Zhang De Lian, Shi Tian, Yao Xiao Guang, Li Mei, Mulalibike Heizhati, Li Xiu Fang, Wen Lu, Yao Ling, He Yuan Yuan, Wang Ying Chun, Hong Jing, Li Nan Fang
Hypertension Institute of Xinjiang,Hypertension Center of the People's Hospital of Xinjiang Uygur Autonomous Region,Urumqi 830001,China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2020 Feb 28;42(1):16-23. doi: 10.3881/j.issn.1000-503X.11246.
To explore the mechanism of obstructive sleep apnea(OSA) by assessing the association between human TWIK-related acid-sensitive K channel-1(TASK-1) gene and OSA. A total of 164 patients with severe OSA and 171 patients without OSA were recruited from the Hypertension Center of People's Hospital of Xinjiang Uygur Autonomous Region,China,from April to December 2016.Two single nucleotide polymorphisms(rs1275988 and rs2586886) in the TASK-1 gene were selected and genotyped using a Kompetitive Allele Specific PCR genotyping system. In patients with blood potassium <3.95 mmol/L,the distribution of rs1275988 alleles(G .A)(=4.474,=0.034) and recessive model(GG+GA .AA)(=4.327,=0.038) showed significant differences between severe and non-OSA groups.The distribution of rs2586886 alleles(G .A)(=6.345,=0.012) and dominant model(AA+GA .GA)(=4.431,=0.035) showed significant differences between severe and non-OSA groups.The Logistic regression analysis showed that the GG genotype was a risk factor for OSA patients with blood potassium <3.95 mmol/L(=7.854,95% :1.710-36.000,=0.008;=8.849,95% :1.816-43.117,=0.007). Both the GG genotypes of rs1275988 and rs2586886 in the TASK-1 gene may be potential risk factors in severe OSA patients with blood potassium <3.95 mmol/L.Serum potassium>3.95 mmol/L in patients with TASK-1 GG genotype may be conducive to reducing the incidence of severe OSA.
通过评估人类TWIK相关酸敏感钾通道1(TASK-1)基因与阻塞性睡眠呼吸暂停(OSA)之间的关联,探讨OSA的发病机制。2016年4月至12月,从中国新疆维吾尔自治区人民医院高血压中心招募了164例重度OSA患者和171例非OSA患者。选择TASK-1基因中的两个单核苷酸多态性(rs1275988和rs2586886),并使用竞争性等位基因特异性PCR基因分型系统进行基因分型。在血钾<3.95 mmol/L的患者中,rs1275988等位基因(G.A)(χ²=4.474,P=0.034)和隐性模型(GG+GA.AA)(χ²=4.327,P=0.038)在重度OSA组和非OSA组之间的分布存在显著差异。rs2586886等位基因(G.A)(χ²=6.345,P=0.012)和显性模型(AA+GA.GG)(χ²=4.431,P=0.035)在重度OSA组和非OSA组之间的分布存在显著差异。Logistic回归分析显示,GG基因型是血钾<3.95 mmol/L的OSA患者的危险因素(χ²=7.854,95%CI:1.710-36.000,P=0.008;χ²=8.8