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Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
Cardiovascular Disorders Associated With Acromegaly: an Update
Rinsha P V Sherin1, Nicole O Vietor1, Aqueel Usman1
1Division of Endocrinology, Department of Endocrinology, Diabetes and Metabolism, Walter Reed National Military Medical Center, Bethesda, Maryland.
Insights
Acromegaly increases cardiovascular mortality through arrhythmias and sudden cardiac death. Effective treatment improves outcomes, but neoplastic causes are now the leading cause of death.
Area of Science:
- Endocrinology
- Cardiology
- Oncology
Background:
- Acromegaly, characterized by excess growth hormone, significantly elevates cardiovascular mortality.
- Cardiac arrhythmias and sudden cardiac death are primary causes of mortality.
- Acromegalic cardiomyopathy involves biventricular hypertrophy and diastolic dysfunction, excluding other cardiac conditions.
Purpose of the Study:
- To summarize the cardiovascular complications and mortality causes in acromegaly.
- To highlight risk factors and disease associations contributing to cardiovascular morbidity.
- To discuss the impact of modern treatment on patient outcomes.
Main Methods:
- Literature review of cardiovascular complications in acromegaly.
- Analysis of risk factors including age, disease duration, and BMI.
- Evaluation of the association between growth hormone excess duration and cardiac dysfunction.
Main Results:
- Cardiovascular disorders like arrhythmias, cardiomyopathy, and hypertension are prevalent.
- Longer disease duration, not hormone level, correlates with biventricular enlargement and heart failure.
- Improved acromegaly control has reduced cardiovascular mortality.
Conclusions:
- Acromegalic cardiomyopathy is a significant contributor to morbidity and mortality.
- While cardiovascular deaths have decreased with treatment, neoplastic causes are now the primary cause of death.
- Comprehensive management of acromegaly and its comorbidities is crucial for improving patient survival.
Abstract:
The most common causes of increased cardiovascular mortality in acromegaly are cardiac arrhythmias and sudden cardiac death. Acromegalic cardiomyopathy is defined as concentric biventricular hypertrophy and diastolic dysfunction when other cardiac diseases such as hypertension, diabetes mellitus, and arrhythmias-related cardiac disorders have been excluded. This also contributes to significant morbidity and mortality in these patients. The main risk factors contributing to the development of cardiomyopathy include advancing age, disease duration, and body mass index. The duration of growth hormone excess is more closely associated with the development of biventricular enlargement, diastolic dysfunction, heart failure, and valvular disease than the degree of hormone elevation. Additionally, other cardiovascular disorders such as coronary artery disease, arrhythmias, valvular heart diseases, systemic hypertension, atherosclerosis, and rarely congestive cardiac failure are involved in the shortened life span of these patients especially if poorly controlled. Biochemical control of acromegaly with the recently available multimodal treatment along with better management of cardiovascular comorbidities has improved the morbidity and mortality rates of patients with acromegaly. However, with the recent advances in the treatment of acromegaly, neoplastic causes presently remain as the main leading cause of death in these patients.
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