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GWAS Study

Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank.

Campos AI, García-Marín LM, Byrne EM et al.

32060260 PubMed ID
GWAS Study Type
407066 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CA
Campos AI
GL
García-Marín LM
BE
Byrne EM
MN
Martin NG
CG
Cuéllar-Partida G
RM
Rentería ME
Chapter II

Abstract

Summary of the research findings

Although snoring is common in the general population, its aetiology has been largely understudied. Here we report a genetic study on snoring (n ~ 408,000; snorers ~ 152,000) using data from the UK Biobank. We identify 42 genome-wide significant loci, with an SNP-based heritability estimate of ~10% on the liability scale. Genetic correlations with body mass index, alcohol intake, smoking, schizophrenia, anorexia nervosa and neuroticism are observed. Gene-based associations identify 173 genes, including DLEU7, MSRB3 and POC5, highlighting genes expressed in the brain, cerebellum, lungs, blood and oesophagus. We use polygenic scores (PGS) to predict recent snoring and probable obstructive sleep apnoea (OSA) in an independent Australian sample (n ~ 8000). Mendelian randomization analyses suggest a potential causal relationship between high BMI and snoring. Altogether, our results uncover insights into the aetiology of snoring as a complex sleep-related trait and its role in health and disease beyond it being a cardinal symptom of OSA.

151,836 British ancestry cases, 255,230 British ancestry controls

Chapter III

Study Statistics

Key metrics and study information

407066
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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