Ikegawa Shiro
RIKEN, SNP Research Center, Laboratory for Bone and Joint Diseases.
Clin Calcium. 2008 Feb;18(2):162-7.
Osteoarthritis (OA) is the most common human arthritis characterized by the degeneration of articular cartilage. OA is a major concern for aging societies worldwide. Epidemiological and genetic studies have revealed that OA is a polygenic disease. Growth differentiation factor 5 (GDF5 ) is a good candidate gene for OA. We have recently found a novel ENU-mutagenesis mouse that presents early onset OA in the elbow joint in homozygotes. Through case-control association studies, we have found that GDF5 is associated with OA in the Japanese population. A single nucleotide polymorphism (SNP) in the 5'-UTR of GDF5 (+ 104T/C ; rs143383) showed a significant association (p = 1.8 x 10(- 13)) in hip OA. This association was replicated for knee OA in both Japanese and Han Chinese populations as well as in West European Caucasians. This SNP is located in the core promoter of GDF5 and exerted allelic differences on transcription, with the susceptibility allele showing reduced transcriptional activity. Our findings implicate GDF5 as a susceptibility gene for OA in worldwide populations and suggest that decreased GDF5 expression is involved in OA pathogenesis.
骨关节炎(OA)是最常见的人类关节炎,其特征是关节软骨退变。OA是全球老龄化社会的一个主要关注点。流行病学和遗传学研究表明,OA是一种多基因疾病。生长分化因子5(GDF5)是OA的一个良好候选基因。我们最近发现了一种新型的ENU诱变小鼠,其纯合子在肘关节出现早发性OA。通过病例对照关联研究,我们发现GDF5与日本人群的OA相关。GDF5 5'-UTR中的一个单核苷酸多态性(SNP)(+104T/C;rs143383)在髋部OA中显示出显著关联(p = 1.8 x 10(-13))。这种关联在日本和汉族人群以及西欧白种人的膝部OA中也得到了重复验证。该SNP位于GDF5的核心启动子区域,在转录上表现出等位基因差异,易感性等位基因的转录活性降低。我们的研究结果表明GDF5是全球人群中OA的一个易感基因,并提示GDF5表达降低参与了OA的发病机制。