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Synchronized inversion recovery‐spin echo sequences for precise in vivo T 1 measurement of human myocardium: A pilot study on 22 healthy subjects
Author(s) -
Walker P. M.,
Marie P. Y.,
Mezeray C.,
Bessieres M.,
Escanyé J. M.,
Karcher G.,
Danchin N.,
Mattei S.,
Villemot J. P.,
Bertrand A.
Publication year - 1993
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.1910290509
Subject(s) - reproducibility , spin echo , pulse sequence , nuclear magnetic resonance , in vivo , echo time , sequence (biology) , spin–lattice relaxation , pulse (music) , biomedical engineering , nuclear medicine , physics , medicine , magnetic resonance imaging , chemistry , mathematics , radiology , biology , optics , statistics , biochemistry , microbiology and biotechnology , detector , nuclear quadrupole resonance
An ECG‐triggered, two‐sequence MRI technique is proposed for the precise measurement of proton T 1 relaxation times of the human myocardium at a field strength of 0.5 T. The combination of an inversion recovery (IR) sequence and a spin echo (SE) sequence is not new. It is, however, rarely used in quantitative in vivo cardiac studies. Our approach employs a synchronization of the 90° read pulse to the systolic period. In a study of 22 healthy volunteers, the globally measured T 1 value was estimated to be 714 ± 23 ms. Four of the volunteers also underwent additional imaging scans for the purposes of reproducibility assessment. The T 1 precision was found to be 3.9 ± 1.1% for the IR/SE combination and 16.9 ± 5.3% for a combination of SE sequences. Total imaging time for the IR and SE sequences was 19.2 ± 3.0 mins. The relative rapidity of this classic technique and the T 1 precision obtained give this technique an obvious application in the discrimination of normal and diseased myocardium. In the same study, valuable supplementary tissue characterization is provided by T 2 , calculated from the SE sequence. T 2 was evaluated to be 50 ± 3 ms.