Dai Xiaoyu, Wang Chao, Dai Jin, Shi Dongquan, Xu Zhihong, Chen Dongyang, Teng Huajian, Jiang Qing
The Center of Diagnosis and Treatment for Joint Disease, Drum Tower Hospital Affiliated to Medical School of Nanjing University, Zhongshan Road 321, Nanjing, Jiangsu 210008, China ; Joint Research Center for Bone and Joint Disease, Model Animal Research Center (MARC), Nanjing University, Nanjing, Jiangsu 210093, China.
Joint Research Center for Bone and Joint Disease, Model Animal Research Center (MARC), Nanjing University, Nanjing, Jiangsu 210093, China.
Biomed Res Int. 2014;2014:151457. doi: 10.1155/2014/151457. Epub 2014 Mar 17.
Osteoarthritis (OA) is the most prevalent form of arthritis and its multifactorial nature has been increasingly recognized. Genetic factors play an important role in OA etiology and estrogen receptor alpha (ESR1) gene polymorphisms may be involved. This study tried to explore whether the ESR1 gene single nucleotide polymorphisms (SNPs) were associated with primary knee OA in the Chinese Han population. Two SNPs, rs2234693 and rs9340799, were genotyped in 469 cases and 522 controls. Rs2234693 was associated with knee OA in the dominant genetic model (TT + TC versus CC) (P = 0.025) and a higher T allele frequency existed (P = 0.047) among females. The combined genotype (TT + TC) (P = 0.025) and T allele (P = 0.016) were related with mild knee OA only. For rs9340799, A allele was associated with knee OA in all subjects (P = 0.031) and females (P = 0.046). Statistical differences were detected in the dominant genetic model (AA + AG versus GG) among females (P = 0.030). The combined genotype (AA + AG) (P = 0.036) and A allele (P = 0.039) were merely correlated with mild knee OA. ESR1 gene is considerably associated with knee OA etiology in the Chinese Han population.
骨关节炎(OA)是最常见的关节炎形式,其多因素性质已得到越来越多的认识。遗传因素在OA病因中起重要作用,雌激素受体α(ESR1)基因多态性可能与之相关。本研究试图探讨ESR1基因单核苷酸多态性(SNP)是否与中国汉族人群的原发性膝关节OA相关。对469例患者和522例对照进行了rs2234693和rs9340799这两个SNP的基因分型。rs2234693在显性遗传模型(TT + TC与CC)中与膝关节OA相关(P = 0.025),女性中T等位基因频率较高(P = 0.047)。联合基因型(TT + TC)(P = 0.025)和T等位基因(P = 0.016)仅与轻度膝关节OA相关。对于rs9340799,A等位基因在所有受试者(P = 0.031)和女性(P = 0.046)中与膝关节OA相关。在女性的显性遗传模型(AA + AG与GG)中检测到统计学差异(P = 0.030)。联合基因型(AA + AG)(P = 0.036)和A等位基因(P = 0.039)仅与轻度膝关节OA相关。ESR1基因与中国汉族人群的膝关节OA病因密切相关。