Determination of T1-mapping values in structurally normal hearts on the 1.5 T Magnetom Sola MRI system
Détails
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Accès restreint UNIL
Etat: Public
Version: Après imprimatur
Licence: Non spécifiée
Accès restreint UNIL
Etat: Public
Version: Après imprimatur
Licence: Non spécifiée
ID Serval
serval:BIB_2C882D4573B8
Type
Mémoire
Sous-type
(Mémoire de) maîtrise (master)
Collection
Publications
Institution
Titre
Determination of T1-mapping values in structurally normal hearts on the 1.5 T Magnetom Sola MRI system
Directeur⸱rice⸱s
RUTZ T.
Codirecteur⸱rice⸱s
HUGELSHOFER S.
Détails de l'institution
Université de Lausanne, Faculté de biologie et médecine
Statut éditorial
Acceptée
Date de publication
2023
Langue
anglais
Nombre de pages
23
Résumé
Introduction
Cardiac magnetic resonance (CMR) is a non-invasive imaging modality capable of
identifying structural and tissular heart pathology and has a particular interest when
myocardial fibrosis is suspected. Images performed after administration of a
Gadolinium-based contrast agent allow to visualize localized, macroscopic myocardial
scar. Specific myocardial mapping-sequences can detect more diffuse and subtle
pathologies. T1-mapping with extracellular volume (ECV) estimation has proven to be
a robust and reproducible method to detect microscopic interstitial fibrosis. In order to
be able to detect pathology, establishment of reference values in normal hearts is
recommended for every specific MR-system and T1-mapping sequence.
Method
Subjects without known cardiovascular risk factors nor heart disease and with a normal
CMR study were retrospectively included. On a 1.5T scanner, an ECG-triggered
modified Look-Locker inversion recovery sequence which is a standard T1-mapping
sequence was acquired on a short-axis basal slice of the left ventricle (LV). Native and
post-contrast myocardial T1 relaxation time was measured, and ECV calculated for six
LV- segments as well as mean values for the whole short-axis slice.
3
Results
Fifty patients (age 43 ± 15y, 36% male) were included. Left ventricular end-diastolic
volume and mass were 78±14 ml/m2 and 94 ± 27 g, respectively. Mean native T1-
mapping and ECV values for the left ventricle were 982 ± 35 (range 886-1051 msec)
and 22.9 ± 2.7% (16.6-28.3%), respectively. Women had significantly higher mean T1
and ECV values than men (987 ± 35ms vs 966 ± 31ms, p=0.04; 24 ± 2% vs 21 ± 3%,
p<0.001). Native T1 and ECV values didn’t change with age: <40 years; N=19, 987±
30ms, 23 ±3%; 40-60 years, N=24, 983 ± 33ms, ECV 24 ± 2%; > 60 years, N=5, 969
± 46ms, ECV 22±3%; p=0.23/0.18.
Conclusion
In a low-risk group of subjects with a normal CMR study, native T1 mapping values
were 982 ± 35ms and ECV 22.9 % ± 2.7%. Female subjects had a slightly higher mean
native T1 and ECV value than men, however, T1 and ECV do not appear to change
with age.
Cardiac magnetic resonance (CMR) is a non-invasive imaging modality capable of
identifying structural and tissular heart pathology and has a particular interest when
myocardial fibrosis is suspected. Images performed after administration of a
Gadolinium-based contrast agent allow to visualize localized, macroscopic myocardial
scar. Specific myocardial mapping-sequences can detect more diffuse and subtle
pathologies. T1-mapping with extracellular volume (ECV) estimation has proven to be
a robust and reproducible method to detect microscopic interstitial fibrosis. In order to
be able to detect pathology, establishment of reference values in normal hearts is
recommended for every specific MR-system and T1-mapping sequence.
Method
Subjects without known cardiovascular risk factors nor heart disease and with a normal
CMR study were retrospectively included. On a 1.5T scanner, an ECG-triggered
modified Look-Locker inversion recovery sequence which is a standard T1-mapping
sequence was acquired on a short-axis basal slice of the left ventricle (LV). Native and
post-contrast myocardial T1 relaxation time was measured, and ECV calculated for six
LV- segments as well as mean values for the whole short-axis slice.
3
Results
Fifty patients (age 43 ± 15y, 36% male) were included. Left ventricular end-diastolic
volume and mass were 78±14 ml/m2 and 94 ± 27 g, respectively. Mean native T1-
mapping and ECV values for the left ventricle were 982 ± 35 (range 886-1051 msec)
and 22.9 ± 2.7% (16.6-28.3%), respectively. Women had significantly higher mean T1
and ECV values than men (987 ± 35ms vs 966 ± 31ms, p=0.04; 24 ± 2% vs 21 ± 3%,
p<0.001). Native T1 and ECV values didn’t change with age: <40 years; N=19, 987±
30ms, 23 ±3%; 40-60 years, N=24, 983 ± 33ms, ECV 24 ± 2%; > 60 years, N=5, 969
± 46ms, ECV 22±3%; p=0.23/0.18.
Conclusion
In a low-risk group of subjects with a normal CMR study, native T1 mapping values
were 982 ± 35ms and ECV 22.9 % ± 2.7%. Female subjects had a slightly higher mean
native T1 and ECV value than men, however, T1 and ECV do not appear to change
with age.
Mots-clé
Cardiovascular magnetic resonance, T1-mapping, extracellular volume, diffuse interstitial fibrosis, gender differences
Création de la notice
09/08/2024 10:02
Dernière modification de la notice
09/08/2024 14:54