Journal of Cardiovascular Magnetic Resonance (Jun 2021)

The impact of Wilson disease on myocardial tissue and function: a cardiovascular magnetic resonance study

  • Janek Salatzki,
  • Isabelle Mohr,
  • Jannick Heins,
  • Mert H. Cerci,
  • Andreas Ochs,
  • Oliver Paul,
  • Johannes Riffel,
  • Florian André,
  • Kristóf Hirschberg,
  • Matthias Müller-Hennessen,
  • Evangelos Giannitsis,
  • Matthias G. Friedrich,
  • Uta Merle,
  • Karl Heinz Weiss,
  • Hugo A. Katus,
  • Marco Ochs

DOI
https://doi.org/10.1186/s12968-021-00760-1
Journal volume & issue
Vol. 23, no. 1
pp. 1 – 16

Abstract

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Abstract Background Systemic effects of altered serum copper processing in Wilson Disease (WD) might induce myocardial copper deposition and consequently myocardial dysfunction and structural remodeling. This study sought to investigate the prevalence, manifestation and predictors of myocardial tissue abnormalities in WD patients. Methods We prospectively enrolled WD patients and an age-matched group of healthy individuals. We applied cardiovascular magnetic resonance (CMR) to analyze myocardial function, strain, and tissue characteristics. A subgroup analysis of WD patients with predominant neurological (WD-neuro + ) or hepatic manifestation only (WD-neuro − ) was performed. Results Seventy-six patients (37 years (27–49), 47% women) with known WD and 76 age-matched healthy control subjects were studied. The prevalence of atrial fibrillation in WD patients was 5% and the prevalence of symptomatic heart failure was 2.6%. Compared to healthy controls, patients with WD had a reduced left ventricular global circumferential strain (LV-GCS), and also showed abnormalities consistent with global and regional myocardial fibrosis. WD-neuro + patients presented with more severe structural remodeling and functional impairment when compared to WD-neuro − patients. Conclusions In a large cohort, WD was not linked to a distinct cardiac phenotype except CMR indexes of myocardial fibrosis. More research is warranted to assess the prognostic implications of these findings. Trial registration: This trial is registered at the local institutional ethics committee (S-188/2018).

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