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 in | World journal of gastroenterology : WJG Vol. 13; no. 15; pp. 2205 - 2208 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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 |