Incidence and Pattern of Aminotransferase Elevation During Anti-Hypertensive Therapy With Angiotensin-II Receptor Blockers
- PMID: 35996932
- PMCID: PMC9424746
- DOI: 10.3346/jkms.2022.37.e255
Incidence and Pattern of Aminotransferase Elevation During Anti-Hypertensive Therapy With Angiotensin-II Receptor Blockers
Abstract
Background: Angiotensin type II receptor blockers (ARBs) are the most widely used anti-hypertensive drugs. This study aimed to elucidate the likelihood and pattern of ARB-induced liver injury in a hospital-based cohort.
Methods: Data of patients receiving fimasartan (n = 5,543), candesartan (n = 6,406), valsartan (n = 6,040), and losartan (n = 9,126) were retrieved from the clinical data warehouse of two tertiary hospitals. Patients with alanine aminotransferase (ALT) levels > 5 times the upper normal limit were assessed according to the Roussel Uclaf Causality Assessment Method (RUCAM).
Results: A total of 27,115 patients were enrolled, including 14,630 (54.0%) men, with a mean age of 64.6 years (standard deviation, 13.6). During 31,717 person-years of ARB therapy, serum ALT levels > 120 IU/L were found in 558 (2.1%) person-years, and levels > 200 IU/L were found in 155 (0.6%) person-years. The incidence of ALT elevation > 120 IU/L per 106 cumulative defined daily doses was 6.6, 3.6, 3.9, and 4.0 in the fimasartan, candesartan, valsartan, and losartan groups, respectively (P = 0.002). An ALT level > 200 IU/L with RUCAM score ≥ 6 was found in 20 patients, suggesting probable drug-induced liver injury for 11 (0.2%) patients receiving fimasartan, five (0.1%) receiving candesartan, four (0.1%) receiving valsartan, and none receiving losartan (P < 0.001).
Conclusion: Approximately 2% of patients receiving ARB therapy had significant ALT elevation (4.24/106 cumulative defined daily doses [cDDDs]), which was associated with probable ARB-related liver injury in 0.07% of patients (0.15/106 cDDDs). Elevation of ALT was more commonly associated with fimasartan than the other ARBs. Clinicians should be aware of the possibility of ARB-related ALT elevation in patients with unexplained chronic abnormal ALT.
Keywords: Alanine Transaminase; Angiotensin II Type 2 Receptor Blockers; Chemical and Drug Induced Liver Injury; Fimasartan; Liver Function Tests.
© 2022 The Korean Academy of Medical Sciences.
Conflict of interest statement
The authors have no potential conflicts of interest to disclose.
Figures
Similar articles
-
Efficacy and tolerability of fimasartan, a new angiotensin receptor blocker, compared with losartan (50/100 mg): a 12-week, phase III, multicenter, prospective, randomized, double-blind, parallel-group, dose escalation clinical trial with an optional 12-week extension phase in adult Korean patients with mild-to-moderate hypertension.Clin Ther. 2012 Mar;34(3):552-568, 568.e1-9. doi: 10.1016/j.clinthera.2012.01.024. Epub 2012 Mar 3. Clin Ther. 2012. PMID: 22381711 Clinical Trial.
-
Comparative effect of angiotensin II type I receptor blockers on serum uric acid in hypertensive patients with type 2 diabetes mellitus: a retrospective observational study.Cardiovasc Diabetol. 2013 Nov 4;12:159. doi: 10.1186/1475-2840-12-159. Cardiovasc Diabetol. 2013. PMID: 24180232 Free PMC article.
-
Clinical pharmacokinetics of angiotensin II (AT1) receptor blockers in hypertension.J Hum Hypertens. 2000 Apr;14 Suppl 1:S73-86. doi: 10.1038/sj.jhh.1000991. J Hum Hypertens. 2000. PMID: 10854085 Review.
-
Fimasartan-induced liver injury in a patient with no adverse reactions on other types of angiotensin II receptor blockers: A case report.Medicine (Baltimore). 2017 Nov;96(47):e8905. doi: 10.1097/MD.0000000000008905. Medicine (Baltimore). 2017. PMID: 29382024 Free PMC article.
-
Newly emerging pharmacologic differences in angiotensin II receptor blockers.Am J Hypertens. 2000 Jan;13(1 Pt 2):18S-24S. doi: 10.1016/s0895-7061(99)00250-2. Am J Hypertens. 2000. PMID: 10678284 Review.
Cited by
-
Physiologically based pharmacokinetic modeling of candesartan to predict the exposure in hepatic and renal impairment and elderly populations.Ther Adv Drug Saf. 2023 Dec 25;14:20420986231220222. doi: 10.1177/20420986231220222. eCollection 2023. Ther Adv Drug Saf. 2023. PMID: 38157240 Free PMC article.
-
Two-Drug Combinations Therapy of Different Doses of Valsartan Existing Diverse Significance for Hypertensive Patients.Rev Cardiovasc Med. 2023 Jun 29;24(7):187. doi: 10.31083/j.rcm2407187. eCollection 2023 Jul. Rev Cardiovasc Med. 2023. PMID: 39077003 Free PMC article.
-
Crosstalk: Biochemical Signatures and Clinical Implications in Rare Hereditary Hemolytic Anemias (Hereditary Spherocytosis).Curr Pharm Des. 2025;31(19):1551-1561. doi: 10.2174/0113816128326588241211063917. Curr Pharm Des. 2025. PMID: 39865824
-
Are Angiotensin II Receptor Blockers Really Safe From Aminotransferase Elevation or Drug-Induced Liver Injury?J Korean Med Sci. 2022 Aug 22;37(33):e261. doi: 10.3346/jkms.2022.37.e261. J Korean Med Sci. 2022. PMID: 35996936 Free PMC article. No abstract available.
References
-
- Sindone A, Erlich J, Lee C, Newman H, Suranyi M, Roger SD. Cardiovascular risk reduction in hypertension: angiotensin-converting enzyme inhibitors, angiotensin receptor blockers. Where are we up to? Intern Med J. 2016;46(3):364–372. - PubMed
-
- Reports and Data. Angiotensin II receptor blockers market analysis, by type (Azilsartan, Candesartan, Eprosartan, Irbesartan, Losartan, Olmesartan, Telmisartan, Valsartan) by application (Hypertension, Cardiovascular risks) forecasts to 2028. [Updated 2021]. [Accessed April 8, 2022]. https://www.reportsanddata.com/report-detail/angiotensin-ii-receptor-blo... .
-
- The Korean Society of Hypertension - Hypertension Epidemiology Research Working Group. Korea hypertension fact sheet 2021. [Updated 2021]. [Accessed April 8, 2022]. https://www.koreanhypertension.org/reference/guide?mode=read&idno=4581 .
-
- Losartan. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. Bethesda, MD, USA: National Institute of Diabetes and Digestive and Kidney Diseases; 2012-. [Updated 2017]. [Accessed April 8, 2022]. https://www.ncbi.nlm.nih.gov/books/NBK547842 . - PubMed
-
- Valsartan. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. Bethesda, MD, USA: National Institute of Diabetes and Digestive and Kidney Diseases; 2012-. [Updated 2017]. [Accessed April 8, 2022]. https://www.ncbi.nlm.nih.gov/books/NBK547944 . - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical