Vol 26, No 6 (2019)
Original articles — Clinical cardiology
Published online: 2018-10-19

open access

Page views 2179
Article views/downloads 997
Get Citation

Connect on Social Media

Connect on Social Media

Right atrial pathology in arrhythmogenic right ventricular dysplasia

Guoliang Li12, Guy H. Fontaine1, Shuanliang Fan3, Yang Yan4, Peter K. Bode5, Firat Duru6, Robert Frank1, Ardan M. Saguner6
Pubmed: 30394508
Cardiol J 2019;26(6):736-743.

Abstract

Background: Atrial fibrillation (AF) is the most common atrial arrhythmia in arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD). Considering the histologic changes known in the right ventricular (RV) in ARVD, the aim of the present study was to examine right atrial (RA) pathology in patients with ARVD. Methods: Histology of RA and RV was assessed from autopsy material in 3 patients with ARVD without persistent atrial arrhythmia. RA histology in 3 patients with permanent AF without ARVD and 5 patients without cardiovascular disease was also studied. Staining with hematoxylin phloxine saffron was performed for the ARVD patients to identify fibrosis, and hematoxylin-eosin for identification of lymphocytes. Masson’s trichrome staining was performed for control groups taken from a collection of standard glass slides. Results: In all 3 ARVD cases, RA anomalies were observed that revealed a reduction of cardiomyocytes, the presence of adipocytes, some of them inside the mediomural atrial layer and interstitial fibrosis. In 2 ARVD cases, interstitial fibrosis was also associated with a focus of replacement fibrosis, which was also observed in patients with permanent AF without ARVD. The histologic specimen of the RA and RV from the control group without cardiovascular disease did not display any evidence of fat or fibrosis with a preserved cardiomyocyte architecture. Conclusions: A similar histopathological substrate, as can be observed in the RV of patients with ARVD can also be seen in the RA of these patients. This may explain the high prevalence of atrial arrhythmias, particularly AF, in patients with ARVD.

Article available in PDF format

View PDF Download PDF file

References

  1. Fontaine G, Guiraudon G, Frank R, et al. Stimulation studies and eicardial maing in ventricular tachycardia: study of mechanisms and selection for surgery. In: Kulbertus H, editor.: Lancaster. MTP Pub. 1977: 334–350.
  2. Marcus FI, Fontaine GH, Guiraudon G, et al. Right ventricular dysplasia: a report of 24 adult cases. Circulation. 1982; 65(2): 384–398.
  3. Calkins H, Corrado D, Marcus F. Risk stratification in arrhythmogenic right ventricular cardiomyopathy. Circulation. 2017; 136(21): 2068–2082.
  4. Lopez-Ayala JM, Pastor-Quirante F, Gonzalez-Carrillo J, et al. Genetics of myocarditis in arrhythmogenic right ventricular dysplasia. Heart Rhythm. 2015; 12(4): 766–773.
  5. Bowles NE, Ni J, Marcus F, et al. The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy. J Am Coll Cardiol. 2002; 39(5): 892–895.
  6. Saguner AM, Roland F, Li GL, et al. 1933Superimposed myocarditis leading to heart transplantation in a young patient with arrhythmogenic right ventricular dysplasia. Eur Heart J. 2017; 38(suppl_1).
  7. Tonet JL, Castro-Miranda R, Iwa T, et al. Frequency of supraventricular tachyarrhythmias in arrhythmogenic right ventricular dysplasia. Am J Cardiol. 1991; 67(13): 1153.
  8. Saguner AM, Ganahl S, Kraus A, et al. Clinical role of atrial arrhythmias in patients with arrhythmogenic right ventricular dysplasia. Circ J. 2014; 78(12): 2854–2861.
  9. Wu L, Guo J, Zheng L, et al. Atrial remodeling and atrial tachyarrhythmias in arrhythmogenic right ventricular cardiomyopathy. Am J Cardiol. 2016; 118(5): 750–753.
  10. Vila J, Pariaut R, Moïse NS, et al. Structural and molecular pathology of the atrium in boxer arrhythmogenic right ventricular cardiomyopathy. J Vet Cardiol. 2017; 19(1): 57–67.
  11. Fontaine G, Fornes P, Hebert JL. Ventricular tachycardia in arrhythmogenic right ventricular cardiomyoathies. In: Zies D, Jalife J, editors. Cardiac Electrohysiology: From Cell to Bedside (4th edition). Saunders, Philadelphia 2004 : 588–600.
  12. Paul M, Rahbar K, Gerss J, et al. Microvascular dysfunction in nonfailing arrhythmogenic right ventricular cardiomyopathy. Eur J Nucl Med Mol Imaging. 2012; 39(3): 416–420.
  13. Bonny A, Lellouche N, Ditah I, et al. C-reactive protein in arrhythmogenic right ventricular dysplasia/cardiomyopathy and relationship with ventricular tachycardia. Cardiol Res Pract. 2010; 2010.
  14. Spoladore R, Fisicaro A, Faccini A, et al. Coronary microvascular dysfunction in primary cardiomyopathies. Heart. 2014; 100(10): 806–813.
  15. Haemers P, Hamdi H, Guedj K, et al. Atrial fibrillation is associated with the fibrotic remodelling of adipose tissue in the subepicardium of human and sheep atria. Eur Heart J. 2017; 38(1): 53–61.
  16. Saguner AM, Brunckhorst C, Duru F. Atrial arrhythmias in arrhythmogenic cardiomyopathy: at the beginning or at the end of the disease story? Reply. Circ J. 2015; 79(2): 447.
  17. Platonov PG, Christensen AH, Holmqvist F, et al. Abnormal atrial activation is common in patients with arrhythmogenic right ventricular cardiomyopathy. J Electrocardiol. 2011; 44(2): 237–241.