St. Clare's Mercy Hospital, St. John's, Newfoundland A1C 5B8, Canada.
J Rheumatol. 2011 Mar;38(3):564-6. doi: 10.3899/jrheum.101123.
Psoriasis and psoriatic arthritis (PsA) are heterogeneous diseases. While both have a strong genetic basis, it is strongest for PsA, where fewer investigators are studying its genetics. Over the last year the number of independent genetic loci associated with psoriasis has substantially increased, mostly due to completion of multiple genome-wide association studies (GWAS) in psoriasis. At least 2 GWAS efforts are now under way in PsA to identify novel genes in this disease; a metaanalysis of genome-wide scans and further studies must follow to examine the genetics of disease expression, epistatic interaction, and gene-environment interaction. In the long term, it is anticipated that genome-wide sequencing is likely to generate another wave of novel genes in PsA. At the annual meeting of the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) in Stockholm, Sweden, in 2009, members discussed issues and challenges regarding the advancement of the genetics of PsA; results of those discussions are summarized here.
银屑病和银屑病关节炎(PsA)是异质性疾病。虽然两者都有很强的遗传基础,但在 PsA 中,遗传基础更强,研究其遗传学的研究人员却较少。在过去的一年中,与银屑病相关的独立遗传位点数量大大增加,这主要是由于完成了多项银屑病全基因组关联研究(GWAS)。目前至少有 2 项 PsA 的 GWAS 工作正在进行,以确定该疾病中的新基因;必须进行全基因组扫描的荟萃分析和进一步的研究,以检查疾病表型、上位性相互作用和基因-环境相互作用的遗传学。从长远来看,预计全基因组测序很可能会在 PsA 中产生另一波新基因。在 2009 年瑞典斯德哥尔摩举行的银屑病和银屑病关节炎研究和评估组织(GRAPPA)年会上,成员们讨论了推进 PsA 遗传学的问题和挑战;这里总结了这些讨论的结果。