Distribution of white matter hyperintensity in cerebral hemorrhage and healthy aging

Yi-Cheng Zhu1, Hugues Chabriat, Ophélia Godin

  • 1Department of Neurology, Peking Union Medical College Hospital, Beijing, China.

Journal of Neurology
|August 31, 2011
PubMed

Insights

Cerebral amyloid angiopathy (CAA) is linked to occipital white matter lesions, suggesting vascular pathology drives white matter damage. This study found more occipital-dominant white matter hyperintensities in lobar intracerebral hemorrhage patients compared to controls.

Area of Science:

  • Neurology
  • Neuroradiology
  • Genetics

Background:

  • White matter hyperintensities (WMH) are common in aging and cerebrovascular disease.
  • Cerebral amyloid angiopathy (CAA) is a leading cause of lobar intracerebral hemorrhage (ICH), particularly in older adults.
  • The distribution of WMH may reflect underlying pathologies like CAA.

Purpose of the Study:

  • To compare the severity and distribution of white matter T2-hyperintensities (WMH) in the frontal and occipital lobes between patients with lobar ICH (suspected CAA), hypertension-related deep ICH, and healthy controls.
  • To investigate the association between WMH distribution, overall WMH burden, and the apolipoprotein E (APOE) ε4 allele.

Main Methods:

  • Retrospective analysis of MRI scans from 102 patients with lobar ICH (possible/probable CAA), 99 with deep ICH (hypertension), and 159 healthy elderly controls.
  • Visual assessment of WMH severity in frontal and occipital lobes using a standardized MRI score.
  • Calculation of the frontal-occipital (FO) gradient to quantify WMH distribution differences.

Main Results:

  • Patients with lobar ICH showed a significantly higher proportion of occipital-dominant WMH (FO gradient ≤-2) compared to healthy controls (13.7% vs. 5.7%, p=0.03).
  • Occipital-dominant WMH was associated with a greater overall WMH burden (p=0.0006) and a higher prevalence of the APOE ε4 allele (45.8% vs. 19.4%, p=0.04).
  • Hypertension-related deep ICH patients were not explicitly compared for FO gradient in this abstract.

Conclusions:

  • The findings support the predilection of CAA for posterior brain regions.
  • White matter lesions may preferentially develop in areas with significant vascular pathology, particularly in CAA.
  • WMH distribution and APOE ε4 status may serve as indicators of underlying cerebrovascular disease mechanisms.