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首页> 外文期刊>Medicine. >Targeted sequencing analysis of the adiponectin gene identifies variants associated with obstructive sleep apnoea in Chinese Han population
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Targeted sequencing analysis of the adiponectin gene identifies variants associated with obstructive sleep apnoea in Chinese Han population

机译:脂联素基因的靶向测序分析可鉴定与中国汉族人群阻塞性睡眠呼吸暂停相关的变异

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摘要

Obstructive sleep apnoea (OSA) is a prevalent sleep disorder considered as an independent risk factor for cardiovascular consequences. It has a strong genetic background and is associated with hypoadiponectinaemia. Target sequencing of whole ADIPONQ gene was performed in 340 participants including 247 patients with OSA and 93 non-OSA participants. Polysomnography was used to diagnose OSA. The associations between variants and OSA were determined by multivariate regression analysis. Thirteen single nucleotide polymorphisms of ADIPOQ were identified in all subjects. Genotype frequencies at rs4686803 ( P = .034), rs3774262 ( P = .034), and rs2082940 ( P = .045) were significantly different between OSA and non-OSA groups. Individuals carrying the CT/TT genotypes of rs4686803, GA/AA genotypes of rs3774262, and CT/TT genotypes of rs1063537 were associated with 2.295-, 2.295- and 2.155-fold increased risk of OSA respectively in dominant model, after adjusting for confounding effects. The subjects with the rs2082940 CC genotype were associated with decreased risk of OSA (OR: 0.455) in recessive model. Additionally, the apnoea–hypopnea index (AHI) was significantly increased in rs3774262 (GA/AA) ( P = .001), rs4686803 (CT/TT) ( P = .001), and rs1063537 (CT/TT) ( P = .004) genotype individuals than those with rs3774262 (GG), rs4686803 (CC), and rs1063537 (CC) genotypes, respectively. The AHI was significantly decreased in individuals with ADIPOQ rs2082940 CC genotypes than in those with the CT and TT genotype ( P = .007). Moreover, the stratified analysis found that the genotype of rs3774262 (GA/AA), rs4686803 (CT/TT), and rs1063537 (CT/TT) variants were associated with increased risk of OSA by 2.935-, 2.935- and 2.786-fold in overweight participants. The genotype of rs2082940 CC variants was associated with decreased risk of OSA (OR: 0.373) in overweight participants compared with rs2082940 CT/ TT genotypes. ADIPOQ variants rs3774262, rs4686803, rs10 63537, and rs2082940 were associated with the prevalence of OSA in Chinese Han individuals.
机译:阻塞性睡眠呼吸暂停(OSA)是一种普遍的睡眠障碍,被认为是导致心血管后果的独立危险因素。它具有很强的遗传背景,并与低脂连蛋白血症有关。在340名参与者(包括247名OSA患者和93名非OSA参与者)中进行了整个ADIPONQ基因的目标测序。多导睡眠图用于诊断OSA。通过多元回归分析确定变体与OSA之间的关联。在所有受试者中鉴定出十三种ADIPOQ的单核苷酸多态性。 OSA组和非OSA组之间的rs4686803(P = .034),rs3774262(P = .034)和rs2082940(P = .045)的基因型频率显着不同。调整混杂效应后,携带rs4686803的CT / TT基因型,rs3774262的GA / AA基因型和rs1063537的CT / TT基因型的个体在显性模型中分别使OSA风险增加2.295、2.295和2.155倍。 。在隐性模型中,具有rs2082940 CC基因型的受试者与OSA风险降低相关(OR:0.455)。此外,在rs3774262(GA / AA)(P = .001),rs4686803(CT / TT)(P = .001)和rs1063537(CT / TT)中,呼吸暂停低通气指数(AHI)显着增加(P = .004)基因型个体,而分别具有rs3774262(GG),rs4686803(CC)和rs1063537(CC)基因型的个体。具有ADIPOQ rs2082940 CC基因型的个体的AHI显着低于具有CT和TT基因型的个体(P = .007)。此外,分层分析发现,rs3774262(GA / AA),rs4686803(CT / TT)和rs1063537(CT / TT)变体的基因型与OSA风险增加相关,分别为2.935-,2.935-和2.786-倍超重的参与者。与rs2082940 CT / TT基因型相比,超重参与者中rs2082940 CC变体的基因型与OSA风险降低(OR:0.373)相关。 ADIPOQ变体rs3774262,rs4686803,rs10 63537和rs2082940与中国汉族人群OSA的患病率相关。

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