Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
Brian E Cade,
Han Chen,
Adrienne M Stilp,
Tin Louie,
Sonia Ancoli-Israel,
Raanan Arens,
Richard Barfield,
Jennifer E Below,
Jianwen Cai,
Matthew P Conomos,
Daniel S Evans,
Alexis C Frazier-Wood,
Sina A Gharib,
Kevin J Gleason,
Daniel J Gottlieb,
David R Hillman,
W Craig Johnson,
David J Lederer,
Jiwon Lee,
Jose S Loredo,
Hao Mei,
Sutapa Mukherjee,
Sanjay R Patel,
Wendy S Post,
Shaun M Purcell,
Alberto R Ramos,
Kathryn J Reid,
Ken Rice,
Neomi A Shah,
Tamar Sofer,
Kent D Taylor,
Timothy A Thornton,
Heming Wang,
Kristine Yaffe,
Phyllis C Zee,
Craig L Hanis,
Lyle J Palmer,
Jerome I Rotter,
Katie L Stone,
Gregory J Tranah,
James G Wilson,
Shamil R Sunyaev,
Cathy C Laurie,
Xiaofeng Zhu,
Richa Saxena,
Xihong Lin and
Susan Redline
PLOS Genetics, 2019, vol. 15, issue 4, 1-31
Abstract:
Sleep disordered breathing (SDB)-related overnight hypoxemia is associated with cardiometabolic disease and other comorbidities. Understanding the genetic bases for variations in nocturnal hypoxemia may help understand mechanisms influencing oxygenation and SDB-related mortality. We conducted genome-wide association tests across 10 cohorts and 4 populations to identify genetic variants associated with three correlated measures of overnight oxyhemoglobin saturation: average and minimum oxyhemoglobin saturation during sleep and the percent of sleep with oxyhemoglobin saturation under 90%. The discovery sample consisted of 8,326 individuals. Variants with p
Date: 2019
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pgen00:1007739
DOI: 10.1371/journal.pgen.1007739
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