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Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature
BACKGROUND: The microvasculature, the smallest blood vessels in the body, has key roles in maintenance of organ health and tumorigenesis. The retinal fundus is a window for human in vivo noninvasive assessment of the microvasculature. Large-scale complementary machine learning-based assessment of th...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746912/ https://www.ncbi.nlm.nih.gov/pubmed/34743558 http://dx.doi.org/10.1161/CIRCULATIONAHA.121.057709 |
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author | Zekavat, Seyedeh Maryam Raghu, Vineet K. Trinder, Mark Ye, Yixuan Koyama, Satoshi Honigberg, Michael C. Yu, Zhi Pampana, Akhil Urbut, Sarah Haidermota, Sara O’Regan, Declan P. Zhao, Hongyu Ellinor, Patrick T. Segrè, Ayellet V. Elze, Tobias Wiggs, Janey L. Martone, James Adelman, Ron A. Zebardast, Nazlee Del Priore, Lucian Wang, Jay C. Natarajan, Pradeep |
author_facet | Zekavat, Seyedeh Maryam Raghu, Vineet K. Trinder, Mark Ye, Yixuan Koyama, Satoshi Honigberg, Michael C. Yu, Zhi Pampana, Akhil Urbut, Sarah Haidermota, Sara O’Regan, Declan P. Zhao, Hongyu Ellinor, Patrick T. Segrè, Ayellet V. Elze, Tobias Wiggs, Janey L. Martone, James Adelman, Ron A. Zebardast, Nazlee Del Priore, Lucian Wang, Jay C. Natarajan, Pradeep |
author_sort | Zekavat, Seyedeh Maryam |
collection | PubMed |
description | BACKGROUND: The microvasculature, the smallest blood vessels in the body, has key roles in maintenance of organ health and tumorigenesis. The retinal fundus is a window for human in vivo noninvasive assessment of the microvasculature. Large-scale complementary machine learning-based assessment of the retinal vasculature with phenome-wide and genome-wide analyses may yield new insights into human health and disease. METHODS: We used 97 895 retinal fundus images from 54 813 UK Biobank participants. Using convolutional neural networks to segment the retinal microvasculature, we calculated vascular density and fractal dimension as a measure of vascular branching complexity. We associated these indices with 1866 incident International Classification of Diseases–based conditions (median 10-year follow-up) and 88 quantitative traits, adjusting for age, sex, smoking status, and ethnicity. RESULTS: Low retinal vascular fractal dimension and density were significantly associated with higher risks for incident mortality, hypertension, congestive heart failure, renal failure, type 2 diabetes, sleep apnea, anemia, and multiple ocular conditions, as well as corresponding quantitative traits. Genome-wide association of vascular fractal dimension and density identified 7 and 13 novel loci, respectively, that were enriched for pathways linked to angiogenesis (eg, vascular endothelial growth factor, platelet-derived growth factor receptor, angiopoietin, and WNT signaling pathways) and inflammation (eg, interleukin, cytokine signaling). CONCLUSIONS: Our results indicate that the retinal vasculature may serve as a biomarker for future cardiometabolic and ocular disease and provide insights into genes and biological pathways influencing microvascular indices. Moreover, such a framework highlights how deep learning of images can quantify an interpretable phenotype for integration with electronic health record, biomarker, and genetic data to inform risk prediction and risk modification. |
format | Online Article Text |
id | pubmed-8746912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-87469122022-01-14 Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature Zekavat, Seyedeh Maryam Raghu, Vineet K. Trinder, Mark Ye, Yixuan Koyama, Satoshi Honigberg, Michael C. Yu, Zhi Pampana, Akhil Urbut, Sarah Haidermota, Sara O’Regan, Declan P. Zhao, Hongyu Ellinor, Patrick T. Segrè, Ayellet V. Elze, Tobias Wiggs, Janey L. Martone, James Adelman, Ron A. Zebardast, Nazlee Del Priore, Lucian Wang, Jay C. Natarajan, Pradeep Circulation Original Research Articles BACKGROUND: The microvasculature, the smallest blood vessels in the body, has key roles in maintenance of organ health and tumorigenesis. The retinal fundus is a window for human in vivo noninvasive assessment of the microvasculature. Large-scale complementary machine learning-based assessment of the retinal vasculature with phenome-wide and genome-wide analyses may yield new insights into human health and disease. METHODS: We used 97 895 retinal fundus images from 54 813 UK Biobank participants. Using convolutional neural networks to segment the retinal microvasculature, we calculated vascular density and fractal dimension as a measure of vascular branching complexity. We associated these indices with 1866 incident International Classification of Diseases–based conditions (median 10-year follow-up) and 88 quantitative traits, adjusting for age, sex, smoking status, and ethnicity. RESULTS: Low retinal vascular fractal dimension and density were significantly associated with higher risks for incident mortality, hypertension, congestive heart failure, renal failure, type 2 diabetes, sleep apnea, anemia, and multiple ocular conditions, as well as corresponding quantitative traits. Genome-wide association of vascular fractal dimension and density identified 7 and 13 novel loci, respectively, that were enriched for pathways linked to angiogenesis (eg, vascular endothelial growth factor, platelet-derived growth factor receptor, angiopoietin, and WNT signaling pathways) and inflammation (eg, interleukin, cytokine signaling). CONCLUSIONS: Our results indicate that the retinal vasculature may serve as a biomarker for future cardiometabolic and ocular disease and provide insights into genes and biological pathways influencing microvascular indices. Moreover, such a framework highlights how deep learning of images can quantify an interpretable phenotype for integration with electronic health record, biomarker, and genetic data to inform risk prediction and risk modification. Lippincott Williams & Wilkins 2021-11-08 2022-01-11 /pmc/articles/PMC8746912/ /pubmed/34743558 http://dx.doi.org/10.1161/CIRCULATIONAHA.121.057709 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited. |
spellingShingle | Original Research Articles Zekavat, Seyedeh Maryam Raghu, Vineet K. Trinder, Mark Ye, Yixuan Koyama, Satoshi Honigberg, Michael C. Yu, Zhi Pampana, Akhil Urbut, Sarah Haidermota, Sara O’Regan, Declan P. Zhao, Hongyu Ellinor, Patrick T. Segrè, Ayellet V. Elze, Tobias Wiggs, Janey L. Martone, James Adelman, Ron A. Zebardast, Nazlee Del Priore, Lucian Wang, Jay C. Natarajan, Pradeep Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature |
title | Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature |
title_full | Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature |
title_fullStr | Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature |
title_full_unstemmed | Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature |
title_short | Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature |
title_sort | deep learning of the retina enables phenome- and genome-wide analyses of the microvasculature |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746912/ https://www.ncbi.nlm.nih.gov/pubmed/34743558 http://dx.doi.org/10.1161/CIRCULATIONAHA.121.057709 |
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