Prevalence of Orthopedic Manifestations in Patients With Cardiac Amyloidosis With a Focus on Shoulder Pathologies

Alyssa Basdavanos1, Mathew S Maurer2, Lauren Ives1

  • 1Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.

Insights

Transthyretin cardiac amyloidosis (ATTR-CA) patients show higher rates of shoulder pathologies than other cardiac amyloidosis types. Early orthopedic manifestations may aid in earlier ATTR-CA diagnosis and treatment.

Area of Science:

  • Cardiology
  • Orthopedics
  • Genetics

Background:

  • Transthyretin cardiac amyloidosis (ATTR-CA) is a restrictive cardiomyopathy.
  • ATTR-CA is linked to orthopedic issues preceding cardiac symptoms.
  • Prevalence of shoulder pathologies in cardiac amyloidosis (CA) is understudied.

Purpose of the Study:

  • To investigate the prevalence of shoulder pathologies in patients with CA.
  • To compare orthopedic manifestations between ATTR-CA and light-chain CA (AL-CA).
  • To assess if orthopedic issues can aid in early CA identification.

Main Methods:

  • Single-center, retrospective, case-control study.
  • Analyzed 1,310 patients with CA (830 ATTR-CA, 480 AL-CA).
  • Compared CA patients to age-matched general population data for arthroplasty odds.

Main Results:

  • ATTR-CA patients had significantly more shoulder pathologies and orthopedic manifestations than AL-CA patients (p <0.001).
  • Patients aged 60+ with ATTR-CA had 6.05x higher odds of shoulder arthroplasty vs. controls.
  • Patients aged 60+ with AL-CA had 1.63x higher odds of shoulder arthroplasty vs. controls.

Conclusions:

  • Shoulder and other orthopedic pathologies are common in ATTR-CA.
  • These findings may facilitate earlier identification of CA patients.
  • Earlier diagnosis can lead to timely intervention and treatment.

Related Concept Videos

Rheumatic Heart Disease I: Introduction01:23

Rheumatic Heart Disease I: Introduction

Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
29
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies01:22

Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies

The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
43
Atherosclerosis II: Clinical Manifestations and Diagnostic Tests01:27

Atherosclerosis II: Clinical Manifestations and Diagnostic Tests

Atherosclerosis is a progressive disorder that leads to the thickening and narrowing of arterial walls due to plaque buildup. This condition can cause various symptoms depending on the arteries affected:Coronary Artery Disease (CAD): This condition affects the coronary arteries and may lead to chest pain (angina), shortness of breath (dyspnea), heart attacks, and other heart disease symptoms.Cerebrovascular Disease: This affects blood flow to the brain, causing transient ischemic attacks (TIAs)...
26
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...
17
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...
31
Coronary Artery Disease III: Clinical Manifestations01:30

Coronary Artery Disease III: Clinical Manifestations

Coronary Artery Disease (CAD) is a primary health risk worldwide, leading to significant morbidity and mortality. The condition arises from the buildup of atherosclerotic plaques within the coronary arteries, resulting in diminished blood supply to the heart muscle.The clinical manifestations of CAD vary widely, from asymptomatic stages to severe, life-threatening conditions. Understanding these manifestations is crucial for early diagnosis and effective management.Angina Pectoris: The Warning...
24