Infarct Laterality Patterns in Relation to A1 Segment Hypoplasia/Aplasia According to Etiological Subtype

Junpei Nagasawa1, Tatsuhiro Yokoyama1, Ryuichi Okamoto1

  • 1Department of Neurology, Toho University Faculty of Medicine, Tokyo 143-8541, Japan.

Brain Sciences
|May 27, 2026
PubMed

Insights

Anatomical variations in the Circle of Willis A1 segment, like hypoplasia or aplasia, did not show a significant link to stroke laterality in this study. Further research with larger sample sizes is needed to confirm these exploratory findings.

Area of Science:

  • Neurology
  • Vascular Neurology
  • Neuroimaging

Background:

  • The Circle of Willis (CoW) is crucial for collateral cerebral circulation.
  • Anatomical variations, specifically A1 segment hypoplasia or aplasia, can impact cerebral hemodynamics.
  • The role of these variations in cerebral infarction distribution is debated.

Purpose of the Study:

  • To investigate the association between A1 segment hypoplasia/aplasia and infarct laterality.
  • To analyze this association across different etiological stroke subtypes: lacunar, cardioembolic stroke (CES), and embolic stroke of undetermined source (ESUS).

Main Methods:

  • Retrospective analysis of 198 patients with unilateral anterior circulation infarction.
  • Assessment of the Circle of Willis using magnetic resonance angiography (MRA).
  • Definition of A1 hypoplasia (<1 mm diameter) and aplasia (non-visualization); identification of minor (affected) and dominant (contralateral) sides.

Main Results:

  • 30% of patients exhibited A1 hypoplasia or aplasia, with similar prevalence across lacunar, ESUS, and CES subtypes.
  • Infarcts occurred on the A1 dominant side in 53% (lacunar), 55% (ESUS), and 75% (CES) of cases.
  • The observed differences in infarct laterality did not reach statistical significance (p=0.43), likely due to limited sample size.

Conclusions:

  • Prevalence of A1 segment hypoplasia/aplasia was consistent across studied stroke types.
  • No statistically significant association was found between A1 variations and infarct laterality.
  • Findings are inconclusive due to sample size limitations, suggesting the need for further hypothesis-generating research.

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