY, 2002, 122 (04) :854-866
[3]   CLINICALLY SILENT INFLAMMATORY GUT LESIONS IN UNDIFFERENTIATED SPONDYLOARTHROPATHIES [J].
ALTOMONTE, L ;
ZOLI, A ;
VENEZIANI, A ;
MIRONE, L ;
SANTACESARIA, G ;
CHIARELLI, C ;
FEDERICO, F ;
MASSI, G ;
MAGARO, M .
CLINICAL RHEUMATOLOGY, 1994, 13 (04) :565-570
[4]  
ARNOTT IDR, 2004, GENES IMMUN 0610
[5]   Macrophages expressing the scavenger receptor CD163: a link between immune alterations of the gut and synovial inflammation in spondyloarthropathy [J].
Baeten, D ;
Demetter, P ;
Cuvelier, CA ;
Kruithof, E ;
Van Damme, N ;
De Vos, M ;
Veys, EM ;
De Keyser, F .
JOURNAL OF PATHOLOGY, 2002, 196 (03) :343-350
[6]   Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan [J].
Bonen, DK ;
Ogura, Y ;
Nicolae, DL ;
Inohara, N ;
Saab, L ;
Tanabe, T ;
Chen, FF ;
Foster, SJ ;
Duerr, RH ;
Brant, SR ;
Cho, JH ;
Nuñez, G .
GASTROENTEROLOGY, 2003, 124 (01) :140-146
[7]  
Borgiani P, 2002, EUR J DERMATOL, V12, P540
[8]  
Braun J, 1998, ARTHRITIS RHEUM-US, V41, P58, DOI 10.1002/1529-0131(199801)41:1<58::AID-ART8>3.3.CO
[9]  
2-7
[10]   Familial and genetic aspects of spondyloarthropathy [J].
Breban, M ;
Said-Nahal, R ;
Hugot, JP ;
Miceli-Richard, C .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 2003, 29 (03) :575-+