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Relationship between zinc finger protein 36 (ZFP36) gene polymorphisms and obstructive sleep apnea.

Authors :
Zhang Y
Li NF
Abulikemu S
Zhang DL
Wang YC
Kong JQ
Nuer GL
Yan ZT
Li HJ
Zhang JH
Zhang XY
Source :
Genetics and molecular research : GMR [Genet Mol Res] 2015 Jun 18; Vol. 14 (2), pp. 6733-43. Date of Electronic Publication: 2015 Jun 18.
Publication Year :
2015

Abstract

Recent data have indicated that inflammation may have an important correlation with obstructive sleep apnea (OSA). Studies have indicated a relationship between OSA and TNF-α gene polymorphisms. Zinc finger protein 36 (ZFP36) regulates TNF-α mRNAs. However, ZFP36 gene polymorphisms have not been investigated in OSA. Therefore, we conducted the present case-control study to assess whether variances in ZFP36 gene polymorphisms account for differences in TNF-α levels in patients with moderate-to-severe OSA. This case-control study aims to investigate the relationship between genetic variations in the ZFP36 gene and moderate-to-severe OSA. Three common single nucleotide polymorphisms of the ZFP36 gene (rs251864, rs3746083, and rs17879933) were evaluated in a group of patients with moderate-to-severe OSA (N = 408) and in a control group (N = 394) by using TaqMan polymerase chain reaction analysis. The moderate-to-severe OSA group and the control group exhibited significant differences in the distributions of rs251864 and rs17879933 genotypes and alleles (P < 0.05). TNF-α levels were significantly different not only among the three rs251864 genotypes but also between the II genotype and the DD + ID genotypes of rs17879933. However, no significant differences in sleep apnea parameters in the three ZFP36 gene polymorphisms were observed. Logistic regression analyses demonstrated that TNF-α and the three ZFP36 gene polymorphisms were not independently associated with OSA. ZFP36 might be involved in TNF-α regulation. However, ZFP36 gene variants were not independent risk factors for moderate-to-severe OSA.

Details

Language :
English
ISSN :
1676-5680
Volume :
14
Issue :
2
Database :
MEDLINE
Journal :
Genetics and molecular research : GMR
Publication Type :
Academic Journal
Accession number :
26125882
Full Text :
https://doi.org/10.4238/2015.June.18.17