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Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly
Acromegaly is an uncommon systematic endocrine disease caused by the hypersecretion of human growth hormone and, consequently, of insulin-like growth factor-1 during adulthood. Acromegaly could cause a typical cardiomyopathy characterized by left ventricular hypertrophy associated with diastolic dys...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648583/ https://www.ncbi.nlm.nih.gov/pubmed/37959322 http://dx.doi.org/10.3390/jcm12216857 |
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author | Nemes, Attila Kormányos, Árpád Ambrus, Nóra Lengyel, Csaba Valkusz, Zsuzsanna |
author_facet | Nemes, Attila Kormányos, Árpád Ambrus, Nóra Lengyel, Csaba Valkusz, Zsuzsanna |
author_sort | Nemes, Attila |
collection | PubMed |
description | Acromegaly is an uncommon systematic endocrine disease caused by the hypersecretion of human growth hormone and, consequently, of insulin-like growth factor-1 during adulthood. Acromegaly could cause a typical cardiomyopathy characterized by left ventricular hypertrophy associated with diastolic dysfunction, which later could progress to systolic dysfunction. Moreover, some valvular and vascular abnormalities are also associated with acromegaly. This present review aims to summarize available information regarding acromegaly-associated abnormalities in myocardial, valvular, and vascular structural and functional properties and their relationship to disease activity and treatment options. |
format | Online Article Text |
id | pubmed-10648583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106485832023-10-30 Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly Nemes, Attila Kormányos, Árpád Ambrus, Nóra Lengyel, Csaba Valkusz, Zsuzsanna J Clin Med Review Acromegaly is an uncommon systematic endocrine disease caused by the hypersecretion of human growth hormone and, consequently, of insulin-like growth factor-1 during adulthood. Acromegaly could cause a typical cardiomyopathy characterized by left ventricular hypertrophy associated with diastolic dysfunction, which later could progress to systolic dysfunction. Moreover, some valvular and vascular abnormalities are also associated with acromegaly. This present review aims to summarize available information regarding acromegaly-associated abnormalities in myocardial, valvular, and vascular structural and functional properties and their relationship to disease activity and treatment options. MDPI 2023-10-30 /pmc/articles/PMC10648583/ /pubmed/37959322 http://dx.doi.org/10.3390/jcm12216857 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Nemes, Attila Kormányos, Árpád Ambrus, Nóra Lengyel, Csaba Valkusz, Zsuzsanna Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly |
title | Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly |
title_full | Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly |
title_fullStr | Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly |
title_full_unstemmed | Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly |
title_short | Myocardial, Valvular, and Vascular Structural and Functional Properties in Acromegaly |
title_sort | myocardial, valvular, and vascular structural and functional properties in acromegaly |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648583/ https://www.ncbi.nlm.nih.gov/pubmed/37959322 http://dx.doi.org/10.3390/jcm12216857 |
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