Journal
JOURNAL OF NEUROLOGY
Volume 267, Issue 3, Pages 721-730Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s00415-019-09620-6
Keywords
4D flow MRI; Pulsatile index; Pulsatility; Small vessel disease; White matter hyperintensities
Categories
Funding
- Swedish Research Council [2017-04949, 2015-05616] Funding Source: Swedish Research Council
- Hjärt-Lungfonden [20140592, 20110383] Funding Source: Medline
- Vetenskapsrådet [2017-04949, 2015-05616] Funding Source: Medline
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Cerebral small vessel disease (SVD) is a major cause of stroke and cognitive impairment. However, the underlying mechanisms behind SVD are still poorly understood. High cerebral arterial pulsatility has been suggested as a possible cause of SVD. In population studies, arterial pulsatility has been linked to white matter hyperintensities (WMH), cerebral atrophy, and cognitive impairment, all features of SVD. In stroke, pulsatility data are scarce and contradictory. The aim of this study was to investigate the relationship between arterial pulsatility and SVD in stroke patients. With a cross-sectional design, 89 patients with acute ischemic stroke or TIA were examined with MRI. A neuropsychological assessment was performed 1 year later. Using 4D flow MRI, pulsatile indices (PI) were calculated for the internal carotid artery (ICA) and middle cerebral artery (M1, M3). Flow volume pulsatility (FVP), a measure corresponding to the cyclic expansion of the arterial tree, was calculated for the same locations. These parameters were assessed for associations with WMH volume, brain volume and cognitive function. ICA-FVP was associated with WMH volume (beta = 1.67, 95% CI: [0.1, 3.24], p = 0.037). M1-PI and M1-FVP were associated with decreasing cognitive function (beta = - 4.4, 95% CI: [- 7.7, - 1.1], p = 0.009 and beta = - 13.15, 95% CI: [- 24.26, - 2.04], p = 0.02 respectively). In summary, this supports an association between arterial pulsatility and SVD in stroke patients, and provides a potential target for further research and preventative treatment. FVP may become a useful biomarker for assessing pulsatile stress with PCMRI and 4D flow MRI.
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