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GWAS Study

A Polygenic Risk Score Based on a Cardioembolic Stroke Multitrait Analysis Improves a Clinical Prediction Model for This Stroke Subtype.

Cárcel-Márquez J, Muiño E, Gallego-Fabrega C et al.

35872910 PubMed ID
GWAS Study Type
362661 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CJ
Cárcel-Márquez J
ME
Muiño E
GC
Gallego-Fabrega C
CN
Cullell N
LM
Lledós M
LL
Llucià-Carol L
ST
Sobrino T
CF
Campos F
CJ
Castillo J
FM
Freijo M
AJ
Arenillas JF
OV
Obach V
ÁJ
Álvarez-Sabín J
MC
Molina CA
RM
Ribó M
JJ
Jiménez-Conde J
RJ
Roquer J
ML
Muñoz-Narbona L
LE
Lopez-Cancio E
MM
Millán M
DR
Diaz-Navarro R
VC
Vives-Bauza C
SG
Serrano-Heras G
ST
Segura T
IL
Ibañez L
HL
Heitsch L
DP
Delgado P
DR
Dhar R
KJ
Krupinski J
DR
Delgado-Mederos R
PL
Prats-Sánchez L
CP
Camps-Renom P
BN
Blay N
SL
Sumoy L
DC
de Cid R
MJ
Montaner J
CC
Cruchaga C
LJ
Lee JM
MJ
Martí-Fàbregas J
FI
Férnandez-Cadenas I
Chapter II

Abstract

Summary of the research findings

Occult atrial fibrillation (AF) is one of the major causes of embolic stroke of undetermined source (ESUS). Knowing the underlying etiology of an ESUS will reduce stroke recurrence and/or unnecessary use of anticoagulants. Understanding cardioembolic strokes (CES), whose main cause is AF, will provide tools to select patients who would benefit from anticoagulants among those with ESUS or AF. We aimed to discover novel loci associated with CES and create a polygenetic risk score (PRS) for a more efficient CES risk stratification.

362,661 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

362661
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
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.