Premium
TNFRSF1A polymorphisms and their role in multiple sclerosis susceptibility and severity in the Slovak population
Author(s) -
Javor Juraj,
Shawkatová Ivana,
Ďurmanová Vladimíra,
Párnická Zuzana,
Čierny Daniel,
Michalik Jozef,
ČopíkováCudráková Daniela,
Smahová Barbora,
Gmitterová Karin,
Peterajová Ľubica,
Bucová Mária
Publication year - 2018
Publication title -
international journal of immunogenetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.41
H-Index - 47
eISSN - 1744-313X
pISSN - 1744-3121
DOI - 10.1111/iji.12388
Subject(s) - medicine , genotype , multiple sclerosis , odds ratio , allele , genetic predisposition , snp , disease , population , immunology , single nucleotide polymorphism , gastroenterology , genetics , biology , gene , environmental health
Tumour necrosis factor (TNF)‐mediated signalling plays a key role in inflammatory and neurodegenerative processes leading to the development of multiple sclerosis (MS). Recent studies have highlighted the role of tumour necrosis factor receptor superfamily member 1A (TNFRSF1A) gene encoding the type 1 TNF receptor in the genetic predisposition to MS. This study aimed to validate the association of TNFRSF1A rs1800693 and rs4149584 polymorphisms with susceptibility to MS in the Slovak population and analyse their influence on age at disease onset, severity, and disability progression. Polymerase chain reaction–restriction fragment length polymorphism method was used to genotype both TNFRSF1A polymorphisms in 541 MS patients and 724 healthy controls. Logistic regression analysis revealed a significantly increased risk of developing MS for the carriers of rs1800693 C allele (TC + CC vs. TT: p corr = 0.005; OR = 1.61; 95% CI = 1.23–2.12), irrespective of sex and carriage of the major MS risk allele HLA‐DRB1*15:01 . On the other hand, no association could be found between rs4149584 and MS risk (GA + AA vs. GG: p corr = 1.00; OR = 1.25; 95% CI = 0.71–2.21). Moreover, neither polymorphism was significantly associated with age at disease onset, MS Severity Score (MSSS) or MS Progression Index (PI) in any of the inheritance models. In conclusion, our results provide support for a sex‐ and HLA‐DRB1*15:01 ‐independent association of TNFRSF1A rs1800693 SNP with MS susceptibility, but not with age at disease onset, severity or rate of disability accumulation.