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Association study of genetic variations of inflammatory biomarkers with susceptibility and severity of obstructive sleep apnea

机译:炎症生物标志物遗传变异与阻塞性睡眠呼吸暂停的敏感性生物标志物的遗传变异研究

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Background Obstructive sleep apnea (OSA) increases health risks of cardiovascular disease and stroke. Both genetic factors and environmental exposures contribute to the occurrence of OSA. The purpose of this study was to determine the role of four functional inflammatory single nucleotide polymorphisms (SNPs) ( VWF rs1063856, IL‐6 rs1800796, TNF rs1800629, and CRP rs2794521) in the susceptibility and severity of OSA. Methods A case–control study of OSA among Chinese population was conducted. Genotyping was performed using ABI TaqMan SNP genotyping technique. Results We found VWF rs1063856 (OR?=?1.50, 95% CIs?=?1.10–2.04; p ?=?0.010), IL‐6 rs1800796 (OR?=?1.32, 95% CIs?=?1.11–1.56; p ?=?0.002), TNF rs1800629 (OR?=?1.44, 95% CIs?=?1.13–1.83; p ?=?0.003), and CRP rs2794521 (OR?=?1.27, 95% CIs?=?1.04–1.55; p ?=?0.021) were all significantly associated with increased susceptibility of OSA, while VWF rs1063856 (OR?=?1.75, 95% CIs?=?1.18–2.62; p ?=?0.006), IL‐6 rs1800796 (OR?=?1.39, 95% CIs?=?1.10–1.76; p ?=?0.006) were associated with the severity of OSA. Conclusions Our study indicated that functional variants of inflammatory biomarkers could cause the occurrence of OSA and influence the severity of OSA. These findings further support that inflammatory cytokines were closely related to the occurrence and development of OSA.
机译:背景技术阻塞性睡眠呼吸暂停(OSA)增加了心血管疾病和中风的健康风险。遗传因素和环境暴露都有助于OSA的发生。本研究的目的是确定四种功能性炎症单核苷酸多态性(SNP)(VWF RS1063856,IL-6 RS1800796,TNF RS1800629和CRP RS2794521)在OSA的易感性和严重程度中的作用。方法对中国人群OSA案例对照研究。使用ABI Taqman SNP基因分型技术进行基因分型。结果我们找到了VWF RS1063856(或?=?1.50,95%CIS?=?1.10-2.04; P?= 0.010),IL-6 RS1800796(或?=?1.32,95%CIS?=?1.11-1.56; p?= 0.002),TNF RS1800629(或?1.44,95%CIS?=?1.13-1.83; p?= 0.003)和CRP RS2794521(或?=?1.27,95%CIS?=?1.04 -1.55; p?= 0.021)与OSA的易感性增加显着相关,而VWF RS1063856(或?=?1.75,95%CIS?=?1.18-2.62; P?=?0.006),IL-6 RS1800796 (或?=?1.39,95%cis?=?1.10-1.76; p?= 0.006)与OSA的严重程度有关。结论我们的研究表明,炎症生物标志物的功能变体可能导致OSA的发生并影响OSA的严重程度。这些发现进一步支持炎症细胞因子与OSA的发生和发展密切相关。

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