Small vessel disease burden and risk of recurrent cerebrovascular events in patients with lacunar stroke and intracerebral haemorrhage attributable to deep perforator arteriolopathy

Author:

Goeldlin Martina B12ORCID,Vynckier Jan13,Mueller Madlaine12,Drop Boudewijn1ORCID,Maamari Basel1,Vonlanthen Noah1,Siepen Bernhard M12,Hakim Arsany4ORCID,Kaesmacher Johannes4,Jesse Christopher Marvin5,Mueller Mandy D5,Meinel Thomas R1ORCID,Beyeler Morin12ORCID,Clénin Leander1,Gralla Jan4,Z’Graggen Werner15ORCID,Bervini David5,Arnold Marcel1,Fischer Urs16ORCID,Seiffge David J1ORCID

Affiliation:

1. Department of Neurology, Inselspital Bern University Hospital and University of Bern, Bern, Switzerland

2. Graduate School for Health Sciences, University of Bern, Bern, Switzerland

3. Department of Neurology, Onze-Lieve-Vrouwziekenhuis Aalst, Aalst, Belgium

4. University Institute for Diagnostic and Interventional Neuroradiology, Inselspital Bern University Hospital and University of Bern, Bern, Switzerland

5. Department of Neurosurgery, Inselspital Bern University Hospital and University of Bern, Bern, Switzerland

6. Department of Neurology, University Hospital Basel, Basel, Switzerland

Abstract

Introduction: Deep perforator arteriolopathy (DPA) causes intracerebral haemorrhage (ICH) and lacunar strokes (LS). We compare patient characteristics, MRI findings and clinical outcomes among patients with deep ICH and LS. Patients and methods: We included patients with MRI-confirmed LS or ICH in the basal ganglia, thalamus, internal capsule or brainstem from the Bernese Stroke Registry. We assessed MRI small vessel disease (SVD) markers, SVD burden score, modified Rankin Scale (mRS) and ischaemic stroke or ICH at 3 months. Results: We included 716 patients, 117 patients (16.3%) with deep ICH (mean age (SD) 65.1 (±15.2) years, 37.1% female) and 599 patients (83.7%) with LS (mean age (SD) 69.7 (±13.6) years, 39.9% female). Compared to LS, deep ICH was associated with a higher SVD burden score (median (IQR) 2 (1–2) vs 1 (0–2)), aORshift 3.19, 95%CI 2.15–4.75). Deep ICH patients had more often cerebral microbleeds (deep ICH: 71.6% vs LS: 29.2%, p < 0.001, median count (IQR) 4(2–12) vs 2(1–6)) and a higher prevalence of lacunes (deep ICH: 60.5% vs LS: 27.4% p < 0.001). At 3 months, deep ICH was associated with higher mRS (aORshift 2.16, 95%CI 1.21–3.87). Occurrence of ischaemic stroke was numerically but not significantly higher in deep ICH (4.3% vs 2.9%; p = 0.51). One patient (1.1%) with ICH but none with LS suffered ICH recurrence. Discussion/Conclusion: DPA manifesting as ICH is associated with more severe MRI SVD burden and worse outcome compared to LS. The short-term risks of subsequent ischaemic stroke and recurrent ICH are similar in ICH and LS patients. This implies potential consequences for future secondary prevention strategies.

Funder

Young Talents in Clinical Research Beginner Grant

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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