Clinical Phenotypes of Patients With Ischemic Cardiomyopathy After Percutaneous Coronary Intervention

Daisuke Nakamura1, Isamu Mizote1, Tomoharu Dohi1

  • 1Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine.

Insights

Latent class analysis identified three distinct phenotypes of ischemic cardiomyopathy (ICM) in patients undergoing percutaneous coronary intervention (PCI). Phenotype 2 showed significantly lower mortality and heart failure hospitalization risks, suggesting tailored treatments for ICM subtypes.

Area of Science:

  • Cardiology
  • Medical Informatics
  • Clinical Research

Background:

  • Percutaneous coronary intervention (PCI) is a treatment option for patients with ischemic cardiomyopathy (ICM) at high risk for surgery.
  • The effectiveness of PCI in ICM is debated, possibly due to the condition's heterogeneity.
  • Latent class analysis (LCA) can identify distinct patient subgroups based on clinical features.

Purpose of the Study:

  • To characterize ischemic cardiomyopathy (ICM) phenotypes using latent class analysis (LCA).
  • To assess clinical outcomes, including mortality and heart failure hospitalization, across identified ICM phenotypes after percutaneous coronary intervention (PCI).
  • To explore the role of left ventricular reverse remodeling (LVRR) in different ICM phenotypes.

Main Methods:

  • Latent class analysis (LCA) was applied to clinical data from 492 patients with left ventricular ejection fraction <50% who underwent PCI.
  • Primary outcomes were all-cause mortality and heart failure (HF) hospitalization.
  • Phenotypes were characterized by clinical features, and outcomes were compared across groups.

Main Results:

  • Three distinct ICM phenotypes were identified.
  • Phenotype 1: severe chronic kidney disease, hemodialysis (n=101). Phenotype 2: male, early-onset ICM, lifestyle diseases, high BMI (n=192). Phenotype 3: older adults, atrial fibrillation, mitral regurgitation, high BNP (n=199).
  • Phenotype 2 had significantly lower combined mortality and HF hospitalization risk. LVRR was associated with better outcomes only in Phenotype 3.

Conclusions:

  • Distinct clinical outcomes and LVRR patterns exist across ICM phenotypes post-PCI.
  • These findings suggest underlying mechanisms vary among ICM phenotypes.
  • Personalized treatment strategies targeting specific ICM phenotypes may improve outcomes.
Abstract

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...
64
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,...
30
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations01:19

Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations

The pathophysiology of Acute Coronary Syndrome [ACD] involves several key processes:The main underlying cause of ACD is atherosclerosis, a chronic inflammatory disease characterized by the buildup of lipid-laden plaques within the coronary arteries.As the atherosclerotic plaque grows in the coronary artery, it may become unstable due to the formation of a lipid-rich core and a thin fibrous cap. Inflammatory cells within the plaque, such as macrophages, secrete enzymes that degrade the...
50
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
71
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...
40
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
26