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Published on: August 30, 2022
Acromegaly and the cardiovascular system
Gaetano Lombardi1, Mariano Galdiero, Renata S Auriemma
1Department of Molecular and Clinical Endocrinology and Oncology, Federico II University of Naples, Naples, Italy. gaelomba@unina.it
Insights
Acromegaly causes heart problems like cardiomyopathy due to excess growth hormone. Early diagnosis and treatment can improve heart function and reduce risks.
Area of Science:
- Endocrinology
- Cardiology
Background:
- Acromegaly, caused by excess growth hormone (GH) and insulin-like growth factor-I (IGF-I), leads to significant cardiovascular risks.
- The condition involves a specific cardiomyopathy, impacting heart function from early stages.
Purpose of the Study:
- To summarize the cardiovascular manifestations of acromegaly.
- To highlight the impact of GH/IGF-I excess on cardiac structure and function.
- To emphasize the importance of early diagnosis and cardiac evaluation in acromegaly management.
Main Methods:
- Review of existing literature on acromegaly and its cardiovascular complications.
- Analysis of the pathophysiological mechanisms linking GH/IGF-I excess to cardiac changes.
- Discussion of diagnostic and therapeutic implications.
Main Results:
- Acromegaly presents with a hyperkinetic syndrome (high heart rate, increased cardiac output) early on.
- Untreated or poorly treated acromegaly can lead to concentric biventricular hypertrophy, diastolic dysfunction, and heart failure.
- Rhythm disturbances, valve dysfunction, and worsening cardiomyopathy are common, especially with comorbidities like diabetes and hypertension.
Conclusions:
- Cardiovascular disease is a major cause of morbidity and mortality in acromegaly.
- Controlling GH/IGF-I levels through surgery or pharmacotherapy can improve cardiac mass and function.
- Early diagnosis and comprehensive cardiac assessment are crucial for managing acromegaly patients.
Abstract:
Acromegaly is characterized by an increased cardiovascular morbidity and mortality. In fact, growth hormone and insulin-like growth factor-I excess induces a specific cardiomyopathy. The heart is involved from the very early stages of the disease in which the hyperkinetic syndrome (high heart rate and increased systolic output) takes place. Frequently, if the disease is untreated for many years or unsuccessfully treated, concentric biventricular hypertrophy and diastolic dysfunction can develop and, at least, lead to diastolic congestive heart failure. Rhythm disturbances and valve dysfunction are also frequently described in acromegaly. The coexistence of other complications, such as diabetes and arterial hypertension, can induce the worsening of acromegalic cardiomyopathy. Control of acromegaly by surgery or pharmacotherapy could improve cardiovascular morbidity thanks to decreasing left ventricular mass and reducing cardiac dysfunction. In conclusion, an early diagnosis and a careful evaluation of cardiac function, morphology and activity seem to be mandatory in acromegaly.
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