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Nonrigid active shape model-based registration framework for motion correction of cardiac T1 mapping.


ABSTRACT: PURPOSE:Accurate reconstruction of myocardial T1 maps from a series of T1 -weighted images consists of cardiac motions induced from breathing and diaphragmatic drifts. We propose and evaluate a new framework based on active shape models to correct for motion in myocardial T1 maps. METHODS:Multiple appearance models were built at different inversion time intervals to model the blood-myocardium contrast and brightness changes during the longitudinal relaxation. Myocardial inner and outer borders were automatically segmented using the built models, and the extracted contours were used to register the T1 -weighted images. Data acquired from 210 patients using a free-breathing acquisition protocol were used to train and evaluate the proposed framework. Two independent readers evaluated the quality of the T1 maps before and after correction using a four-point score. The mean absolute distance and Dice index were used to validate the registration process. RESULTS:The testing data set from 180 patients at 5 short axial slices showed a significant decrease of mean absolute distance (from 3.3?±?1.6 to 2.3?±?0.8?mm, P?

SUBMITTER: El-Rewaidy H 

PROVIDER: S-EPMC5941305 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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Nonrigid active shape model-based registration framework for motion correction of cardiac T<sub>1</sub> mapping.

El-Rewaidy Hossam H   Nezafat Maryam M   Jang Jihye J   Nakamori Shiro S   Fahmy Ahmed S AS   Nezafat Reza R  

Magnetic resonance in medicine 20180103 2


<h4>Purpose</h4>Accurate reconstruction of myocardial T<sub>1</sub> maps from a series of T<sub>1</sub> -weighted images consists of cardiac motions induced from breathing and diaphragmatic drifts. We propose and evaluate a new framework based on active shape models to correct for motion in myocardial T<sub>1</sub> maps.<h4>Methods</h4>Multiple appearance models were built at different inversion time intervals to model the blood-myocardium contrast and brightness changes during the longitudinal  ...[more]

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