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Complicaciones cardiovasculares asociadas a la acromegalia. Estado del arte.

Authors :
Concepción-Zavaleta, Marcio
Muñoz-Moreno, Juan
Quispe-Flores, María
Rafael-Robles, Luciana
Lobato-Jeri, Carlos
Ramos-Yataco, Anthony
Concepción-Urteaga, Luis
Paz-Ibarra, José
Source :
Archivos de Cardiología de México. oct-dic2022, Vol. 92 Issue 4, p495-503. 9p.
Publication Year :
2022

Abstract

Acromegaly is a rare disease, mainly caused by a pituitary tumor secreting growth hormone. It is characterized by slow progression and is associated with a multisystemic involvement, being the cardiovascular system, one of the most involved, even reaching, more than 10 years ago, to represent the main cause of death. Cardiovascular complications develop as a result of elevated blood concentrations of growth hormone and insulin-like growth factor 1, which exert direct and indirect effects on the endothelium, large vessels, kidney and cardiomyocytes; causing arterial hypertension, valve disease, cardiac arrhythmia and a specific heart disease called acromegalic cardiomyopathy. After the literature overview related to the pathophysiology, clinical manifestations, diagnosis and treatment of cardiovascular involvement, we found that from a cardiovascular point of view, patients with acromegaly can range from an asymptomatic state to severe cardiac dysfunction, being the biochemical markers and imaging studies diagnostic tools that allow assessment the degree of cardiovascular disease in order to provide individualized treatment. The normalization of growth hormone and insulin-like growth factor 1 levels improves cardiovascular parameters, and therefore its prognosis. [ABSTRACT FROM AUTHOR]

Details

Language :
Spanish
ISSN :
14059940
Volume :
92
Issue :
4
Database :
Academic Search Index
Journal :
Archivos de Cardiología de México
Publication Type :
Academic Journal
Accession number :
160320517
Full Text :
https://doi.org/10.24875/ACM.21000339