How do age, sex, and valve phenotype affect fibro-calcific remodeling in calcific aortic valve disease?
549 patients with calcific aortic valve disease, comprising a multidetector computed tomography cohort (n=411, 37% women) and a histological cohort of explanted aortic valves (n=138, 50% women), divided by age (<60 or ≥60 years) and valve phenotype (bicuspid vs tricuspid).
Aortic valve calcification density (via MDCT) and collagen content/fibrosis (via histology)surrogate
In calcific aortic valve disease, women exhibit less calcification and more fibrotic remodeling than men, regardless of age or valve phenotype, suggesting sex-specific mechanisms of valve degeneration.
Background In calcific aortic valve disease on tricuspid aortic valves (TAVs), men have higher aortic valve calcification and less fibrosis than women. However, little is known in bicuspid aortic valves (BAV). We thus aimed to investigate the impact of age, sex, and valve phenotype (TAVs versus BAVs) on fibro-calcific remodeling in calcific aortic valve disease. Methods and Results We included 2 cohorts: 411 patients who underwent multidetector computed tomography (37% women) for aortic valve calcification density assessment and 138 explanted aortic valves (histological cohort; 50% women). The cohorts were divided in younger (P≤0.01). Moreover, in women, younger patients with BAV had the lowest aortic valve calcification density (both P=0.02). In multivariate analysis, aortic valve calcification density correlated with age (β estimate±standard error: 6.5±1.8; P=0.0004) and male sex (109.2±18.4; PP=0.07). Women presented a higher collagen content than men (77.8±10.8 versus 69.9±12.9%; PP≤0.05), while no difference was observed between men. Conclusions In calcific aortic valve disease, women had less calcification and more fibrotic remodeling than men, regardless of the phenotype of the valve or age of the patient. Moreover, younger women with BAVs had less valve calcification. Thus, mineralization/fibrosis of the aortic valve is likely to have sex/age-specific mechanisms and be influenced by the valve morphology.
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Martine Voisine
Montreal Heart Institute
Maxime Hervault
Institut Universitaire de Cardiologie et de Pneumologie de Québec
Mylène Shen
Structural Heart Disease
Journal of the American Heart Association
SHILAP Revista de lepidopterología
Université Laval
Institut Universitaire de Cardiologie et de Pneumologie de Québec
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Voisine et al. (Fri,) studied this question.
synapsesocial.com/papers/69d5725975589c71d767e733 — DOI: https://doi.org/10.1161/jaha.119.015610
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