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Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report

BACKGROUND: In women with evidence of ischemia and no obstructive coronary artery disease the underlying mechanism is most often attributed to coronary microvascular dysfunction. Higher rates of adverse cardiovascular events, specifically heart failure with preserved ejection fraction, are present i...

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Autores principales: Joung, Sandy, Wei, Janet, Nelson, Michael D., Aldiwani, Haider, Shufelt, Chrisandra, Tamarappoo, Balaji, Berman, Daniel, Thomson, Louise E. J., Bairey Merz, C. Noel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501452/
https://www.ncbi.nlm.nih.gov/pubmed/31056078
http://dx.doi.org/10.1186/s13256-019-2074-z
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author Joung, Sandy
Wei, Janet
Nelson, Michael D.
Aldiwani, Haider
Shufelt, Chrisandra
Tamarappoo, Balaji
Berman, Daniel
Thomson, Louise E. J.
Bairey Merz, C. Noel
author_facet Joung, Sandy
Wei, Janet
Nelson, Michael D.
Aldiwani, Haider
Shufelt, Chrisandra
Tamarappoo, Balaji
Berman, Daniel
Thomson, Louise E. J.
Bairey Merz, C. Noel
author_sort Joung, Sandy
collection PubMed
description BACKGROUND: In women with evidence of ischemia and no obstructive coronary artery disease the underlying mechanism is most often attributed to coronary microvascular dysfunction. Higher rates of adverse cardiovascular events, specifically heart failure with preserved ejection fraction, are present in women with coronary microvascular dysfunction, leading to the hypothesis that coronary microvascular dysfunction may contribute to the progression of heart failure with preserved ejection fraction. CASE SUMMARY: A 55-year-old, Caucasian woman with a past medical history of chest pain and shortness of breath was referred to our tertiary care center and diagnosed as having coronary microvascular dysfunction by invasive coronary reactivity testing. After 10 years of follow-up care for coronary microvascular dysfunction, she presented to an emergency room in acute heart failure and was diagnosed as having heart failure with preserved ejection fraction. DISCUSSION: The current case report provides a specific example in support of existing studies that demonstrate that coronary microvascular dysfunction may be a precursor of heart failure with preserved ejection fraction. Further research is needed to establish causality and management. TRIAL REGISTRATION: Clinical Trial Registration: ClinicalTrials.gov Identifier: NCT02582021.
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spelling pubmed-65014522019-05-10 Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report Joung, Sandy Wei, Janet Nelson, Michael D. Aldiwani, Haider Shufelt, Chrisandra Tamarappoo, Balaji Berman, Daniel Thomson, Louise E. J. Bairey Merz, C. Noel J Med Case Rep Case Report BACKGROUND: In women with evidence of ischemia and no obstructive coronary artery disease the underlying mechanism is most often attributed to coronary microvascular dysfunction. Higher rates of adverse cardiovascular events, specifically heart failure with preserved ejection fraction, are present in women with coronary microvascular dysfunction, leading to the hypothesis that coronary microvascular dysfunction may contribute to the progression of heart failure with preserved ejection fraction. CASE SUMMARY: A 55-year-old, Caucasian woman with a past medical history of chest pain and shortness of breath was referred to our tertiary care center and diagnosed as having coronary microvascular dysfunction by invasive coronary reactivity testing. After 10 years of follow-up care for coronary microvascular dysfunction, she presented to an emergency room in acute heart failure and was diagnosed as having heart failure with preserved ejection fraction. DISCUSSION: The current case report provides a specific example in support of existing studies that demonstrate that coronary microvascular dysfunction may be a precursor of heart failure with preserved ejection fraction. Further research is needed to establish causality and management. TRIAL REGISTRATION: Clinical Trial Registration: ClinicalTrials.gov Identifier: NCT02582021. BioMed Central 2019-05-06 /pmc/articles/PMC6501452/ /pubmed/31056078 http://dx.doi.org/10.1186/s13256-019-2074-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Joung, Sandy
Wei, Janet
Nelson, Michael D.
Aldiwani, Haider
Shufelt, Chrisandra
Tamarappoo, Balaji
Berman, Daniel
Thomson, Louise E. J.
Bairey Merz, C. Noel
Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
title Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
title_full Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
title_fullStr Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
title_full_unstemmed Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
title_short Progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
title_sort progression of coronary microvascular dysfunction to heart failure with preserved ejection fraction: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501452/
https://www.ncbi.nlm.nih.gov/pubmed/31056078
http://dx.doi.org/10.1186/s13256-019-2074-z
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