Is Complement Factor H Tyr402His Variant a Potential Cause of Ankylosing Spondylitis?

被引:0
作者
Pehlivan, Sacide [1 ]
Akaltun, Mazlum Serdar [2 ]
Pehlivan, Mustafa [3 ]
Gursoy, Savas [2 ]
Nursal, Ayse Feyda [4 ]
机构
[1] Istanbul Univ, Dept Med Biol, Fac Med, Istanbul, Turkey
[2] Gaziantep Univ, Dept Phys Med & Rehabil, Fac Med, Gaziantep, Turkey
[3] Gaziantep Univ, Dept Haematol, Fac Med, Gaziantep, Turkey
[4] Hitit Univ, Dept Med Genet, Fac Med, Corum, Turkey
来源
HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI | 2020年 / 58卷 / 02期
关键词
Ankylosing spondylitis; complement factor H; variant; RHEUMATOID-ARTHRITIS; SYNOVIAL-FLUIDS; ASSOCIATION; ACTIVATION; RISK; SUSCEPTIBILITY; POLYMORPHISMS; SYSTEM; GENE; DNA;
D O I
10.4274/haseki.galenos.2020.5783
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: Ankylosing spondylitis (AS) is an autoimmune disease caused by chronic inflammatory response. Complement system is the major component of the innate immune defence. In this study, we investigated the potential association between complement factor H (CFH) gene Tyr402His variant (rs1061170) with AS in a Turkish population. Methods: Seventy-eight AS patients and 80 healthy individuals were enrolled in the present study as case and control subjects, respectively. The Tyr402His variant of CFH gene was analysed by PCR-RFLP method. Results: There was no statistically significant difference between AS patients and healthy controls in terms of CFH Tyr402His genotype and allele frequencies. However, the visual analogue scale (VAS) daytime and the AS Quality of Life (ASQoL) were significantly different according to CFH Tyr402His genotype distribution (p=0.032 and p=0.036, respectively). VAS of daytime and ASQoL were higher in subjects carrying Tyr402His variant Tyr/Tyr + Tyr/His genotypes compared to those carrying His/His genotype. Conclusion: This is the first study evaluating the association between CFH Tyr402His and susceptibility to AS in a Turkish population. Although CFH Tyr402His variant was not considered a candidate gene for AS susceptibility in our samples, some clinical findings seem to be associated with genotype distribution of CFH Tyr402His variant.
引用
收藏
页码:142 / 147
页数:6
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