4.6 Article

Quantitative collagen assessment in right ventricular myectomies form patients with tetralogy of Fallot

Journal

EUROPACE
Volume 23, Issue -, Pages I38-I47

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/europace/euaa389

Keywords

Fibrosis; Histology; Right ventricle; Congenital heart disease Tetralogy of Fallot; Second harmonic generation microscopy

Funding

  1. European Research Council (Advanced Grant CardioNECT) [323099]
  2. Ministry of Science, Research and Arts Baden-Wurttemberg (MWK-BW Sonderlinie Medizin) [3091311631]
  3. German Research Foundation (DFG) [183027722]
  4. DFG [RO-5694/1-1]
  5. German Cardiac Society (DGK)
  6. DFG Collaborative Research Centre (DFG) [SFB 1425, 422681845]
  7. Theo-Rossi di Montelera (TRM) foundation
  8. European Research Council (ERC) [323099] Funding Source: European Research Council (ERC)

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This study aimed to evaluate fibrosis distribution in right ventricular outflow tract (RVOT) myocardium of TOF patients and explore fibrosis quantification using SHGI as an alternative method. The research found high heterogeneity in fibrosis distribution and the need for extended volume analyses for accurate quantification. SHGI provided faster data and enabled collagen anisotropy quantification.
Aims Patients with tetralogy of Fallot (TOF) are often affected by right ventricular fibrosis, which has been associated with arrhythmias. This study aimed to assess fibrosis distribution in right ventricular outflow tract (RVOT) myocardium of TOF patients to evaluate the utility of single histology-section analyses, and to explore the possibility of fibrosis quantification in unlabelled tissue by second harmonic generation imaging (SHGI) as an alternative to conventional histology-based assays. Methods and results We quantified fibrosis in 11 TOF RVOT samples, using a tailor-made automated image analysis method on Picrosirius red-stained sections. In a subset of samples, histology- and SHGI-based fibrosis quantification approaches were compared. Fibrosis distribution was highly heterogeneous, with significant and comparable vari-ability between and within samples. We found that, on average, 67.8 mm(2) of 10 mu m thick, histologically processed tissue per patient had to be analysed for accurate fibrosis quantification. SHGI provided data faster and on live tissue, additionally enabling quantification of collagen anisotropy. Conclusion Given the high intra-individual heterogeneity, fibrosis quantification should not be conducted on single sections of TOF RVOT myectomies. We provide an analysis algorithm for fibrosis quantification in histological images, which enables the required extended volume analyses in these patients.

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