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Phenotype-based management of coronary microvascular dysfunction

40-70% of patients undergoing invasive coronary angiography with signs and symptoms of ischemia are found to have no obstructive coronary artery disease (INOCA). When this heterogeneous group undergo coronary function testing, approximately two-thirds have demonstrable coronary microvascular dysfunc...

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Autores principales: Ang, Daniel Tze Yee, Berry, Colin, Kaski, Juan-Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834338/
https://www.ncbi.nlm.nih.gov/pubmed/35672569
http://dx.doi.org/10.1007/s12350-022-03000-w
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author Ang, Daniel Tze Yee
Berry, Colin
Kaski, Juan-Carlos
author_facet Ang, Daniel Tze Yee
Berry, Colin
Kaski, Juan-Carlos
author_sort Ang, Daniel Tze Yee
collection PubMed
description 40-70% of patients undergoing invasive coronary angiography with signs and symptoms of ischemia are found to have no obstructive coronary artery disease (INOCA). When this heterogeneous group undergo coronary function testing, approximately two-thirds have demonstrable coronary microvascular dysfunction (CMD), which is independently associated with adverse prognosis. There are four distinct phenotypes, or subgroups, each with unique pathophysiological mechanisms and responses to therapies. The clinical phenotypes are microvascular angina, vasospastic angina, mixed (microvascular and vasospastic), and non-cardiac symptoms (reclassification as non-INOCA). The Coronary Vasomotor Disorders International Study Group (COVADIS) have proposed standardized criteria for diagnosis. There is growing awareness of these conditions among clinicians and within guidelines. Testing for CMD can be done using invasive or non-invasive modalities. The CorMicA study advocates the concept of ‘functional angiography’ to guide stratified medical therapy. Therapies broadly fall into two categories: those that modulate cardiovascular risk and those to alleviate angina. Management should be tailored to the individual, with periodic reassessment for efficacy. Phenotype-based management is a worthy endeavor for both patients and clinicians, aligning with the concept of ‘precision medicine’ to improve prognosis, symptom burden, and quality of life. Here, we present a contemporary approach to the phenotype-based management of patients with INOCA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12350-022-03000-w.
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spelling pubmed-98343382023-01-13 Phenotype-based management of coronary microvascular dysfunction Ang, Daniel Tze Yee Berry, Colin Kaski, Juan-Carlos J Nucl Cardiol Theme Articles 40-70% of patients undergoing invasive coronary angiography with signs and symptoms of ischemia are found to have no obstructive coronary artery disease (INOCA). When this heterogeneous group undergo coronary function testing, approximately two-thirds have demonstrable coronary microvascular dysfunction (CMD), which is independently associated with adverse prognosis. There are four distinct phenotypes, or subgroups, each with unique pathophysiological mechanisms and responses to therapies. The clinical phenotypes are microvascular angina, vasospastic angina, mixed (microvascular and vasospastic), and non-cardiac symptoms (reclassification as non-INOCA). The Coronary Vasomotor Disorders International Study Group (COVADIS) have proposed standardized criteria for diagnosis. There is growing awareness of these conditions among clinicians and within guidelines. Testing for CMD can be done using invasive or non-invasive modalities. The CorMicA study advocates the concept of ‘functional angiography’ to guide stratified medical therapy. Therapies broadly fall into two categories: those that modulate cardiovascular risk and those to alleviate angina. Management should be tailored to the individual, with periodic reassessment for efficacy. Phenotype-based management is a worthy endeavor for both patients and clinicians, aligning with the concept of ‘precision medicine’ to improve prognosis, symptom burden, and quality of life. Here, we present a contemporary approach to the phenotype-based management of patients with INOCA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12350-022-03000-w. Springer International Publishing 2022-06-07 2022 /pmc/articles/PMC9834338/ /pubmed/35672569 http://dx.doi.org/10.1007/s12350-022-03000-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Theme Articles
Ang, Daniel Tze Yee
Berry, Colin
Kaski, Juan-Carlos
Phenotype-based management of coronary microvascular dysfunction
title Phenotype-based management of coronary microvascular dysfunction
title_full Phenotype-based management of coronary microvascular dysfunction
title_fullStr Phenotype-based management of coronary microvascular dysfunction
title_full_unstemmed Phenotype-based management of coronary microvascular dysfunction
title_short Phenotype-based management of coronary microvascular dysfunction
title_sort phenotype-based management of coronary microvascular dysfunction
topic Theme Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834338/
https://www.ncbi.nlm.nih.gov/pubmed/35672569
http://dx.doi.org/10.1007/s12350-022-03000-w
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