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Translesional pressure gradient and leptomeningeal collateral status in symptomatic middle cerebral artery stenosis
Author(s) -
Leng X.,
Lan L.,
Ip H. L.,
Fan F.,
Ma S. H.,
Ma K.,
Liu H.,
Yan Z.,
Liu J.,
Abrigo J.,
Soo Y. O. Y.,
Liebeskind D. S.,
Wong K. S.,
Leung T. W.
Publication year - 2018
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/ene.13521
Subject(s) - medicine , middle cerebral artery , cardiology , stenosis , anterior cerebral artery , stroke (engine) , univariate analysis , radiology , computed tomography angiography , internal carotid artery , culprit , angiography , ischemia , multivariate analysis , mechanical engineering , myocardial infarction , engineering
Background and purpose Leptomeningeal collateral ( LMC ) status governs the prognosis of large artery occlusive stroke, although factors determining LMC status are not fully elucidated. The aim was to investigate metrics affecting LMC status in such patients by using computational fluid dynamics ( CFD ) models based on computed tomography angiography ( CTA ). Methods In this cross‐sectional study, patients with recent ischaemic stroke or transient ischaemic attack attributed to atherosclerotic M1 middle cerebral artery ( MCA ) stenosis (50%–99%) were recruited. Demographic, clinical and imaging data of these patients were collected. Ipsilesional LMC status was graded as good or poor by assessing the laterality of anterior and posterior cerebral arteries in CTA . A CFD model based on CTA was constructed to reflect focal hemodynamics in the distal internal carotid artery, M1 MCA and A1 anterior cerebral artery. Pressure gradients were calculated across culprit MCA stenotic lesions in CFD models. Predictors for good LMC status were sought in univariate and multivariate analyses. Results Amongst the 85 patients enrolled (mean age 61.5 ± 10.9 years), 38 (44.7%) had good ipsilesional LMC status. The mean pressure gradient across MCA lesions was 14.8 ± 18.1 mmHg. Advanced age ( P = 0.030) and a larger translesional pressure gradient ( P = 0.029) independently predicted good LMC s. A lower fasting blood glucose level also showed a trend for good LMC s ( P = 0.058). Conclusions Our study suggested a correlation between translesional pressure gradient and maturation of LMC s in intracranial atherosclerotic disease. Further studies with more exquisite and dynamic monitoring of cerebral hemodynamics and LMC evolution are needed to verify the current findings.