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Genetics of rheumatoid arthritis: time for a change!

机译:类风湿关节炎的遗传学:改变的时候了!

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PURPOSE OF REVIEW: To review recent progress in the genetics of rheumatoid arthritis (RA) and discuss the implications for understanding the pathogenesis of the disease as well as clinical application. RECENT FINDINGS: Protection against anticitrullinated protein antibody (ACPA) positive RA was shown to be associated wit DRB1*1301. Genome-wide association studies (GWASs) added about 10 new loci to the list of already more than 20 loci associated with RA, so the list is now over 30. Typing for the known risk loci is not helpful for prediction of the risk for RA. It is remarkable how few functional studies have been published. SUMMARY: Known genetic factors explain 50-60% of the genetic variance for susceptibility to ACPA-positive and 30-50% for ACPA-negative RA. Searching for the remaining missing or hidden heritability is in all probability not going to yield much for prediction and/or targeted intervention. Therefore, I conclude that if you want to find more genes you should have a lot of patience, time and money, stop with convential GWAS and invest in large-scale sequencing of selected patients and controls. I have a better suggestion, however: use the information that is already available to perform functional studies in order to understand the mechanism of the known associations!
机译:审查的目的:审查类风湿关节炎(RA)的遗传学的最新进展,并讨论对理解疾病的发病机理和临床应用的意义。最近的发现:DRB1 * 1301与抗瓜氨酸蛋白抗体(ACPA)阳性RA的保护作用有关。全基因组关联研究(GWAS)在与RA相关的已经超过20个基因座的列表中添加了大约10个新基因座,因此该列表现在超过30个。键入已知的风险基因座无助于预测RA的风险。值得注意的是,很少有功能研究发表。摘要:已知的遗传因素解释了50-60%的遗传变异对ACPA阳性易感性和30-50%的ACPA阴性RA。搜索剩余的遗漏或隐藏的遗传力很可能不会为预测和/或目标干预带来很多收益。因此,我得出的结论是,如果您想找到更多的基因,则应该有足够的耐心,时间和金钱,请停止使用常规的GWAS,并投资于选定患者和对照的大规模测序。但是,我有一个更好的建议:使用已经可用的信息进行功能研究,以了解已知关联的机制!

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