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Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression

BACKGROUND: ACC/AHA guidelines recognize the progressive nature of heart failure (HF). Patients with risk factors (Stage A) are at risk for developing asymptomatic cardiac dysfunction (Stage B), which may then lead to symptomatic HF (Stage C). As such, therapies targeting abnormalities in stages A a...

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Autores principales: Taher, Riad, Sara, Jaskanwal D., Toya, Takumi, Borlaug, Barry A., Lerman, Lilach O., Lerman, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385446/
https://www.ncbi.nlm.nih.gov/pubmed/32743042
http://dx.doi.org/10.1016/j.ijcha.2020.100584
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author Taher, Riad
Sara, Jaskanwal D.
Toya, Takumi
Borlaug, Barry A.
Lerman, Lilach O.
Lerman, Amir
author_facet Taher, Riad
Sara, Jaskanwal D.
Toya, Takumi
Borlaug, Barry A.
Lerman, Lilach O.
Lerman, Amir
author_sort Taher, Riad
collection PubMed
description BACKGROUND: ACC/AHA guidelines recognize the progressive nature of heart failure (HF). Patients with risk factors (Stage A) are at risk for developing asymptomatic cardiac dysfunction (Stage B), which may then lead to symptomatic HF (Stage C). As such, therapies targeting abnormalities in stages A and B may protect against development of symptomatic HF. peripheral endothelial dysfunction (PED) is an independent predictor of adverse outcomes in patients with stage C HF. The aim of the current study was to evaluate whether PED might be associated with Stage B HF, where therapeutic interventions to prevent progression might be more efficacious. METHODS: We performed a retrospective cross-sectional analysis of patients who were referred for routine cardiovascular evaluation that included an assessment of peripheral endothelial function with reactive hyperemia-peripheral arterial tonometry. Individuals in this study underwent routine clinically indicated echocardiography within 2 months of testing for PED. Patients with clinical HF were excluded. RESULTS: The study included 355 patients (mean age 51.5 ± 14.6 years, 231 (65.1%) female). There was a significant association between PED and Stage B HF (Odds Ratio (OR) 6.38; P < 0.0001) that persisted after stratifying by sex. In multivariate analyses PED was significantly associated with Stage B HF (OR 5.33; P = 0.0038), and was also associated with progression to overt stage C HF (OR 4.63; P = 0.033). CONCLUSION: Peripheral endothelial dysfunction is risk factor for Stage B HF, even in low risk individuals. Further study is warranted to better understand the mechanistic basis of PED in HF to reduce the risk of symptomatic progression.
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spelling pubmed-73854462020-07-30 Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression Taher, Riad Sara, Jaskanwal D. Toya, Takumi Borlaug, Barry A. Lerman, Lilach O. Lerman, Amir Int J Cardiol Heart Vasc Original Paper BACKGROUND: ACC/AHA guidelines recognize the progressive nature of heart failure (HF). Patients with risk factors (Stage A) are at risk for developing asymptomatic cardiac dysfunction (Stage B), which may then lead to symptomatic HF (Stage C). As such, therapies targeting abnormalities in stages A and B may protect against development of symptomatic HF. peripheral endothelial dysfunction (PED) is an independent predictor of adverse outcomes in patients with stage C HF. The aim of the current study was to evaluate whether PED might be associated with Stage B HF, where therapeutic interventions to prevent progression might be more efficacious. METHODS: We performed a retrospective cross-sectional analysis of patients who were referred for routine cardiovascular evaluation that included an assessment of peripheral endothelial function with reactive hyperemia-peripheral arterial tonometry. Individuals in this study underwent routine clinically indicated echocardiography within 2 months of testing for PED. Patients with clinical HF were excluded. RESULTS: The study included 355 patients (mean age 51.5 ± 14.6 years, 231 (65.1%) female). There was a significant association between PED and Stage B HF (Odds Ratio (OR) 6.38; P < 0.0001) that persisted after stratifying by sex. In multivariate analyses PED was significantly associated with Stage B HF (OR 5.33; P = 0.0038), and was also associated with progression to overt stage C HF (OR 4.63; P = 0.033). CONCLUSION: Peripheral endothelial dysfunction is risk factor for Stage B HF, even in low risk individuals. Further study is warranted to better understand the mechanistic basis of PED in HF to reduce the risk of symptomatic progression. Elsevier 2020-07-23 /pmc/articles/PMC7385446/ /pubmed/32743042 http://dx.doi.org/10.1016/j.ijcha.2020.100584 Text en © 2020 The Authors http://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
Taher, Riad
Sara, Jaskanwal D.
Toya, Takumi
Borlaug, Barry A.
Lerman, Lilach O.
Lerman, Amir
Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
title Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
title_full Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
title_fullStr Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
title_full_unstemmed Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
title_short Peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
title_sort peripheral endothelial dysfunction is a novel risk factor for systolic dysfunction and heart failure progression
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7385446/
https://www.ncbi.nlm.nih.gov/pubmed/32743042
http://dx.doi.org/10.1016/j.ijcha.2020.100584
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