Bicuspid Aortic Valve in 2 Model Species and Review of the Literature

dc.centroFacultad de Cienciases_ES
dc.contributor.authorFernández-Corujo, Borja
dc.contributor.authorSoto-Navarrete, María Teresa
dc.contributor.authorLópez-García, Alejandro
dc.contributor.authorLópez-Unzu, Miguel A.
dc.contributor.authorDurán-Boyero, Ana Carmen
dc.contributor.authorFernández-Domínguez, María Carmen
dc.date.accessioned2024-02-07T13:09:08Z
dc.date.available2024-02-07T13:09:08Z
dc.date.created2024
dc.date.issued2020-02-21
dc.departamentoBiología Animal
dc.description.abstractBicuspid aortic valve (BAV) is the most common human congenital cardiac malformation. Although the etiology is unknown for most patients, formation of the 2 main BAV anatomic types (A and B) has been shown to rely on distinct morphogenetic mechanisms. Animal models of BAV include 2 spontaneous hamster strains and 27 genetically modified mouse strains. To assess the value of these models for extrapolation to humans, we examined the aortic valve anatomy of 4340 hamsters and 1823 mice from 8 and 7 unmodified strains, respectively. In addition, we reviewed the literature describing BAV in nonhuman mammals. The incidences of BAV types A and B were 2.3% and 0.03% in control hamsters and 0% and 0.3% in control mice, respectively. Hamsters from the spontaneous model had BAV type A only, whereas mice from 2 of 27 genetically modified strains had BAV type A, 23 of 27 had BAV type B, and 2 of 27 had both BAV types. In both species, BAV incidence was dependent on genetic background. Unlike mice, hamsters had a wide spectrum of aortic valve morphologies. We showed interspecific differences in the occurrence of BAV between humans, hamsters, and mice that should be considered when studying aortic valve disease using animal models. Our results suggest that genetic modifiers play a significant role in both the morphology and incidence of BAV. We propose that mutations causing anomalies in specific cardiac morphogenetic processes or cell lineages may lead to BAV types A, B, or both, depending on additional genetic, environmental, and epigenetic factorses_ES
dc.description.sponsorshipJunta de Andalucía (grant P10-CTS-6068). Ministerio de Ciencia, Innovación y Universidades (grant CGL2017-85090-P and fellowships FPU15/03209 to M.A.L.-U. and PRE2018-083176 to M.T.S.-N.). Sistema Nacional de Garantía Juvenil (contract UMAJI75 to M.T.S.-N.). FEDER funds.es_ES
dc.identifier.citationFernández B, Soto-Navarrete MT, López-García A, López-Unzu MÁ, Durán AC, Fernández MC. Bicuspid Aortic Valve in 2 Model Species and Review of the Literature. Veterinary Pathology. 2020;57(2):321-331.es_ES
dc.identifier.doi10.1177/0300985819900018
dc.identifier.urihttps://hdl.handle.net/10630/30007
dc.language.isospaes_ES
dc.publisherSage Publications INCes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectVálvula aórticaes_ES
dc.subjectCardiopatía congénitaes_ES
dc.subjectEnfermedades - Etiologíaes_ES
dc.subjectRatoneses_ES
dc.subjectHámstereses_ES
dc.subject.otherAnatomyes_ES
dc.subject.otherBicuspid aortic valvees_ES
dc.subject.otherCongenital heart defectses_ES
dc.subject.otherEtiologyes_ES
dc.subject.otherHamsterses_ES
dc.subject.otherMousees_ES
dc.subject.otherQuadricuspid aortic valvees_ES
dc.subject.otherReviewes_ES
dc.titleBicuspid Aortic Valve in 2 Model Species and Review of the Literaturees_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication025b48ac-64ac-4520-9fff-78c59c8bb114
relation.isAuthorOfPublication3ca36874-bacf-43c1-8c7f-09280cfc9cc7
relation.isAuthorOfPublication.latestForDiscoveryd7f1c2c4-9c7f-44b8-83a3-6aa3ebf45c1e

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