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T(1) mapping in cardiac MRI

Quantitative myocardial and blood T(1) have recently achieved clinical utility in numerous pathologies, as they provide non-invasive tissue characterization with the potential to replace invasive biopsy. Native T(1) time (no contrast agent), changes with myocardial extracellular water (edema, focal...

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Detalles Bibliográficos
Autores principales: Radenkovic, Dina, Weingärtner, Sebastian, Ricketts, Lewis, Moon, James C., Captur, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487768/
https://www.ncbi.nlm.nih.gov/pubmed/28623475
http://dx.doi.org/10.1007/s10741-017-9627-2
Descripción
Sumario:Quantitative myocardial and blood T(1) have recently achieved clinical utility in numerous pathologies, as they provide non-invasive tissue characterization with the potential to replace invasive biopsy. Native T(1) time (no contrast agent), changes with myocardial extracellular water (edema, focal or diffuse fibrosis), fat, iron, and amyloid protein content. After contrast, the extracellular volume fraction (ECV) estimates the size of the extracellular space and identifies interstitial disease. Spatially resolved quantification of these biomarkers (so-called T(1) mapping and ECV mapping) are steadily becoming diagnostic and prognostically useful tests for several heart muscle diseases, influencing clinical decision-making with a pending second consensus statement due mid-2017. This review outlines the physics involved in estimating T(1) times and summarizes the disease-specific clinical and research impacts of T(1) and ECV to date. We conclude by highlighting some of the remaining challenges such as their community-wide delivery, quality control, and standardization for clinical practice.