Department of Geriatric Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
J Bone Miner Metab. 2010 Mar;28(2):220-6. doi: 10.1007/s00774-009-0124-0. Epub 2009 Oct 2.
HTRA1 (high-temperature requirement A1) has been implicated in the modulation of various disease pathologies. HTRA1 expression is upregulated in osteoarthritic joints, suggesting that it may contribute to the development of this debilitating disease. Moreover, recent reports have shown that the rs11200638, a single nucleotide polymorphism (SNP) in the promoter region of the HTRA1 gene, is strongly associated with an increased prevalence of age-related macular degeneration (AMD). In the present study, we examined the expression of the HTRA1 in human primary chondrocytes and an association between the rs11200638 SNP and radiographic features of spinal disc degeneration in 513 postmenopausal Japanese women. HTRA1 mRNA was detected and increased by TGF-beta treatment in human primary chondrocytes. As an association study of rs11200638 SNP in the HTRA1 gene, the subjects without the G allele (AA; n = 89) had a significantly higher spinal disc space narrowing score than the subjects bearing at least one G allele (GG + GA; n = 424) (P = 0.0292). We found that subjects without the G allele (AA) were significantly overrepresented in the subjects having a higher (> or =4) disc space narrowing score (P = 0.013; odds ratio 1.97; 95% confidence interval 1.15-3.37 by logistic regression analysis). A genetic variation at the HTRA1 gene promoter locus is associated with spinal disc degeneration, suggesting an involvement of the HTRA1 gene in osteoarthritis.
HTRA1(高温需求 A1)已被牵连到各种疾病病理学的调节中。HTRA1 在骨关节炎关节中的表达上调,表明它可能有助于这种使人衰弱的疾病的发展。此外,最近的报告表明,HTRA1 基因启动子区域的单核苷酸多态性(SNP)rs11200638 与年龄相关性黄斑变性(AMD)的患病率增加密切相关。在本研究中,我们检查了人原代软骨细胞中 HTRA1 的表达,以及 rs11200638 SNP 与 513 名绝经后日本女性脊柱椎间盘退变的放射学特征之间的关联。在人原代软骨细胞中,HTRA1 mRNA 被 TGF-β处理检测到并增加。作为 HTRA1 基因 rs11200638 SNP 的关联研究,没有 G 等位基因(AA;n = 89)的受试者的脊柱椎间盘狭窄评分明显高于至少携带一个 G 等位基因(GG + GA;n = 424)的受试者(P = 0.0292)。我们发现,没有 G 等位基因(AA)的受试者在具有较高(≥4)椎间盘狭窄评分的受试者中明显过多(P = 0.013;逻辑回归分析的优势比为 1.97;95%置信区间为 1.15-3.37)。HTRA1 基因启动子区域的遗传变异与脊柱椎间盘退变相关,表明 HTRA1 基因参与骨关节炎。