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首页> 外文期刊>BioMed research international >The Effect of Bradykinin B2 Receptor Polymorphisms on the Susceptibility and Severity of Osteoarthritis in a Chinese Cohort
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The Effect of Bradykinin B2 Receptor Polymorphisms on the Susceptibility and Severity of Osteoarthritis in a Chinese Cohort

机译:缓激肽B2受体多态性对中国人群骨关节炎的敏感性和严重性的影响

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摘要

Background. The B2-bradykinin receptor (BDKRB2) has been reported to associate with onset and development of Osteoarthritis (OA); however, the role of BDKRB2 genetic polymorphisms in OA remains unknown.Method. A total of 245 patients with primary knee OA and 264 healthy volunteer were recruited. BDKRB2 gene polymorphisms, −58T/C and +9/−9 bp polymorphisms, were genotyped.Results. The genotype distributions and allele frequencies of +9/−9 bp polymorphisms significantly differed between OA and control subjects. Logistic regression analysis showed carriers with −9/−9 genotype had a significantly increased risk for knee OA compared with the +9/+9 genotype (adjustedOR=2.356,P<0.001). The OR for −9 allele carriage was significantly higher than +9 allele carriage (adjustedOR=1.52,P<0.001). The +9/−9 bp polymorphisms also determined the OA radiographic severity. The presence of −9 bp was associated with severer OA. The −58T/C polymorphisms did not affect OA risk and severity.Conclusion. The +9/−9 bp polymorphisms of BDKRB2 gene may be used as a genetic marker for the susceptibility and severity of OA.
机译:背景。据报道,B2-缓激肽受体(BDKRB2)与骨关节炎(OA)的发生和发展有关。然而,BDKRB2基因多态性在OA中的作用仍然未知。总共招募了245例原发性膝关节炎患者和264名健康志愿者。对BDKRB2基因多态性-58T / C和+ 9 / -9-9bp多态性进行基因分型。 + 9 / −9 bp多态性的基因型分布和等位基因频率在OA和对照组之间存在显着差异。 Logistic回归分析显示,与+ 9 / + 9基因型相比,具有-9 / -9基因型的携带者患膝OA的风险显着增加(校正OR = 2.356,P <0.001)。 -9个等位基因支架的OR显着高于+9个等位基因支架的OR(调整后的OR = 1.52,P <0.001)。 + 9 / −9 bp多态性还决定了OA的放射学严重程度。 -9 bp的存在与更严重的OA有关。 −58T / C多态性不影响OA的风险和严重性。 BDKRB2基因的+ 9 / −9 bp多态性可以用作OA易感性和严重性的遗传标记。

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