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炎症和生物力学因素在钙化性主动脉瓣疾病中内皮-间质相互作用的作用机制。

Inflammatory and Biomechanical Drivers of Endothelial-Interstitial Interactions in Calcific Aortic Valve Disease.

机构信息

Meinig School of Biomedical Engineering, Cornell University, Ithaca NY.

出版信息

Circ Res. 2021 Apr 30;128(9):1344-1370. doi: 10.1161/CIRCRESAHA.121.318011. Epub 2021 Apr 29.


DOI:10.1161/CIRCRESAHA.121.318011
PMID:
Abstract

Calcific aortic valve disease is dramatically increasing in global burden, yet no therapy exists outside of prosthetic replacement. The increasing proportion of younger and more active patients mandates alternative therapies. Studies suggest a window of opportunity for biologically based diagnostics and therapeutics to alleviate or delay calcific aortic valve disease progression. Advancement, however, has been hampered by limited understanding of the complex mechanisms driving calcific aortic valve disease initiation and progression towards clinically relevant interventions.

摘要

钙化性主动脉瓣疾病在全球范围内的负担显著增加,但除了人工瓣膜置换术之外,尚无其他治疗方法。越来越多的年轻和活跃的患者需要替代治疗。研究表明,有机会利用基于生物学的诊断和治疗方法来减轻或延缓钙化性主动脉瓣疾病的进展。然而,由于对驱动钙化性主动脉瓣疾病发生和向临床相关干预进展的复杂机制的理解有限,进展受到了阻碍。

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[2]
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[3]
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[4]
Risk of Retinal Vascular Occlusive Disease in Patients with Aortic Stenosis: A Nationwide Korean Cohort Study.

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[5]
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[6]
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[7]
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J Cardiovasc Dev Dis. 2025-4-3

[8]
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Cardiovasc Ther. 2025-4-7

[9]
Unveiling the Angiogenic Potential and Functional Decline of Valve Interstitial Cells During Calcific Aortic Valve Stenosis Progression.

J Cell Mol Med. 2025-4

[10]
Y chromosome-linked UTY modulates sex differences in valvular fibroblast methylation in response to nanoscale extracellular matrix cues.

Sci Adv. 2025-3-14

本文引用的文献

[1]
Hydrogen sulfide inhibits aortic valve calcification in heart via regulating RUNX2 by NF-κB, a link between inflammation and mineralization.

J Adv Res. 2020-7-21

[2]
Chronic High Glucose Concentration Induces Inflammatory and Remodeling Changes in Valvular Endothelial Cells and Valvular Interstitial Cells in a Gelatin Methacrylate 3D Model of the Human Aortic Valve.

Polymers (Basel). 2020-11-25

[3]
Human Aortic Valve Interstitial Cells Display Proangiogenic Properties During Calcific Aortic Valve Disease.

Arterioscler Thromb Vasc Biol. 2021-1

[4]
Cell-Type Transcriptome Atlas of Human Aortic Valves Reveal Cell Heterogeneity and Endothelial to Mesenchymal Transition Involved in Calcific Aortic Valve Disease.

Arterioscler Thromb Vasc Biol. 2020-10-22

[5]
Transforming growth factor-β1 promotes fibrosis but attenuates calcification of valvular tissue applied as a three-dimensional calcific aortic valve disease model.

Am J Physiol Heart Circ Physiol. 2020-9-28

[6]
Sex-Specific Features of Calcific Aortic Valve Disease.

Int J Mol Sci. 2020-8-6

[7]
Caffeic Acid Phenethyl Ester Ameliorates Calcification by Inhibiting Activation of the AKT/NF-κB/NLRP3 Inflammasome Pathway in Human Aortic Valve Interstitial Cells.

Front Pharmacol. 2020-7-7

[8]
Calcific Aortic Valve Disease-Natural History and Future Therapeutic Strategies.

Front Pharmacol. 2020-5-13

[9]
Endothelial-to-Mesenchymal Transition in Calcific Aortic Valve Disease.

Acta Cardiol Sin. 2020-5

[10]
Repair of the rheumatic mitral valve: Is the controversy over?

Asian Cardiovasc Thorac Ann. 2020-9

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