Genetic variants of rs1275988 and rs2586886 in TWIK-related acidsensitive K+ channel-1 gene may be potential risk factors for obese patients with obstructive sleep apnea
10.1097/CM9.0000000000000401
- Author:
Tian SHI
1
,
2
;
Xiao-Guang YAO
1
,
2
;
Mei LI
1
,
2
;
Mulalibieke HEIZHATI
1
,
2
;
Xiu-Fang LI
1
,
2
;
Lu WEN
1
,
2
;
Yuan-Yuan HE
1
,
2
;
Ling YAO
1
,
2
;
Ying-Chun WANG
1
,
2
;
Jing HONG
1
,
2
;
Nan-Fang LI
1
,
2
Author Information
1. Center for Hypertension of People’s Hospital of Xinjiang Uygur Autonomous Region
2. Hypertension Institute of Xinjiang, Urumqi, Xinjiang 830001, China
- Publication Type:Journal Article
- Keywords:
Potassium channels;
Obstructive sleep apnea;
Single nucleotide polymorphism;
Body mass index
- From:
Chinese Medical Journal
2019;132(17):2059-2065
- CountryChina
- Language:English
-
Abstract:
Background:The pathogenesis of obstructive sleep apnea (OSA) remains not fully understood. This study aimed to explore the mechanism of OSA by assessing the association between the human tandem of P domains in a weak inwardly rectifying K+ channel (TWIK)-related acid-sensitive K+ channel-1 (TASK-1) gene and OSA.
Methods:A total of 164 patients with severe OSA and 171 patients without OSA were recruited from the Center for Hypertension of People’s Hospital of Xinjiang Uygur Autonomous Region (China) from April to December in 2016. Two single nucleotide polymorphisms (rs1275988 and rs2586886) in the TASK-1 gene were selected and genotyped using a kompetitive allele specific polymerase chain reaction genotyping system. Clinical-pathological characteristics and genotype data were compared between the severe and non-OSA groups to explore the association between TASK-1 gene polymorphism and severe OSA.
Results:There were no significant differences in genotype distribution, allele frequency, and the recessive and dominant model of the two selected single nucleotide polymorphisms (rs1275988 and rs2586886) between the severe and non-OSA groups in the total population (P < 0.05). However, for patients with a body mass index (BMI) ≥28 kg/m2, the distribution of genotypes and alleles, and the recessive model (GG + GA vs. AA) exhibited significant differences between the severe and non-OSA group (for genotypes: P = 0.014 and P = 0.026; for alleles: P = 0.006 and P = 0.011; for the recessive model: P = 0.005 and P = 0.009, respectively). The simple logistic regression analysis revealed that the GG genotype was a risk factor for OSA. The odds ratio (OR) and 95% confidence intervals (CI) were 4.902 (1.582–15.186, P = 0.006) for rs1275988 and 4.420 (1.422–13.734, P = 0.010) for rs2586886, respectively. In multivariate logistic regression analysis, the combination of GG genotypes of rs1275988 with BMI ≥28 kg/m2 increased the risk of severe OSA (OR = 8.916, 95% CI 4.506–17.645, P < 0.001).
Conclusion:Both the GG genotype of rs1275988 and GG genotype of rs2586886 in the TASK-1 gene may play as potential risk factors in obese patients with OSA.
