Genetic Biomarkers as Predictors of Response to Tocilizumab in Rheumatoid Arthritis: A Systematic Review and Meta-Analysis

被引:4
|
作者
Janahiraman, Sivakami [1 ,2 ]
Too, Chun Lai [3 ]
Lee, Kai Wei [4 ]
Shahril, Nor Shuhaila [5 ]
Leong, Chee Onn [6 ,7 ]
机构
[1] Int Med Univ, Sch Postgrad Studies, Kuala Lumpur 57000, Malaysia
[2] Minist Hlth Malaysia, Hosp Selayang, Pharm Dept, Selayang 68100, Malaysia
[3] Minist Hlth Malaysia, Inst Med Res, Immunogenet Unit, Natl Inst Hlth Complex, Shah Alam 40170, Selangor, Malaysia
[4] Univ Tunku Abdul Rahman, Fac Med & Hlth Sci, Dept Preclin Sci, Kajang 31900, Malaysia
[5] Minist Hlth Malaysia, Hosp Putrajaya, Med Dept, Putrajaya 62250, Malaysia
[6] Int Med Univ, Ctr Canc & Stem Cell Res Dev & Innovat IRDI, Inst Res, Kuala Lumpur 57000, Malaysia
[7] AGTC Genom, Kuala Lumpur 57000, Malaysia
基金
美国国家卫生研究院;
关键词
rheumatoid arthritis; tocilizumab; genetic; polymorphisms; predictor; treatment response; INTERLEUKIN-6 RECEPTOR GENE; IL-6; RECEPTOR; SOLUBLE IL-6; POLYMORPHISMS; PHARMACOGENETICS; ASSOCIATION; COMBINATION; STRATEGY; RISK;
D O I
10.3390/genes13071284
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rheumatoid arthritis (RA) is a lifelong, debilitating disease which incredibly impacts a patient's quality of life if not treated to the optimal target. The clinical response of tocilizumab, an interleukin-6 (IL-6) inhibitor, is associated with several gene polymorphisms, particularly targeting the IL-6 pathway. This systematic review and meta-analysis seeks to investigate genetic biomarkers that predict the treatment outcome of tocilizumab therapy in RA patients. After evaluating the quality of retrieved records, five studies were chosen to carry out a quantitative synthesis involving 591 participants. We analysed genetic markers of IL-6R single nucleotide polymorphism (SNP)s rs12083537, rs2228145 and rs4329505, FCGR3A, CD69, GALNT18 and FCGR2A. A plausible finding based on meta-analysis revealed that RA patients with homozygous AA genotype for rs12083537 polymorphism of the IL-6R gene demonstrate a better response to TCZ treatment as opposed to homozygous and heterozygous patients with the G allele. Nonetheless, limitations in evaluating the available studies by meta-analysis include a lack of studies with dissimilarities in study design and outcome definitions, small sample sizes with low statistical power and heterogeneity of cohorts, a restricted the number of tested SNPs and small effects for the selected variants. Inconsistent finding remains as a great challenge to forge ahead towards personalised medicine for RA management.
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页数:14
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