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Original Research Article | OPEN ACCESS

Genetic polymorphisms of osteopontin in association with ankylosing spondylitis in a chinese population

Xiu-fang Wang, Yi Cai

Department of Pain, The Central Hospital of Wuhan, Wuhan, Hubei Province, 430021, China;

For correspondence:-  Yi Cai   Email: 187076605@qq.com

Received: 7 August 2015        Accepted: 5 November 2015        Published: 27 December 2015

Citation: Wang X, Cai Y. Genetic polymorphisms of osteopontin in association with ankylosing spondylitis in a chinese population. Trop J Pharm Res 2015; 14(12):2319-2323 doi: 10.4314/tjpr.v14i12.24

© 2015 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To determine the association of osteopontin (OPN) polymorphisms with ankylosing spondylitis (AS).
Methods: A total of 120 cases diagnosed with AS and 106 age- and sex-matched healthy controls were recruited. All the patients were human leukocyte antigen (HLA)-B27 positive. Three single nucleotide polymorphisms were genotyped using direct sequencing
Results: The T allele at -443 SNP had significantly higher frequency in AS patients (0.1875) than the controls (0.1085, p < 0.01). The rate of CT+TT genotype in AS patients was significantly higher than those with CC genotype compared with the control (p < 0.01).
Conclusion: SNP at -443 of OPN gene can serve as a candidate genetic marker to evaluate the risk of AS, thus indicating that subjects who carry T allele have a significantly higher risk of developing AS.

Keywords: Genetic polymorphism, Ankylosing spondylitis, Osteopontin, Sequencing

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