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希腊人群中NOS2A基因启动子区域多态性与原发性膝骨关节炎的关联

Association of Polymorphisms in the Promoter Region of NOS2A Gene with Primary Knee Osteoarthritis in the Greek Population.

作者信息

Leonidou Andreas, Lepetsos Panagiotis, Kenanidis Eustathios, Macheras George, Tzetis Maria, Potoupnis Michael, Tsiridis Eleftherios

机构信息

Orthopaedics and Trauma, Aristotle University Medical School, Thessaloniki, GRC.

Trauma and Orthopedics, KAT Hospital, Athens, GRC.

出版信息

Cureus. 2020 Jan 27;12(1):e6780. doi: 10.7759/cureus.6780.

Abstract

Introduction A new emerging role of nitric oxide (NO) in the aetiology of osteoarthritis (OA) has been reported. Inducible NO synthase (iNOS), produced by chondrocytes, is the major source of NO in the osteoarthritic cartilage. The aim of this study is to evaluate the potential association between the -1173C/T (rs9282799), -1026 C/A (rs 2779249) and -954G/C (rs1800482) single nucleotide polymorphisms (SNPs) in the promoter of the iNOS gene (NOS2A) and the incidence of knee OA in Greek population. Methods Ninety-six patients with primary knee OA were included in the study along with 44 controls. Genotypes were identified using polymerase chain reaction (PCR) and DNA sequencing techniques. Allelic and genotypic frequencies were compared between patients and controls. Results None of the -1173C/T, -1026 C/A and -954G/C SNPs were detected in the studied population, either in patients or controls. However, another SNP was identified at the site -1056 at the promoter region, where the initial G allele was substituted by the T allele. Interestingly, the TT genotype was completely absent in controls, but was detected in six patients with a 6.2% observed frequency. The difference between patients and controls was not statistically significant (p-value = 0.18). In male OA patients, the observed frequency of the TT genotype was higher (28.6%) in comparison to the 0% of the male controls (p-value = 0.1). The frequency of the G allele was 0.82 in controls and 0.78 in OA patients (p-value = 0.53). Conclusions The present study demonstrates that the 954G/C, -1026C/A, -1056G/T and -1173C/T SNPs of the NOS2A gene are not a risk factor for primary knee OA in Greek population. Moreover, -954G/C, -1026C/A and -1173C/T are rare, if not completely absent, in the Greek population. Additional research is mandatory in order to investigate the association of these SNPs with OA in different ethnic populations.

摘要

引言 一氧化氮(NO)在骨关节炎(OA)病因学中的新作用已被报道。软骨细胞产生的诱导型一氧化氮合酶(iNOS)是骨关节炎软骨中NO的主要来源。本研究旨在评估希腊人群中iNOS基因(NOS2A)启动子区的-1173C/T(rs9282799)、-1026 C/A(rs 2779249)和-954G/C(rs1800482)单核苷酸多态性(SNP)与膝骨关节炎发病率之间的潜在关联。

方法 本研究纳入了96例原发性膝骨关节炎患者和44例对照。使用聚合酶链反应(PCR)和DNA测序技术鉴定基因型。比较患者和对照之间的等位基因和基因型频率。

结果 在研究人群中,无论是患者还是对照,均未检测到-1173C/T、-1026 C/A和-954G/C SNP。然而,在启动子区域的-1056位点发现了另一个SNP,其中初始的G等位基因被T等位基因取代。有趣的是,对照中完全没有TT基因型,但在6例患者中检测到,观察频率为6.2%。患者和对照之间的差异无统计学意义(p值=0.18)。在男性OA患者中,TT基因型的观察频率(28.6%)高于男性对照的0%(p值=0.1)。G等位基因在对照中的频率为0.82,在OA患者中的频率为0.78(p值=0.53)。

结论 本研究表明,NOS基因的954G/C、-1026C/A、-1056G/T和-1173C/T SNP不是希腊人群原发性膝骨关节炎的危险因素。此外,-954G/C、-1026C/A和-1173C/T在希腊人群中即使不是完全不存在也是罕见的。为了研究这些SNP与不同种族人群OA的关联,必须进行更多的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d30e/7045981/b6e755d0f035/cureus-0012-00000006780-i01.jpg

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