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Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project

BACKGROUND: While autoimmune rheumatic diseases (ARDs) have been linked with coronary microvascular dysfunction (CMD), the relationship between ARD and CMD in women with signs and symptoms of ischemia and no obstructive arteries (INOCA) are not well described. We hypothesized that among women with C...

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Autores principales: Chen, Melanie T., Chang, Joseph, Manchanda, Ashley S., Cook-Wiens, Galen, Shufelt, Chrisandra L., Anderson, R. David, Petersen, John W., Naik, Dhaval R., Thomson, Louise E. J., Berman, Daniel S., Handberg, Eileen M., Pepine, Carl J., Bairey Merz, C. Noel, Wei, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266277/
https://www.ncbi.nlm.nih.gov/pubmed/37324629
http://dx.doi.org/10.3389/fcvm.2023.1155914
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author Chen, Melanie T.
Chang, Joseph
Manchanda, Ashley S.
Cook-Wiens, Galen
Shufelt, Chrisandra L.
Anderson, R. David
Petersen, John W.
Naik, Dhaval R.
Thomson, Louise E. J.
Berman, Daniel S.
Handberg, Eileen M.
Pepine, Carl J.
Bairey Merz, C. Noel
Wei, Janet
author_facet Chen, Melanie T.
Chang, Joseph
Manchanda, Ashley S.
Cook-Wiens, Galen
Shufelt, Chrisandra L.
Anderson, R. David
Petersen, John W.
Naik, Dhaval R.
Thomson, Louise E. J.
Berman, Daniel S.
Handberg, Eileen M.
Pepine, Carl J.
Bairey Merz, C. Noel
Wei, Janet
author_sort Chen, Melanie T.
collection PubMed
description BACKGROUND: While autoimmune rheumatic diseases (ARDs) have been linked with coronary microvascular dysfunction (CMD), the relationship between ARD and CMD in women with signs and symptoms of ischemia and no obstructive arteries (INOCA) are not well described. We hypothesized that among women with CMD, those with ARD history have greater angina, functional limitations, and myocardial perfusion compromise compared to those without ARD history. METHODS: Women with INOCA and confirmed CMD by invasive coronary function testing were included from the Women's Ischemia Syndrome Evaluation-Coronary Vascular Dysfunction (WISE-CVD) project (NCT00832702). Seattle Angina Questionnaire (SAQ), Duke Activity Status Index (DASI), and cardiac magnetic resonance myocardial perfusion reserve index (MPRI) were collected at baseline. Chart review was performed to confirm self-reported ARD diagnosis. RESULTS: Of the 207 women with CMD, 19 (9%) had a confirmed history of ARD. Compared to those without ARD, women with ARD were younger (p = 0.04). In addition, they had lower DASI-estimated metabolic equivalents (p = 0.03) and lower MPRI (p = 0.008) but similar SAQ scores. There was a trend towards increased nocturnal angina and stress-induced angina in those with ARD (p = 0.05 for both). Invasive coronary function variables were not significantly different between groups. CONCLUSIONS: Among women with CMD, women with a history of ARD had lower functional status and worse myocardial perfusion reserve compared to women without ARD. Angina-related health status and invasive coronary function were not significantly different between groups. Further studies are warranted to understand mechanisms contributing to CMD among women with ARDs with INOCA.
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spelling pubmed-102662772023-06-15 Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project Chen, Melanie T. Chang, Joseph Manchanda, Ashley S. Cook-Wiens, Galen Shufelt, Chrisandra L. Anderson, R. David Petersen, John W. Naik, Dhaval R. Thomson, Louise E. J. Berman, Daniel S. Handberg, Eileen M. Pepine, Carl J. Bairey Merz, C. Noel Wei, Janet Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: While autoimmune rheumatic diseases (ARDs) have been linked with coronary microvascular dysfunction (CMD), the relationship between ARD and CMD in women with signs and symptoms of ischemia and no obstructive arteries (INOCA) are not well described. We hypothesized that among women with CMD, those with ARD history have greater angina, functional limitations, and myocardial perfusion compromise compared to those without ARD history. METHODS: Women with INOCA and confirmed CMD by invasive coronary function testing were included from the Women's Ischemia Syndrome Evaluation-Coronary Vascular Dysfunction (WISE-CVD) project (NCT00832702). Seattle Angina Questionnaire (SAQ), Duke Activity Status Index (DASI), and cardiac magnetic resonance myocardial perfusion reserve index (MPRI) were collected at baseline. Chart review was performed to confirm self-reported ARD diagnosis. RESULTS: Of the 207 women with CMD, 19 (9%) had a confirmed history of ARD. Compared to those without ARD, women with ARD were younger (p = 0.04). In addition, they had lower DASI-estimated metabolic equivalents (p = 0.03) and lower MPRI (p = 0.008) but similar SAQ scores. There was a trend towards increased nocturnal angina and stress-induced angina in those with ARD (p = 0.05 for both). Invasive coronary function variables were not significantly different between groups. CONCLUSIONS: Among women with CMD, women with a history of ARD had lower functional status and worse myocardial perfusion reserve compared to women without ARD. Angina-related health status and invasive coronary function were not significantly different between groups. Further studies are warranted to understand mechanisms contributing to CMD among women with ARDs with INOCA. Frontiers Media S.A. 2023-05-30 /pmc/articles/PMC10266277/ /pubmed/37324629 http://dx.doi.org/10.3389/fcvm.2023.1155914 Text en © 2023 Chen, Chang, Manchanda, Cook-Wiens, Shufelt, Anderson, Petersen, Naik, Thomson, Berman, Handberg, Pepine, Bairey Merz and Wei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Chen, Melanie T.
Chang, Joseph
Manchanda, Ashley S.
Cook-Wiens, Galen
Shufelt, Chrisandra L.
Anderson, R. David
Petersen, John W.
Naik, Dhaval R.
Thomson, Louise E. J.
Berman, Daniel S.
Handberg, Eileen M.
Pepine, Carl J.
Bairey Merz, C. Noel
Wei, Janet
Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project
title Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project
title_full Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project
title_fullStr Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project
title_full_unstemmed Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project
title_short Autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the Women's Ischemia Syndrome Evaluation—Coronary Vascular Dysfunction (WISE-CVD) project
title_sort autoimmune rheumatic diseases in women with coronary microvascular dysfunction: a report from the women's ischemia syndrome evaluation—coronary vascular dysfunction (wise-cvd) project
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266277/
https://www.ncbi.nlm.nih.gov/pubmed/37324629
http://dx.doi.org/10.3389/fcvm.2023.1155914
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