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Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy

BACKGROUND: Peripartum cardiomyopathy (PPCM) is idiopathic pregnancy‐associated heart failure (HF) with reduced left ventricular ejection fraction (LVEF). We aimed to assess arterial stiffness and left ventricular (LV) function in women recovered from PPCM compared with controls. METHODS: Twenty‐two...

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Autores principales: Johansson, Magnus C., Barasa, Anders, Basic, Carmen, Nyberg, Gunnar, Schaufelberger, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756804/
https://www.ncbi.nlm.nih.gov/pubmed/33068494
http://dx.doi.org/10.1111/cpf.12671
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author Johansson, Magnus C.
Barasa, Anders
Basic, Carmen
Nyberg, Gunnar
Schaufelberger, Maria
author_facet Johansson, Magnus C.
Barasa, Anders
Basic, Carmen
Nyberg, Gunnar
Schaufelberger, Maria
author_sort Johansson, Magnus C.
collection PubMed
description BACKGROUND: Peripartum cardiomyopathy (PPCM) is idiopathic pregnancy‐associated heart failure (HF) with reduced left ventricular ejection fraction (LVEF). We aimed to assess arterial stiffness and left ventricular (LV) function in women recovered from PPCM compared with controls. METHODS: Twenty‐two PPCM patients were compared with 15 age‐matched controls with previous uncomplicated pregnancies. Eleven of the patients were at inclusion in the study recovered and off medication since at least 6 months and still free from cardiovascular symptoms with normal LVEF and normal NT‐proBNP. All underwent echocardiography, including LV strain, left atrial (LA) reservoir strain and tissue Doppler early diastolic velocity (e´) and non‐invasive assessment for arterial stiffness and central aortic systolic blood pressure (AoBP) at rest and immediately postexercise. RESULTS: The patients off medication showed alterations compared with controls. AoBP was higher (120 ± 9 mm Hg vs. 104 ± 13 mm Hg; p = .001), a difference which persisted postexercise. The arterial elastance was higher (1.9 ± 0.4 mm Hg/ml vs. 1.3 ± 0.2 mm Hg/ml; p < .001), while there were lower e´ septal (8.9 ± 1.7 cm/s vs. 11.0 ± 1.1 cm/s; p = 0. 002), LV global strain (18.7 ± 3.9% vs. 23.1 ± 1.6%; p = .004) and LA reservoir strain (24.8 ± 9.1% vs. 37.7 ± 6.3%; p = .002). CONCLUSIONS: Compared with healthy controls, PPCM patients considered recovered and off medication had increased arterial stiffness, decreased LV longitudinal function and reduced LA function.
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spelling pubmed-77568042020-12-28 Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy Johansson, Magnus C. Barasa, Anders Basic, Carmen Nyberg, Gunnar Schaufelberger, Maria Clin Physiol Funct Imaging Original Articles BACKGROUND: Peripartum cardiomyopathy (PPCM) is idiopathic pregnancy‐associated heart failure (HF) with reduced left ventricular ejection fraction (LVEF). We aimed to assess arterial stiffness and left ventricular (LV) function in women recovered from PPCM compared with controls. METHODS: Twenty‐two PPCM patients were compared with 15 age‐matched controls with previous uncomplicated pregnancies. Eleven of the patients were at inclusion in the study recovered and off medication since at least 6 months and still free from cardiovascular symptoms with normal LVEF and normal NT‐proBNP. All underwent echocardiography, including LV strain, left atrial (LA) reservoir strain and tissue Doppler early diastolic velocity (e´) and non‐invasive assessment for arterial stiffness and central aortic systolic blood pressure (AoBP) at rest and immediately postexercise. RESULTS: The patients off medication showed alterations compared with controls. AoBP was higher (120 ± 9 mm Hg vs. 104 ± 13 mm Hg; p = .001), a difference which persisted postexercise. The arterial elastance was higher (1.9 ± 0.4 mm Hg/ml vs. 1.3 ± 0.2 mm Hg/ml; p < .001), while there were lower e´ septal (8.9 ± 1.7 cm/s vs. 11.0 ± 1.1 cm/s; p = 0. 002), LV global strain (18.7 ± 3.9% vs. 23.1 ± 1.6%; p = .004) and LA reservoir strain (24.8 ± 9.1% vs. 37.7 ± 6.3%; p = .002). CONCLUSIONS: Compared with healthy controls, PPCM patients considered recovered and off medication had increased arterial stiffness, decreased LV longitudinal function and reduced LA function. John Wiley and Sons Inc. 2020-11-06 2021-01 /pmc/articles/PMC7756804/ /pubmed/33068494 http://dx.doi.org/10.1111/cpf.12671 Text en © 2020 The Authors. Clinical Physiology and Functional Imaging published by John Wiley & Sons Ltd on behalf of Scandinavian Society of Clinical Physiology and Nuclear Medicine This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Johansson, Magnus C.
Barasa, Anders
Basic, Carmen
Nyberg, Gunnar
Schaufelberger, Maria
Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
title Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
title_full Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
title_fullStr Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
title_full_unstemmed Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
title_short Increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
title_sort increased arterial stiffness and reduced left ventricular long‐axis function in patients recovered from peripartum cardiomyopathy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756804/
https://www.ncbi.nlm.nih.gov/pubmed/33068494
http://dx.doi.org/10.1111/cpf.12671
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