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Enlarged translesional pressure gradient drives recruitment of leptomeningeal collaterals in medically treated patients with symptomatic middle cerebral artery stenosis

  • Yuying Liu
  • , Xuan Tian
  • , Jill Abrigo
  • , Shuang Li
  • , Yu Liu
  • , Linfang Lan
  • , Haipeng Liu
  • , Bonaventure Yiu Ming Ip
  • , Sze Ho Ma
  • , Karen Ka Yan Ma
  • , Florence Sin Ying Fan
  • , Vincent Hing Lung Ip
  • , Yannie Oi Yan Soo
  • , Howan Leung
  • , Vincent Chung Tong Mok
  • , Thomas Wai Hong Leung
  • , Xinyi Leng
    • Chinese University of Hong Kong
    • Prince of Wales Hospital Hong Kong
    • First Affiliated Hospital of Sun Yat-sen University

    Research output: Contribution to journalArticlepeer-review

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    Abstract

    Aims: Evolution patterns and contributing factors of leptomeningeal collaterals (LMCs) in symptomatic intracranial atherosclerotic stenosis (sICAS) remain elusive. Methods: Patients with atherosclerotic M1 middle cerebral artery (MCA-M1) stenosis (50%–99%), who were treated medically and had CT angiography (CTA) at baseline and 1 year, were recruited. LMC status was determined by the laterality of distal vessels in anterior and posterior cerebral artery territories in baseline and 1-year CTA. Computational fluid dynamics models were constructed based on baseline and 1-year CTA, to quantify post-stenotic to pre-stenotic pressure ratio (PR) in MCA-M1 lesions. Decreased PR over 1 year indicated enlarged translesional pressure gradient. Results: Among 33 patients (median age 62 years), 18 (54.5%) and 15 (45.5%) had good and poor baseline LMCs; 11 (33.3%) and 22 (66.7%) had good and poor 1-year LMCs. Twelve (36.4%), 16 (48.5%) and 5 (15.2%) patients had worse, similar and better LMCs at 1 year versus baseline. Sixteen (48.5%) patients had decreased PR over 1 year, associated with good LMCs at 1 year (adjusted odds ratio 6.40; p=0.038), independent of baseline LMC status. Conclusion: LMCs may evolve over time in medically treated sICAS patients, when an enlarged translesional pressure gradient may be a driving force.
    Original languageEnglish
    Pages (from-to)326-334
    Number of pages9
    JournalCerebrovascular Diseases
    Volume55
    Issue number3
    Early online date1 Jul 2025
    DOIs
    Publication statusPublished - Jul 2025

    Bibliographical note

    Publisher Copyright:
    © 2025 The Author(s). Published by S. Karger AG, Basel.

    Funding

    This study was supported by General Research Fund (Ref No. 14106019) and Early Career Scheme (Ref No. 24103122), Hong Kong Research Grants Council; Kwok Tak Seng Centre for Stroke Research and Intervention; and Li Ka Shing Institute of Health Sciences.

    Funders
    Chinese University of Hong Kong
    Research Grants Council, University Grants Committee

      Keywords

      • Computational fluid dynamics
      • Hemodynamics
      • Intracranial atherosclerotic stenosis
      • Ischemic stroke
      • Leptomeningeal collaterals

      ASJC Scopus subject areas

      • Neurology
      • Clinical Neurology
      • Cardiology and Cardiovascular Medicine

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