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Genetic polymorphisms of NOS2 and predisposition to fracture non-union: A case control study based on Han Chinese population

机译:NOS2基因多态性与骨折不愈合的易感性:基于汉族人群的病例对照研究

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摘要

A non-union, especially atrophic non-unions, is a permanent failure of healing following a fracture and can be difficult to treat. Approximately 5–10% of fractures will result in a non-union during the healing process. non-unions can be classified into two types: atrophic non-union which is often due to impaired bone healing with a potential biological mechanism, and hypertrophic non-union which is due to inadequate fixation after fracture. Genetic variations also play an important role in the fracture healing response. Previous studies based on animal models have indicated that NOS2 might be greatly involved in the bone fracture healing process. In this case-control study, 346 nonunion patients were compared to 883 patients with normal fracture healing to investigate the potential genetic association between NOS2 and the fracture healing process using study subjects of Chinese Han ancestry. Twenty-seven single nucleotide polymorphisms (SNPs) covering NOS2 were genotyped in our study subjects and analyzed. In addition to the single marker-based analysis, we performed a gene-by-environment analysis to examine the potential interactions between genetic polymorphisms and some environmental factors. SNP rs2297514 showed significant association with the fracture healing process after adjusting for age and gender (OR = 1.38, P = 0.0005). Our results indicated that the T allele of rs2297514 significantly increased the risk of a non-union during the fracture healing process by 38% compared to the C allele. Further stratification analyses conducted for this SNP using data from subgroups classified by different sites of fracture indicated that significance could only be observed in the tibial diaphysis subgroup (N = 428, OR = 1.77, P = 0.0007) but not other groups including femur diaphysis, humeral shaft, ulnar shaft, and femur neck. Gene-by-environment interaction analyses of the three environmental factors showed no significant results. In this study, rs2297514 was significantly associated with the non-union status of fracture healing using a large Chinese population-based study sample. Our findings replicated those of a previous preliminary study and offered strong evidence linking NOS2 and fracture healing.
机译:骨不连,特别是萎缩性骨不连,是骨折后永久性的愈合失败,可能难以治疗。大约5–10%的骨折会导致愈合过程中骨不连。骨不连可以分为两种类型:萎缩性骨不连(通常是由于具有潜在生物学机制的骨愈合受损)和肥大性骨不连(由于骨折后固定不充分所致)。遗传变异在骨折愈合反应中也起着重要作用。先前基于动物模型的研究表明,NOS2可能在骨折愈合过程中起很大作用。在本病例对照研究中,将346例不愈合的患者与883例骨折愈合正常的患者进行比较,以中国汉族研究对象调查NOS2与骨折愈合过程之间的潜在遗传关联。在我们的研究对象中对覆盖NOS2的27个单核苷酸多态性(SNP)进行了基因分型并进行了分析。除了基于单个标记的分析之外,我们还进行了逐个基因的分析,以检查遗传多态性与某些环境因素之间的潜在相互作用。调整年龄和性别后,SNP rs2297514与骨折愈合过程密切相关(OR = 1.38,P = 0.0005)。我们的结果表明,与C等位基因相比,rs2297514的T等位基因显着增加了骨折愈合过程中发生骨不连的风险。使用从不同骨折部位分类的亚组的数据对该SNP进行的进一步分层分析表明,仅在胫骨干sub端亚组中可以观察到显着性(N = 428,OR = 1.77,P = 0.0007),而其他组(包括股骨干physi端)肱骨干,尺骨干和股骨颈。三种环境因素的基因逐环境相互作用分析均未显示明显结果。在这项研究中,使用大量基于中国人群的研究样本,rs2297514与骨折愈合的不愈合状态显着相关。我们的研究结果重复了先前的初步研究,并提供了将NOS2与骨折愈合联系起来的有力证据。

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