Greater periventricular white matter hyperintensity severity in basilar artery branch atheromatous disease

Po-Chen Lin1,2, Feng-Chi Chang2,3, Hui-Chi Huang1,4

  • 1Department of Neurology, Taipei Veterans General Hospital, No. 201 Sec.2, Shihpai Road, Peitou, Taipei, 11217, Taiwan.

BMC Neurology
|July 19, 2017
PubMed

Insights

Basilar artery branch atheromatous disease (BABAD) is linked to more severe white matter hyperintensity (WMH) in periventricular regions, independent of other risk factors. This association suggests small vessel issues may play a role in BABAD, impacting patient prognosis.

Area of Science:

  • Neurology
  • Vascular Neurology
  • Neuroimaging

Background:

  • Basilar artery branch atheromatous disease (BABAD) is a frequent cause of posterior circulation stroke (PCS).
  • The relationship between white matter hyperintensity (WMH), a marker of small vessel disease (SVD), and BABAD remains unclear.
  • Understanding this association is crucial for stroke etiology and management.

Purpose of the Study:

  • To investigate the association between WMH severity and BABAD.
  • To compare WMH severity in BABAD patients versus those with large-artery atherosclerotic stenosis (LAA) and non-stroke subjects (NS).
  • To evaluate the prognostic value of WMH severity in BABAD patients.

Main Methods:

  • Retrospective analysis of PCS patients from the Taipei Veterans General Hospital Stroke Registry (2010-2014).
  • WMH severity assessed using the Scheltens scale.
  • Multivariate analyses compared WMH severity across BABAD, LAA, and NS groups and evaluated WMH's impact on 3-month prognosis in BABAD.

Main Results:

  • The study included 151 BABAD, 97 LAA, and 78 NS patients.
  • BABAD patients exhibited significantly greater periventricular WMH severity compared to LAA and NS groups, independent of vascular risk factors.
  • Increased periventricular WMH severity was a predictor of poor 3-month functional outcomes in BABAD patients (OR=3.21, p=0.028).

Conclusions:

  • This study establishes a novel, independent association between WMH and BABAD.
  • Findings suggest that small vessel abnormalities, beyond lipohyalinosis, may contribute to BABAD pathophysiology.
  • Future management of BABAD should consider both large and small vessel protection strategies.
Abstract

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