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dc.contributor.author | Weiss, Dar | es_ES |
dc.contributor.author | Cavinato, Cristina | es_ES |
dc.contributor.author | Gray, Authia | es_ES |
dc.contributor.author | Ramachandra, Abhay B. | es_ES |
dc.contributor.author | Avril, Stephane | es_ES |
dc.contributor.author | Humphrey, Jay D. | es_ES |
dc.contributor.author | Latorre, Marcos | es_ES |
dc.date.accessioned | 2023-01-30T19:01:06Z | |
dc.date.available | 2023-01-30T19:01:06Z | |
dc.date.issued | 2020-12-04 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/191511 | |
dc.description.abstract | [EN] Arterial tortuosity manifests in many conditions, including hypertension, genetic mutations predisposing to thoracic aortopathy, and vascular aging. Despite evidence that tortuosity disrupts efficient blood flow and that it may be an important clinical biomarker, underlying mechanisms remain poorly understood but are widely appreciated to be largely biomechanical. Many previous studies suggested that tortuosity may arise via an elastic structural buckling instability, but the novel experimental-computational approach used here suggests that tortuosity arises from mechanosensitive, cell-mediated responses to local aberrations in the microstructural integrity of the arterial wall. In particular, computations informed by multimodality imaging show that aberrations in elastic fiber integrity, collagen alignment, and collagen turnover can lead to a progressive loss of structural stability that entrenches during the development of tortuosity. Interpreted in this way, microstructural defects or irregularities of the arterial wall initiate the condition and hypertension is a confounding factor. | es_ES |
dc.description.sponsorship | This work was supported by grants from the U.S. NIH (R01 HL105297, P01 HL134605, and U01 HL142518) | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | American Association for the Advancement of Science | es_ES |
dc.relation.ispartof | Science Advances | es_ES |
dc.rights | Reconocimiento (by) | es_ES |
dc.subject | Tortuosity | es_ES |
dc.title | Mechanics-driven mechanobiological mechanisms of arterial tortuosity | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1126/sciadv.abd3574 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/NIH//R01 HL105297//Mechanisms Underlying the Progression of Arterial Stiffness in Hypertension/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/NIH//P01 HL134605 //Endothelial Mechanotransduction in Thoracic Aneurysm Formation and Progression/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/NIH//U01 HL142518//Multimodality imaging-driven multifidelity modeling of aortic dissection/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.description.bibliographicCitation | Weiss, D.; Cavinato, C.; Gray, A.; Ramachandra, AB.; Avril, S.; Humphrey, JD.; Latorre, M. (2020). Mechanics-driven mechanobiological mechanisms of arterial tortuosity. Science Advances. 6(49):1-26. https://doi.org/10.1126/sciadv.abd3574 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1126/sciadv.abd3574 | es_ES |
dc.description.upvformatpinicio | 1 | es_ES |
dc.description.upvformatpfin | 26 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 6 | es_ES |
dc.description.issue | 49 | es_ES |
dc.identifier.eissn | 2375-2548 | es_ES |
dc.identifier.pmid | 33277255 | es_ES |
dc.identifier.pmcid | PMC7821897 | es_ES |
dc.relation.pasarela | S\472453 | es_ES |
dc.contributor.funder | National Institutes of Health, EEUU | es_ES |
dc.subject.ods | 03.- Garantizar una vida saludable y promover el bienestar para todos y todas en todas las edades | es_ES |