Literature DB >> 19524188

Association of CTLA-4 gene polymorphism with Graves' disease and ophthalmopathy in Iranian patients.

Alireza Esteghamati1, Omid Khalilzadeh, Zahra Mobarra, Mehdi Anvari, Maryam Tahvildari, Hoda Mojazi Amiri, Armin Rashidi, Ghasem Solgi, Kazem Parivar, Behrouz Nikbin, Aliakbar Amirzargar.   

Abstract

BACKGROUND: The cytotoxic T lymphocyte associated antigen-4 (CTLA-4) gene, is one of the candidate genes for susceptibility to Graves' disease. This study aimed to investigate the association of Graves' disease and Graves' ophthalmopathy with polymorphisms at position +49 in exon 1 and positions -318 and -1147 in the promoter region of CTLA-4 gene in Iranian patients.
METHODS: A total of 205 unrelated Iranian patients with Graves' disease who were referred to the outpatient endocrine clinic of a large university general hospital and 103 sex-matched healthy controls were included in this study. Venous blood was obtained, genomic DNA was extracted by a salting out method, and the polymorphisms at positions +49, -318 and -1147 of the CTLA-4 gene were determined using the PCR-restriction fragment length polymorphism method (PCR-RFLP). Genotype and allele frequencies were determined.
RESULTS: The frequency of the G allele at position +49 was significantly higher in patients with Graves' disease than in the control group (27.1% vs. 15.1%, OR=2.096, 95%CI=1.350-3.253 and p<0.01). Significant trends were not seen for the other two polymorphisms studied. In patients with ophthalmopathy, the frequency of the G allele at position +49 was higher than in those without ophthalmopathy (33.8% vs. 20.0%, OR=2.043, 95%CI=1.304-3.202 and p<0.01).
CONCLUSION: The results of this study suggest that the G allele at position +49 in exon1 of the CTLA-4 gene is associated with Graves' disease and Graves' ophthalmopathy in Iranian patients.

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Year:  2009        PMID: 19524188     DOI: 10.1016/j.ejim.2008.12.005

Source DB:  PubMed          Journal:  Eur J Intern Med        ISSN: 0953-6205            Impact factor:   4.487


  12 in total

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2.  [Association between CTLA-4 gene polymorphism and Henoch-Schönlein purpura in children].

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Authors:  Omid Khalilzadeh; Sina Noshad; Armin Rashidi; Aliakbar Amirzargar
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4.  Associations of CTLA4 Gene Polymorphisms with Graves' Ophthalmopathy: A Meta-Analysis.

Authors:  Pengfei Du; Xiaojie Ma; Changjiang Wang
Journal:  Int J Genomics       Date:  2014-07-09       Impact factor: 2.326

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Authors:  Jwu Jin Khong; Kathryn P Burdon; Yi Lu; Kate Laurie; Lefta Leonardos; Paul N Baird; Srujana Sahebjada; John P Walsh; Adam Gajdatsy; Peter R Ebeling; Peter Shane Hamblin; Rosemary Wong; Simon P Forehan; Spiros Fourlanos; Anthony P Roberts; Matthew Doogue; Dinesh Selva; Grant W Montgomery; Stuart Macgregor; Jamie E Craig
Journal:  BMC Genomics       Date:  2016-11-18       Impact factor: 3.969

6.  Association between rs3087243 and rs231775 polymorphism within the cytotoxic T-lymphocyte antigen 4 gene and Graves' disease: a case/control study combined with meta-analyses.

Authors:  Yaqin Tu; Guorun Fan; Yu Dai; Tianshu Zeng; Fei Xiao; Lulu Chen; Wen Kong
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Authors:  Natacha Turck; Simone Eperon; Maria De Los Angeles Gracia; Aurélie Obéric; Mehrad Hamédani
Journal:  Dis Markers       Date:  2018-03-15       Impact factor: 3.434

8.  Association of Cytotoxic T Lymphocyte Antigen-4 Gene Polymorphisms with Psoriasis Vulgaris: A Case-Control Study in Turkish Population.

Authors:  Hatice Gül Dursun; Hüseyin Osman Yılmaz; Recep Dursun; Sevsen Kulaksızoğlu
Journal:  J Immunol Res       Date:  2018-04-23       Impact factor: 4.818

9.  Association between the CTLA-4 +49A/G polymorphism and Graves' disease: A meta-analysis.

Authors:  Xiaoyu Si; Xiufeng Zhang; Wenru Tang; Ying Luo
Journal:  Exp Ther Med       Date:  2012-06-20       Impact factor: 2.447

10.  The associations between the polymorphisms in the CTLA-4 gene and the risk of Graves' disease in the Chinese population.

Authors:  Liang Du; Jiqiao Yang; Jichong Huang; Yaxian Ma; Haichuan Wang; Tianyuan Xiong; Zhangpeng Xiang; Yonggang Zhang; Jin Huang
Journal:  BMC Med Genet       Date:  2013-04-19       Impact factor: 2.103

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