Apoptosis-related Fas and FasL gene polymorphisms' associations with knee osteoarthritis

11Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.
Get full text

Abstract

To investigate the associations between Fas and FasL gene polymorphisms and susceptibility to knee osteoarthritis. Genomic DNA was obtained from 146 patients with knee osteoarthritis and 102 healthy controls. Genotype distributions and allelic frequencies of four polymorphisms of Fas (-670 G>A rs1800682, -1377 G>A rs2234767) and FasL (IVS2nt-124 A>G rs5030772, -844 T>C rs763110) genes were compared between the groups. Thereafter, this association was investigated between patients and controls of the same sex. There were significant differences between patients with knee osteoarthritis and controls regarding the genotype distributions and allelic frequencies of Fas-1377 G>A polymorphism (P = 0.0001 and P = 0.005, respectively). The Fas-1377 GG genotype and G allele were significantly more frequent in patients with knee osteoarthritis than in controls. Genotype distributions and allelic frequencies of Fas-670 G>A, FasL-844 T>C, and FasL IVS2nt-124 A>G polymorphisms did not differ between the groups (P > 0.05). However, there were no significant differences between patients and controls of the same sex (P > 0.05). These findings suggest that the Fas-1377 G>A polymorphism in the Fas gene related with apoptosis may contribute to susceptibility to knee osteoarthritis in the Turkish population. There is a need for further studies to evaluate the role of apoptosis in large cohorts. © 2013 Springer-Verlag Berlin Heidelberg.

Cite

CITATION STYLE

APA

Sezgin, M., Barlas, I. Ö., Yildir, S., Türköz, G., Ankarali, H. Ç., Şahin, G., & Erdal, M. E. (2013). Apoptosis-related Fas and FasL gene polymorphisms’ associations with knee osteoarthritis. Rheumatology International, 33(8), 2039–2043. https://doi.org/10.1007/s00296-013-2688-1

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free