PFKP and GPC6 Variants Were Correlated with Alcohol-Induced Femoral Head Necrosis Risk in the Chinese Han Population.

Pharmacogenomics and Personalized Medicine Pub Date : 2022-09-09 eCollection Date: 2022-01-01 DOI:10.2147/PGPM.S369957
Chang Liu, Xuan Liu, Xiaolin Li
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Abstract

Background: Osteonecrosis of the femoral head (ONFH) is a common joint disease caused by excessive drinking, genetic factors, etc. The purpose of this study was to investigate the association between PFKP and GPC6 variants and alcohol-induced ONFH (AIONFH) risk in the Chinese Han population.

Methods: This study genotyped 9 selected single nucleotide polymorphisms (SNPs) in 402 males by Agena MassARRAY Assay. By calculating odds ratios (ORs) and 95% confidence intervals (CIs), we assessed the effect of gene polymorphisms on AIONFH occurrence. False-positive report probability (FPRP) analysis and power were also used to evaluate the significant results. Multifactor dimensionality reduction (MDR) software was also utilized to predict the association between the selected SNPs and AIONFH risk.

Results: The overall analysis showed that PFKP rs10903966 and GPC6 rs7320969 were correlated with AIONFH risk. GPC6 rs4773724 was associated with a reduced risk of AIONFH, while individuals with GPC6 rs9523981 CC genotype had a higher risk of AIONFH than individuals with the other genotypes among people under 42 years old. Based on stratified analysis of necrotic sites, rs7320969 was related to a decreased risk of AIONFH, while rs10903966 and rs9523981 were related to an increased risk of AIONFH. In addition, rs1008993 and rs7320969 were observed to be linked to AIONFH risk in patients at different clinical stages. Meanwhile, there were significant differences in TC, TG, platelet, ApoA1 and ApoB levels among subjects with different genotypes of rs1008993, rs9523981, rs7320969 and rs59624626. The results of MDR showed that rs11251720 and rs7320969 may play a synergistic role in predicting the risk of AIONFH.

Conclusion: PFKP rs10903966 and GPC6 rs9523981 were associated with an increased risk of AIONFH, while GPC6 (rs7320969 and rs4773724) were correlated with a decreased risk of AIONFH. This result will need further experiments to verify.

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PFKP和GPC6变异与中国汉族人群酒精性股骨头坏死风险相关
背景:股骨头坏死(Osteonecrosis of femoral head, ONFH)是一种常见的关节疾病,由过量饮酒、遗传等因素引起。本研究的目的是调查中国汉族人群中PFKP和GPC6变异与酒精诱导的ONFH (AIONFH)风险之间的关系。方法:采用Agena MassARRAY法对402例男性的9个单核苷酸多态性(snp)进行基因分型。通过计算比值比(ORs)和95%置信区间(CIs),我们评估了基因多态性对AIONFH发生的影响。假阳性报告概率(FPRP)分析和功率也用于评估显著性结果。还利用多因素降维(MDR)软件预测所选snp与AIONFH风险之间的关系。结果:综合分析显示PFKP rs10903966和GPC6 rs7320969与AIONFH风险相关。在42岁以下人群中,GPC6 rs4773724基因型与AIONFH风险降低相关,而GPC6 rs9523981 CC基因型个体的AIONFH风险高于其他基因型个体。基于坏死部位分层分析,rs7320969与AIONFH风险降低相关,rs10903966和rs9523981与AIONFH风险升高相关。此外,rs1008993和rs7320969被观察到与不同临床阶段患者的AIONFH风险相关。同时,不同rs1008993、rs9523981、rs7320969、rss59624626基因型的受试者TC、TG、血小板、ApoA1、ApoB水平存在显著差异。MDR结果显示rs11251720和rs7320969可能在预测AIONFH风险中发挥协同作用。结论:PFKP rs10903966和GPC6 rs9523981与AIONFH发生风险增加相关,而GPC6 rs7320969和rs4773724与AIONFH发生风险降低相关。这一结果需要进一步的实验来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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