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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.
Background:
Peripartum cardiomyopathy (PPCM) is a potentially life-threatening condition. The histological characteristics of PPCM as risk factors for poor outcomes have not been thoroughly investigated. This study evaluated the pathological findings of PPCM, with a particular focus on inflammatory factors such as tenascin-C (TNC) and interleukin-6, which may predict left ventricular dysfunction and the prognosis of PPCM.
Methods And Results:
We conducted a retrospective single-center observational study involving endomyocardial biopsies (from 27 patients) as clinically diagnosed PPCM. We assessed the association between the histology and cardiac events, namely cardiac death, left ventricular assist device implantation, and/or heart transplantation. During the median follow-up period of 2,100 days, 7 (25.9%) composite events were documented. Kaplan-Meier survival curves demonstrated that patients with advanced cardiac fibrosis had significantly poorer long-term outcomes than those with mild cardiac fibrosis (log-rank P=0.0003). Furthermore, TNC-positive patients with advanced fibrosis had significantly worse event-free survival than TNC-negative patients with advanced fibrosis and patients with mild fibrosis (Bonferroni-adjusted P=0.016 and P<0.0001, respectively). Interleukin-6 expression was higher in cardiac tissue from PPCM patients who were TNC positive (P=0.03).
Conclusions:
Cardiac histopathology in PPCM patients can predict long-term prognosis; both advanced fibrosis and immunohistochemical TNC expression are associated with poor prognosis.
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