心脏手术后腹部并发症的遗传预测因素:一项前瞻性研究

Q4 Medicine
D. Belov, O.S. Abramovskikh, M.A. Zotova, Y. Loginova, A.A. Fokin
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引用次数: 0

摘要

导言:预测术后腹部并发症是心脏外科一直关注的问题。确定遗传预测因子将有助于更好地了解术后并发症的病理生理机制及其预防:确定心脏手术后腹部并发症的遗传预测因素:方法:在联邦心血管外科中心(车里雅宾斯克)进行了一项前瞻性研究,涉及 72 名腹部并发症患者和 102 名无腹部并发症的对照组。根据 PLINK 软件包(1.9 版)中的 SNP-HWE 算法,使用精确法评估了基因型分布是否符合 Hardy-Weinberg 分布。为了确定与腹部并发症风险相关的标记基因,对每个多态性基因评估了 6 种模型:等位基因、共显性基因、显性基因、隐性基因、过显性基因和对数加性基因。为了分析 IL6(rs1800795)、TNF(rs1800629)和 SERPINE1(rs1799768)基因的 SNPs,使用 Syntol CJSC(俄罗斯莫斯科)生产的引物和探针,按照生产商的说明,在 Rotor-Gene 6000 检测循环器(Corbett Research Pty Ltd., Mortlake, Australia)上进行了实时聚合酶链反应(PCR)。分析 IL1B (rs1143634), CXCL8 (rs4073), IL10 (rs1800872), APOE (rs429358), FABP2 (rs1799883), NOS3 (rs1799983), VEGFA (rs699947) 基因的 SNPs、使用 TestGene LLC(俄罗斯乌里扬诺夫斯克)生产的引物和探针,按照生产商的说明在 DTprime 4 分析仪(DNA-Technology,俄罗斯莫斯科)上进行了实时 PCR 检测。TLR3基因SNP(rs3775291)的测定是在DTprime 4设备上使用TestGene LLC试剂盒,根据熔解曲线进行实时PCR测定:结果:发现IL1B rs1143634和FABP2 rs1799883这两个基因与腹部并发症的风险有关。经多重比较调整后,只有 FABP2 rs1799883 仍具有统计学意义。FABP2 基因的 rs1799883 多态性可被视为腹部并发症风险的预测因子,并可在共显模型和显性模型中进行评估,其 p 值相似(分别为 0.003 和 0.002)。总之,对所获数据的分析表明,腹部并发症的风险与基因组中突变等位基因 C 的存在有关,这可能是由于其显性作用。具体而言,在显性模型中,几率比为 3.53(95% CI 1.62 至 7.70):结论:腹部并发症风险最重要的标记是IL1B(rs1143634)和FABP2(rs1799883)基因,其中FABP2(rs1799883)在调整多重比较后仍具有统计学意义。其多态性作为腹部并发症的预测因子,可在共显模型和显性模型中进行评估。2023年6月13日收到。2023 年 11 月 28 日修订。2023年11月29日接受。资助:本研究由俄罗斯科学基金会资助,项目编号:22-25-20016,https://rscf.ru/project/22-25-20016/ 利益冲突:作者声明无利益冲突。作者贡献构思和研究设计:O.S. Abramovskikh, A.A. Fokin, D.V. Belov数据收集和分析:Yu.V. Loginova数据收集和分析:Yu.V. Loginova 统计分析:M.A. ZotovaM.A. Zotova撰写文章:D.V. Belov文章的严格修订:Yu.V. LoginovaFinal revision of the article:Yu.V. LoginovaFinal approval of the version to be published:D.V. Belov, O.S. Abramovskikh, M.A. Zotova, Yu.V. Loginova, A.A. Fokin
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic predictors of abdominal complications after cardiac surgery: a prospective study
Introduction: The prediction of postoperative abdominal complications is a continuing concern in the cardiac surgery. Identifying genetic predictors will allow a better understanding of the pathophysiological mechanisms underlying postoperative disorders and their prevention.Objective: To identify genetic predictors of abdominal complications after heart surgery.Methods: A prospective study was carried out at the Federal Center for Cardiovascular Surgery (Chelyabinsk) involving 72 patients with abdominal complications and 102 controls without such complications. The distribution of genotypes was assessed for adherence to the Hardy-Weinberg distribution using the exact method according to the SNP-HWE algorithm in the PLINK package (version 1.9). To identify marker genes associated with the risk of abdominal complications, 6 models were evaluated for each polymorphic gene: allelic, codominant, dominant, recessive, overdominant, and log-additive. To analyze the SNPs of the IL6 (rs1800795), TNF (rs1800629), and SERPINE1 (rs1799768) genes, real-time polymerase chain reaction (PCR) was performed on a Rotor-Gene 6000 detecting cycler (Corbett Research Pty Ltd., Mortlake, Australia) using primers and probes manufactured by Syntol CJSC (Moscow, Russia) according to the manufacturer's instructions. To analyze the SNPs of the IL1B (rs1143634), CXCL8 (rs4073), IL10 (rs1800872), APOE (rs429358), FABP2 (rs1799883), NOS3 (rs1799983), VEGFA (rs699947) genes, real-time PCR was performed on a DTprime 4 analyzer (DNA-Technology, Moscow, Russia) using primers and probes manufactured by TestGene LLC (Ulyanovsk, Russia) according to the manufacturer's instructions. The determination of the SNP of the TLR3 gene (rs3775291) relied on real-time PCR according to melting curves using TestGene LLC reagent kits on a DTprime 4 device.Results: Two genes, IL1B rs1143634 and FABP2 rs1799883, were found to be associated with the risk of abdominal complications. Following the adjustment for multiple comparisons, only FABP2 rs1799883 remained statistically significant. The rs1799883 polymorphism of the FABP2 gene can be considered a predictor of the risk of abdominal complications and can be evaluated within the codominant and dominant models, which exhibit similar p-values (0.003 and 0.002, respectively). Overall, the analysis of the obtained data suggests that the risk of abdominal complications is associated with the presence of the mutant allele C in the genome, likely due to its dominance. Specifically, in the dominant model, the odds ratio was 3.53 (95% CI 1.62 to 7.70).Conclusion: The most significant markers of the risk of abdominal complications were the IL1B (rs1143634) and FABP2 (rs1799883) genes, of which FABP2 (rs1799883) remained statistically significant after adjusting for multiple comparisons. Its polymorphism as a predictor of abdominal complications can be evaluated within the codominant and dominant models. Received 13 June 2023. Revised 28 November 2023. Accepted 29 November 2023. Funding: The study was supported by the Russian Science Foundation, project No. 22-25-20016, https://rscf.ru/project/22-25-20016/ Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsConception and study design: O.S. Abramovskikh, A.A. Fokin, D.V. BelovData collection and analysis: Yu.V. LoginovaStatistical analysis: M.A. ZotovaDrafting the article: D.V. BelovCritical revision of the article: Yu.V. LoginovaFinal approval of the version to be published: D.V. Belov, O.S. Abramovskikh, M.A. Zotova, Yu.V. Loginova, A.A. Fokin
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Patologiya krovoobrashcheniya i kardiokhirurgiya
Patologiya krovoobrashcheniya i kardiokhirurgiya Medicine-Cardiology and Cardiovascular Medicine
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12 weeks
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