A randomised controlled trial of rosuvastatin for the prevention of aminoglycoside-induced kidney toxicity in children with cystic fibrosis.

Stephen J McWilliam, Anna Rosala-Hallas, Ashley P Jones, Victoria Shaw, William Greenhalf, Thomas Jaki, Alan R Smyth, Rosalind L Smyth, Munir Pirmohamed

Journal: Scientific reports 2020;10(1):1796

PMID: 32020028

Abstract

The PROteKT study tested the hypothesis that rosuvastatin can inhibit aminoglycoside-induced nephrotoxicity in children with Cystic Fibrosis (CF). This open label, parallel group, randomised controlled trial recruited children and young people aged 6 to 18 years with CF at 13 paediatric CF treatment centres in the UK. Participants were randomised equally to either receive oral rosuvastatin (10 mg once daily) or no intervention (control) throughout clinically indicated treatment with intravenous tobramycin. The primary outcome was the difference between the groups in mean fold-change in urinary Kidney Injury Molecule-1 (KIM-1). Fifty (rosuvastatin n = 23, control n = 27) participants were recruited between May 2015 and January 2017. Primary outcome data was available for 88% (rosuvastatin n = 20, control n = 24). The estimated mean treatment difference in the geometric mean-fold change of normalised KIM-1 was 1.08 (95% CI 0.87-1.35, p = 0.48). In total there were 12 adverse reactions, all mild, reported by five participants randomised to rosuvastatin, and one serious adverse event in each group. Whilst no protective effect of rosuvastatin was seen, there was a lower than expected level of nephrotoxicity in the cohort. Therefore, we can neither confirm nor refute the hypothesis that rosuvastatin protects against aminoglycoside nephrotoxicity.

Address: Department of Women's and Children's Health, University of Liverpool, Liverpool, Merseyside, United Kingdom. [email protected].; Clinical Trials Research Centre, University of Liverpool, a member of the Liverpool Health Partners, Liverpool, Merseyside, United Kingdom.; Institute of Translational Medicine, University of Liverpool, Liverpool, Merseyside, United Kingdom.; Department of Mathematics and Statistics, Lancaster University, Lancaster, United Kingdom.; Division of Child Health, Obstetrics & Gynaecology, University of Nottingham, Nottingham, United Kingdom.; University College London, Great Ormond Street Institute of Child Health, London, United Kingdom.; Department of Molecular and Clinical Pharmacology, and MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, Merseyside, United Kingdom.
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