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Test-retest reliability of arterial spin labelling for cerebral blood flow in older adults with small vessel disease.

Binnie, LR; Pauls, MMH; Benjamin, P; Dhillon, M-PK; Betteridge, S; Clarke, B; Ghatala, R; Hainsworth, FAH; Howe, FA; Khan, U; et al. Binnie, LR; Pauls, MMH; Benjamin, P; Dhillon, M-PK; Betteridge, S; Clarke, B; Ghatala, R; Hainsworth, FAH; Howe, FA; Khan, U; Kruuse, C; Madigan, JB; Moynihan, B; Patel, B; Pereira, AC; Rostrup, E; Shtaya, ABY; Spilling, CA; Trippier, S; Williams, R; Isaacs, JD; Barrick, TR; Hainsworth, AH (2022) Test-retest reliability of arterial spin labelling for cerebral blood flow in older adults with small vessel disease. Transl Stroke Res, 13 (4). pp. 583-594. ISSN 1868-601X https://doi.org/10.1007/s12975-021-00983-5
SGUL Authors: Hainsworth, Atticus Henry Barrick, Thomas Richard Isaacs, Jeremy Howe, Franklyn Arron

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Abstract

Cerebral small vessel disease (SVD) is common in older people and is associated with lacunar stroke, white matter hyperintensities (WMH) and vascular cognitive impairment. Cerebral blood flow (CBF) is reduced in SVD, particularly within white matter.Here we quantified test-retest reliability in CBF measurements using pseudo-continuous arterial spin labelling (pCASL) in older adults with clinical and radiological evidence of SVD (N=54, mean (SD): 66.9 (8.7) years, 15 females/39 males). We generated whole-brain CBF maps on two visits at least 7 days apart (mean (SD): 20 (19), range 7-117 days).Test-retest reliability for CBF was high in all tissue types, with intra-class correlation coefficient [95%CI]: 0.758 [0.616, 0.852] for whole brain, 0.842 [0.743, 0.905] for total grey matter, 0.771 [0.636, 0.861] for deep grey matter (caudate-putamen and thalamus), 0.872 [0.790, 0.923] for normal-appearing white matter (NAWM) and 0.780 [0.650, 0.866] for WMH (all p<0.001). ANCOVA models indicated significant decline in CBF in total grey matter, deep grey matter and NAWM with increasing age and diastolic blood pressure (all p<0.001). CBF was lower in males relative to females (p=0.013 for total grey matter, p=0.004 for NAWM).We conclude that pCASL has high test-retest reliability as a quantitative measure of CBF in older adults with SVD. These findings support the use of pCASL in routine clinical imaging and as a clinical trial endpoint.All data come from the PASTIS trial, prospectively registered at: https://eudract.ema.europa.eu (2015-001235-20, registered 13/05/2015), http://www.clinicaltrials.gov (NCT02450253, registered 21/05/2015).

Item Type: Article
Additional Information: © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Keywords: Arterial spin labelling, Cerebral blood flow, Small vessel disease, Vascular aging, White matter lesions
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Transl Stroke Res
ISSN: 1868-601X
Language: eng
Dates:
DateEvent
August 2022Published
26 January 2022Published Online
22 December 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
20140901Alzheimer's Drug Discovery FoundationUNSPECIFIED
20140901UK Alzheimer SocietyUNSPECIFIED
CL-2015-16-001National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 35080734
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113995
Publisher's version: https://doi.org/10.1007/s12975-021-00983-5

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