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

dc.contributor.authorFernández, Borja
dc.contributor.authorSoto-Navarrete, María Teresa
dc.contributor.authorLópez-García, Alejandro
dc.contributor.authorLópez-Unzu, Miguel Ángel
dc.contributor.authorDurán, Ana Carmen
dc.contributor.authorFernández, M Carmen
dc.date.accessioned2023-02-08T14:41:45Z
dc.date.available2023-02-08T14:41:45Z
dc.date.issued2020-02-21
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 factors.
dc.identifier.doi10.1177/0300985819900018
dc.identifier.essn1544-2217
dc.identifier.pmid32079504
dc.identifier.unpaywallURLhttps://journals.sagepub.com/doi/pdf/10.1177/0300985819900018
dc.identifier.urihttp://hdl.handle.net/10668/15138
dc.issue.number2
dc.journal.titleVeterinary pathology
dc.journal.titleabbreviationVet Pathol
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.page.number321-331
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.pubmedtypeReview
dc.rights.accessRightsopen access
dc.subjectanatomy
dc.subjectbicuspid aortic valve
dc.subjectcongenital heart defects
dc.subjectetiology
dc.subjecthamsters
dc.subjectmouse
dc.subjectquadricuspid aortic valve
dc.subjectreview
dc.subject.meshAnimals
dc.subject.meshAortic Valve
dc.subject.meshBicuspid Aortic Valve Disease
dc.subject.meshCricetinae
dc.subject.meshDisease Models, Animal
dc.subject.meshHumans
dc.subject.meshIncidence
dc.subject.meshMice
dc.subject.meshMutation
dc.subject.meshRetrospective Studies
dc.titleBicuspid Aortic Valve in 2 Model Species and Review of the Literature.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number57
dspace.entity.typePublication

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