Objectives: This study aimed to simulate the aerodynamics and to identify the spatial correlation between anatomical and functional stenoses in Crouzon syndrome patients.
Methods: Six patients of Crouzon syndrome were included. Computational fluid dynamics (CFD) was utilized to simulate airflow dynamics, and characteristics, including the velocity, pressure intensity, wall shear stress, airflow resistance and streamline, were extracted for quantitative analysis both in overall and regionally. Structural stenosis was defined at the minimum cross-sectional area, while functional stenosis was identified at the point of maximum airflow velocity. The spatial distances between the Frankfurt plane and structural/functional stenosis were calculated and compared.
Results: Structural stenosis occurred in the palatopharynx, while the highest inspiratory resistance and peak airflow velocity during expiration identified the glossopharynx as the functional stenosis site. A steep increase in negative pressure and a significant increase in wall shear stress could be observed surrounding the functional stenosis. The intensity and diffusion range of wall shear stress are positively correlated with age. Notably, the functional stenosis was consistently 5 mm below the structural stenosis (P < 0.05).
Conclusions: CFD effectively visualized both overall and regional aerodynamics of Crouzon syndrome, providing a novel method for functional airway evaluation. The spatial distributions of structural and functional stenoses did not strictly correspond; the structural stenosis was located on the palatopharynx, while the functional stenosis was on the glossopharynx. The wall shear stress worsens pathologically with age, aggravating functional stenosis to structural stenosis. Therefore, functional stenosis should also be addressed in airway management to ensure therapeutic effectiveness.
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http://dx.doi.org/10.1016/j.jcms.2025.02.005 | DOI Listing |
JACC Cardiovasc Interv
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Department of Cardiology and Vascular Medicine, West German Heart and Vascular Center, University of Duisburg-Essen, Essen, Germany.
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Shu Chien-Gene Lay Department of Bioengineering, University of California San Diego, La Jolla, CA 92093, USA.
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Alkaptonuria is an extremely rare disorder of tyrosine metabolism caused by an autosomal recessive enzymatic deficiency of homogentisic acid (HGA) oxidase, causing its accumulation in collagenous structures, especially in hyaline cartilage. It is characterized by a triad of homogentisic aciduria, bluish-black discoloration of connective tissues (ochronosis) and arthropathy of the spine and large weight-bearing joints. Several clinical manifestations were described including coronary and valvular calcification, aortic stenosis, limited chest expansion, and renal, urethral and prostate calculi as well as ocular and cutaneous pigmentation.
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Cardiology Department, Fethi Sekin City Hospital, Elazığ, Turkey.
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Department of Neurology, The First Affiliated Hospital of Shandong First Medical University and Shandong Provincial Qianfoshan Hospital, Shandong Institute of Neuroimmunology, Jinan, China.
Small and dense LDL cholesterol (sdLDL-C) and apolipoprotein B (ApoB) have important roles in promoting the development of atherosclerosis and are highly correlated with the degree of atherosclerosis. Several studies have found differences in anterior and posterior circulation strokes and in the mechanisms of their atherosclerosis, but little research has been done on the relationship of sdLDL-C and ApoB to atherosclerotic stenosis in anterior and posterior circulation strokes. We analyzed the correlation between sdLDL-C and ApoB and the degree of arterial stenosis in patients with posterior circulation stroke.
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