TY - JOUR
T1 - Markers of Myocardial Damage Predict Mortality in Patients With Aortic Stenosis
AU - Kwak, Soongu
AU - Everett, Russell J.
AU - Treibel, Thomas A.
AU - Yang, Seokhun
AU - Hwang, Doyeon
AU - Ko, Taehoon
AU - Williams, Michelle C.
AU - Bing, Rong
AU - Singh, Trisha
AU - Joshi, Shruti
AU - Lee, Heesun
AU - Lee, Whal
AU - Kim, Yong Jin
AU - Chin, Calvin W.L.
AU - Fukui, Miho
AU - Al Musa, Tarique
AU - Rigolli, Marzia
AU - Singh, Anvesha
AU - Tastet, Lionel
AU - Dobson, Laura E.
AU - Wiesemann, Stephanie
AU - Ferreira, Vanessa M.
AU - Captur, Gabriella
AU - Lee, Sahmin
AU - Schulz-Menger, Jeanette
AU - Schelbert, Erik B.
AU - Clavel, Marie Annick
AU - Park, Sung Ji
AU - Rheude, Tobias
AU - Hadamitzky, Martin
AU - Gerber, Bernhard L.
AU - Newby, David E.
AU - Myerson, Saul G.
AU - Pibarot, Phillipe
AU - Cavalcante, João L.
AU - McCann, Gerry P.
AU - Greenwood, John P.
AU - Moon, James C.
AU - Dweck, Marc R.
AU - Lee, Seung Pyo
N1 - Publisher Copyright:
© 2021
PY - 2021/8/10
Y1 - 2021/8/10
N2 - Background: Cardiovascular magnetic resonance (CMR) is increasingly used for risk stratification in aortic stenosis (AS). However, the relative prognostic power of CMR markers and their respective thresholds remains undefined. Objectives: Using machine learning, the study aimed to identify prognostically important CMR markers in AS and their thresholds of mortality. Methods: Patients with severe AS undergoing AVR (n = 440, derivation; n = 359, validation cohort) were prospectively enrolled across 13 international sites (median 3.8 years’ follow-up). CMR was performed shortly before surgical or transcatheter AVR. A random survival forest model was built using 29 variables (13 CMR) with post-AVR death as the outcome. Results: There were 52 deaths in the derivation cohort and 51 deaths in the validation cohort. The 4 most predictive CMR markers were extracellular volume fraction, late gadolinium enhancement, indexed left ventricular end-diastolic volume (LVEDVi), and right ventricular ejection fraction. Across the whole cohort and in asymptomatic patients, risk-adjusted predicted mortality increased strongly once extracellular volume fraction exceeded 27%, while late gadolinium enhancement >2% showed persistent high risk. Increased mortality was also observed with both large (LVEDVi >80 mL/m2) and small (LVEDVi ≤55 mL/m2) ventricles, and with high (>80%) and low (≤50%) right ventricular ejection fraction. The predictability was improved when these 4 markers were added to clinical factors (3-year C-index: 0.778 vs 0.739). The prognostic thresholds and risk stratification by CMR variables were reproduced in the validation cohort. Conclusions: Machine learning identified myocardial fibrosis and biventricular remodeling markers as the top predictors of survival in AS and highlighted their nonlinear association with mortality. These markers may have potential in optimizing the decision of AVR.
AB - Background: Cardiovascular magnetic resonance (CMR) is increasingly used for risk stratification in aortic stenosis (AS). However, the relative prognostic power of CMR markers and their respective thresholds remains undefined. Objectives: Using machine learning, the study aimed to identify prognostically important CMR markers in AS and their thresholds of mortality. Methods: Patients with severe AS undergoing AVR (n = 440, derivation; n = 359, validation cohort) were prospectively enrolled across 13 international sites (median 3.8 years’ follow-up). CMR was performed shortly before surgical or transcatheter AVR. A random survival forest model was built using 29 variables (13 CMR) with post-AVR death as the outcome. Results: There were 52 deaths in the derivation cohort and 51 deaths in the validation cohort. The 4 most predictive CMR markers were extracellular volume fraction, late gadolinium enhancement, indexed left ventricular end-diastolic volume (LVEDVi), and right ventricular ejection fraction. Across the whole cohort and in asymptomatic patients, risk-adjusted predicted mortality increased strongly once extracellular volume fraction exceeded 27%, while late gadolinium enhancement >2% showed persistent high risk. Increased mortality was also observed with both large (LVEDVi >80 mL/m2) and small (LVEDVi ≤55 mL/m2) ventricles, and with high (>80%) and low (≤50%) right ventricular ejection fraction. The predictability was improved when these 4 markers were added to clinical factors (3-year C-index: 0.778 vs 0.739). The prognostic thresholds and risk stratification by CMR variables were reproduced in the validation cohort. Conclusions: Machine learning identified myocardial fibrosis and biventricular remodeling markers as the top predictors of survival in AS and highlighted their nonlinear association with mortality. These markers may have potential in optimizing the decision of AVR.
KW - aortic valve stenosis
KW - magnetic resonance imaging
KW - random survival forest
UR - http://www.scopus.com/inward/record.url?scp=85111065201&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2021.05.047
DO - 10.1016/j.jacc.2021.05.047
M3 - Article
C2 - 34353531
AN - SCOPUS:85111065201
SN - 0735-1097
VL - 78
SP - 545
EP - 558
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 6
ER -