No association of the cytotoxic T-lymphocyte associated gene CTLA4 +49A/G polymorphisms with Crohn's disease and ulcerative colitis in Hungarian population samples

The goal of the current work was to analyse the prevalence of the +49A/G variant of the cytotoxic T-lymphocyte antigen 4 gene (CTLA4) in Hungarian patients with Crohnos disease (CD) and ulcerative colitis (UC). A total of 130 unrelated subjects with CD and 150 with UC, and 170 matched controls were...

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Published inWorld journal of gastroenterology : WJG Vol. 13; no. 15; pp. 2205 - 2208
Main Authors Magyari, Lili, Faragó, Bernadett, Bene, Judit, Horvatovich, Katalin, Lakner, Lilla, Varga, Márta, Figler, Mária, Gasztonyi, Beáta, Mózsik, Gyula, Melegh, Béla
Format Journal Article
LanguageEnglish
Published United States Department of Medical Genetics and Child Development, University of Pécs, Pécs, Hungary%Department of Medical Genetics and Child Development, University of Pécs, Pécs, Hungary 21.04.2007
MTA PTE Clinical Genetics Research Group of the Hungarian Academy of Sciences at the University of Pécs, Pécs,Hungary%Markusovszky Hospital, Department of Medicine and Gastroenterology, Szombathely, Hungary%Réthy Pál Hospital, 3rd Department of Medicine and Gastroenterology, Békéscsaba, Hungary%1st Department of Medicine, School of Medicine, University of Pécs, Pécs, Hungary%Department of Gastroenterology, Zala County Hospital, Zalaegerszeg, Hungary
Baishideng Publishing Group Co., Limited
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Summary:The goal of the current work was to analyse the prevalence of the +49A/G variant of the cytotoxic T-lymphocyte antigen 4 gene (CTLA4) in Hungarian patients with Crohnos disease (CD) and ulcerative colitis (UC). A total of 130 unrelated subjects with CD and 150 with UC, and 170 matched controls were genotyped for the single nucleotide polymorphism (SNP). The genotypes were determined by using PCR/RFLP test. The G allele frequency and the prevalence of the GG genotype were 38.1% and 12.3% in the CD group, 40.6% and 18.6% in the UC patients, and 37.4% and 15.9% in the control group, respectively. The results of the current study show that carriage of the +49G SNP in heterozygous or in homozygous form does not confer risk either for CD or for UC in the Hungarian population.
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Correspondence to: Dr. Béla Melegh, Professor of Medical Genetics and Pediatrics, Department of Medical Genetics and Child Development, University of Pécs, H-7624 Pécs, Szigeti 12, Hungary. bela.melegh@aok.pte.hu
Telephone: +36-72-536427 Fax: +36-72-536427
Author contributions: All authors contributed equally to the work.
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v13.i15.2205