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Systemic complications of acromegaly: epidemiology, pathogenesis, and management
Annamaria Colao1, Diego Ferone, Paolo Marzullo
1Department of Molecular and Clinical Endocrinology and Oncology, Federico II University of Naples, 80131 Naples, Italy. colao@unina.it
Insights
Acromegaly significantly increases mortality due to cardiovascular and respiratory issues. Effective treatment of acromegaly improves these systemic complications, including heart problems and sleep apnea.
Area of Science:
- Endocrinology
- Internal Medicine
- Cardiology
Background:
- Acromegaly, a disorder caused by excess growth hormone (GH) and insulin-like growth factor-I (IGF-I), leads to significant systemic complications.
- Cardiovascular and respiratory diseases are major contributors to increased mortality in acromegaly patients.
Purpose of the Study:
- To review the systemic complications associated with acromegaly.
- To discuss the impact of acromegaly on cardiovascular, respiratory, neoplastic, and musculoskeletal systems.
- To evaluate the benefits of treatment on these complications.
Main Methods:
- This is a review article synthesizing existing research on acromegaly complications.
- Information was gathered from various investigations focusing on mortality, morbidity, and treatment outcomes.
Main Results:
- Biventricular hypertrophy is the most common cardiac complication, independent of hypertension. Diastolic and systolic dysfunction, arrhythmias, and hypertension are prevalent.
- Respiratory disorders, including sleep apnea, contribute to mortality but improve with GH/IGF-I control.
- Increased risk of colonic polyps is noted, while arthropathy is a major cause of disability, potentially reversible in early stages.
Conclusions:
- Acromegaly treatment, via surgery or pharmacotherapy (e.g., somatostatin analogs), effectively reduces cardiovascular and respiratory morbidity.
- Controlling GH and IGF-I hypersecretion is crucial for managing systemic complications and improving patient outcomes.
- Early intervention for arthropathy is recommended to prevent irreversible functional disability.
Abstract:
This review focuses on the systemic complications of acromegaly. Mortality in this disease is increased mostly because of cardiovascular and respiratory diseases, although currently neoplastic complications have been questioned as a relevant cause of increased risk of death. Biventricular hypertrophy, occurring independently of hypertension and metabolic complications, is the most frequent cardiac complication. Diastolic and systolic dysfunction develops along with disease duration; and other cardiac disorders, such as arrhythmias, valve disease, hypertension, atherosclerosis, and endothelial dysfunction, are also common in acromegaly. Control of acromegaly by surgery or pharmacotherapy, especially somatostatin analogs, improves cardiovascular morbidity. Respiratory disorders, sleep apnea, and ventilatory dysfunction are also important contributors in increasing mortality and are advantageously benefitted by controlling GH and IGF-I hypersecretion. An increased risk of colonic polyps, which more frequently recur in patients not controlled after treatment, has been reported by several independent investigations, although malignancies in other organs have also been described, but less convincingly than at the gastrointestinal level. Finally, the most important cause of morbidity and functional disability of the disease is arthropathy, which can be reversed at an initial stage, but not if the disease is left untreated for several years.
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