TY - JOUR
T1 - Prognostic value of cardiac magnetic resonance feature tracking strain in aortic stenosis
AU - Tsampasian, Vasiliki
AU - Merinopoulos, Ioannis
AU - Ravindrarajah, Thuwarahan
AU - Ring, Liam
AU - Heng, Ee Ling
AU - Prasad, Sanjay
AU - Vassiliou, Vassilios S.
N1 - Funding Information: This work was supported by the Rosetrees Trust (V.S.V. and S.K.P.), the National Institute for Health Research (NIHR) Cardiovascular Biomedical Research Unit (CBRU) of Royal Brompton and Harefield NHS Trust and Imperial College London (E.L.H., V.S.V. and S.K.P.) and NIHR Doctoral Research Fellowship (V.T., Ref NIHR303306). The views expressed in this publication are those of the authors and not those of the funders.
PY - 2024/1/19
Y1 - 2024/1/19
N2 - Background: Recent data have suggested that global longitudinal strain (GLS) could be useful for risk stratification of patients with severe aortic stenosis (AS). In this study, we aimed to investigate the prognostic role of GLS in patients with AS and also its incremental value in relation to left ventricular ejection fraction (LVEF) and late gadolinium enhancement (LGE). Methods: We analysed all consecutive patients with AS and LGE-CMR in our institution. Survival data were obtained from office of national statistics, a national body where all deaths in England are registered by law. Death certificates were obtained from the general register office. Results: Some 194 consecutive patients with aortic stenosis were investigated with CMR at baseline and followed up for 7.3 ± 4 years. On multivariate Cox regression analysis, only increasing age remained significant for both all-cause and cardiac mortality, while LGE (any pattern) retained significance for all-cause mortality and had a trend to significance for cardiac mortality. Kaplan–Meier survival analysis demonstrated that patients in the best and middle GLS tertiles had significantly better mortality compared to patients in the worst GLS tertiles. Importantly though, sequential Cox proportional-hazard analysis demonstrated that GLS did not have significant incremental prognostic value for all-cause mortality or cardiac mortality in addition to LVEF and LGE. Conclusions: Our study has demonstrated that age and LGE but not GLS are significant poor prognostic indicators in patients with moderate and severe AS.
AB - Background: Recent data have suggested that global longitudinal strain (GLS) could be useful for risk stratification of patients with severe aortic stenosis (AS). In this study, we aimed to investigate the prognostic role of GLS in patients with AS and also its incremental value in relation to left ventricular ejection fraction (LVEF) and late gadolinium enhancement (LGE). Methods: We analysed all consecutive patients with AS and LGE-CMR in our institution. Survival data were obtained from office of national statistics, a national body where all deaths in England are registered by law. Death certificates were obtained from the general register office. Results: Some 194 consecutive patients with aortic stenosis were investigated with CMR at baseline and followed up for 7.3 ± 4 years. On multivariate Cox regression analysis, only increasing age remained significant for both all-cause and cardiac mortality, while LGE (any pattern) retained significance for all-cause mortality and had a trend to significance for cardiac mortality. Kaplan–Meier survival analysis demonstrated that patients in the best and middle GLS tertiles had significantly better mortality compared to patients in the worst GLS tertiles. Importantly though, sequential Cox proportional-hazard analysis demonstrated that GLS did not have significant incremental prognostic value for all-cause mortality or cardiac mortality in addition to LVEF and LGE. Conclusions: Our study has demonstrated that age and LGE but not GLS are significant poor prognostic indicators in patients with moderate and severe AS.
KW - aortic stenosis
KW - cardiovascular magnetic resonance
KW - ejection fraction
KW - global longitudinal strain
KW - late gadolinium enhancement
UR - http://www.scopus.com/inward/record.url?scp=85183165948&partnerID=8YFLogxK
U2 - 10.3390/jcdd11010030
DO - 10.3390/jcdd11010030
M3 - Article
AN - SCOPUS:85183165948
VL - 11
JO - Journal of Cardiovascular Development and Disease
JF - Journal of Cardiovascular Development and Disease
SN - 2308-3425
IS - 1
M1 - 30
ER -