Psoriatic arthritis and CARD15 gene polymorphisms:: No evidence for association in the Italian population

被引:32
作者
Giardina, E [1 ]
Novelli, G
Costanzo, A
Nisticò, S
Bulli, C
Sinibaldi, C
Sorgi, ML
Chimenti, S
Pallone, F
Taccari, E
Borgiani, P
机构
[1] Univ Roma Tor Vergata, Ctr Excellence Genom Risk Assessment Mutifactoria, Sch Med, Rome, Italy
[2] Univ Arkansas Med Sci, Dept Cardiovasc Med, Little Rock, AR 72205 USA
[3] Univ Roma Tor Vergata, Dept Dermatol, Rome, Italy
[4] Univ Roma La Sapienza, Dept Appl Clin & Med Therapy, Rheumatol Unit, Rome, Italy
关键词
D O I
10.1111/j.0022-202X.2004.22524.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Psoriatic arthritis (PsA) has been defined as an inflammatory arthritis associated with psoriasis that may affect as many as 30% of psoriasis patients. Epidemiological study reported strong familial clustering of PsA although the precise etiology of PsA is poorly understood. Recently, a genomewide linkage scan in PsA revealed a LOD score of 2.17 on chromosome 16q and provided strong evidence for a paternal imprinting effect. That region surrounds a psoriasis susceptibility locus including the CARD15 gene which has convincingly been shown to confer susceptibility to Crohn's disease. The existence of a common susceptibility gene for psoriasis/PsA and Crohn disease was recently demonstrated by evidence of association of CARD15 polymorphisms with PsA. To confirm these results in an independent population, we analyzed a data set of 193 Italian PsA patients and 150 controls for CARD15 polymorphisms (R702W, G908R and leu1007finsC) previously demonstrated associated with PsA. Here we report no evidence for association in the examined population for CARD15 polymorphisms, suggesting that the positive association previously reported in a genetically isolated population was the result of a linkage disequilibrium due to a founder effect.
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页码:1106 / 1107
页数:2
相关论文
共 13 条
[1]  
Borgiani P, 2002, EUR J DERMATOL, V12, P540
[2]   THE EUROPEAN-SPONDYLARTHROPATHY-STUDY-GROUP PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SPONDYLARTHROPATHY [J].
DOUGADOS, M ;
VANDERLINDEN, S ;
JUHLIN, R ;
HUITFELDT, B ;
AMOR, B ;
CALIN, A ;
CATS, A ;
DIJKMANS, B ;
OLIVIERI, I ;
PASERO, G ;
VEYS, E ;
ZEIDLER, H .
ARTHRITIS AND RHEUMATISM, 1991, 34 (10) :1218-1227
[3]   Current concepts in psoriatic arthritis [J].
Gladman, DD .
CURRENT OPINION IN RHEUMATOLOGY, 2002, 14 (04) :361-366
[4]   Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease [J].
Hugot, JP ;
Chamaillard, M ;
Zouali, H ;
Lesage, S ;
Cézard, JP ;
Belaiche, J ;
Almer, S ;
Tysk, C ;
O'Morain, CA ;
Gassull, M ;
Binder, V ;
Finkel, Y ;
Cortot, A ;
Modigliani, R ;
Laurent-Puig, P ;
Gower-Rousseau, C ;
Macry, J ;
Colombel, JF ;
Sahbatou, M ;
Thomas, G .
NATURE, 2001, 411 (6837) :599-603
[5]   A susceptibility gene for psoriatic arthritis maps to chromosome 16q: Evidence for imprinting [J].
Karason, A ;
Gudjonsson, JE ;
Upmanyu, R ;
Antonsdottir, AA ;
Hauksson, VB ;
Runasdottir, EH ;
Jonsson, HH ;
Gudbjartsson, DF ;
Frigge, ML ;
Kong, A ;
Stefansson, K ;
Valdimarsson, H ;
Gulcher, JR .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (01) :125-131
[6]   FAMILIAL OCCURRENCE OF PSORIATIC ARTHRITIS [J].
MOLL, JMH ;
WRIGHT, V .
ANNALS OF THE RHEUMATIC DISEASES, 1973, 32 (03) :181-201
[7]   Lack of association between NOD2 3020InsC frameshift mutation and psoriasis [J].
Nair, RP ;
Stuart, P ;
Ogura, Y ;
Inohara, N ;
Chia, NVC ;
Young, L ;
Henseler, T ;
Jenisch, S ;
Christophers, E ;
Voorhees, JJ ;
Nuñez, G ;
Elder, JT .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (06) :1671-1672
[8]   Evidence for two psoriasis susceptibility loci (HLA and 17q) and two novel candidate regions (16q and 20p) by genome-wide scan [J].
Nair, RP ;
Henseler, T ;
Jenisch, S ;
Stuart, P ;
Bichakjian, CK ;
Lenk, W ;
Westphal, E ;
Guo, SW ;
Christophers, E ;
Voorhees, JJ ;
Elder, JT .
HUMAN MOLECULAR GENETICS, 1997, 6 (08) :1349-1356
[9]   Psoriasis in the community: Prevalence, severity and patients' beliefs and attitudes towards the disease [J].
Nevitt, GJ ;
Hutchinson, PE .
BRITISH JOURNAL OF DERMATOLOGY, 1996, 135 (04) :533-537
[10]   The Newfoundland population: a unique resource for genetic investigation of complex diseases [J].
Rahman, P ;
Jones, A ;
Curtis, J ;
Bartlett, S ;
Peddle, L ;
Fernandez, BA ;
Freimer, NB .
HUMAN MOLECULAR GENETICS, 2003, 12 :R167-R172