Menu
Currency
GWAS Study

High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease.

Tcheandjieu C, Xiao K, Tejeda H et al.

35637384 PubMed ID
GWAS Study Type
133 Participants
88 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TC
Tcheandjieu C
XK
Xiao K
TH
Tejeda H
LJ
Lynch JA
RS
Ruotsalainen S
BT
Bellomo T
PM
Palnati M
JR
Judy R
KD
Klarin D
KR
Kember RL
VS
Verma S
PA
Palotie A
DM
Daly M
RM
Ritchie M
RD
Rader DJ
RM
Rivas MA
AT
Assimes T
TP
Tsao P
DS
Damrauer S
PJ
Priest JR
Chapter II

Abstract

Summary of the research findings

Enlargement of the aorta is an important risk factor for aortic aneurysm and dissection, a leading cause of morbidity in the developed world. Here we performed automated extraction of ascending aortic diameter from cardiac magnetic resonance images of 36,021 individuals from the UK Biobank, followed by genome-wide association. We identified lead variants across 41 loci, including genes related to cardiovascular development (HAND2, TBX20) and Mendelian forms of thoracic aortic disease (ELN, FBN1). A polygenic score significantly predicted prevalent risk of thoracic aortic aneurysm and the need for surgical intervention for patients with thoracic aneurysm across multiple ancestries within the UK Biobank, FinnGen, the Penn Medicine Biobank and the Million Veterans Program (MVP). Additionally, we highlight the primary causal role of blood pressure in reducing aortic dilation using Mendelian randomization. Overall, our findings provide a roadmap for using genetic determinants of human anatomy to understand cardiovascular development while improving prediction of diseases of the thoracic aorta.

133 East Asian ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

133
Total Participants
GWAS
Study Type
No
Replicated
East Asian, European, African American or Afro-Caribbean, Sub-Saharan African, South Asian
Ancestry
U.K.
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.