Tenascin-C and Fibrosis as Prognostic Predictors of Peripartum Cardiomyopathy - A Histopathological Study

Kisaki Amemiya1, Junko Nakashima2, Keiko Ohta-Ogo1

  • 1Department of Pathology, National Cerebral and Cardiovascular Center.

Insights

Histopathology in peripartum cardiomyopathy (PPCM) predicts outcomes. Advanced fibrosis and tenascin-C (TNC) expression in cardiac tissue are linked to poorer prognosis in PPCM patients.

Area of Science:

  • Cardiology
  • Pathology
  • Immunohistochemistry

Background:

  • Peripartum cardiomyopathy (PPCM) is a severe heart condition.
  • Histological factors predicting PPCM outcomes require further investigation.
  • This study focuses on inflammatory markers like tenascin-C (TNC) and interleukin-6 in PPCM prognosis.

Purpose of the Study:

  • To evaluate PPCM pathological findings.
  • To identify histological risk factors for poor outcomes.
  • To assess the predictive value of TNC and interleukin-6 for left ventricular dysfunction and prognosis.

Main Methods:

  • Retrospective observational study of 27 PPCM patients.
  • Analysis of endomyocardial biopsies.
  • Assessment of cardiac events and correlation with fibrosis and TNC/interleukin-6 expression.

Main Results:

  • Advanced cardiac fibrosis correlated with significantly poorer long-term outcomes.
  • TNC-positive patients with advanced fibrosis had worse event-free survival.
  • Higher interleukin-6 expression was observed in TNC-positive PPCM patients.

Conclusions:

  • Cardiac histopathology is a predictor of long-term prognosis in PPCM.
  • Advanced fibrosis and TNC expression are associated with adverse outcomes.
  • TNC may play a role in PPCM pathogenesis and prognosis.
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...
708
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...
802
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,...
757
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...
816
Myocarditis I: Introduction01:21

Myocarditis I: Introduction

Myocarditis is inflammation of the myocardium, which is the muscular layer of the heart.EtiologyMyocarditis has a diverse etiology, including a wide range of infectious and non-infectious causes:Infectious CausesViral: Common viruses include Coxsackie A and B, adenovirus, parvovirus B19, enteroviruses, and influenza A.Bacterial: Examples include infections caused by Streptococcus, Staphylococcus, and Mycoplasma species.Rickettsial: Infections like Rocky Mountain spotted fever can result in...
574
Pericarditis IV: Nursing Management01:25

Pericarditis IV: Nursing Management

Pericarditis, an inflammation of the pericardium, necessitates diligent nursing management to ensure effective patient care and recovery. The initial step in managing pericarditis is a comprehensive patient medical assessment.The patient reports chest pain aggravated by breathing, coughing, and swallowing, which worsens when lying supine. The pain often improves when sitting up and leaning forward. Additional symptoms may include fever, malaise, and, in severe cases, signs of heart failure.
547