Strictly Lobar Microbleeds Reflect Amyloid Angiopathy Regardless of Cerebral and Cerebellar Compartments

Young Hee Jung1, Hyemin Jang2,3, Seong Beom Park2,3

  • 1Department of Neurology, Myongji Hospital, Hanyang University, Goyang, Korea (Y.H.J).

Stroke
|November 17, 2020
PubMed
Abstract

Insights

Strictly lobar cerebral and cerebellar microbleeds indicate cerebral amyloid angiopathy. Combinations of lobar and deep microbleeds suggest hypertensive arteriopathy, regardless of location. This research differentiates microbleed origins.

Area of Science:

  • Neurology
  • Neuroradiology
  • Cerebrovascular Diseases

Background:

  • Cerebral amyloid angiopathy (CAA) and hypertensive arteriopathy are common causes of microbleeds.
  • Distinguishing between CAA and hypertensive arteriopathy is crucial for understanding disease progression and treatment.
  • Lobar cerebellar microbleeds, alone or with deep microbleeds, require further investigation to determine their underlying pathology.

Purpose of the Study:

  • To investigate whether lobar cerebellar microbleeds, with or without deep microbleeds, are associated with cerebral amyloid angiopathy (CAA) or hypertensive arteriopathy.
  • To differentiate the underlying pathologies of various microbleed distributions in the brain.

Main Methods:

  • Categorized 71 patients with suspected CAA markers into four groups based on microbleed distribution: strictly lobar cerebral (L), lobar cerebral and lobar cerebellar (L/LCbll), lobar cerebral, cerebellar, and deep (L/Cbll/D), and lobar cerebral and deep (L/D).
  • Further categorized patients with cerebellar microbleeds into strictly lobar cerebellar and dentate nucleus groups.
  • Compared clinical characteristics, amyloid-beta (Aβ) positron emission tomography (PET) positivity, MRI CAA markers, and cerebral small vessel disease burden across groups.

Main Results:

  • Aβ positivity was significantly higher in the L and L/LCbll groups (81.8%, 84.6%) compared to L/Cbll/D and L/D groups (37.5%, 29.4%).
  • Lacune numbers were lower in the L and L/LCbll groups (1.7±3.3, 1.7±2.6) than in the L/Cbll/D and L/D groups (8.0±10.3, 13.4±17.7).
  • The strictly lobar cerebellar group showed higher Aβ positivity (75%) and lower lacune counts (2.3±3.7) than the dentate nucleus group (28.6%, 8.6±1.2).

Conclusions:

  • Strictly lobar cerebral and cerebellar microbleeds are associated with cerebral amyloid angiopathy.
  • Concurrent lobar and deep microbleeds indicate hypertensive arteriopathy, irrespective of the specific brain compartments involved.

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