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Acetaminophen treatment in children and adults with spinal muscular atrophy: a lower tolerance and higher risk of hepatotoxicity.

Authors :
Naume, Marie Mostue
Zhao, Qiaolin
Haslund-Krog, Sissel Sundell
Krag, Thomas
Winter, Brenda C.M. de
Revsbech, Karoline Lolk
Vissing, John
Holst, Helle
Møller, Morten Hylander
Hornsyld, Tessa Munkeboe
Dunø, Morten
Hoei-Hansen, Christina Engel
Born, Alfred Peter
Bo Jensen, Per
Cathrine Ørngreen, Mette
Source :
Neuromuscular Disorders. Jan2024, Vol. 34, p9-18. 10p.
Publication Year :
2024

Abstract

• Patients with spinal muscular atrophy (SMA) may be at increased risk of acetaminophen-induced hepatotoxicity due to low skeletal muscle mass. • Patients with SMA have a lower clearance of acetaminophen compared to healthy controls. • One SMA patient had increased liver biomarkers after only two days of acetaminophen treatment. • We recommend giving pediatric doses of acetaminophen (15 mg/kg/dose) to adult SMA patients with a maximum of 4000 mg/day. • We recommend monitoring standard liver biomarkers of ALT, GGT and LDH after first-time treatment of acetaminophen. Acute liver failure has been reported sporadically in patients with spinal muscular atrophy (SMA) and other neuromuscular disorders with low skeletal muscle mass receiving recommended dosages of acetaminophen. It is suggested that low skeletal muscle mass may add to the risk of toxicity. We aimed to describe the pharmacokinetics and safety of acetaminophen in patients with SMA. We analyzed acetaminophen metabolites and liver biomarkers in plasma from SMA patients and healthy controls (HC) every hour for six or eight hours on day 1 and day 3 of treatment with therapeutic doses of acetaminophen. Twelve patients with SMA (six adults and six children) and 11 HC participated in the study. Adult patients with SMA had significantly lower clearance of acetaminophen compared to HC (14.1 L/h vs. 21.5 L/h). Formation clearance of acetaminophen metabolites, glucuronide, sulfate, and oxidative metabolites were two-fold lower in the patients compared to HC. The liver transaminases and microRNAs increased nine-fold in one adult SMA patient after two days of treatment. The other patients and HC did not develop abnormal liver biomarkers. In this study, patients with SMA had lower clearance and slower metabolism of acetaminophen, and one patient developed liver involvement. We recommend giving 15 mg/kg/dose to SMA adults (with a maximum of 4000 mg/day) and monitoring standard liver biomarkers 48 h after first-time treatment of acetaminophen. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09608966
Volume :
34
Database :
Academic Search Index
Journal :
Neuromuscular Disorders
Publication Type :
Academic Journal
Accession number :
174915039
Full Text :
https://doi.org/10.1016/j.nmd.2023.11.005