Published April 16, 2019
| Version v1
Journal article
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Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep
Creators
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Cade, Brian E.1
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Chen, Han2
- Stilp, Adrienne M.3
- Louie, Tin3
- Ancoli-Israel, Sonia4
- Arens, Raanan5
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Barfield, Richard1
- Below, Jennifer E.6
- Cai, Jianwen7
- Conomos, Matthew P.3
- Evans, Daniel S.8
- Frazier-Wood, Alexis C.9
- Gharib, Sina A.3
- Gleason, Kevin J.10
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Gottlieb, Daniel J.11
- Hillman, David R.12
- Johnson, W. Craig3
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Lederer, David J.13
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Lee, Jiwon11
- Loredo, Jose S.4
- 1. Harvard University
- 2. University of Texas Health Science Center at Houston
- 3. University of Washington
- 4. University of California San Diego
- 5. Albert Einstein College of Medicine
- 6. Vanderbilt University
- 7. University of North Carolina at Chapel Hill
- 8. California Pacific Medical Center Research Institute
- 9. Baylor College of Medicine
- 10. University of Chicago
- 11. Brigham and Women's Hospital
- 12. Sir Charles Gairdner Hospital
- 13. Columbia University
Description
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 < 1 × 10−6 were analyzed in a replication group of 14,410 individuals. We identified 3 significantly associated regions, including 2 regions in multi-ethnic analyses (2q12, 10q22). SNPs in the 2q12 region associated with minimum SpO2 (rs78136548 p = 2.70 × 10−10). SNPs at 10q22 were associated with all three traits including average SpO2 (rs72805692 p = 4.58 × 10−8). SNPs in both regions were associated in over 20,000 individuals and are supported by prior associations or functional evidence. Four additional significant regions were detected in secondary sex-stratified and combined discovery and replication analyses, including a region overlapping Reelin, a known marker of respiratory complex neurons.These are the first genome-wide significant findings reported for oxyhemoglobin saturation during sleep, a phenotype of high clinical interest. Our replicated associations with HK1 and IL18R1 suggest that variants in inflammatory pathways, such as the biologically-plausible NLRP3 inflammasome, may contribute to nocturnal hypoxemia.
Data availability
Full meta-analysis results are freely available from http://www.sleepdisordergenetics.org/informational/data
Files
journal.pgen.1007739.pdf
Additional details
Identifiers
- DOI
- 10.1371/journal.pgen.1007739
- Other
- oai:uchicago.tind.io:6304
Funding
- National Institutes of Health
- K01-HL135405-01
- National Institutes of Health
- R01-HL113338-04
- National Institutes of Health
- R35-HL135818-01
- American Thoracic Society Foundation
- National Institutes of Health
- 5-R01-HL046380-15
- National Institutes of Health
- 5-KL2-RR024990-05
- National Heart, Lung, and Blood Institute
- N01-HC-55015
- National Heart, Lung, and Blood Institute
- N01-HC-55018
- National Heart, Lung, and Blood Institute
- N01-HC-55016
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- National Institute of Neurological Disorders and Stroke
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- National Center for Advancing Translational Sciences
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- National Institute on Minority Health and Health Disparities
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- National Institute of Diabetes and Digestive and Kidney Diseases
- National Institute of Neurological Disorders and Stroke
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- HL56984
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- National Institute on Aging
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- National Institutes of Health
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- Sir Charles Gairdner and Hollywood Private Hospital Research Foundations
- University of Texas Health Science Center at Houston
- Western Australian Sleep Disorders Research Institute
- University of Western Australia
- Ontario Institute for Cancer Research
- University of Toronto
- McLaughlin Centre Accelerator Grant