TY - JOUR
T1 - Intracranial Atherosclerotic Burden and Cerebral Parenchymal Changes at 7T MRI in Patients With Transient Ischemic Attack or Ischemic Stroke
AU - Lindenholz, Arjen
AU - de Bresser, Jeroen
AU - van der Kolk, Anja G
AU - van der Worp, H Bart
AU - Witkamp, Theodoor D
AU - Hendrikse, Jeroen
AU - van der Schaaf, Irene C
N1 - Funding Information:
Funding. The research of JH has received funding from the European Research Council under the European Union's Horizon 2020 Programme (H2020)/ERC grant agreement no. 637024 (HEARTOFSTROKE).
Funding Information:
The research of JH has received funding from the European Research Council under the European Union’s Horizon
Publisher Copyright:
© Copyright © 2021 Lindenholz, de Bresser, van der Kolk, van der Worp, Witkamp, Hendrikse and van der Schaaf.
PY - 2021/5/6
Y1 - 2021/5/6
N2 - The relevance of intracranial vessel wall lesions detected with MRI is not fully established. In this study (trial identification number: NTR2119; www.trialregister.nl), 7T MRI was used to investigate if a higher vessel wall lesion burden is associated with more cerebral parenchymal changes in patients with ischemic stroke or transient ischemic attack (TIA). MR images of 82 patients were assessed for the number of vessel wall lesions of the large intracranial arteries and for cerebral parenchymal changes, including the presence and number of cortical, small subcortical, and deep gray matter infarcts; lacunes of presumed vascular origin; cortical microinfarcts; and periventricular and deep white matter hyperintensities (WMHs). Regression analyses showed that a higher vessel wall lesion burden was associated with the presence of small subcortical infarcts, lacunes of presumed vascular origin, and deep gray matter infarcts (relative risk 1.18; 95% CI, 1.03-1.35) and presence of moderate-to-severe periventricular WMHs (1.21; 95% CI, 1.03-1.42), which are all manifestations of small vessel disease (SVD). The burden of enhancing vessel wall lesions was associated with the number of cortical microinfarcts only (1.48; 95% CI, 1.04-2.11). These results suggest an interrelationship between large vessel wall lesion burden and cerebral parenchymal manifestations often linked to SVD or, alternatively, that vascular changes occur in both large and small intracranial arteries simultaneously.
AB - The relevance of intracranial vessel wall lesions detected with MRI is not fully established. In this study (trial identification number: NTR2119; www.trialregister.nl), 7T MRI was used to investigate if a higher vessel wall lesion burden is associated with more cerebral parenchymal changes in patients with ischemic stroke or transient ischemic attack (TIA). MR images of 82 patients were assessed for the number of vessel wall lesions of the large intracranial arteries and for cerebral parenchymal changes, including the presence and number of cortical, small subcortical, and deep gray matter infarcts; lacunes of presumed vascular origin; cortical microinfarcts; and periventricular and deep white matter hyperintensities (WMHs). Regression analyses showed that a higher vessel wall lesion burden was associated with the presence of small subcortical infarcts, lacunes of presumed vascular origin, and deep gray matter infarcts (relative risk 1.18; 95% CI, 1.03-1.35) and presence of moderate-to-severe periventricular WMHs (1.21; 95% CI, 1.03-1.42), which are all manifestations of small vessel disease (SVD). The burden of enhancing vessel wall lesions was associated with the number of cortical microinfarcts only (1.48; 95% CI, 1.04-2.11). These results suggest an interrelationship between large vessel wall lesion burden and cerebral parenchymal manifestations often linked to SVD or, alternatively, that vascular changes occur in both large and small intracranial arteries simultaneously.
KW - intracranial arteries
KW - intracranial atherosclerosis
KW - intracranial vessel wall MR imaging
KW - large vessel disease
KW - small vessel disease
KW - white matter hyperintensity
UR - http://www.scopus.com/inward/record.url?scp=85106174975&partnerID=8YFLogxK
U2 - 10.3389/fneur.2021.637556
DO - 10.3389/fneur.2021.637556
M3 - Article
C2 - 34025551
SN - 1664-2295
VL - 12
SP - 1
EP - 10
JO - Frontiers in Neurology
JF - Frontiers in Neurology
M1 - 637556
ER -