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Deep learning enables genetic analysis of the human thoracic aorta

  • James P. Pirruccello
  • , Mark D. Chaffin
  • , Elizabeth L. Chou
  • , Stephen J. Fleming
  • , Honghuang Lin
  • , Mahan Nekoui
  • , Shaan Khurshid
  • , Samuel F. Friedman
  • , Alexander G. Bick
  • , Alessandro Arduini
  • , Lu Chen Weng
  • , Seung Hoan Choi
  • , Amer Denis Akkad
  • , Puneet Batra
  • , Nathan R. Tucker
  • , Amelia W. Hall
  • , Carolina Roselli
  • , Emelia J. Benjamin
  • , Shamsudheen K. Vellarikkal
  • , Rajat M. Gupta
  • Christian M. Stegmann, Dejan Juric, James R. Stone, Ramachandran S. Vasan, Jennifer E. Ho, Udo Hoffmann, Steven A. Lubitz, Anthony A. Philippakis, Mark E. Lindsay, Patrick T. Ellinor

Producción científica: Articlerevisión exhaustiva

Resumen

Enlargement or aneurysm of the aorta predisposes to dissection, an important cause of sudden death. We trained a deep learning model to evaluate the dimensions of the ascending and descending thoracic aorta in 4.6 million cardiac magnetic resonance images from the UK Biobank. We then conducted genome-wide association studies in 39,688 individuals, identifying 82 loci associated with ascending and 47 with descending thoracic aortic diameter, of which 14 loci overlapped. Transcriptome-wide analyses, rare-variant burden tests and human aortic single nucleus RNA sequencing prioritized genes including SVIL, which was strongly associated with descending aortic diameter. A polygenic score for ascending aortic diameter was associated with thoracic aortic aneurysm in 385,621 UK Biobank participants (hazard ratio = 1.43 per s.d., confidence interval 1.32–1.54, P = 3.3 × 10−20). Our results illustrate the potential for rapidly defining quantitative traits with deep learning, an approach that can be broadly applied to biomedical images.

Idioma originalEnglish (US)
Páginas (desde-hasta)40-51
Número de páginas12
PublicaciónNature Genetics
Volumen54
N.º1
DOI
EstadoPublished - ene 2022
Publicado de forma externa

ASJC Scopus subject areas

  • Genetics

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