PTPN22 C1858T and the risk of psoriasis: a meta-analysis

被引:13
作者
Chen, Yu-Fu [2 ]
Chang, Jeffrey S. [1 ]
机构
[1] Natl Hlth Res Inst, Natl Inst Canc Res, Tainan 70456, Taiwan
[2] Show Chwan Mem Hosp, Dept Dermatol, Changhua, Taiwan
关键词
Psoriasis; Psoriatic arthritis; PTPN22; Meta-analysis; TYROSINE-PHOSPHATASE; RHEUMATOID-ARTHRITIS; GENE; ASSOCIATION; EPIDEMIOLOGY; POPULATION; POLYMORPHISMS; VARIANTS;
D O I
10.1007/s11033-012-1630-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Psoriasis is a chronic autoimmune skin disease with both environmental and genetic risk factors. Previous studies of the association between psoriasis and PTPN22 C1858T (rs2476601), a gain of function variant associated with a stronger inhibitory effect of T-lymphocytes, have produced inconsistent results. The purpose of the current study is to evaluate the association between PTPN22 C1858T and psoriasis using meta-analysis to: (1) have a sufficient sample size for detecting a weak association; and (2) to explore the heterogeneity between studies. A meta-analysis based on random-effects model was performed with ten studies (3,334 psoriasis cases and 5,753 controls) identified from a literature search. A non-significantly positive association between psoriasis and the PTPN22 T1858 was observed [summary allelic odds ratio (OR) = 1.15, 95 % confidence interval (CI): 1.00-1.33] and the association appears stronger among subjects with psoriatic arthritis (summary allelic OR = 1.23, 95 % CI: 1.00-1.52). A null association between PTPN22 T1858 and early-onset psoriasis was observed (summary allelic OR = 1.08, 95 % CI: 0.92-1.28). The current analysis showed a non-significantly positive association between psoriasis and the PTPN22 T1858 allele, and the association appeared stronger among subjects with psoriatic arthritis. Future studies of psoriasis should incorporate gene-environment interaction in the analysis and pay attention to the heterogeneity of psoriasis cases and bias associated with population stratification.
引用
收藏
页码:7861 / 7870
页数:10
相关论文
共 33 条
[1]  
[Anonymous], SYSTEMATIC REV HLTH
[2]   Cutting Edge: The PTPN22 Allelic Variant Associated with Autoimmunity Impairs B Cell Signaling [J].
Arechiga, Adrian F. ;
Habib, Tania ;
He, Yantao ;
Zhang, Xian ;
Zhang, Zhong-Yin ;
Funk, Andrew ;
Buckner, Jane H. .
JOURNAL OF IMMUNOLOGY, 2009, 182 (06) :3343-3347
[3]  
Bradburn M.J., 2004, UPDATED NEW COMMANDS
[4]   Why is PTPN22 a good candidate susceptibility gene for autoimmune disease? [J].
Burn, Garth L. ;
Svensson, Lena ;
Sanchez-Blanco, Cristina ;
Saini, Manoj ;
Cope, Andrew P. .
FEBS LETTERS, 2011, 585 (23) :3689-3698
[5]   Association of functional variants of PTPN22 and tp53 in psoriatic arthritis:: a case-control study [J].
Butt, C ;
Peddle, L ;
Greenwood, C ;
Hamilton, S ;
Gladman, D ;
Rahman, P .
ARTHRITIS RESEARCH & THERAPY, 2006, 8 (01)
[6]   PTPN22 genetic variation:: Evidence for multiple variants associated with rheumatoid arthritis [J].
Carlton, VEH ;
Hu, XL ;
Chokkalingam, AP ;
Schrodi, SJ ;
Brandon, R ;
Alexander, HC ;
Chang, M ;
Catanese, JJ ;
Leong, DU ;
Ardlie, KG ;
Kastner, DL ;
Seldin, MF ;
Criswell, LA ;
Gregersen, PK ;
Beasley, E ;
Thomson, G ;
Amos, CI ;
Begovich, AB .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 77 (04) :567-581
[7]   Familial aggregation of psoriatic arthritis [J].
Chandran, V. ;
Schentag, C. T. ;
Brockbank, J. E. ;
Pellett, F. J. ;
Shanmugarajah, S. ;
Toloza, S. M. A. ;
Rahman, P. ;
Gladman, D. D. .
ANNALS OF THE RHEUMATIC DISEASES, 2009, 68 (05) :664-667
[8]   Geoepidemiology and environmental factors of psoriasis and psoriatic arthritis [J].
Chandran, Vinod ;
Raychaudhuri, Siba P. .
JOURNAL OF AUTOIMMUNITY, 2010, 34 (03) :J314-J321
[9]   Genetic polymorphisms in PTPN22, PADI-4, and CTLA-4 and risk for rheumatoid arthritis in two longitudinal cohort studies:: evidence of gene-environment interactions with heavy cigarette smoking [J].
Costenbader, Karen H. ;
Chang, Shun-Chiao ;
De Vivo, Immaculata ;
Plenge, Robert ;
Karlson, Elizabeth W. .
ARTHRITIS RESEARCH & THERAPY, 2008, 10 (03)
[10]   Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection:: the PTPN22 620W allele associates with multiple autoimmune phenotypes [J].
Criswell, LA ;
Pfeiffer, KA ;
Lum, RF ;
Gonzales, B ;
Novitzke, J ;
Moser, KL ;
Begovich, AB ;
Carlton, VEH ;
Li, W ;
Lee, AT ;
Ortmann, W ;
Behrens, TW ;
Gregersen, PK .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (04) :561-571