Hepatotoxicity of Statins as Determined by Serum Alanine Aminotransferase in a Pediatric Cohort With Dyslipidemia.
Journal
Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
pubmed:
20
10
2018
medline:
26
3
2020
entrez:
19
10
2018
Statut:
ppublish
Résumé
The aim of the study was to evaluate the hepatotoxicity of statins, as determined by serum alanine aminotransferase (ALT), in children and adolescents with dyslipidemia in real-world clinical practice. Clinical and laboratory data were prospectively collected between September 2010 and March 2014. We compared ALT levels between patients prescribed versus not prescribed 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase inhibitors (statins), and then compared ALT before and after initiation of statins. Over the 3.5-year observation period, there were 2704 ALT measurements among 943 patients. The mean age was 14 years; 54% were boys, 47% obese, and 208 patients were treated with statins. Median follow-up after first ALT was 18 months. The mean (SD) ALT in statin and non-statin users was 23 (20) U/L and 28 (28) U/L, respectively. In models adjusted for age, sex, and race, ALT was 2.1 U/L (95% CI 0.1 to 4.4; P = 0.04) lower among statin users, which was attenuated after adjustment for weight category. Patients started on statins during the observation period did not demonstrate an increase in ALT over time (ALT 0.9 U/L [95% confidence interval -5.2 to 3.4] increase per year; P = 0.7). In our study population, we did not observe a higher burden of ALT elevations among pediatric patients on statins as compared to those with dyslipidemia who are not on statins, supporting the hepatic safety of statin use in childhood.
Identifiants
pubmed: 30334928
doi: 10.1097/MPG.0000000000002174
pmc: PMC6344263
mid: NIHMS1508852
doi:
Substances chimiques
Hydroxymethylglutaryl-CoA Reductase Inhibitors
0
Alanine Transaminase
EC 2.6.1.2
Types de publication
Evaluation Study
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
175-181Subventions
Organisme : NHLBI NIH HHS
ID : K23 HL111335
Pays : United States
Organisme : NHLBI NIH HHS
ID : K99 HL136875
Pays : United States
Références
Am J Gastroenterol. 2010 May;105(5):978-80
pubmed: 20445507
J Pediatr Gastroenterol Nutr. 2017 Feb;64(2):319-334
pubmed: 28107283
J Clin Lipidol. 2015 Nov-Dec;9(6):741-750
pubmed: 26687694
Hepatology. 2005 Apr;41(4):690-5
pubmed: 15789367
J Am Coll Cardiol. 2010 Mar 16;55(11):1121-6
pubmed: 20223367
Cardiol Clin. 2015 May;33(2):257-65
pubmed: 25939298
MMWR Morb Mortal Wkly Rep. 2010 Jan 22;59(2):29-33
pubmed: 20094024
Drugs. 2012 Apr 16;72(6):759-72
pubmed: 22512364
Pediatrics. 2007 Feb;119(2):370-80
pubmed: 17272627
Circulation. 2014 Jun 24;129(25 Suppl 2):S1-45
pubmed: 24222016
Cochrane Database Syst Rev. 2010 Jul 07;(7):CD006401
pubmed: 20614444
JAMA. 1999 Jan 13;281(2):137-44
pubmed: 9917116
Am J Med Sci. 2010 Aug;340(2):89-93
pubmed: 20588181
Lancet. 2010 Dec 4;376(9756):1916-22
pubmed: 21109302
Cochrane Database Syst Rev. 2013 Jan 31;(1):CD004816
pubmed: 23440795
Circulation. 2002 Oct 22;106(17):2231-7
pubmed: 12390953
J Pediatr. 2003 Jul;143(1):74-80
pubmed: 12915827
Pediatrics. 2011 Dec;128 Suppl 5:S213-56
pubmed: 22084329
J Clin Lipidol. 2014 May-Jun;8(3 Suppl):S47-57
pubmed: 24793441
BMC Med. 2014 Mar 22;12:51
pubmed: 24655568
Endocrinol Metab Clin North Am. 2016 Mar;45(1):117-28
pubmed: 26893001