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GWAS Study

Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease.

Kurniansyah N, Strausz SJ, Chittoor G et al.

40472801 PubMed ID
GWAS Study Type
182017 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KN
Kurniansyah N
SS
Strausz SJ
CG
Chittoor G
GS
Gupta S
JA
Justice AE
HY
Hrytsenko Y
KB
Keenan BT
CB
Cade BE
SB
Spitzer BW
WH
Wang H
HJ
Huffman J
MM
Moll MR
HB
Haring B
JS
Jung SY
RL
Raffield LM
KR
Kaplan R
RJ
Rotter JI
RS
Rich SS
GS
Gharib SA
BT
Bartz TM
LP
Liu PY
CH
Chen H
FM
Fornage M
HL
Hou L
LD
Levy D
MA
Morrison AC
OH
Ochs-Balcom HM
PB
Psaty BM
WP
Wilson PWF
CK
Cho K
PA
Pack AI
OH
Ollila HM
RS
Redline S
GD
Gottlieb DJ
ST
Sofer T
Chapter II

Abstract

Summary of the research findings

Obstructive sleep apnoea (OSA) is a common chronic condition, with obesity its strongest risk factor. Polygenic scores (PGSs) summarise the genetic liability to phenotype and can provide insights into relationships between phenotypes. Recently, large datasets that include genetic data and OSA status became available, providing an opportunity to utilise PGS approaches to study the genetic relationship between OSA and other phenotypes, while differentiating OSA-specific from obesity-specific genetic factors.

182,017 European ancestry, East Asian ancestry, African American or Afro-Caribbean, or Hispanic or Latin American females

Chapter III

Study Statistics

Key metrics and study information

182017
Total Participants
GWAS
Study Type
No
Replicated
European, East Asian, African American or Afro-Caribbean, Hispanic or Latin American
Ancestry
U.S., Finland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.