Advances in Research on the Cardiovascular Complications of Acromegaly

Han Yang1,2, Huiwen Tan1, He Huang3

  • 1Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, China.

Frontiers in Oncology
|April 19, 2021
PubMed

Insights

Acromegaly patients face high risks of heart complications like hypertension and cardiomyopathy due to excess growth hormone (GH) and insulin-like growth factor 1 (IGF-1). Early diagnosis and treatment of acromegaly can prevent heart disease and premature death.

Area of Science:

  • Endocrinology
  • Cardiology
  • Internal Medicine

Background:

  • Acromegaly, caused by excess growth hormone (GH) and insulin-like growth factor 1 (IGF-1), frequently leads to cardiovascular complications.
  • These complications significantly increase mortality risk in affected individuals.

Purpose of the Study:

  • To summarize the cardiovascular complications associated with acromegaly.
  • To discuss the pathophysiology and risk factors contributing to cardiac issues in acromegaly.
  • To highlight the importance of early diagnosis and treatment for preventing adverse cardiovascular outcomes.

Main Methods:

  • Review of existing literature on acromegaly and cardiovascular complications.
  • Analysis of the characteristics of acromegalic cardiomyopathy, including biventricular hypertrophy and diastolic dysfunction.
  • Identification of key risk factors such as age, disease duration, and coexisting cardiovascular conditions.

Main Results:

  • Hypertension and cardiomyopathy are the predominant cardiovascular complications in acromegaly.
  • Acromegalic cardiomyopathy is characterized by concentric biventricular hypertrophy and diastolic dysfunction.
  • Arrhythmia and heart valve disease are also common, with pathophysiology linked to sustained GH and IGF-1 excess.

Conclusions:

  • Cardiovascular complications are a major cause of morbidity and mortality in acromegaly.
  • Factors like age, disease duration, and elevated GH/IGF-1 levels are critical.
  • Timely diagnosis and management of acromegaly are essential for mitigating cardiac risks and improving survival.

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
119
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
121
Coronary Artery Disease I: Introduction01:30

Coronary Artery Disease I: Introduction

Coronary Artery Disease (CAD): An Overview with Scientific InsightsCoronary Artery Disease (CAD), often referred to as C-A-D, is a prevalent blood vessel disorder classified under the broader category of atherosclerosis. Atherosclerosis is a pathological process characterized by the hardening and narrowing of arteries due to the accumulation of atherosclerotic plaques. These plaques are composed of cholesterol, fatty substances, inflammatory cells, calcium, and fibrin, reducing blood flow to...
588
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
166
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
104
Hypertension III: Clinical Manifestations and Diagnostic Studies01:30

Hypertension III: Clinical Manifestations and Diagnostic Studies

Hypertension is asymptomatic and also referred to as the "silent killer" until it progresses to a severe stage or causes target organ disease. Patients may experience symptoms stemming from the strain on blood vessels and tissues in various organs or the heart's increased workload.Physical exams might show no abnormalities other than high blood pressure. Signs of vascular damage, when present, correspond to the organs supplied by the affected vessels, leading to target organ damage. For...
172