Uitterlinden A G, Burger H, Huang Q, Odding E, Duijn C M, Hofman A, Birkenhäger J C, van Leeuwen J P, Pols H A
Department of Internal Medicine III, Erasmus University Medical School, 3000 DR Rotterdam, The Netherlands.
J Clin Invest. 1997 Jul 15;100(2):259-63. doi: 10.1172/JCI119530.
Osteoporosis and osteoarthritis are age-related disorders of the skeleton with genetic components. Low bone density is a risk factor for osteoporotic fracture while osteoarthritis is associated with increased bone density. The 1,25-dihydroxyvitamin D3 receptor (VDR) gene locus was previously found to be associated with bone density. We therefore studied the relationship between radiographic osteoarthritis at the knee and VDR genotype in a population-based sample (n = 846), using molecular haplotyping of anonymous intragenic DNA polymorphisms. Radiographic osteoarthritis was defined using the Kellgren score, which is based on the assessment of osteophytes and joint space narrowing (JSN). We show that one VDR haplotype allele is significantly overrepresented in individuals with knee osteoarthritis and associated with a 2.27-fold increased relative risk (95% confidence interval 1.46, 3.52). Adjustment for bone density at the femoral neck did not change these results, indicating that the association is not mediated by bone density. The association appeared to be largely explained by the presence of osteophytes rather than JSN. Our results indicate a role of the VDR gene in the pathogenesis of osteophytes while linkage disequilibrium with another nearby gene, i.e., the collagen type IIa1 gene encoding the most abundant protein in cartilage, might contribute to the association.
骨质疏松症和骨关节炎是与年龄相关的骨骼疾病,具有遗传成分。低骨密度是骨质疏松性骨折的危险因素,而骨关节炎与骨密度增加有关。先前发现1,25-二羟基维生素D3受体(VDR)基因位点与骨密度有关。因此,我们在一个基于人群的样本(n = 846)中,使用匿名基因内DNA多态性的分子单倍型分析,研究了膝关节影像学骨关节炎与VDR基因型之间的关系。影像学骨关节炎采用Kellgren评分定义,该评分基于对骨赘和关节间隙变窄(JSN)的评估。我们发现,一种VDR单倍型等位基因在膝关节骨关节炎患者中显著过度表达,并且与相对风险增加2.27倍相关(95%置信区间1.46, 3.52)。对股骨颈骨密度进行校正后,这些结果并未改变,表明这种关联不是由骨密度介导的。这种关联似乎主要由骨赘的存在而非JSN来解释。我们的结果表明VDR基因在骨赘发病机制中起作用,而与另一个附近基因(即编码软骨中最丰富蛋白质的IIa1型胶原基因)的连锁不平衡可能促成了这种关联。