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https://hdl.handle.net/11499/7176
Title: | PTPN22 gene polymorphism in Takayasu's arteritis | Authors: | Sahin, N. Aksu, K. Kamali, S. Bicakcigil, M. Özbalkan, Z. Fresko, I. Özer, H. |
Keywords: | PTPN22 Single nucleotide polymorphism Takayasu's arteritis adenine guanine protein tyrosine phosphatase adult amino acid substitution angiography aorta arch syndrome article autoimmunity case control study controlled study enzyme degradation female gene amplification gene frequency genetic association genetic polymorphism genetic screening genetic susceptibility genotype heterozygosity human human cell major clinical study male polymerase chain reaction population genetics priority journal prognosis restriction fragment length polymorphism single nucleotide polymorphism Turkey (republic) Adult Case-Control Studies Female Gene Frequency Genetic Predisposition to Disease Heterozygote Humans Male Middle Aged Polymorphism, Restriction Fragment Length Polymorphism, Single Nucleotide Protein Tyrosine Phosphatase, Non-Receptor Type 22 Takayasu Arteritis Turkey |
Abstract: | Objective. Takayasu's arteritis (TA) is a chronic, rare granulomatous panarteritis of unknown aetiology involving mainly the aorta and its major branches. In this study, genetic susceptibility to TA has been investigated by screening the functional single nucleotide polymorphism (SNP) of PTPN22 gene encoding the lymphoid-specific protein tyrosine phosphatase. Methods. Totally, 181 patients with TA and 177 healthy controls are genotyped by PCR-RFLP method for the SNP rs2476601 (A/G) of PTPN22 gene. Polymorphic region was amplified by PCR and digested with Xcm I enzyme. Results. Detected frequencies of heterozygous genotype (AG) were 5.1% (9/177) in control group and 3.8% (7/181) in TA group (P = 0.61, odds ratio: 0.75, 95% CI: 0.3, 2.0). No association with angiographic type, vascular involvement or prognosis of TA was observed either. Conclusion. The distribution of PTPN22 polymorphism did not reveal any association with TA in Turkey. © The Author 2008. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. | URI: | https://hdl.handle.net/11499/7176 https://doi.org/10.1093/rheumatology/ken106 |
ISSN: | 1462-0324 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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