Vaes R B A, Rivadeneira F, Kerkhof J M, Hofman A, Pols H A P, Uitterlinden A G, van Meurs J B J
Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, The Netherlands.
Ann Rheum Dis. 2009 Nov;68(11):1754-60. doi: 10.1136/ard.2008.099655. Epub 2008 Nov 24.
A polymorphism (rs143383; T to C) near the GDF5 gene has been associated with height and osteoarthritis (OA), but debate exists about whether its primary biological action is directed to cartilage or bone.
To study the association between genetic variation in the GDF5 region and radiographic osteoarthritis (ROA) susceptibility, height, bone size parameters and fracture risk in a large population-based cohort of Caucasian elderly subjects.
6365 men and women had genotype data available. ROA was defined as a Kellgren/Lawrence (K/L) score > or =2 for hand, knee and hip joints. CTX-II levels, height, bone mineral density (BMD), bone size and fracture risk were also assessed.
rs143383 and three highly correlated single nucleotide polymorphisms (SNPs) in the GDF5 region were found to be independently associated with OA, height, bone size and fracture risk in women. Women with homozygotes for the rs143383 C allele had a 37% lower risk for hand OA (p = 8 x 10(-6)) and a 28% lower risk for knee OA (p = 0.003). In addition, they were 1.1 cm taller (p = 0.001), had a larger hip axis length (HAL) (p = 4 x 10(-4)) and had a 29% increased risk of incident non-vertebral fractures (p = 0.02). No associations with hip OA or BMD were detected. No associations were found in men.
This population-based study shows that GDF5 gene variants are associated with hand OA, knee OA and fracture risk in elderly women. It also replicates previous association between GDF5 variation and height. Furthermore, our findings for HAL suggest that GDF5 action is primarily directed to the long bones, rather than the axial skeleton.
生长分化因子5(GDF5)基因附近的一个多态性位点(rs143383;T突变为C)与身高和骨关节炎(OA)有关,但关于其主要生物学作用是针对软骨还是骨骼存在争议。
在一个以白种人老年人群为基础的大型队列中,研究GDF5区域的基因变异与放射学骨关节炎(ROA)易感性、身高、骨大小参数及骨折风险之间的关联。
6365名男性和女性有可用的基因型数据。ROA定义为手部、膝关节和髋关节的凯尔格伦/劳伦斯(K/L)评分≥2。还评估了Ⅱ型胶原C端肽(CTX-II)水平、身高、骨密度(BMD)、骨大小和骨折风险。
发现rs143383以及GDF5区域的三个高度相关的单核苷酸多态性(SNP)与女性的OA、身高、骨大小和骨折风险独立相关。rs143383 C等位基因纯合子的女性患手部OA的风险降低37%(p = 8×10⁻⁶),患膝关节OA的风险降低28%(p = 0.003)。此外,她们身高高1.1厘米(p = 0.001),髋轴长度(HAL)更大(p = 4×10⁻⁴),发生非椎体骨折的风险增加29%(p = 0.02)。未检测到与髋关节OA或BMD的关联。在男性中未发现关联。
这项基于人群的研究表明,GDF5基因变异与老年女性的手部OA、膝关节OA及骨折风险相关。它还重复了先前GDF5变异与身高之间的关联。此外,我们关于HAL的研究结果表明,GDF5的作用主要针对长骨,而非中轴骨骼。