Effects of Acquisition Parameter Modifications and Field Strength on the Reproducibility of Brain Perfusion Measurements Using Arterial Spin-Labeling.


Journal

AJNR. American journal of neuroradiology
ISSN: 1936-959X
Titre abrégé: AJNR Am J Neuroradiol
Pays: United States
ID NLM: 8003708

Informations de publication

Date de publication:
01 2021
Historique:
received: 23 04 2020
accepted: 17 08 2020
pubmed: 14 11 2020
medline: 23 3 2021
entrez: 13 11 2020
Statut: ppublish

Résumé

Although the added diagnostic value of arterial spin-labeling is shown in various cerebral pathologies, its use in clinical practice is limited. To encourage clinical adoption of ASL, we investigated the reproducibility of CBF measurements and the effects of variations in acquisition parameters compared to the recommended ASL implementation. Thirty-four volunteers (mean age, 57.8 ± 17.0 years; range, 22-80 years) underwent two separate sessions (1.5T and 3T scanners from a single vendor) using a 15-channel head coil. Both sessions contained repeated 3D and 2D pseudocontinuous arterial spin-labeling scans using vendor-recommended acquisition parameters (recommendation paper-based), followed by three 3D pseudocontinuous arterial spin-labeling scans, two with postlabeling delays of 1600  and 2000 ms and one with increased spatial resolution. All scans were single postlabeling delay. Intrasession (identical acquisitions, scanned five minutes apart) and intersession (first 2D and 3D acquisitions of two sessions) reproducibility was examined as well as the effect of parameter variations on CBF. Intrasession CBF reproducibility was similar across image readouts and field strengths (within-subject coefficient of variation between 4.0% and 6.7%). Intersession within-subject coefficient of variation ranged from 6.6% to 14.8%. At 3T, the 3D acquisition with a higher spatial resolution resulted in less mixing of GM and WM signal, thus decreasing the bias in GM CBF between the 2D and 3D acquisitions (ΔCBF = 2.49 mL/100g/min [ Arterial spin-labeling imaging is reproducible at both field strengths, and the reproducibility is not significantly correlated with age. Furthermore, 3T tolerates more acquisition parameter variations and allows more extensive optimizations so that 3D and 2D acquisitions can be compared.

Sections du résumé

BACKGROUND AND PURPOSE
Although the added diagnostic value of arterial spin-labeling is shown in various cerebral pathologies, its use in clinical practice is limited. To encourage clinical adoption of ASL, we investigated the reproducibility of CBF measurements and the effects of variations in acquisition parameters compared to the recommended ASL implementation.
MATERIALS AND METHODS
Thirty-four volunteers (mean age, 57.8 ± 17.0 years; range, 22-80 years) underwent two separate sessions (1.5T and 3T scanners from a single vendor) using a 15-channel head coil. Both sessions contained repeated 3D and 2D pseudocontinuous arterial spin-labeling scans using vendor-recommended acquisition parameters (recommendation paper-based), followed by three 3D pseudocontinuous arterial spin-labeling scans, two with postlabeling delays of 1600  and 2000 ms and one with increased spatial resolution. All scans were single postlabeling delay. Intrasession (identical acquisitions, scanned five minutes apart) and intersession (first 2D and 3D acquisitions of two sessions) reproducibility was examined as well as the effect of parameter variations on CBF.
RESULTS
Intrasession CBF reproducibility was similar across image readouts and field strengths (within-subject coefficient of variation between 4.0% and 6.7%). Intersession within-subject coefficient of variation ranged from 6.6% to 14.8%. At 3T, the 3D acquisition with a higher spatial resolution resulted in less mixing of GM and WM signal, thus decreasing the bias in GM CBF between the 2D and 3D acquisitions (ΔCBF = 2.49 mL/100g/min [
CONCLUSIONS
Arterial spin-labeling imaging is reproducible at both field strengths, and the reproducibility is not significantly correlated with age. Furthermore, 3T tolerates more acquisition parameter variations and allows more extensive optimizations so that 3D and 2D acquisitions can be compared.

Identifiants

pubmed: 33184068
pii: ajnr.A6856
doi: 10.3174/ajnr.A6856
pmc: PMC7814799
doi:

Substances chimiques

Spin Labels 0

Types de publication

Clinical Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109-115

Informations de copyright

© 2021 by American Journal of Neuroradiology.

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Auteurs

K P A Baas (KPA)

From the Department of Radiology and Nuclear Medicine (K.P.A.B., A.J.N.), Amsterdam University Medical Center, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands k.p.baas@amsterdamumc.nl.

J Petr (J)

Institute of Radiopharmaceutical Cancer Research (J.P.), Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.
Department of Biomedical Engineering (J.P., H.J.M.M.M.), Institute Hall, Rochester Institute of Technology, Rochester, New York.

J P A Kuijer (JPA)

Department of Radiology and Nuclear Medicine (J.P.A.K., H.J.M.M.M.), Amsterdam University Medical Center, VU University Medical Center, Amsterdam, the Netherlands.

A J Nederveen (AJ)

From the Department of Radiology and Nuclear Medicine (K.P.A.B., A.J.N.), Amsterdam University Medical Center, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.

H J M M Mutsaerts (HJMM)

Department of Biomedical Engineering (J.P., H.J.M.M.M.), Institute Hall, Rochester Institute of Technology, Rochester, New York.
Department of Radiology and Nuclear Medicine (J.P.A.K., H.J.M.M.M.), Amsterdam University Medical Center, VU University Medical Center, Amsterdam, the Netherlands.
Department of Radiology and Nuclear Medicine (H.J.M.M.M.), University Hospital Ghent, Ghent, Belgium.

K C C van de Ven (KCC)

BIU MR (K.C.C.v.d.V.), Philips Healthcare, Best, the Netherlands.

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