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NOS3 多态性与股骨头坏死的关系。

Association between NOS3 polymorphisms and osteonecrosis of the femoral head.

机构信息

a Department of Orthopaedics , Weifang Traditional Chinese Hospital , Weifang , China.

b Department of Orthopaedics , Eighty-ninth Hospital of the Chinese People's Liberation Army , Weifang , China.

出版信息

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):1423-1427. doi: 10.1080/21691401.2019.1593995.

Abstract

PURPOSE

This study aimed to detect the association between nitric oxide synthase 3 (NOS3) gene polymorphisms (rs1799983 and rs3918181) and the susceptibility to osteonecrosis of the femoral head (ONFH).

METHODS

Total 88 ONFH patients (55 non-traumatic ONFH and 33 traumatic ONFH) and 90 healthy controls were recruited in this case-control study. Polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) was adopted for genotyping NOS3 rs1799983 and rs3918181 polymorphisms. χ test was used to calculate differences in genotype and allele frequencies of NOS3 gene polymorphisms between the cases and controls. Relative risk of ONFH was represented using odds ratios (ORs) with corresponding 95% confidence intervals (CIs).

RESULTS

The T allele of the polymorphism rs1799983 showed significantly different frequencies between ONFH patients and control groups (p = .046) and carrying this allele significantly decreased the disease risk (OR = 0.521, 95%CI = 0.272-0.997), especially for non-traumatic ONFH (OR = 0.408, 95%CI = 0.179-0.929, p = .029). But genotype frequencies of the polymorphism rs1799983 had no obvious difference between the compared two groups (p > .05 for all). There was no remarkable association between NOS3 rs3918181 polymorphism and NOFH risk (p > .05 for all).

CONCLUSIONS

NOS3 rs1799983 polymorphism is obviously associated with ONFH and its T allele may be a protective factor against ONFH occurrence in Chinese Han population.

摘要

目的

本研究旨在检测一氧化氮合酶 3(NOS3)基因多态性(rs1799983 和 rs3918181)与股骨头坏死(ONFH)易感性之间的关联。

方法

本病例对照研究纳入了 88 例 ONFH 患者(55 例非创伤性 ONFH 和 33 例创伤性 ONFH)和 90 名健康对照。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对 NOS3 rs1799983 和 rs3918181 多态性进行基因分型。χ²检验用于计算 NOS3 基因多态性在病例组和对照组之间的基因型和等位基因频率差异。ONFH 的相对风险用比值比(ORs)及其 95%置信区间(CIs)表示。

结果

多态性 rs1799983 的 T 等位基因在 ONFH 患者和对照组之间的频率有显著差异(p=0.046),携带该等位基因显著降低了疾病风险(OR=0.521,95%CI=0.272-0.997),尤其是对于非创伤性 ONFH(OR=0.408,95%CI=0.179-0.929,p=0.029)。但是,多态性 rs1799983 的基因型频率在两组比较之间没有明显差异(p>0.05)。NOS3 rs3918181 多态性与 ONFH 风险之间没有明显的关联(p>0.05)。

结论

NOS3 rs1799983 多态性与 ONFH 明显相关,其 T 等位基因可能是汉族人群中发生 ONFH 的保护因素。

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