Please use this identifier to cite or link to this item: https://doi.org/10.3390/ani10101906
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dc.titleLarge animal models of heart failure: Reduced vs. preserved ejection fraction
dc.contributor.authorCharles, C.J.
dc.contributor.authorRademaker, M.T.
dc.contributor.authorScott, N.J.A.
dc.contributor.authorRichards, A.M.
dc.date.accessioned2021-08-27T02:35:47Z
dc.date.available2021-08-27T02:35:47Z
dc.date.issued2020
dc.identifier.citationCharles, C.J., Rademaker, M.T., Scott, N.J.A., Richards, A.M. (2020). Large animal models of heart failure: Reduced vs. preserved ejection fraction. Animals 10 (10) : 1-12. ScholarBank@NUS Repository. https://doi.org/10.3390/ani10101906
dc.identifier.issn2076-2615
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/199696
dc.description.abstractHeart failure (HF) is the final common end point of multiple metabolic and cardiovascular diseases and imposes a significant health care burden worldwide. Despite significant improvements in clinical management and outcomes, morbidity and mortality remain high and there remains an indisputable need for improved treatment options. The pathophysiology of HF is complex and covers a spectrum of clinical presentations from HF with reduced ejection fraction (HFrEF) (?40% EF) through to HF with preserved EF (HFpEF), with HFpEF patients demonstrating a reduced ability of the heart to relax despite an EF maintained above 50%. Prior to the last decade, the majority of clinical trials and animal models addressed HFrEF. Despite growing efforts recently to understand underlying mechanisms of HFpEF and find effective therapies for its treatment, clinical trials in patients with HFpEF have failed to demonstrate improvements in mortality. A significant obstacle to therapeutic innovation in HFpEF is the absence of preclinical models including large animal models which, unlike rodents, permit detailed instrumentation and extensive imaging and sampling protocols. Although several large animal models of HFpEF have been reported, none fulfil all the features present in human disease and few demonstrate progression to frank decompensated HF. This review summarizes well-established models of HFrEF in pigs, dogs and sheep and discusses attempts to date to model HFpEF in these species. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
dc.publisherMDPI AG
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2020
dc.subjectAnimal model
dc.subjectEjection fraction
dc.subjectHeart failure
dc.subjectHFpEF
dc.subjectHFrEF
dc.subjectOvine
dc.subjectPorcine
dc.typeReview
dc.contributor.departmentSURGERY
dc.description.doi10.3390/ani10101906
dc.description.sourcetitleAnimals
dc.description.volume10
dc.description.issue10
dc.description.page1-12
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