TY - GEN
T1 - Clustering Disease Trajectories in Contrastive Feature Space for Biomarker Proposal in Age-Related Macular Degeneration
AU - Holland, Robbie
AU - Leingang, Oliver
AU - Holmes, Christopher
AU - Anders, Philipp
AU - Kaye, Rebecca
AU - Riedl, Sophie
AU - Paetzold, Johannes C.
AU - Ezhov, Ivan
AU - Bogunović, Hrvoje
AU - Schmidt-Erfurth, Ursula
AU - Scholl, Hendrik P.N.
AU - Sivaprasad, Sobha
AU - Lotery, Andrew J.
AU - Rueckert, Daniel
AU - Menten, Martin J.
N1 - Publisher Copyright:
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023.
PY - 2023
Y1 - 2023
N2 - Age-related macular degeneration (AMD) is the leading cause of blindness in the elderly. Current grading systems based on imaging biomarkers only coarsely group disease stages into broad categories that lack prognostic value for future disease progression. It is widely believed that this is due to their focus on a single point in time, disregarding the dynamic nature of the disease. In this work, we present the first method to automatically propose biomarkers that capture temporal dynamics of disease progression. Our method represents patient time series as trajectories in a latent feature space built with contrastive learning. Then, individual trajectories are partitioned into atomic sub-sequences that encode transitions between disease states. These are clustered using a newly introduced distance metric. In quantitative experiments we found our method yields temporal biomarkers that are predictive of conversion to late AMD. Furthermore, these clusters were highly interpretable to ophthalmologists who confirmed that many of the clusters represent dynamics that have previously been linked to the progression of AMD, even though they are currently not included in any clinical grading system.
AB - Age-related macular degeneration (AMD) is the leading cause of blindness in the elderly. Current grading systems based on imaging biomarkers only coarsely group disease stages into broad categories that lack prognostic value for future disease progression. It is widely believed that this is due to their focus on a single point in time, disregarding the dynamic nature of the disease. In this work, we present the first method to automatically propose biomarkers that capture temporal dynamics of disease progression. Our method represents patient time series as trajectories in a latent feature space built with contrastive learning. Then, individual trajectories are partitioned into atomic sub-sequences that encode transitions between disease states. These are clustered using a newly introduced distance metric. In quantitative experiments we found our method yields temporal biomarkers that are predictive of conversion to late AMD. Furthermore, these clusters were highly interpretable to ophthalmologists who confirmed that many of the clusters represent dynamics that have previously been linked to the progression of AMD, even though they are currently not included in any clinical grading system.
KW - Age-related macular degeneration
KW - Biomarker discovery
KW - Clustering
KW - Contrastive learning
KW - Disease trajectories
UR - http://www.scopus.com/inward/record.url?scp=85174746122&partnerID=8YFLogxK
U2 - 10.1007/978-3-031-43990-2_68
DO - 10.1007/978-3-031-43990-2_68
M3 - Conference contribution
AN - SCOPUS:85174746122
SN - 9783031439896
T3 - Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
SP - 724
EP - 734
BT - Medical Image Computing and Computer Assisted Intervention – MICCAI 2023 - 26th International Conference, Proceedings
A2 - Greenspan, Hayit
A2 - Greenspan, Hayit
A2 - Madabhushi, Anant
A2 - Mousavi, Parvin
A2 - Salcudean, Septimiu
A2 - Duncan, James
A2 - Syeda-Mahmood, Tanveer
A2 - Taylor, Russell
PB - Springer Science and Business Media Deutschland GmbH
T2 - 26th International Conference on Medical Image Computing and Computer-Assisted Intervention, MICCAI 2023
Y2 - 8 October 2023 through 12 October 2023
ER -