Transcriptional Active Parvovirus B19 Infection Predicts Adverse Long-Term Outcome in Patients with Non-Ischemic Cardiomyopathy
by
,
and
Felicitas Escher
1,2,3,*
,
Ganna Aleshcheva
1,
Heiko Pietsch
1,2,3,
Christian Baumeier
1,
Ulrich M. Gross
1,
Benedikt Norbert Schrage
4,5,
Dirk Westermann
4,5,
Claus-Thomas Bock
6,7 and
Heinz-Peter Schultheiss
1
1
Institute of Cardiac Diagnostics and Therapy, IKDT GmbH, 12203 Berlin, Germany
2
Department of Internal Medicine and Cardiology, Campus Virchow-Klinikum, Charité-Universitaetsmedizin Berlin, Corporate Member of Freie Universitaet Berlin and Humboldt-Universitaet zu Berlin, 13353 Berlin, Germany
3
DZHK (German Centre for Cardiovascular Research), Partner Site Berlin, 13353 Berlin, Germany
4
Department of Cardiology, University Heart and Vascular Center Hamburg, 20246 Hamburg, Germany
5
DZHK (German Center for Cardiovascular Research), Partner Site Hamburg/Lübeck/Kiel, 20246 Hamburg, Germany
6
Department of Infectious Diseases, Division of Viral Gastroenteritis and Hepatitis Pathogens and Enteroviruses, Robert Koch Institute, 13353 Berlin, Germany
7
Institute of Tropical Medicine, University of Tuebingen, 72074 Tuebingen, Germany
*
Author to whom correspondence should be addressed.
Biomedicines 2021, 9(12), 1898; https://doi.org/10.3390/biomedicines9121898
Submission received: 2 November 2021 / Revised: 22 November 2021 / Accepted: 10 December 2021 / Published: 14 December 2021
(This article belongs to the Special Issue Cardiomyopathies：From Molecular Basis to Therapy)
Abstract
:
Parvovirus B19 (B19V) is the predominant cardiotropic virus currently found in endomyocardial biopsies (EMBs). However, direct evidence showing a causal relationship between B19V and progression of inflammatory cardiomyopathy are still missing. The aim of this study was to analyze the impact of transcriptionally active cardiotropic B19V infection determined by viral RNA expression upon long-term outcomes in a large cohort of adult patients with non-ischemic cardiomyopathy in a retrospective analysis from a prospective observational cohort. In total, the analyzed study group comprised 871 consecutive B19V-positive patients (mean age 50.0 ± 15.0 years) with non-ischemic cardiomyopathy who underwent EMB. B19V-positivity was ascertained by routine diagnosis of viral genomes in EMBs. Molecular analysis of EMB revealed positive B19V transcriptional activity in n = 165 patients (18.9%). Primary endpoint was all-cause mortality in the overall cohort. The patients were followed up to 60 months. On the Cox regression analysis, B19V transcriptional activity was predictive of a worse prognosis compared to those without actively replicating B19V (p = 0.01). Moreover, multivariable analysis revealed transcriptional active B19V combined with inflammation [hazard ratio 4.013, 95% confidence interval 1.515–10.629 (p = 0.005)] as the strongest predictor of impaired survival even after adjustment for age and baseline LVEF (p = 0.005) and independently of viral load. The study demonstrates for the first time the pathogenic clinical importance of B19V with transcriptional activity in a large cohort of patients. Transcriptionally active B19V infection is an unfavourable prognostic trigger of adverse outcome. Our findings are of high clinical relevance, indicating that advanced diagnostic differentiation of B19V positive patients is of high prognostic importance.
1. Introduction
Viral infection of the heart can cause myocarditis and dilated inflammatory cardiomyopathy (DCMi) [1,2]. Following infection, patients may develop a chronic autoimmune inflammatory reaction [3,4,5]. Clinical outcome is determined by the interplay between virulence and host immune response, and may range from subclinical disease to congestive heart failure [6]. Enterovirus- and adenovirus persistence is proven to be associated with an increased mortality [7]. In recent decades, a shift has been observed to parvovirus B19 (B19V), a single-stranded DNA virus and member of the Parvoviridae family, genus Erythroparvovirus [8], as the most frequently found cardiotropic virus in endomyocardial biopsies (EMBs) [9,10]. Despite this common detection of B19V in EMBs, prognostic relevance of B19V prevalence has been denied so far [11]. Previous clinical studies suggested that B19V presence determined by viral genomes is an unspecific bystander and may have no prognostic value in myocarditis and DCMi [12]. However, primarily experimental data suggest a relevant effect of B19V on the development of myocarditis and DCMi [13,14].
Due to the virus receptor distribution, B19V persist lifelong within bone marrow precursor cells, and are causative in the vascular endothelium [15], leading to persistent B19V infection [16,17,18]. It is known that endothelial cells represent specific targets in B19V-associated myocarditis [19]. As the B19V infection of endothelial cells is associated with a symptomatic endothelial dysfunction [17,20,21], it has been reported with atherosclerosis, vasospasms, and progression of coronary vasculopathy, limiting organ transplant survival [14,22,23,24,25]. Thus, a causal relationship between parvovirus B19V-related infection of vascular endothelial cells and inflammation can be suspected [26].
Assessing the replicative status by measuring transcriptional activity of B19V is the most accurate way to determine active B19V infection in the heart [27], as the presence of B19V genome in the heart itself can indicate a latent virus without replicative activity [10].
B19V with transcriptional activity is expected to cause cardiac inflammation, damage and dysfunction, since altered cardiac gene expression has been demonstrated in patients with transcriptional activity in comparison to control patients and myocarditis patients with latent B19V [28].
In order to gain more specific insight into the pathophysiological significance of B19V infection in the development of DCMi and more detailed insights into the long-term effects of B19V with or without transcriptional activity, we conducted a retrospective study of a prospective large observational cohort of adult patients who had underwent EMB with proof of B19V-positivity, following them for up to 60 months and comparing their outcomes with respect to EMB analysis. The aim of this study was to analyze for the first time the prognostic role of transcriptional active B19V infection on long-term outcomes.
2. Materials and Methods
2.1. Total Study Cohort
The analyzed group comprised of 871 B19V-positive patients with clinical evidence of symptomatic heart failure underwent an EMB for clear diagnosis [29,30]. The patients included in this study were evaluated by means of extensive EMB diagnostics. The diagnosis of B19V positivity was made by B19V-specific nested PCR of viral genomes. Coronary artery disease was excluded angiographically in all patients prior to EMB. The patients complained about symptoms of heart failure with fatigue, reduced physical capacity or dyspnea on exertion, and cardiac dysfunction.
Patients with myocardial virus infections other than B19V or coinfections such as enteroviruses, adenoviruses, or herpesviruses were excluded from this study [31]. Patients with other co-morbidities and known cardiac involvement were also excluded. Active myocarditis and storage diseases (amyloid, lime, iron) have been excluded by histological staining using Azan, hematoxylin eosin, EvG, and PAS.
All diagnostic procedures and evaluation were obtained using standardized protocols and questionnaires, respectively [32]. The median time from debut of first symptoms to diagnostic biopsy was six months. Indication of EMB was based on heart failure symptoms and reduced left ventricular ejection fraction (LVEF), resulting in the suspected diagnosis of chronic myocarditis/inflammatory cardiomyopathy [33].
The study endpoint was time to all-cause death. Occurrence of the endpoint (death) was determined through direct knowledge of the patient’s status, contact with family members, or inquiries at the registration office. The overall observation period was at mean 11.91 months (96% CI of mean 10.7–13.0 months).
In a subgroup analysis of n = 222 patients, an additional LVEF measurement was taken after a follow-up period mean 21.4 months (96% CI of mean 19.1–23.6 months) and analyzed. LVEF baseline and at follow-up was determined by echocardiography. LVEF deterioration has been defined as Δ-LVEF, i.e., the difference between follow-up and baseline LVEF ≥−5%. Lack of improvement of LV function was determined as consistent LV dysfunction <35% at baseline and follow-up.
2.2. Analysis of EMB
2.2.1. Analysis of Viral Nucleic Acids in EMB, Genomic DNA Isolation from EMBs
EMB were analyzed in the CAP-accredited laboratory IKDT (Institute for Cardiac Diagnostic and Therapy Berlin, Germany) by molecular workup: Genomic DNA from RNAlater (Ambion, Austin, Texas, USA) fixed EMBs was extracted by Puregene Mousetail Kit (Gentra, Minneapolis, Minnesota, USA). After isolation the amount of isolated DNA was quantified by a specialised Quantifiler TaqMan assay (Applied Biosystems, Darmstadt, Germany), in order to calculate and standardize estimation of the virus load in small EMBs (viral genomes per µg of isolated human genomic DNA) [9].
2.2.2. Detection of Viral Genomes in EMBs by Nested-PCR and Sequencing
2.2.3. Measurement of Viral DNA Load by Quantitative Real-Time PCR (TaqMan QPCR)
Subsequent calculation of viral DNA load was performed by ratio of estimated viral genome copy number in TaqMan assay to amount of incorporated human DNA amount measured by Quantifiler TaqMan assay (Applied Biosystems, Darmstadt, Germany) [28].
2.2.4. RNA Isolation, Reverse Transcription (RT) and TaqMan QPCR for Measurement of Viral Transcripts
Total RNA was isolated from endomyocardial biopsies using Trizol reagent (Invitrogen, Karlsruhe, Germany), treated with DNAse (PeqLab, Erlangen, Germany) to remove any traces of genomic DNA and reverse-transcribed to cDNA with the High capacity Kit (Applied Biosystems, Darmstadt, Germany) using random hexamers.
2.2.5. Histological and Immunohistochemical Staining for Assessment of Inflammation
Histology was developed by hematoxylin eosin staining in light microscopy. Immunohistochemistry was used for the characterization of inflammatory infiltrates and carried out on RNA-later fixation. Stainings were quantified by digital image analysis as described previously [35]. Intramyocardial inflammation was assigned according to the ESC statement [33] by CD3+ t-lymphocytes/mm2 (Dako, Glostrup, Denmark), CD11a+/LFA-1+ lymphocytes/mm2 (Immuno Tools, Friesoythe, Germany), CD11b+/Mac-1+ macrophages/mm2 (ImmunoTools, Friesoythe, Germany), and CD45R0+ T memory cells (Dako, Glostrup, Denmark). Stainings were quantified by digital image analysis as described previously [35].
2.3. Ethical Approval
The study was performed within the CRC Transregio 19 (NCT02970227) approved by the by Institutional Ethics Committee (Charité Berlin). Informed written consent was obtained from each study patient and the protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki.
2.4. Statistical Analysis
All analyses were performed using R 3.5.3 and GraphPad Prism 9. Qualitative data were compared conducting the χ2-test. The Student’s t-test was used to analyze continuous variables. Results are presented as mean ± standard deviation or given as median value (10th, 90th percentile). Survival curves were generated according to the Kaplan-Meier method and compared with the log-rank statistic. The initial time point for each survival analysis was the date of myocardial biopsy. To analyze the association between transcriptional activity and inflammation with all-cause mortality, multivariable Cox regression models were fitted with adjustments for age and baseline-LVEF. A probability value of p < 0.05 was considered statistically significant.
3. Results
3.1. Total Patient Cohort
The study group was comprised of 871 consecutive B19V-positive patients who underwent EMB performed at first admission.
The baseline data of patient characteristics and EMB analyses are given in Table 2. The cohort comprised EMBs from n = 555 (63.7%) male and n = 316 (36.2%) female patients at a mean age of 50.0 ± 15.0 years. The mean LVEF was 48.6 ± 20.0 % at baseline. The patient complaints for symptoms of heart failure included reduced physical capacity (85.1%) and NYHA II 54.37%/NYHA III 31.70%/NYHA IV 4.5%.
In the molecular biological analysis of 871 EMBs, B19V-positive transcriptional activity was detected in 165 patients, (18.9%) preferably men (64.8%) of the mean age of 50.0 ± 15.0 years old with mean LVEF of 44.9.0 ± 19.2% at baseline (Table 2).
According to the immunohistochemical analyses, intramyocardial inflammation was detected in 436 patients (50.1%). Quantification of infiltrative cells did not yield a significant difference regarding B19V-RNA+ vs. B19V-RNA− in the total cohort. Intramyocardial inflammatory infiltration was preferentially found in the neighborhood of small vessels (Figure 1).
3.2. Predictors of Outcome
3.2.1. B19V Viral Load
As the B19V copy numbers above 500 copies/μg isolated DNA have been considered as being clinically relevant [14], we determined a quantitative measurement of the B19V DNA copy numbers. Neither the mean virus loads nor the frequency of patients with viral copy numbers below or above 500 copies/μg isolated DNA (Figure 2) were significantly different. The same holds true if the threshold was set at 1000 copies (p = 0.602) or 2000 copies (p = 0.795). This indicates that the virus load alone has no direct impact on the outcome.
As a next step, B19V transcriptional activity and copy numbers were evaluated. B19V DNA copy numbers were significantly elevated in patients with transcriptional activity (B19V-RNA+) (Figure 3), however, there was no correlation between DNA load and extent of viral transcription (mRNA copy number) p = 0.3.
3.2.2. B19V Transcriptional Activity
After examining of transcriptional activity in the patient cohort as the main result of our study on the Kaplan–Meier curve analysis, B19V transcriptional activity was predictive of a worse prognosis, compared to those without actively replicating B19V (p = 0.01 by the log-rank test) (Figure 4).
We could confirm via the Cox regression analysis a significant difference in mortality rate in patients negative for B19V transcriptional activity with vs. without inflammation (p = 0.03). Corresponding to our main statement, the cohort of patients with B19V-RNA+ with inflammation exhibited a significantly worse prognosis in contrast to patients with B19V-RNA− with inflammation in the total cohort (p = 0.04).
Moreover, the majority of fatal causalities was found in patients with actively replicated B19V and inflammation. In the multivariable Cox regression analysis, transcriptionally active B19V combined with inflammation [hazard ratio 4.013, 95% confidence interval 1.515–10.629 (p = 0.005)] was the strongest predictor and was associated with higher mortality as compared to the absence of transcriptional activity and the absence of inflammation; even after adjustment for age and baseline LVEF (Table 3).
3.2.3. Subgroup Analysis
In a subgroup analysis of n = 222 patients with haemodynamic measurements after a long follow-up period, a Cox analysis of composite end-point including LVEF deterioration, lack of improvement of LV function, and all-cause mortality confirmed significant association between B19V transcriptional activity and the combined end-point (0.0002). Interestingly, this subgroup analysis also showed a significant difference in the groups with and without transcriptional activity even without inflammation in EMB (p = 0.03 by the log-rank test) (Table 4, Figure 5).
4. Discussion
In this study, we demonstrated for the first time in a large cohort of patients with B19V infection in EMB that viral B19V genomes in the presence of replicative intermediates (viral RNAs) are related to adverse long-term clinical outcomes. This is the first demonstration of the clinical pathophysiological significance of B19V with transcriptional activity as contrasted with latent B19V.
B19V as the predominant pathogen currently detected in EMBs of patients with DCMi is underestimated from a clinical perspective. Its wide circulation generally leads to a diminished appreciation of its pathogenetic potential. Over the last decade, B19V has frequently been linked to the pathogenesis of DCMi and its progression towards dilated cardiomyopathy (DCM) [36]. Nevertheless, direct evidence showing a causal relationship between B19V cardiac presence and disease progression of B19V-associated DCMi were missing until now.
Due to our large collective of adult B19V positive patients, in this study we were able to demonstrate for the first time that B19V has a clinical relevance associated with evidence of transcriptional activity in EMBs. To gain more information on the clinical relevance of B19V with and without viral RNA transcriptional activity, we followed B19V-positive patients with reduced LVEF up to 60 months. On Cox regression analysis, B19V transcriptional activity was predictive of a worse prognosis, compared to those without actively replicating B19V. Moreover, this effect is exacerbated in the presence of inflammation. In the multivariable analysis, transcriptional active B19V combined with inflammation proved to be the strongest predictor of impaired survival. In addition, we conducted a subgroup Cox analysis with composite end-point confirmed significant association between B19V transcriptional activity and LV deterioration or lack of improvement of LV function even without inflammation in EMB.
Due to elevated B19V copy numbers in patients with DCM/DCMi in comparison to controls, 500 virus copies have been considered as a clinically important threshold value [14]. In inflamed and uninflamed hearts, copy numbers of the B19V genome and elevated copy numbers above 500 copies/µg isolated DNA were neither different nor associated with an impaired clinical outcome. This is in line with the general clinical experience that the load of B19V per se does not correlate with the clinical course or complaints of patients with heart failure [21].
Interestingly, and in contrast to other cardiotropic viruses, B19V exclusively targets vascular endothelial cells [20,37]. If infected cells are injured by a lytic virus infection or by the antiviral immune response, replaceable endothelial cells but not irreplaceable cardiomyocytes are destroyed. In addition, myocardial inflammation in response to viral infection was found to be associated with increased endothelial expression of the human leucocyte antigen system and adhesion molecules [19,38]. The presence of B19V remained a single independent predictor for reduced cardiac vascular density in patients with cardiomyopathy. This result demonstrates the importance of B19V infection for reduced coronary blood flow leading to ischemia and endothelial dysfunction. This is an explanation as to why acute endothelial cell B19V-infection is associated with a cardiac microvascular impairment mimicking myocardial infarction [39,40,41]. It would also be in line with reports on progressive alterations of the vasculature and reduced survival of transplanted hearts in B19V-positive children or improvement of endothelial cell function upon antiviral treatment strategies [20,22,42]. In contrast to enteroviral and adenoviral infections which are acquired at any age, B19V permanently resides in the bone marrow and vascular endothelial cells after primary infection [43]. It is caused by endogenous B19V-infected bone marrow derived endothelia progenitor cells which are released into the bloodstream during vascular repair [16,20]. In this respect, the EMB proof of B19V in adults constitutes a completely distinct disease entity.
The importance of testing viral presence for further treatment has been shown in a retrospective analysis by Frustaci in which viral persistence was associated with detrimental outcomes in patients with myocarditis receiving immunosuppressive therapy [44]. Proofing of transcriptional activity of B19V is therefore mandatory to differentiate between latent and active viral persistence and avoiding potential incorrect therapeutic decisions.
Primary antiviral therapeutic options already exist. Recently, we were able to show that clinical symptoms in patients with enterovirus and adenovirus genomes improved during antiviral treatment with interferon-β [45]. Moreover, suppression of B19V transcriptional activity by nucleoside analogue telbivudine treatment improved hemodynamic and clinical outcomes significantly [46]. In- vitro data provided an anti-apoptotic effect of this nucleoside analogue through normalization of BIRC3 levels in B19V-induced apoptosis, and thereby protected cells from B19V damage [47].
Limitation of the Study
The major limitation of this study is the lack of randomization. This was a retrospective analysis of data from a prospective observational cohort and, as such, the possible effect of selection bias cannot be denied. The cohort was only adjusted to B19V-positive patients with or without detectable replicative intermediates of B19V confirmed by measurement of B19V RNA transcripts. In this design, unmeasured confounding cannot be ruled out.
5. Conclusions
Among patients with B19V genomes in EMB, in this study we were able to demonstrate for the first time that B19V with transcriptional activity is clinically relevant. Transcriptionally active B19V is associated with progressive cardiac dysfunction and impaired survival.
Compentency in medical knowledge: Our study has high and immediate clinical impact, since B19V is the most frequently found cardiotropic virus in EMBs. Testing of replicative status of B19V is a prerequisite for further therapeutic decisions. The findings reported here highlight the importance of an advanced diagnostic approach with inclusion of B19V transcriptional activity into the routine evaluation of EMBs, especially if inflammation is detected. This is of particular importance because initiation of an immunosuppressive therapy leads to a significantly worse prognosis in the case of an additional active viral infection.
Translational outlook: Comprehensive, standardized diagnostic differentiation of endomyocardial B19V infections with biological and prognostic relevance (including viral replication and ongoing inflammation) seems to be the key approach for both an updated diagnostic classification of B19V associated viral cardiomyopathy and a more meaningful selection of candidates for future innovative anti-viral immunomodulatory treatment strategies and randomized studies, which are urgently needed.
Author Contributions
Conceptualization, F.E., H.-P.S.; methodology, H.-P.S., G.A., H.P., B.N.S., C.B., U.M.G., C.-T.B. and F.E.; investigation, H.-P.S., F.E., G.A.; data curation, H.P., G.A. and F.E.; writing—original draft preparation, F.E., C.-T.B., G.A., H.P.; writing—review and editing, H.-P.S., C.-T.B., G.A., H.P., C.B., B.N.S., D.W. and F.E.; visualization, H.P. and F.E.; supervision, H.-P.S., C.-T.B. and F.E.; project administration, H.-P.S.; funding acquisition, H.-P.S., F.E. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by grants of the CRC Transregio 19 (NCT02970227), ERA-Net on Cardiovascular Diseases (ERA-CVD; JTC2016-40-158), and a ProFIT grant of the Investitionsbank Berlin/cofounded of EFRE (No. 10169096, 10169098, 10169028).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Data analyses were performed within the CRC Transregio 19 (NCT02970227) approved by the by Institutional Ethics Committee (Charité Berlin). Informed consent was obtained from all subjects involved in the study. The protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki.
Data Availability Statement
The data presented in this study are available on request from the corresponding author.
Acknowledgments
Figures were created at the Institute for cardiac diagnostic and therapy (IKDT) Berlin, Germany. For excellent work, we thank Kitty Winter, Jenny Klostermann, Susanne Ochmann, Katrin Errami (IKDT Berlin, Germany), and Hannes Jarmuth (Charite, Berlin).
Conflicts of Interest
The authors declare no conflict of interest.
References
- Esfandiarei, M.; McManus, B.M. Molecular Biology and Pathogenesis of Viral Myocarditis. Annu. Rev. Pathol. Mech. Dis. 2008, 3, 127–155. [Google Scholar] [CrossRef]
- Schultheiss, H.-P.; Fairweather, D.L.; Caforio, A.L.P.; Escher, F.; Hershberger, R.E.; Lipshultz, S.E.; Liu, P.P.; Matsumori, A.; Mazzanti, A.; McMurray, J.; et al. Dilated cardiomyopathy. Nat. Rev. Dis. Prim. 2019, 5, 32. [Google Scholar] [CrossRef]
- Rose, N.R.; Neu, N.; Neumann, D.A.; Herskowitz, A. Myocarditis: A Postinfectious Autoimmune Disease. In New Concepts in Viral Heart Disease; Springer: Berlin/Heidelberg, Germany, 1988. [Google Scholar]
- Fairweather, D.; Frisancho-Kiss, S.; Rose, N.R. Viruses as adjuvants for autoimmunity: Evidence from Coxsackievirus-induced myocarditis. Rev. Med. Virol. 2005, 15, 17–27. [Google Scholar] [CrossRef] [PubMed]
- Schultheiss, H.-P.; Baumeier, C.; Pietsch, H.; Bock, C.T.; Poller, W.; Escher, F. Cardiovascular consequences of viral infections: From COVID to other viral diseases. Cardiovasc. Res. 2021, 117, 2610–2623. [Google Scholar] [CrossRef] [PubMed]
- Corsten, M.F.; Schroen, B.; Heymans, S. Inflammation in viral myocarditis: Friend or foe? Trends Mol. Med. 2012, 18, 426–437. [Google Scholar] [CrossRef]
- Kühl, U.; Lassner, D.; von Schlippenbach, J.; Poller, W.; Schultheiss, H.-P. Interferon-Beta Improves Survival in Enterovirus-Associated Cardiomyopathy. J. Am. Coll. Cardiol. 2012, 60, 1295–1296. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Rogo, L.D.; Mokhtari-Azad, T.; Kabir, M.H.; Rezaei, F. Human parvovirus B19: A review. Acta Virol. 2014, 58, 199–213. [Google Scholar] [CrossRef] [PubMed]
- Kühl, U.; Lassner, D.; Pauschinger, M.; Gross, U.M.; Seeberg, B.; Noutsias, M.; Poller, W.; Schultheiss, H.-P. Prevalence of erythrovirus genotypes in the myocardium of patients with dilated cardiomyopathy. J. Med. Virol. 2008, 80, 1243–1251. [Google Scholar] [CrossRef]
- Verdonschot, J.A.J.; Cooper, L.T.; Heymans, S.R.B. Parvovirus B19 in Dilated Cardiomyopathy: There Is More Than Meets the Eye. J. Card. Fail. 2019, 25, 64–66. [Google Scholar] [CrossRef] [PubMed]
- Hjalmarsson, C.; Liljeqvist, J.-Å.; Lindh, M.; Karason, K.; Bollano, E.; Oldfors, A.; Andersson, B. Parvovirus B19 in Endomyocardial Biopsy of Patients With Idiopathic Dilated Cardiomyopathy: Foe or Bystander? J. Card. Fail. 2019, 25, 60–63. [Google Scholar] [CrossRef] [PubMed]
- Angelini, A.; Calzolari, V.; Calabrese, F.; Boffa, G.M.; Maddalena, F.; Chioin, R.; Thiene, G. Myocarditis mimicking acute myocardial infarction: Role of endomyocardial biopsy in the differential diagnosis. Heart 2000, 84, 245–250. [Google Scholar] [CrossRef] [Green Version]
- Schmidt-Lucke, C.; Zobel, T.; Escher, F.; Tschöpe, C.; Lassner, D.; Kühl, U.; Gubbe, K.; Volk, H.-D.; Schultheiss, H.-P. Human Parvovirus B19 (B19V) Up-regulates CXCR4 Surface Expression of Circulating Angiogenic Cells: Implications for Cardiac Ischemia in B19V Cardiomyopathy. J. Infect. Dis. 2018, 217, 456–465. [Google Scholar] [CrossRef]
- Bock, C.-T.; Klingel, K.; Kandolf, R. Human Parvovirus B19–Associated Myocarditis. N. Engl. J. Med. 2010, 362, 1248–1249. [Google Scholar] [CrossRef] [PubMed]
- Bowles, N.E.; Vallejo, J. Viral causes of cardiac inflammation. Curr. Opin. Cardiol. 2003, 18, 182–188. [Google Scholar] [CrossRef] [PubMed]
- Schmidt-Lucke, C.; Escher, F.; Van Linthout, S.; Kühl, U.; Miteva, K.; Ringe, J.; Zobel, T.; Schultheiss, H.-P.; Tschöpe, C. Cardiac Migration of Endogenous Mesenchymal Stromal Cells in Patients with Inflammatory Cardiomyopathy. Mediat. Inflamm. 2015, 2015, 308185. [Google Scholar] [CrossRef] [PubMed]
- Yilmaz, A.; Mahrholdt, H.; Athanasiadis, A.; Vogelsberg, H.; Meinhardt, G.; Voehringer, M.; Kispert, E.-M.; Deluigi, C.; Baccouche, H.; Spodarev, E.; et al. Coronary vasospasm as the underlying cause for chest pain in patients with PVB19 myocarditis. Heart 2008, 94, 1456. [Google Scholar] [CrossRef] [PubMed]
- Schenk, T.; Enders, M.; Pollak, S.; Hahn, R.; Huzly, D. High Prevalence of Human Parvovirus B19 DNA in Myocardial Autopsy Samples from Subjects without Myocarditis or Dilative Cardiomyopathy. J. Clin. Microbiol. 2009, 47, 106. [Google Scholar] [CrossRef] [Green Version]
- Crea, F.; Camici, P.G.; Bairey Merz, C.N. Coronary microvascular dysfunction: An update. Eur. Heart J. 2014, 35, 1101–1111. [Google Scholar] [CrossRef] [Green Version]
- Schmidt-Lucke, C.; Spillmann, F.; Bock, T.; Kühl, U.; Van Linthout, S.; Schultheiss, H.-P.; Tschöpe, C. Interferon Beta Modulates Endothelial Damage in Patients with Cardiac Persistence of Human Parvovirus B19 Infection. J. Infect. Dis. 2010, 201, 936–945. [Google Scholar] [CrossRef]
- Tschope, C.; Bock, C.-T.; Kasner, M.; Noutsias, M.; Westermann, D.; Schwimmbeck, P.-L.; Pauschinger, M.; Poller, W.-C.; Kühl, U.; Kandolf, R.; et al. High Prevalence of Cardiac Parvovirus B19 Infection in Patients With Isolated Left Ventricular Diastolic Dysfunction. Circulation 2005, 111, 879–886. [Google Scholar] [CrossRef] [Green Version]
- Breinholt, J.P.; Moulik, M.; Dreyer, W.J.; Denfield, S.W.; Kim, J.J.; Jefferies, J.L.; Rossano, J.W.; Gates, C.M.; Clunie, S.K.; Bowles, K.R.; et al. Viral epidemiologic shift in inflammatory heart disease: The increasing involvement of parvovirus B19 in the myocardium of pediatric cardiac transplant patients. J. Heart Lung Transplant. 2010, 29, 739–746. [Google Scholar] [CrossRef] [Green Version]
- Liu, S.-C.; Tsai, C.-T.; Wu, C.-K.; Yu, M.-F.; Wu, M.-Z.; Lin, L.-I.; Wang, S.-S.; Hwang, J.-J.; Tseng, Y.-Z.; Chiang, F.-T.; et al. Human Parvovirus B19 Infection in Patients with Coronary Atherosclerosis. Arch. Med. Res. 2009, 40, 612–617. [Google Scholar] [CrossRef] [PubMed]
- Barzon, L.; Murer, L.; Pacenti, M.; Biasol, M.A.; Della Vella, M.; Benetti, E.; Zanon, G.F.; Palù, G. Investigation of Intrarenal Viral Infections in Kidney Transplant Recipients Unveils an Association between Parvovirus B19 and Chronic Allograft Injury. J. Infect. Dis. 2009, 199, 372–380. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Pankuweit, S.; Klingel, K. Viral myocarditis: From experimental models to molecular diagnosis in patients. Heart Fail. Rev. 2013, 18, 683–702. [Google Scholar] [CrossRef] [PubMed]
- Magro, C.M.; Crowson, A.N.; Dawood, M.; Nuovo, G.J. Parvoviral infection of endothelial cells and its possible role in vasculitis and autoimmune diseases. J. Rheumatol. 2002, 29, 1227. [Google Scholar]
- Rigopoulos, G.A.; Klutt, B.; Matiakis, M.; Apostolou, A.; Mavrogeni, S.; Noutsias, M. Systematic Review of PCR Proof of Parvovirus B19 Genomes in Endomyocardial Biopsies of Patients Presenting with Myocarditis or Dilated Cardiomyopathy. Viruses 2019, 11, 566. [Google Scholar] [CrossRef] [Green Version]
- Kuhl, U.; Lassner, D.; Dorner, A.; Rohde, M.; Escher, F.; Seeberg, B.; Hertel, E.; Tschope, C.; Skurk, C.; Gross, U.M.; et al. A distinct subgroup of cardiomyopathy patients characterized by transcriptionally active cardiotropic erythrovirus and altered cardiac gene expression. Basic Res. Cardiol. 2013, 108, 372. [Google Scholar] [CrossRef]
- Thiene, G.; Bruneval, P.; Veinot, J.; Leone, O. Diagnostic use of the endomyocardial biopsy: A consensus statement. Virchows Arch. 2013, 463, 1–5. [Google Scholar] [CrossRef] [PubMed]
- Leone, O.; Veinot, J.P.; Angelini, A.; Baandrup, U.T.; Basso, C.; Berry, G.; Bruneval, P.; Burke, M.; Butany, J.; Calabrese, F.; et al. 2011 Consensus statement on endomyocardial biopsy from the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology. Cardiovasc. Pathol. 2012, 21, 245–274. [Google Scholar] [CrossRef]
- Kuühl, U.; Pauschinger, M.; Noutsias, M.; Seeberg, B.; Bock, T.; Lassner, D.; Poller, W.; Kandolf, R.; Schultheiss, H.-P. High Prevalence of Viral Genomes and Multiple Viral Infections in the Myocardium of Adults With “Idiopathic” Left Ventricular Dysfunction. Circulation 2005, 111, 887–893. [Google Scholar] [CrossRef] [Green Version]
- Angelow, A.; Weitmann, K.; Schmidt, M.; Schwedler, S.; Vogt, H.; Havemann, C.; Staudt, A.; Felix, S.B.; Stangl, K.; Klingel, K.; et al. The German Transregional Collaborative Research Centre ‘Inflammatory Cardiomyopathy—Molecular Pathogenesis and Therapy’. Cardiology 2009, 113, 222–230. [Google Scholar] [CrossRef]
- Caforio, A.L.P.; Pankuweit, S.; Arbustini, E.; Basso, C.; Gimeno-Blanes, J.; Felix, S.B.; Fu, M.; Heliö, T.; Heymans, S.; Jahns, R.; et al. Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur. Heart J. 2013, 34, 2636–2648. [Google Scholar] [CrossRef] [PubMed]
- Pietsch, H.; Escher, F.; Aleshcheva, G.; Lassner, D.; Bock, C.-T.; Schultheiss, H.-P. Detection of parvovirus mRNAs as markers for viral activity in endomyocardial biopsy-based diagnosis of patients with unexplained heart failure. Sci. Rep. 2020, 10, 22354. [Google Scholar] [CrossRef] [PubMed]
- Escher, F.; Kühl, U.; Lassner, D.; Poller, W.; Westermann, D.; Pieske, B.; Tschöpe, C.; Schultheiss, H.-P. Long-term outcome of patients with virus-negative chronic myocarditis or inflammatory cardiomyopathy after immunosuppressive therapy. Clin. Res. Cardiol. 2016, 105, 1011–1020. [Google Scholar] [CrossRef] [PubMed]
- Bogomolovas, J.; Šimoliunas, E.; Rinkunaite, I.; Smalinskaite, L.; Podkopajev, A.; Bironaite, D.; Weis, C.A.; Marx, A.; Bukelskiene, V.; Gretz, N.; et al. A Novel Murine Model of Parvovirus Associated Dilated Cardiomyopathy Induced by Immunization with VP1-Unique Region of Parvovirus B19. BioMed Res. Int. 2016, 2016, 1627184. [Google Scholar] [CrossRef] [Green Version]
- Schmidt-Lucke, C.; Zobel, T.; Schrepfer, S.; Kuhl, U.; Wang, D.; Klingel, K.; Becher, P.M.; Fechner, H.; Pozzuto, T.; Van Linthout, S.; et al. Impaired Endothelial Regeneration Through Human Parvovirus B19-Infected Circulating Angiogenic Cells in Patients with Cardiomyopathy. J. Infect. Dis. 2015, 212, 1070–1081. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Zakrzewska, K.; Cortivo, R.; Tonello, C.; Panfilo, S.; Abatangelo, G.; Giuggioli, D.; Ferri, C.; Corcioli, F.; Azzi, A. Human parvovirus B19 experimental infection in human fibroblasts and endothelial cells cultures. Virus Res. 2005, 114, 1–5. [Google Scholar] [CrossRef] [PubMed]
- Kühl, U.; Pauschinger, M.; Bock, T.; Klingel, K.; Schwimmbeck, P.; Seeberg, B.; Krautwurm, L.; Poller, W.; Schultheiss, H.; Kandolf, R. Parvovirus B19 Infection Mimicking Acute Myocardial Infarction. Circulation 2003, 108, 945–950. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bültmann, B.D.; Klingel, K.; Sotlar, K.; Bock, C.T.; Baba, H.A.; Sauter, M.; Kandolf, R. Fatal parvovirus B19–associated myocarditis clinically mimicking ischemic heart disease: An endothelial cell–mediated disease. Hum. Pathol. 2003, 34, 92–95. [Google Scholar] [CrossRef] [PubMed]
- Bultmann, B.; Sotlar, K.; Klingel, K. Parvovirus B19. N. Engl. J. Med. 2004, 350, 2006–2007. [Google Scholar] [CrossRef]
- Moulik, M.; Breinholt, J.P.; Dreyer, W.J.; Kearney, D.L.; Price, J.F.; Clunie, S.K.; Moffett, B.S.; Kim, J.J.; Rossano, J.W.; Jefferies, J.L.; et al. Viral Endomyocardial Infection Is an Independent Predictor and Potentially Treatable Risk Factor for Graft Loss and Coronary Vasculopathy in Pediatric Cardiac Transplant Recipients. J. Am. Coll. Cardiol. 2010, 56, 582–592. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Norja, P.; Hokynar, K.; Aaltonen, L.-M.; Chen, R.; Ranki, A.; Partio, E.K.; Kiviluoto, O.; Davidkin, I.; Leivo, T.; Eis-Hübinger, A.M.; et al. Bioportfolio: Lifelong persistence of variant and prototypic erythrovirus DNA genomes in human tissue. Proc. Natl. Acad. Sci. USA 2006, 103, 7450–7453. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Frustaci, A.; Chimenti, C.; Calabrese, F.; Pieroni, M.; Thiene, G.; Maseri, A. Immunosuppressive therapy for active lymphocytic myocarditis: Virological and immunologic profile of responders versus nonresponders. Circulation 2003, 107, 857–863. [Google Scholar] [CrossRef]
- Schultheiss, H.-P.; Piper, C.; Sowade, O.; Waagstein, F.; Kapp, J.-F.; Wegscheider, K.; Groetzbach, G.; Pauschinger, M.; Escher, F.; Arbustini, E.; et al. Betaferon in chronic viral cardiomyopathy (BICC) trial: Effects of interferon-β treatment in patients with chronic viral cardiomyopathy. Clin. Res. Cardiol. 2016, 105, 763–773. [Google Scholar] [CrossRef] [PubMed]
- Schultheiss, H.-P.; Bock, T.; Pietsch, H.; Aleshcheva, G.; Baumeier, C.; Fruhwald, F.; Escher, F. Nucleoside Analogue Reverse Transcriptase Inhibitors Improve Clinical Outcome in Transcriptional Active Human Parvovirus B19-Positive Patients. J. Clin. Med. 2021, 10, 1928. [Google Scholar] [CrossRef] [PubMed]
- Zobel, T.; Bock, C.T.; Kuhl, U.; Rohde, M.; Lassner, D.; Schultheiss, H.P.; Schmidt-Lucke, C. Telbivudine Reduces Parvovirus B19-Induced Apoptosis in Circulating Angiogenic Cells. Viruses 2019, 11, 227. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1. Representative images if (Immuno-) histopathological findings from endomycardial biopsies of B19V positive patients. (A). H&E staining. Patient with B19V with transcriptional activity and inflammation. Inflammatory cellular infiltrates in between myocytes preferentially in the neighborhood of small vessels. Nuclei and cytoplasm of myocytes vary in diameter. (B). H&E staining. Patient with B19 V without transcriptional activity without inflammation. Varying diameter of myocytes. (C). Immunohistological staining of increased CD3 positive T lymphocytes near small vessels between myocytes with some variation of diameter in a patient with B19V with transcriptional activity. (D). Immunohistological staining of low CD3 positive T lymphocytes infiltration in a patient with B19V without transcriptional activity. Scale bars: 50 µm.
Figure 1. Representative images if (Immuno-) histopathological findings from endomycardial biopsies of B19V positive patients. (A). H&E staining. Patient with B19V with transcriptional activity and inflammation. Inflammatory cellular infiltrates in between myocytes preferentially in the neighborhood of small vessels. Nuclei and cytoplasm of myocytes vary in diameter. (B). H&E staining. Patient with B19 V without transcriptional activity without inflammation. Varying diameter of myocytes. (C). Immunohistological staining of increased CD3 positive T lymphocytes near small vessels between myocytes with some variation of diameter in a patient with B19V with transcriptional activity. (D). Immunohistological staining of low CD3 positive T lymphocytes infiltration in a patient with B19V without transcriptional activity. Scale bars: 50 µm.
Figure 2. Kaplan-Meier plots in total patient cohort for all-cause mortality. Five-year outcome of B19V-positive patients with copy numbers above or below 500 copies/μg isolated DNA.
Figure 2. Kaplan-Meier plots in total patient cohort for all-cause mortality. Five-year outcome of B19V-positive patients with copy numbers above or below 500 copies/μg isolated DNA.
Figure 3. Box blot showing high statistical difference between B19V copy numbers in B19V-RNA+ (n = 165) vs. B19V-RNA− (n = 706) (** p = 0.006). B19V = parvovirus B19; B19V-RNA+ = B19V with transcriptional activity; B19V-RNA− = B19V without transcriptional activity.
Figure 3. Box blot showing high statistical difference between B19V copy numbers in B19V-RNA+ (n = 165) vs. B19V-RNA− (n = 706) (** p = 0.006). B19V = parvovirus B19; B19V-RNA+ = B19V with transcriptional activity; B19V-RNA− = B19V without transcriptional activity.
Figure 4. Kaplan-Meier plots in total patient cohort for all-cause mortality. Five-year mortality of B19V-positive patients in dependence of B19V and transcriptional activity. The mortality rate was higher in patients with transcriptional activity (n = 165) compared to those without transcriptional activity (n = 706).
Figure 4. Kaplan-Meier plots in total patient cohort for all-cause mortality. Five-year mortality of B19V-positive patients in dependence of B19V and transcriptional activity. The mortality rate was higher in patients with transcriptional activity (n = 165) compared to those without transcriptional activity (n = 706).
Figure 5. Kaplan-Meier plots for composite end-point LV deterioration and all-cause mortality. In a subgroup analysis of n = 222 patients with haemodynamic measurements after a long follow-up period, a Cox analysis confirmed significant association between B19V transcriptional activity and LVEF deterioration, lack of improvement of LV function, and higher mortality even without inflammation in EMB (p = 0.03).
Figure 5. Kaplan-Meier plots for composite end-point LV deterioration and all-cause mortality. In a subgroup analysis of n = 222 patients with haemodynamic measurements after a long follow-up period, a Cox analysis confirmed significant association between B19V transcriptional activity and LVEF deterioration, lack of improvement of LV function, and higher mortality even without inflammation in EMB (p = 0.03).
Table 1. Primer sequences used for detection of B19V.
| Primer/Probe Name | Nucleotide Sequence (5′–3′) |
|---|---|
| NS1-FW | TCCCTGGAATWAATGCAGATGC |
| NS1-RV | CACTGCTGCTGAYACTGGTGTCT |
| NS1-probe | 6FAM-ACCTCCAAACCACCCCAATTGTCACA-TAMRA |
| VP1-FW | TGTAAGATGCAGCCCTGACATG |
| VP1-RV | GAGGGCATCTGCATTAATTCCA |
| VP1-probe | 6FAM-TGGTGTAATGCACAAAGCTGG-TAMRA |
Note: B19V = parvovirus B19; FW = forward; NS1 = nonstructural B19 protein NS1; RV = reverse; VP1 = structural B19V protein VP1.
Table 2. Clinical characteristics and EMB analysis at baseline with and without transcriptional activity in total patient cohort.
Table 2. Clinical characteristics and EMB analysis at baseline with and without transcriptional activity in total patient cohort.
| Clinical Characteristics | All Patients | With Replicative Intermediates (B19V-RNA+) | Without Replicative Intermediates (B19V-RNA−) |
|---|---|---|---|
| Number of patients, n (%) | 871 (100) | 165 (18.9) | 706 (81.1) |
| Sex, n (%) | 555 (63.7) male 316 (36.2) female |
107 (64.8) male 58 (35.1) female |
448 (63.4) male 258 (36.5) female |
| Age, mean ± SD (years) | 50.0 ± 15.0 | 50.0 ± 15.0 | 49.0 ± 15.0 |
| LVEF, mean ± SD (%) | 48.6 ± 20.0 | 44.90 ± 19.2 | 49.4 ± 18.6 a |
| LVEDD, mean ± SD (mm) | 56.7 ± 9.1 | 58.0 ± 9.6 | 55.8 ± 9.7 a |
| LVESD, mean ± SD (mm) | 40.4 ± 12.3 | 42.4 ± 13.2 | 41.0 ± 12.7 |
| infection preceding onset of symptoms <12 weeks (%), n = 429 | 52.5 | 56.0 | 50.5 |
| - flue like (%) | 38.9 | 45.4 | 35.4 |
| - pneumonia (%) | 8.4 | 6.6 | 9.4 |
| - gastrointestinal (%) | 1.6 | 0.7 | 2.2 |
| - other (%) | 3.5 | 3.3 | 3.6 |
| Complaints at baseline biopsy | |||
| Reduced physical capacity (%) | 85.1 | 90.5 | 82.1 |
| NYHA II/III/IV (%) | 54.3/31.7/4.5 | 56.4/29.1/5.1 | 50.1/34.2/3.7 |
| Angina at rest (%) | 22.4 | 26.7 | 20.1 |
| Angina on exertion (%) | 40.1 | 41.0 | 39.2 |
| Palpitation (%) | 8.5 | 6.8 | 10.8 |
| Systolic blood pressure, mean ± SD (mmHg) | 118 ± 18 | 115 ± 18 | 117 ± 17 |
| Diastolic blood pressure, mean ± SD (mmHg) | 74 ± 11 | 74 ± 11 | 74 ± 1 |
| Peripheral edema (%) | 29.4 | 30.9 | 28.6 |
| Medication, n | |||
| - β-blockers | 48.7 | 47.9 | 49.1 |
| - ACE inhibitors/ARB | 71.8 | 72.2 | 71.9 |
| - diuretic agents | 52.2 | 50.1 | 53.1 |
| Biopsy (inflammatory cell counts) | |||
| CD3+, mean ± SD (cells/mm2) | 7.4 ± 12.0 | 7.2 ± 6.9 | 7.5 ± 13.0 |
| CD45RO+, mean ± SD (cells/mm2) | 21.5 ± 21.8 | 23.8 ± 19.2 | 21.0 ± 22.4 |
| LFA-1+, mean ± SD (cells/mm2) | 17.4 ± 25.0 | 16.8 ± 15.2 | 17.5 ± 26.8 |
| Mac-1+, mean ± SD (cells/mm2) | 34.8 ± 28.0 | 35.3 ± 24.9 | 34.7 ± 28.7 |
Note: ACE inhibitor = angiotensin-converting-enzyme inhibitor; ARB = angiotensin receptor blocker; B19V = Parvovirus B19; CD3 = t cells; CD45R0 = t memory cells; LFA-1 = Lymphocyte function-associated antigen 1; LVEDD = left ventricular end-diastolic diameter, LVEF = left ventricular ejection fraction; LVESD = left ventricular end-systolic diameter; MAC-1 = Macrophage-1 antigen.; NYHA = New York Heart Association. The data are presented as mean ± standard deviation (SD), as %, and as No. of subjects. a Significantly different; B19V-RNA+ vs. B19V-RNA−.
Table 3. Multivariable Cox regression analysis of total patient cohort.
| Unadjusted Cox Model |
Adjusted Cox Model | |||||
|---|---|---|---|---|---|---|
| Group | HR | 95%CI | p-Value | HR | 95%CI | p-Value |
| B19V-RNA+ without inflammation vs. B19V-RNA− without inflammation | 1.020 | 0.223–4.658 | 0.980 | 1.004 | 0.219–4.559 | 0.996 |
| B19V-RNA+ with inflammation vs. B19V-RNA− without inflammation | 3.239 | 1.223–8.575 | 0.018 | 4.013 | 1.515–10.629 | 0.005 |
Note: Cox regression model in total patient cohort with time to death as the dependent variable and B19V replication/inflammation as the independent variable, with additional adjustment for age and ejection fraction at baseline.
Table 4. Subgroup analysis.
| Clinical Characteristics | With Replicative Intermediates (B19V-RNA+) | Without Replicative Intermediates (B19V-RNA−) |
|---|---|---|
| Number of patients, n (%) | 126 | 96 |
| Age, mean ± SD (years) | 48.1 ± 16.4 | 48.3 ± 13.2 |
| LVEF, mean baseline ± SD (%) | 45.5 ± 18.2 | 48.6 ± 19.1 a |
| LVEF, mean follow-up ± SD (%) | 52.0 ± 17.2 b | 56.8 ± 15.3 ab |
| LVEF recovery (%) | 38.0 | 52.0 a |
| LVEDD, mean baseline ± SD (mm) | 55.8 ± 9.5 | 56.2 ± 10.4 |
| LVEDD, mean follow-up ± SD (mm) | 58.1 ± 9.0 | 55.3 ± 10.2 a |
| LVESD, mean baseline ± SD (mm) | 41.4 ± 12.9 | 41.6 ± 14.7 |
| LVESD, mean follow-up ± SD (mm) | 44.9 ± 12.0 | 40.4 ± 14.0 |
| Medication, % | ||
| - β-blockers | 47.5 | 49.2 |
| - ACE inhibitors/ARB | 73.2 | 72.3 |
| - diuretic agents | 51.1 | 53.1 |
| Biopsy (inflammatory cell counts) | ||
| CD3+, mean ± SD (cells/mm2) | 10.3 ± 14 | 9.9 ± 21.3 |
| CD45R0+, mean ± SD (cells/mm2) | 28.5 ± 29.7 | 26.8 ± 72.5 |
| LFA-1+, mean ± SD (cells/mm2) | 23.6 ± 26.6 | 29.6 ± 118 |
| Mac-1+, mean ± SD (cells/mm2) | 43.1 ± 33.9 | 48.6 ± 123.3 |
Note: ACE inhibitor = angiotensin-converting-enzyme inhibitor; ARB = angiotensin receptor blocker; B19V = parvovirus B19; LVEDD = left ventricular end-diastolic diameter, LVEF = left ventricular ejection fraction; LVESD = left ventricular end-systolic diameter; CD3 = t cells; CD45R0 = t memory cells; LFA-1 = Lymphocyte function-associated antigen 1; MAC-1 = Macrophage-1 antigen. The data are presented as mean + standard deviation (SD), as %, and as No. of subjects. a Significantly different; B19V-RNA+ vs. B19V-RNA−. b Significantly different; baseline vs. follow-up.
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Escher, F.; Aleshcheva, G.; Pietsch, H.; Baumeier, C.; Gross, U.M.; Schrage, B.N.; Westermann, D.; Bock, C.-T.; Schultheiss, H.-P. Transcriptional Active Parvovirus B19 Infection Predicts Adverse Long-Term Outcome in Patients with Non-Ischemic Cardiomyopathy. Biomedicines 2021, 9, 1898. https://doi.org/10.3390/biomedicines9121898
AMA Style
Escher F, Aleshcheva G, Pietsch H, Baumeier C, Gross UM, Schrage BN, Westermann D, Bock C-T, Schultheiss H-P. Transcriptional Active Parvovirus B19 Infection Predicts Adverse Long-Term Outcome in Patients with Non-Ischemic Cardiomyopathy. Biomedicines. 2021; 9(12):1898. https://doi.org/10.3390/biomedicines9121898
Chicago/Turabian StyleEscher, Felicitas, Ganna Aleshcheva, Heiko Pietsch, Christian Baumeier, Ulrich M. Gross, Benedikt Norbert Schrage, Dirk Westermann, Claus-Thomas Bock, and Heinz-Peter Schultheiss. 2021. "Transcriptional Active Parvovirus B19 Infection Predicts Adverse Long-Term Outcome in Patients with Non-Ischemic Cardiomyopathy" Biomedicines 9, no. 12: 1898. https://doi.org/10.3390/biomedicines9121898
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