Volume 26, Issue 3 pp. 331-338
Original Research

Hemodynamic Impact of Systolic Blood Pressure and Hematocrit Calculated by Computational Fluid Dynamics in Patients with Intracranial Atherosclerosis

Hyo Suk Nam

Hyo Suk Nam

Department of Neurology, Yonsei University College of Medicine, Seoul, Korea

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Fabien Scalzo

Fabien Scalzo

Neurovascular Imaging Research Core, University of California, Los Angeles, CA

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Xinyi Leng

Xinyi Leng

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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Hing Lung Ip

Hing Lung Ip

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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Hye Sun Lee

Hye Sun Lee

Department of Biostatistics, Yonsei University College of Medicine, Seoul, Korea

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Florence Fan

Florence Fan

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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Xiangyan Chen

Xiangyan Chen

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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Yannie Soo

Yannie Soo

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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Zhongrong Miao

Zhongrong Miao

Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

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Liping Liu

Liping Liu

Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

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Edward Feldmann

Edward Feldmann

Baystate Medical Center Springfield, MA

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Thomas Leung

Thomas Leung

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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Ka Sing Wong

Ka Sing Wong

Department of Medicine and Therapeutics, Chinese University of Hong Kong, Hong Kong SAR, China

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David S. Liebeskind

Corresponding Author

David S. Liebeskind

Neurovascular Imaging Research Core, University of California, Los Angeles, CA

Correspondence: Address correspondence to David S. Liebeskind, MD, Neuroscience Research Building, 635 Charles E Young Drive South, Suite 225, Los Angeles, CA 90095-7334, USA, Tel: 310-963-5539. E-mail [email protected].Search for more papers by this author
First published: 24 November 2015
Citations: 17

Funding: This research was supported by the Leading Foreign Research Institute Recruitment Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (MSIP) (2012027176), a faculty research grant from the Yonsei University College of Medicine for 2014 (6-2014-0181), and the General Research Fund (Reference No. 14117414), Research Grants Council, Hong Kong SAR, China.

Disclosures: D. Liebeskind: Consultant/Advisory Board; Modest; Stryker, Covidien. The other authors have nothing to disclose.

ABSTRACT

OBJECTIVE

Success in clinical trials of intracranial atherosclerosis (ICAS) is related to accurate identification of high-risk patients. Noninvasive computational fluid dynamics (CFD) of stenotic lesions may enhance therapeutic decision-making. We determined whether physiologic parameters change downstream cerebral hemodynamics in patients with ICAS.

METHODS

Consecutive ICAS patients who underwent both CT angiography (CTA) and digital subtraction angiography were enrolled. CFD models were made using CTA source images. Inlet boundary conditions were defined using three ranges of systolic blood pressure (BP) (109.2, 158, and 225 mmHg) and hematocrit (27.3, 40.2, and 48.8). Ratios of pressure, shear strain rates (SSR), and flow velocity across the lesion were calculated using CFD simulations. A linear mixed model was used for the statistical analysis of repeated simulations.

RESULTS

Among the 56 patients, 32 had moderate stenosis (50-69%) and 24 had severe stenosis (70-99%). A linear mixed model revealed that the ratio of pressure was predicted by systolic BP and stenosis group interaction (P = .036). These pressure decreases were associated with systolic BP (P < .001) and stenosis group (P < .001), but not with hematocrit (P = .337). Post-hoc analysis revealed that pressure decreases were more profound in the severe stenosis than the moderate stenosis group when comparing high and low systolic BP (P = .0108). Ratios of SSR and velocity were only associated in the stenosis group.

CONCLUSIONS

Our study showed that systolic BP along with the degree of stenosis was associated with pressure decreases across stenotic lesions. Physiologic conditions may superimpose further changes in post-stenotic or downstream blood flow.

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