Extensive white matter changes predict stroke recurrence up to 5 years after a first-ever ischemic stroke

S Melkas1, G Sibolt, N K J Oksala

  • 1Department of Neurological Sciences, University of Helsinki, and Department of Neurology, Helsinki University Central Hospital, Helsinki, Finland. susanna.melkas@hus.fi

Abstract

Insights

Severe white matter changes (WMCs) indicate a higher risk of recurrent ischemic stroke within five years. WMCs serve as a marker for small vessel disease (SVD) and aid in stroke recurrence risk stratification.

Area of Science:

  • Neurology
  • Radiology
  • Epidemiology

Background:

  • White matter changes (WMCs) are linked to small vessel disease (SVD) and negatively impact cognition, mood, and daily functioning.
  • The association between severe WMCs and recurrent ischemic stroke risk requires further investigation.

Purpose of the Study:

  • To determine if severe WMCs are a risk factor for recurrent ischemic stroke.
  • To evaluate the long-term prognosis of patients with severe WMCs after a first-ever ischemic stroke.

Main Methods:

  • A cohort of 320 patients with first-ever ischemic stroke was followed for 12 years.
  • White matter changes (WMCs) were assessed using MRI and categorized as absent-to-moderate or severe.
  • Multivariate Cox regression analysis was employed to identify independent predictors of stroke recurrence, controlling for confounding factors.

Main Results:

  • Recurrent stroke occurred in 23.8% of patients at 5 years and 39.7% at 12 years.
  • Severe WMCs were associated with a higher 5-year recurrence risk (39.1%) compared to absent-to-moderate WMCs (24.5%).
  • Independent predictors of 5-year recurrent stroke included severe WMCs, atrial fibrillation, hypertension, and peripheral arterial disease.

Conclusions:

  • Severe WMCs predict stroke recurrence within 5 years after an initial ischemic stroke.
  • WMCs can serve as a marker for SVD, summarizing the impact of risk factors on the brain's small vessels.
  • These findings highlight the poor long-term prognosis associated with cerebral SVD.

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