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PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population

BACKGROUND: The aim was to investigate the prevalence of “classical” (predominantly related to alterations in hyperemic MBFs) and “endogen” (predominantly related to alterations in resting MBF) normal coronary microvascular function (nCMF) or coronary microvascular dysfunction (CMD) in a clinical po...

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Autores principales: Bhandiwad, Anita R., Valenta, Ines, Jain, Sudhir, Schindler, Thomas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127120/
https://www.ncbi.nlm.nih.gov/pubmed/37113650
http://dx.doi.org/10.1016/j.ijcha.2023.101206
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author Bhandiwad, Anita R.
Valenta, Ines
Jain, Sudhir
Schindler, Thomas H.
author_facet Bhandiwad, Anita R.
Valenta, Ines
Jain, Sudhir
Schindler, Thomas H.
author_sort Bhandiwad, Anita R.
collection PubMed
description BACKGROUND: The aim was to investigate the prevalence of “classical” (predominantly related to alterations in hyperemic MBFs) and “endogen” (predominantly related to alterations in resting MBF) normal coronary microvascular function (nCMF) or coronary microvascular dysfunction (CMD) in a clinical population without flow-limiting obstructive CAD. METHODS: We prospectively enrolled 239 symptomatic patients with normal pharmacologically-stress and rest myocardial perfusion on (13)N-ammonia PET/CT. (13)N-ammonia PET/CT concurrently assessed myocardial flow reserve (MFR = MBF stress/MBF rest). Normal nCMF was defined by a MFR of ≥ 2.0, while an abnormal MFR of < 2.0 signified CMD. In addition, patients were subgrouped into classical and endogen type of nCMF and CMD, respectively. RESULTS: In the whole study population, CMD was present in 54% (130/239). The classical type was more prevalent than the endogen type of CMD (65% vs 35%, p ≤ 0.008). The classical type of CMD was paralleled by a high prevalence of diabetes mellitus, metabolic syndrome, and obesity, while the endogen type of CMD was accompanied by a higher prevalence of arterial hypertension, obesity, and/or morbid obesity. Further, the classical type of nCMF was more frequently observed that the endogen type (74% vs. 26%, p ≤ 0.007). The endogen type of nCMF was related to lower heart rate and/or arterial blood pressures. CONCLUSIONS: In this contemporary clinical study population, slightly more than half of symptomatic patients had CMD with predominance of the classical type. These observations emphasize the need for standardized reporting of CMD to gear individualized and/or intensified medical treatment to improve symptoms and/or clinical outcome in these patients.
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spelling pubmed-101271202023-04-26 PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population Bhandiwad, Anita R. Valenta, Ines Jain, Sudhir Schindler, Thomas H. Int J Cardiol Heart Vasc Original Paper BACKGROUND: The aim was to investigate the prevalence of “classical” (predominantly related to alterations in hyperemic MBFs) and “endogen” (predominantly related to alterations in resting MBF) normal coronary microvascular function (nCMF) or coronary microvascular dysfunction (CMD) in a clinical population without flow-limiting obstructive CAD. METHODS: We prospectively enrolled 239 symptomatic patients with normal pharmacologically-stress and rest myocardial perfusion on (13)N-ammonia PET/CT. (13)N-ammonia PET/CT concurrently assessed myocardial flow reserve (MFR = MBF stress/MBF rest). Normal nCMF was defined by a MFR of ≥ 2.0, while an abnormal MFR of < 2.0 signified CMD. In addition, patients were subgrouped into classical and endogen type of nCMF and CMD, respectively. RESULTS: In the whole study population, CMD was present in 54% (130/239). The classical type was more prevalent than the endogen type of CMD (65% vs 35%, p ≤ 0.008). The classical type of CMD was paralleled by a high prevalence of diabetes mellitus, metabolic syndrome, and obesity, while the endogen type of CMD was accompanied by a higher prevalence of arterial hypertension, obesity, and/or morbid obesity. Further, the classical type of nCMF was more frequently observed that the endogen type (74% vs. 26%, p ≤ 0.007). The endogen type of nCMF was related to lower heart rate and/or arterial blood pressures. CONCLUSIONS: In this contemporary clinical study population, slightly more than half of symptomatic patients had CMD with predominance of the classical type. These observations emphasize the need for standardized reporting of CMD to gear individualized and/or intensified medical treatment to improve symptoms and/or clinical outcome in these patients. Elsevier 2023-04-18 /pmc/articles/PMC10127120/ /pubmed/37113650 http://dx.doi.org/10.1016/j.ijcha.2023.101206 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Paper
Bhandiwad, Anita R.
Valenta, Ines
Jain, Sudhir
Schindler, Thomas H.
PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
title PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
title_full PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
title_fullStr PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
title_full_unstemmed PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
title_short PET-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
title_sort pet-determined prevalence of coronary microvascular dysfunction and different types in a cardio-metabolic risk population
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10127120/
https://www.ncbi.nlm.nih.gov/pubmed/37113650
http://dx.doi.org/10.1016/j.ijcha.2023.101206
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