Age-related microvascular degeneration in the human cerebral periventricular white matter

Eszter Farkas1, Rob A I de Vos, Gergely Donka

  • 1Department of Anatomy, School of Medicine, University of Szeged, P.O. Box 427, 6701, Szeged, Hungary. farkase@anat-fm.szote.u-szeged.hu

Acta Neuropathologica
|February 3, 2006
PubMed

Insights

Aging causes microvascular degeneration in the brain's white matter (WM), leading to WM lesions. This study reveals age-related changes in microvessels, particularly in the frontal lobe, potentially impacting nutrient supply.

Area of Science:

  • Neurology
  • Pathology
  • Gerontology

Background:

  • White matter (WM) lesions are common in elderly patients and are often attributed to cerebrovascular issues.
  • Understanding the microvascular changes in the aging brain is crucial for explaining WM lesion development.

Purpose of the Study:

  • To investigate the microvascular histopathologic changes in the periventricular white matter (WM) of aging subjects.
  • To correlate these microvascular changes with age and peripheral atherosclerosis.

Main Methods:

  • Quantitative light and electron microscopy were used on post-mortem periventricular WM samples from individuals aged 40-90.
  • Microvascular fibrohyalinosis, basement membrane thickening, vascular density, and intact microvessels were assessed.

Main Results:

  • Microvascular fibrohyalinosis was the most frequent microvascular damage observed in the elderly.
  • Age-related increases in basement membrane pathology and decreases in intact microvessels were noted, especially in frontal and occipital WM.
  • Peripheral atherosclerosis was associated with significant microvascular fibrosis, particularly in the frontal WM.

Conclusions:

  • Age-related microvascular degeneration in periventricular WM may impair nutrient supply, contributing to WM lesions.
  • The frontal lobe appears most vulnerable to WM pathology with advancing age.
  • Peripheral atherosclerosis may serve as a predictive marker for microvascular pathology in the brain's WM.