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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd"><ArticleSet><Article><Journal><PublisherName></PublisherName><JournalTitle>Knowledge &amp; Health</JournalTitle><Volume>9</Volume><Issue>3</Issue><PubDate PubStatus="epublish"><Year>2013</Year><Month>12</Month><Day>16</Day></PubDate></Journal><VernacularTitle>Evaluation of CTLA-4 Exon-1 +49A/G Polymorphism in Systemic Lupus Erythematosus Patients: A Meta Analysis</VernacularTitle><FirstPage>60</FirstPage><LastPage>60</LastPage><ELocationID EIdType="doi">10.1234/knh.v0i0.60</ELocationID><Language>FA</Language><AuthorList><Author><FirstName>Mahdieh</FirstName><LastName>Shojaa</LastName><Affiliation>مرکز تحقیقات استئوپورز دانشگاه علوم پزشکی تهران. mahdieh.shojaa_mw@yahoo.com</Affiliation></Author><Author><FirstName>Mehrdad</FirstName><LastName>Aghaie</LastName></Author><Author><FirstName>Mostafa</FirstName><LastName>Qorbani</LastName></Author><Author><FirstName>Patricia</FirstName><LastName>Khashayar</LastName></Author><Author><FirstName>Abbas Ali</FirstName><LastName>Keshtkar</LastName></Author><Author><FirstName>Ramin</FirstName><LastName>Mohebi</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2013</Year><Month>08</Month><Day>13</Day></PubDate><PubDate PubStatus="accepted"><Year>2013</Year><Month>12</Month><Day>09</Day></PubDate><PubDate PubStatus="revised"><Year>2013</Year><Month>12</Month><Day>02</Day></PubDate></History><Abstract>Introduction: Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) is an important negative regulator of T-cell responses. The49AG polymorphism of the CTLA-4 gene may be associated with systemic lupus erythematosus (SLE) risk, but the results from previous published studies have been inconsistent. We carried out a meta-analysis search to assess this association more precisely.Methods: A systematic search of six electronic databases (Pubmed, Science direct, OVID, Iran doc, Iran medex and SID:Scientefic Information Database) was performed for relevant articles published between 1978 and 2011. The odds ratio (OR) and its 95% confidence interval (95%CI) were used to assess the strength of the association. We evaluated both fixed and random effect models, depending on the presence of between-study heterogeneity. The data were analyzed using STATA software. Results: A total of 15 independent studies on the CTLA-4 gene 49AG polymorphism and SLE, including 1705 cases and 2299 controls were used in the meta-analysis. No significant association was found between 49AG polymorphism and SLE risk in the overall or subgroup analyses.Conclusion: This meta-analysis showed no significant association between 49AG polymorphism and SLE susceptibility. Large-scale and well-designed case-control studies are suggested.</Abstract></Article></ArticleSet>