Non-alcoholic fatty liver disease is associated with early left ventricular dysfunction in childhood acute

Maurizio Delvecchio1, Paola Muggeo1, Mariantonietta Monteduro2

  • 1Department of Biomedicine and Human OncologyPediatric Section, University 'A. Moro' of Bari, Bari, Italy.

Insights

Childhood acute lymphoblastic leukemia (ALL) survivors show a higher rate of non-alcoholic fatty liver disease (NAFLD), linked to early heart problems. Lifestyle interventions are crucial for managing risks in these survivors.

Area of Science:

  • Pediatric Oncology
  • Cardiology
  • Hepatology

Background:

  • Childhood acute lymphoblastic leukemia (ALL) survivors face elevated risks of metabolic and cardiovascular diseases.
  • Non-alcoholic fatty liver disease (NAFLD) is a growing concern in this population.
  • Early detection of NAFLD and associated cardiovascular dysfunction is critical.

Purpose of the Study:

  • To assess the prevalence of NAFLD in childhood ALL survivors.
  • To investigate the association between NAFLD and early cardiovascular dysfunction in these survivors.

Main Methods:

  • A cohort of 53 childhood ALL survivors and 34 controls underwent comprehensive evaluations.
  • Methods included auxological assessment, biochemical assays, and liver, heart, and vascular ultrasound studies.

Main Results:

  • NAFLD was significantly more frequent in ALL survivors (39.6%) compared to controls (11.7%).
  • ALL patients with NAFLD exhibited higher rates of obesity and insulin resistance.
  • ALL survivors showed impaired flow-mediated dilatation, reduced interventricular septum, and lower left ventricular ejection fraction, particularly those with NAFLD.

Conclusions:

  • Childhood ALL survivors have a higher prevalence of NAFLD, which is associated with early left ventricular impairment.
  • Comprehensive cardiac evaluation is mandatory for ALL survivors with fatty liver.
  • Preventing visceral adiposity and addressing metabolic syndrome components through lifestyle interventions are strongly recommended during follow-up.
Abstract

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