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Multicenter Study
. 2013 Jun;84(6):624-9.
doi: 10.1136/jnnp-2012-304434. Epub 2013 Feb 14.

Enlarged perivascular spaces as a marker of underlying arteriopathy in intracerebral haemorrhage: a multicentre MRI cohort study

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Free PMC article
Multicenter Study

Enlarged perivascular spaces as a marker of underlying arteriopathy in intracerebral haemorrhage: a multicentre MRI cohort study

Andreas Charidimou et al. J Neurol Neurosurg Psychiatry. 2013 Jun.
Free PMC article

Abstract

Background and purpose: Small vessel disease (mainly hypertensive arteriopathy and cerebral amyloid angiopathy (CAA)) is an important cause of spontaneous intracerebral haemorrhage (ICH), a devastating and still poorly understood stroke type. Enlarged perivascular spaces (EPVS) are a promising neuroimaging marker of small vessel disease. Based on the underlying arteriopathy distributions, we hypothesised that severe centrum semiovale EPVS are more common in lobar ICH attributed to CAA than other ICH. We evaluated EPVS prevalence, severity and distribution, and their clinical-radiological associations.

Methods: Retrospective multicentre cohort study of 121 ICH patients. Clinical information was obtained using standardised forms. Basal ganglia and centrum semiovale EPVS on T2-weighted MRI (graded 0-4 (>40 EPVS)), white-matter changes, cerebral microbleeds (CMBs) and lacunes were rated using validated scales.

Results: Patients with probable or possible CAA (n=76) had a higher prevalence of severe (>40) centrum semiovale EPVS compared with other ICH patients (35.5% vs 17.8%; p=0.041). In logistic regression age (OR: 1.43; 95% CI 1.01 to 2.02; p=0.045), deep CMBs (OR: 3.27; 95% CI 1.27 to 8.45; p=0.014) and mean white-matter changes score (OR: 1.29; 95% CI 1.17 to 1.43; p<0.0001) were independently associated with increased basal ganglia EPVS severity; only age was associated with increased centrum semiovale EPVS severity (OR: 1.50; 95% CI 1.08 to 2.10; p=0.017).

Conclusions: EPVS are common in ICH. Different mechanisms may account for EPVS according to their anatomical distribution. Severe centrum semiovale EPVS may be secondary to, and indicative of, CAA with value as a new neuroimaging marker. By contrast, basal ganglia EPVS severity is associated with markers of hypertensive arteriopathy.

Keywords: Amyloid; Cerebrovascular Disease; Clinical Neurology; MRI.

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Figures

Figure 1
Figure 1
Axial T2-weighted MRI. (A and B) Dot-like hyperintensities characteristic of enlarged perivascular spaces (EPVS) in the basal ganglia in a patient with spontaneous deep intracerebral haemorrhage (ICH). (C and D) Linear hyperintensities typical of EPVS in the centrum semiovale in a patient with cerebral amyloid angiopathy-related lobar ICH. Note that deep brain regions (eg, basal ganglia) are not affected by EPVS (D).
Figure 2
Figure 2
Age-adjusted prevalence of severe centrum semiovale enlarged perivascular spaces (EPVS) (>40 EPVS) in patients with strictly lobar intracerebral haemorrhage (ICH), attributed to cerebral amyloid angiopathy, compared with other ICH. Age was used as a continuous variable. (For within-group comparisons of the proportion of patients with centrum semiovale EPVS vs basal ganglia EPVS for lobar ICH and other ICH see online supplementary material).

References

    1. Qureshi AI, Mendelow AD, Hanley DF. Intracerebral haemorrhage. Lancet 2009;373:1632–44 - PMC - PubMed
    1. Charidimou A, Gang Q, Werring DJ. Sporadic cerebral amyloid angiopathy revisited: recent insights into pathophysiology and clinical spectrum. J Neurol Neurosurg Psychiatry 2012;83:124–37 - PubMed
    1. Ozturk MH, Aydingoz U. Comparison of MR signal intensities of cerebral perivascular (Virchow-Robin) and subarachnoid spaces. J Comput Assist Tomogr 2002;26:902–4 - PubMed
    1. Marin-Padilla M, Knopman DS. Developmental aspects of the intracerebral microvasculature and perivascular spaces: insights into brain response to late-life diseases. J Neuropathol Exp Neurol 2011;70:1060–9 - PMC - PubMed
    1. Wardlaw JM. Blood-brain barrier and cerebral small vessel disease. J Neurol Sci 2010;299:66–71 - PubMed

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