Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes
Permanent lenke
https://hdl.handle.net/10037/28285Dato
2022-12-31Type
Journal articleTidsskriftartikkel
Peer reviewed
Forfatter
Libiseller-Egger, Julian; Phelan, Jody E.; Attia, Zachi I.; Benavente, Ernest Diez; Campino, Susana; Friedman, Paul A.; Lopez-Jimenez, Francisco; Leon, David A.; Clark, Taane G.Sammendrag
Artifcial intelligence (AI)-based approaches can now use electrocardiograms (ECGs) to provide expertlevel performance in detecting heart abnormalities and diagnosing disease. Additionally, patient age
predicted from ECGs by AI models has shown great potential as a biomarker for cardiovascular age,
where recent work has found its deviation from chronological age (“delta age”) to be associated with
mortality and co-morbidities. However, despite being crucial for understanding underlying individual
risk, the genetic underpinning of delta age is unknown. In this work we performed a genome-wide
association study using UK Biobank data (n=34,432) and identifed eight loci associated with delta
age (p ≤ 5 × 10−8), including genes linked to cardiovascular disease (CVD) (e.g. SCN5A) and (heart)
muscle development (e.g. TTN). Our results indicate that the genetic basis of cardiovascular ageing
is predominantly determined by genes directly involved with the cardiovascular system rather than
those connected to more general mechanisms of ageing. Our insights inform the epidemiology of
CVD, with implications for preventative and precision medicine.
Forlag
Springer NatureSitering
Libiseller-Egger, Phelan, Attia, Benavente, Campino, Friedman, Lopez-Jimenez, Leon, Clark. Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes. Scientific Reports. 2022;12(1)Metadata
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