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Aggravation of left ventricular dysfunction in patients with biopsy-proven cardiac human herpesvirus A and B
1Department of Cardiology and Pneumology, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Berlin, Germany; Institut für Kardiale Diagnostik und Therapie (IKDT), Berlin, Germany.
Insights
Persistent Human Herpesvirus 6 (HHV-6) B infection in the heart is linked to cardiac dysfunction. Clearance of HHV-6 B was associated with improved heart function in patients with inflammatory cardiomyopathy.
Area of Science:
- Cardiology
- Virology
- Immunology
Background:
- Human herpesvirus 6 (HHV-6) A and B are lymphotropic viruses known for lifelong persistence.
- These viruses are primarily linked to non-cardiac conditions but are suspected contributors to myocarditis and cardiomyopathy.
Purpose of the Study:
- To investigate the long-term effects of persistent HHV-6 A and B infections on cardiac function.
- To analyze the spontaneous course of inflammatory cardiomyopathy in patients with HHV-6 persistence using follow-up endomyocardial biopsies.
Main Methods:
- Prospective evaluation of 73 patients with biopsy-proven HHV-6 A/B infection in endomyocardial biopsies (EMBs).
- Follow-up analysis of EMBs and left ventricular ejection fraction (LV-EF) measurements after a median of 8.8 months.
- Investigation of HHV-6 prevalence in peripheral blood cells (PBCs) and identification of infection sites within the myocardium via immunohistochemistry (IHC).
Main Results:
- Cardiac HHV-6 A and B persistence was identified in 73 patients, with HHV-6 B being predominant (95.0%).
- Persistent cardiac HHV-6 B infection significantly correlated with worsened cardiac dysfunction (LV-EF decline).
- Resolution of HHV-6 B persistence was associated with significant improvement in LV-EF.
Conclusions:
- Persistence of cardiac HHV-6 B genomes is a significant factor in cardiac dysfunction.
- Hemodynamic parameters in patients with inflammatory cardiomyopathy improve following HHV-6 B clearance.
Background:
Human herpesvirus 6 (HHV-6) A and B are lymphotropic viruses with life-long persistence, primarily associated with non-cardiac diseases, and discussed as a possible etiologic factor of myocarditis and cardiomyopathy.
Objective:
To analyze the long-term spontaneous course of cardiac patients suffering from suspected inflammatory cardiomyopathy (CMi) with persisting HHV-6 A and B infections by follow-up biopsies.
Study Design:
We prospectively evaluated patients (n=73) with biopsy-proven viral HHV-6 A and B infection in endomyocardial biopsies (EMBs), followed up by reanalysis of EMBs and left ventricular ejection fraction (LV-EF) measurements after a median period of 8.8 months (range 4-73 months). Beyond, we studied HHV-6 prevalence in isolated peripheral blood cells (PBCs) and HHV-6 species in EMBs. HHV-6 species-specific cellular infection sites within the myocardium were identified by immunohistochemistry (IHC).
Results:
We identified 73 patients with cardiac HHV-6 A and B persistence or newly detected in follow-up EMB (95.0% B). Proof of HHV-6 in PBCs was primarily associated with A. Persistence of cardiac HHV-6 B genome was significantly associated with cardiac dysfunction at follow-up (LV-EF deteriorated from 58.2±16.0 to 51.8±17.2%, p<0.001), and LV improvement was observed when HHV-6 B persistence resolved (LV-EF increased from 54.9±15.4 to 60.7±13.1%, p<0.001).
Conclusions:
Persistence of cardiac HHV-6 B genomes was significantly associated with cardiac dysfunction, and hemodynamic parameters improved in association with HHV-6 B clearance.
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