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Deep Learning Model of Diastolic Dysfunction Risk Stratifies the Progression of Early-Stage Aortic Stenosis. | LitMetric

AI Article Synopsis

  • The study explores how a deep learning model can predict the risk of developing aortic stenosis (AS) from the early stage of aortic valve sclerosis by assessing diastolic dysfunction (DD).
  • Researchers evaluated data from 898 participants in the ARIC cohort and validated their findings in two other groups, showing a significant correlation between high DD risk and the development of AS or related health interventions.
  • The results indicate that using deep learning to measure DD effectively stratifies risk in patients, providing a better understanding of how AS progresses.

Article Abstract

Background: The development and progression of aortic stenosis (AS) from aortic valve (AV) sclerosis is highly variable and difficult to predict.

Objectives: The authors investigated whether a previously validated echocardiography-based deep learning (DL) model assessing diastolic dysfunction (DD) could identify the latent risk associated with the development and progression of AS.

Methods: The authors evaluated 898 participants with AV sclerosis from the ARIC (Atherosclerosis Risk In Communities) cohort study and associated the DL-predicted probability of DD with 2 endpoints: 1) the new diagnosis of AS; and 2) the composite of subsequent mortality or AV interventions. Validation was performed in 2 additional cohorts: 1) in 50 patients with mild-to-moderate AS undergoing cardiac magnetic resonance (CMR) imaging and serial echocardiographic assessments; and 2) in 18 patients with AV sclerosis undergoing F-sodium fluoride (NaF) and F-fluorodeoxyglucose positron emission tomography (PET) combined with computed tomography (CT) to assess valvular inflammation and calcification.

Results: In the ARIC cohort, a higher DL-predicted probability of DD was associated with the development of AS (adjusted HR: 3.482 [95% CI: 2.061-5.884]; P < 0.001) and subsequent mortality or AV interventions (adjusted HR: 7.033 [95% CI: 3.036-16.290]; P < 0.001). The multivariable Cox model (incorporating the DL-predicted probability of DD) derived from the ARIC cohort efficiently predicted the progression of AS (C-index: 0.798 [95% CI: 0.648-0.948]) in the CMR cohort. Moreover, the predictions of this multivariable Cox model correlated positively with valvular F-NaF mean standardized uptake values in the PET/CT cohort (r = 0.62; P = 0.008).

Conclusions: Assessment of DD using DL can stratify the latent risk associated with the progression of early-stage AS.

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Source
http://dx.doi.org/10.1016/j.jcmg.2024.07.017DOI Listing

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