Cardiometabolic Risk in Acromegaly: A Review With a Focus on Pasireotide

Acromegaly is a disease due to chronic GH excess and a consequent rise in IGF-1 levels. This rare endocrine condition is associated with metabolic alterations such as hyperglycaemia, dyslipidaemia, and systemic arterial hypertension, which, in addition to GH excess-related cardiovascular changes, pl...

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Published inFrontiers in endocrinology (Lausanne) Vol. 11; p. 28
Main Authors Puglisi, Soraya, Ferraù, Francesco, Ragonese, Marta, Spagnolo, Federica, Cannavò, Salvatore
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 06.02.2020
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Summary:Acromegaly is a disease due to chronic GH excess and a consequent rise in IGF-1 levels. This rare endocrine condition is associated with metabolic alterations such as hyperglycaemia, dyslipidaemia, and systemic arterial hypertension, which, in addition to GH excess-related cardiovascular changes, play critical roles in increasing cardiovascular risk and mortality rates. Biochemical control of acromegaly, achieved by means of surgical, and/or medical treatment, positively impacts on cardiovascular risk factors and metabolic alterations, reducing overall patient mortality. However, treatment modalities of acromegaly and disease control differently impact on glucose homeostasis and lipid changes, and consequently on cardiometabolic risk. In this regard, pasireotide was shown to significantly influence glucose metabolism. This review summarizes the cardiometabolic consequences of acromegaly and its treatment, focusing on available data around the effects of medical therapy with pasireotide on factors that influence cardiometabolic risk.
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Edited by: Marek Bolanowski, Wroclaw Medical University, Poland
This article was submitted to Pituitary Endocrinology, a section of the journal Frontiers in Endocrinology
Reviewed by: Roberto Salvatori, Johns Hopkins University, United States; Luiz Eduardo Armondi Wildemberg, Instituto Estadual do Cérebro Paulo Niemeyer, Brazil
ISSN:1664-2392
1664-2392
DOI:10.3389/fendo.2020.00028