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Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits

Author

Listed:
  • Craig A Glastonbury
  • Sara L Pulit
  • Julius Honecker
  • Jenny C Censin
  • Samantha Laber
  • Hanieh Yaghootkar
  • Nilufer Rahmioglu
  • Emilie Pastel
  • Katerina Kos
  • Andrew Pitt
  • Michelle Hudson
  • Christoffer Nellåker
  • Nicola L Beer
  • Hans Hauner
  • Christian M Becker
  • Krina T Zondervan
  • Timothy M Frayling
  • Melina Claussnitzer
  • Cecilia M Lindgren

Abstract

Genetic studies have recently highlighted the importance of fat distribution, as well as overall adiposity, in the pathogenesis of obesity-associated diseases. Using a large study (n = 1,288) from 4 independent cohorts, we aimed to investigate the relationship between mean adipocyte area and obesity-related traits, and identify genetic factors associated with adipocyte cell size. To perform the first large-scale study of automatic adipocyte phenotyping using both histological and genetic data, we developed a deep learning-based method, the Adipocyte U-Net, to rapidly derive mean adipocyte area estimates from histology images. We validate our method using three state-of-the-art approaches; CellProfiler, Adiposoft and floating adipocytes fractions, all run blindly on two external cohorts. We observe high concordance between our method and the state-of-the-art approaches (Adipocyte U-net vs. CellProfiler: R2visceral = 0.94, P

Suggested Citation

  • Craig A Glastonbury & Sara L Pulit & Julius Honecker & Jenny C Censin & Samantha Laber & Hanieh Yaghootkar & Nilufer Rahmioglu & Emilie Pastel & Katerina Kos & Andrew Pitt & Michelle Hudson & Christof, 2020. "Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits," PLOS Computational Biology, Public Library of Science, vol. 16(8), pages 1-21, August.
  • Handle: RePEc:plo:pcbi00:1008044
    DOI: 10.1371/journal.pcbi.1008044
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