Beneficial effects of nintedanib on cardiomyopathy in patients with systemic sclerosis: a pilot study

Rheumatology (Oxford). 2023 Jul 5;62(7):2550-2555. doi: 10.1093/rheumatology/keac674.

Abstract

Objectives: Nintedanib is an inhibitor of tyrosine kinases that has been shown to slow the progression of interstitial lung disease (ILD), including ILD associated with SSc. The aim of this study was to explore the effect of nintedanib on cardiomyopathy associated with systemic sclerosis (SSc).

Methods: Twenty consecutively hospitalized patients with SSc-ILD were enrolled and prospectively followed. The rate of change at 6 months in cardiac magnetic resonance (CMR) parametric mapping, including myocardial extracellular volume, was primarily evaluated. Other endpoints included changes in CMR functional parameters, echocardiographic parameters, modified Rodnan skin score, serum biomarkers and pulmonary function test.

Results: Nintedanib was administered in 10 patients, whereas the other 10 were treated without nintedanib or watched, according to ILD severity and progression. Baseline values of CMR parametric mapping were not different between the two groups. The rate of change at 6 months in myocardial extracellular volume was highly different, almost divergent, between the nintedanib group and the control group (-1.62% vs +2.00%, P = 0.0001). Among other endpoints, the change in right ventricular ejection fraction was significantly different between the two groups (P = 0.02), with a preferential change in the nintedanib group.

Conclusion: Our data indicate beneficial signals of nintedanib on cardiomyopathy associated with SSc. The anti-fibrotic effect of nintedanib might not be limited to the lung.

Keywords: SSc; cardiomyopathy; myocardial fibrosis; nintedanib.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cardiomyopathies* / complications
  • Cardiomyopathies* / etiology
  • Humans
  • Lung Diseases, Interstitial* / complications
  • Pilot Projects
  • Scleroderma, Systemic* / complications
  • Scleroderma, Systemic* / drug therapy
  • Scleroderma, Systemic* / pathology
  • Stroke Volume
  • Ventricular Function, Right

Substances

  • nintedanib