Wang Y, Chu M, Rong J, Xing B, Zhu L, Zhao Y, Zhuang X, Jiang L
Department of Epidemiology, Nantong University, School of Public Health, Nantong, Jiangsu Province, China.
Department of Orthopedic Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, China.
Bone Joint Res. 2016 May;5(5):169-74. doi: 10.1302/2046-3758.55.2000589.
Previous genome-wide association studies (GWAS) have reported significant association of the single nucleotide polymorphism (SNP) rs8044769 in the fat mass and obesity-associated gene (FTO) with osteoarthritis (OA) risk in European populations. However, these findings have not been confirmed in Chinese populations.
We systematically genotyped rs8044769 and evaluated the association between the genetic variants and OA risk in a case-controlled study including 196 OA cases and 442 controls in a northern Chinese population. Genotyping was performed using the Sequenom MassARRAY iPLEX platform.
We found that the variant T allele of rs8044769 showed no significant association of OA risk (p = 0.791), or association with body mass index (BMI) (pmeta = 0.786) in an additive genetic model. However, we detected a significant interaction between rs8044769 genotypes and BMI on OA risk (p = 0.037), as well as a borderline interaction between rs8044769 genotypes and age on OA risk (p = 0.062).
Our findings indicate that rs8044769 in the FTO gene may not modify individual susceptibility to OA or increased BMI in the Chinese population. Further studies are warranted to validate and extend our findings.Cite this article: Prof L. Jiang. No association of the single nucleotide polymorphism rs8044769 in the fat mass and obesity-associated gene with knee osteoarthritis risk and body mass index: A population-based study in China. Bone Joint Res 2016;5:169-174. DOI: 10.1302/2046-3758.55.2000589.
既往全基因组关联研究(GWAS)报道,在欧洲人群中,脂肪量和肥胖相关基因(FTO)中的单核苷酸多态性(SNP)rs8044769与骨关节炎(OA)风险显著相关。然而,这些研究结果尚未在中国人群中得到证实。
在一项病例对照研究中,我们对rs8044769进行了系统基因分型,并评估了基因变异与OA风险之间的关联。该研究纳入了196例OA患者和442例对照,来自中国北方人群。基因分型采用Sequenom MassARRAY iPLEX平台进行。
我们发现,在加性遗传模型中,rs8044769的变异T等位基因与OA风险无显著关联(p = 0.791),与体重指数(BMI)也无关联(pmeta = 0.786)。然而,我们检测到rs8044769基因型与BMI之间对OA风险存在显著交互作用(p = 0.037),以及rs8044769基因型与年龄之间对OA风险存在临界交互作用(p = 0.062)。
我们的研究结果表明,在中国人群中,FTO基因中的rs8044769可能不会改变个体对OA的易感性或增加BMI。需要进一步研究来验证和扩展我们的研究结果。引用本文:蒋教授。脂肪量和肥胖相关基因中的单核苷酸多态性rs8044769与膝关节骨关节炎风险及体重指数无关联:一项基于中国人群的研究。骨关节研究2016;5:169 - 174。DOI:10.1302/2046 - 3758.55.2000589。