| Title: | Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring |
| Journal: | Sleep |
| Published: | 16 Dec 2022 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/36525587/ |
| DOI: | https://doi.org/10.1093/sleep/zsac308 |
| URL: | https://academic.oup.com/sleep/advance-article-pdf/doi/10.1093/sleep/zsac308/49155966/zsac308.pdf |
| Citations: | 15 (13 in last 2 years) as of 8 Aug 2024 |
Publication 10827
WARNING: the interactive features of this website use CSS3, which your browser does not support. To use the full features of this website, please update your browser.
Abstract
STUDY OBJECTIVES: Despite its association with severe health conditions, the etiology of sleep apnea (SA) remains understudied. This study sought to identify genetic variants robustly associated with SA risk.</p>
METHODS: We performed a genome-wide association study (GWAS) meta-analysis of SA across five cohorts (NTotal = 523 366), followed by a multi-trait analysis of GWAS (multi-trait analysis of genome-wide association summary statistics [MTAG]) to boost power, leveraging the high genetic correlation between SA and snoring. We then adjusted our results for the genetic effects of body mass index (BMI) using multi-trait-based conditional and joint analysis (mtCOJO) and sought replication of lead hits in a large cohort of participants from 23andMe, Inc (NTotal = 1 477 352; Ncases = 175 522). We also explored genetic correlations with other complex traits and performed a phenome-wide screen for causally associated phenotypes using the latent causal variable method.</p>
RESULTS: Our SA meta-analysis identified five independent variants with evidence of association beyond genome-wide significance. After adjustment for BMI, only one genome-wide significant variant was identified. MTAG analyses uncovered 49 significant independent loci associated with SA risk. Twenty-nine variants were replicated in the 23andMe GWAS adjusting for BMI. We observed genetic correlations with several complex traits, including multisite chronic pain, diabetes, eye disorders, high blood pressure, osteoarthritis, chronic obstructive pulmonary disease, and BMI-associated conditions.</p>
CONCLUSION: Our study uncovered multiple genetic loci associated with SA risk, thus increasing our understanding of the etiology of this condition and its relationship with other complex traits.</p>
68 Authors
- Adrian I Campos
- Nathan Ingold
- Yunru Huang
- Brittany L Mitchell
- Pik-Fang Kho
- Xikun Han
- Luis M García-Marín
- Jue-Sheng Ong
- Michelle Agee
- Stella Aslibekyan
- Adam Auton
- Elizabeth Babalola
- Robert K Bell
- Jessica Bielenberg
- Katarzyna Bryc
- Emily Bullis
- Briana Cameron
- Daniella Coker
- Devika Dhamija
- Sayantan Das
- Sarah L Elson
- Teresa Filshtein
- Kipper Fletez-Brant
- Pierre Fontanillas
- Will Freyman
- Pooja M Gandhi
- Karl Heilbron
- Barry Hicks
- David A Hinds
- Karen E Huber
- Ethan M Jewett
- Yunxuan Jiang
- Aaron Kleinman
- Katelyn Kukar
- Keng-Han Lin
- Maya Lowe
- Marie K Luff
- Jennifer C McCreight
- Matthew H McIntyre
- Kimberly F McManus
- Steven J Micheletti
- Meghan E Moreno
- Joanna L Mountain
- Sahar V Mozaffari
- Priyanka Nandakumar
- Elizabeth S Noblin
- Jared O'Connell
- Aaron A Petrakovitz
- G David Poznik
- Anjali J Shastri
- Janie F Shelton
- Jingchunzi Shi
- Suyash Shringarpure
- Chao Tian
- Vinh Tran
- Joyce Y Tung
- Xin Wang
- Wei Wang
- Catherine H Weldon
- Peter Wilton
- Matthew H Law
- Jennifer S Yokoyama
- Nicholas G Martin
- Xianjun Dong
- Gabriel Cuellar-Partida
- Stuart MacGregor
- Stella Aslibekyan
- Miguel E Rentería
1 Application
| Application ID | Title |
|---|---|
| 25331 | Gene mapping and genetic correlation across complex traits |
Enabling scientific discoveries that improve human health