Frontiers in Neurology (Sep 2019)

Location-Specific Association Between Cerebral Microbleeds and Arterial Pulsatility

  • Kun-Hsien Chou,
  • Kun-Hsien Chou,
  • Pei-Ning Wang,
  • Pei-Ning Wang,
  • Pei-Ning Wang,
  • Pei-Ning Wang,
  • Li-Ning Peng,
  • Li-Ning Peng,
  • Li-Kuo Liu,
  • Li-Kuo Liu,
  • Wei-Ju Lee,
  • Wei-Ju Lee,
  • Wei-Ju Lee,
  • Liang-Kung Chen,
  • Liang-Kung Chen,
  • Ching-Po Lin,
  • Ching-Po Lin,
  • Chih-Ping Chung,
  • Chih-Ping Chung

DOI
https://doi.org/10.3389/fneur.2019.01012
Journal volume & issue
Vol. 10

Abstract

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Objective: Increased arterial pulsatility index (API), usually representative of distal vascular resistance, have been linked to cerebral small vessel disease. However, their relationship with cerebral microbleeds (CMBs) is less well-studied. The present study aimed to evaluate the relationship between CMBs and API.Methods: We cross-sectionally evaluated participants from a non-clinical stroke, non-demented community-based population. APIs of cervical internal carotid and vertebral arteries were measured by ultrasonography. CMBs were assessed by susceptibility-weighted-imaging on 3T magnetic resonance imaging (MRI). Subjects were classified according to CMB locations: deep/infratentorial (DI) or strictly lobar (SL) CMB groups. DI-CMB group also included subjects with simultaneous lobar CMBs.Results: Of the 681 subjects [62.2 (8.4) years, 43.5% men] included, CMBs were found in 92 (13.5%) subjects: 57 (8.4%) with DI-CMB and 35 (5.1%) with SL-CMB. The results showed that CMB location influenced their association with API. DI-CMB was significantly associated with elevated API of internal carotid arteries (β = 0.031; 95% confidence interval = 0.002–0.059; P = 0.03), while SL-CMB was significantly associated with elevated API of vertebral arteries (β = 0.050; 95% confidence interval = 0.006–0.094; P = 0.025) in multivariate analyses adjusting for age, sex, cardiovascular risk factors, white matter hyperintensities (WMH), and lacunes.Conclusion: Our study again emphasizes (1) the association between API and cerebral small vessel disease and (2) the pathogenic differences between DI- and SL-CMBs. Our results lead to the postulation that in the presence of CMBs without clinical dysfunction yet, insidious small vascular disorders might already occur with corresponding topography.

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