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The Effect of Potentially Hepatotoxic Medicinal Products on Alanine Transaminase Levels in COVID-19 Patients: A Case–Control Study

Petrov et al., Safety and Risk of Pharmacotherapy, doi:10.30895/2312-7821-2025-458
Feb 2025  
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Case-control study of 1,296 hospitalized COVID-19 patients showing remdesivir associated with significantly increased ALT levels (OR 4.38, p<0.001).
Gérard, Zhou, Wu, Kamo, Choi, Kim show increased risk of acute kidney injury with remdesivir. Leo, Briciu, Muntean, Petrov show increased risk of liver injury with remdesivir.
Petrov et al., 26 Feb 2025, Israel, peer-reviewed, 3 authors. Contact: anastasiya.ryazanova@volgmed.ru.
This PaperRemdesivirAll
The Effect of Potentially Hepatotoxic Medicinal Products on Alanine Transaminase Levels in COVID-19 Patients: A Case–Control Study
Vladimir I Petrov, Anastasia Yu. Ryazanova, Natalia S Tokareva
Safety and Risk of Pharmacotherapy, doi:10.30895/2312-7821-2025-458
РЕЗЮМЕ ВВЕДЕНИЕ. Повышение активности печеночных ферментов часто встречается у пациентов с COVID-19. Разработка индивидуального подбора лекарственных препаратов с целью снижения риска гепатотоксичности требует изучения роли лекарственной терапии в развитии нарушений функции печени у пациентов с COVID-19. ЦЕЛЬ. Выявить наличие и степень выраженности связи между повышением активности аланиновой трансаминазы (АЛТ) и применением потенциально гепатотоксичных препаратов у госпитализированных пациентов с COVID-19 для дифференцированного выбора препаратов с учетом меньшего риска гепатотоксичности в практическом здравоохранении. МАТЕРИАЛЫ И МЕТОДЫ. Проанализированы 1296 медицинских карт пациентов, госпитализированных в инфекционный госпиталь Волгоградской области с диагнозом COVID-19 в 2020-2022 гг. Исследование «случай-контроль» выполнено с использованием метода подбора пар пациентов, идентичных по полу, возрасту, степени тяжести и исходу COVID-19. Среди пациентов с исходной активностью АЛТ <1 или 2 верхней границы нормы (ВГН) отбирали тех, у кого на протяжении всей госпитализации наблюдали повышение активности АЛТ ≥2, 3 и 5 ВГН (группы «случай») и пациентов с активностью АЛТ <2 ВГН (группы «контроль»). РЕЗУЛЬТАТЫ. Шанс обнаружения приема 3 или более лекарственных средств высокого риска лекарственного повреждения печени (ЛС ВР ЛПП) был значимо выше во всех группах «случай» по сравнению с контролем (отношение шансов (ОШ) 2,38 (1,54-3,67), р<0,001 для ≥3 ЛС ВР ЛПП и повышения активности АЛТ >2 ВГН при исходной <1 ВГН, 195 пар; ОШ 2,59 (1,48-4,53), р<0,001 для ≥3 ЛС ВР ЛПП и повышения активности АЛТ >3 ВГН при исходной <1 ВГН, 115 пар). Прием отдельных ЛС также значимо увеличивал риск повышения активности АЛТ >2 ВГН при исходной <1 ВГН (ремдесивир ОШ 4,38 (2,98-6,42), р<0,001; олокизумаб ОШ 7,83 (3,35-18,32), р<0,001; левилимаб ОШ 3,0 (1,19-7,56), р=0,014) и риск повышения активности АЛТ >3 ВГН при исходной <2 ВГН (ремдесивир ОШ 2,0 (1,21-3,30), р=0,006; олокизумаб ОШ 3,94 (2,35-6,62), р<0,001; левилимаб ОШ 2,67 (1,24-5,74), р=0,009). ВЫВОДЫ. Выявлена статистически значимая связь между повышением активности АЛТ и применением нескольких гепатотоксичных ЛС у госпитализированных пациентов с COVID-19. Необходимы проведение дальнейших исследований безопасности ЛС, применяемых для лечения COVID-19, и разработка мер по раннему выявлению и профилактике ЛПП.
Дополнительная информация. Таблица
References
Abajo, Montero, Madurga, Rodríguez, Acute and clinically relevant drug-induced liver injury: A population based case-control study, Br J Clin Pharmacol, doi:10.1111/j.1365-2125.2004.02133.x
Bessone, Dirchwolf, Rodil, Razori, Roma, Review article: Drug-induced liver injury in the context of nonalcoholic fatty liver disease -a physiopathological and clinical integrated view, Aliment Pharmacol Ther, doi:10.1111/apt.14952
Danan, Teschke, Drug-induced liver injury: Why is the Roussel Uclaf Causality Assessment Method (RUCAM) still used 25 years after its launch?, Drug Saf, doi:10.1007/s40264-018-0654-2
Danan, Teschke, RUCAM in drug and herb induced liver injury: The update, Int J Mol Sci, doi:10.3390/ijms17010014
Grjibovski, Ivanov, Gorbatova, Case-control studies in healthcare, Science & Healthcare
Jensen, Lauritzen, Vilstrup, Jepsen, Alanine aminotransferase and 20-year risk of major chronic diseases and death in a healthy cohort aged 30 to 49 years, Clin Epidemiol, doi:10.2147/CLEP.S241292
Li, Liu, Cheng, Yu, Li, COVID-19-associated liver injury: Clinical characteristics, pathophysiological mechanisms and treatment management, Biomed Pharmacother, doi:10.1016/j.biopha.2022.113568
Muhović, Bojović, Bulatović, Vukčević, Ratković et al., First case of drug-induced liver injury associated with the use of tocilizumab in a patient with COVID-19, Liver Int, doi:10.1111/liv.14516
Onakpoya, Heneghan, Aronson, Post-marketing withdrawal of 462 medicinal products because of adverse drug reactions: A systematic review of the world literature, BMC Med, doi:10.1186/s12916-016-0553-2
Papagiouvanni, Kotoulas, Pataka, Spyratos, Porpodis et al., COVID-19 and liver injury: an ongoing challenge, World J Gastroenterol, doi:10.3748/wjg.v29.i2.257
Petrov, Academician of the Russian Academy of Sciences
Petrov, Ayu, Privaltseva, Nekrasov, Polypharmacy in managment of in-patients with novel coronavirus disease (COVID-19), Pharmacy & Pharmacology, doi:10.19163/2307-9266-2022-10-3-267-277
Petrov, Ponomareva, Ivakhnenko, Razvalyaeva, Meshrqi et al., Etiopathogenetic aspects of liver injury in patients with COVID-19, Journal of Volgograd State Medical University, doi:10.19163/1994-9480-2020-4(76)-9-15
Schmilovitz-Weiss, Gingold-Belfer, Boltin, Beloosesky, Meyerovitch et al., Risk of mortality and level of serum alanine aminotransferase among community-dwelling elderly in Israel, Eur J Gastroenterol Hepatol, doi:10.1097/MEG.0000000000001225
Teschke, Méndez-Sánchez, Eickhoff, Liver injury in COV-ID-19 patients with drugs as causatives: A systematic review of 996 DILI cases published 2020/2021 based on RUCAM as causality Безопасность и риск фармакотерапии. 2025 assessment method, Int J Mol Sci, doi:10.3390/ijms23094828
Tokareva, None
Treem, Palmer, Lonjon-Domanec, Seekins, Dimick-Santos et al., Consensus guidelines: Best practic-es for detection, assessment and management of suspected acute drug-induced liver injury during clinical trials in adults with chronic viral hepatitis and adults with cirrhosis secondary to hepatitis B, C and nonalcoholic steatohepatitis, Drug Saf, doi:10.1007/s40264-020-01014-2
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Yu, Ryazanova, None, Cand. Sci. (Med.)
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Литература, None
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Петров, Рязанова, Привальцева, Некрасов, Полипрагмазия при лечении стационарных больных с новой коронавирусной инфекцией COVID-19, Фармация и фармакология
DOI record: { "DOI": "10.30895/2312-7821-2025-458", "ISSN": [ "2619-1164", "2312-7821" ], "URL": "http://dx.doi.org/10.30895/2312-7821-2025-458", "abstract": "<jats:p><jats:bold>INTRODUCTION.</jats:bold> Elevated liver enzyme levels are common in patients with COVID-19. Personalised prescribing to reduce the risk of hepatotoxicity requires studying the role of pharmacotherapy in the development of liver dysfunction in COVID-19 patients.</jats:p><jats:p><jats:bold>AIM.</jats:bold> This study aimed to identify the presence and strength of the relationship between an increase in alanine transaminase (ALT) levels and the use of potentially hepatotoxic medicinal products in hospitalised patients with COVID-19 to provide practising clinicians with a case-specific approach for selecting medicinal products with a lower risk of hepatotoxicity.</jats:p><jats:p><jats:bold>MATERIALS AND METHODS.</jats:bold> The authors analysed 1,296 medical records of COVID-19 patients who had been admitted to a Volgograd Region hospital for infectious diseases in 2020–2022. A case-control study was performed using the pair-matched case–control method, with pairs of patients matched by their sex, age, and COVID-19 severity and outcomes. The authors identified the medical records of COVID-19 patients with baseline alanine transaminase (ALT) levels &lt;1 or 2 times the upper limit of the normal range (ULN) and selected the medical records of the patients who had been having elevated ALT levels ≥2, 3, and 5 ULN (cases) or ALT levels &lt;2 ULN (controls) throughout their hospital stay.</jats:p><jats:p><jats:bold>RESULTS.</jats:bold> There was a significantly higher likelihood of detecting the use of ≥3 medicinal products associated with a high risk of drug-induced liver injury (DILI) in the medical records of all case groups than in those of the controls (odds ratio (OR)=2.38 (1.54–3.67), <jats:italic>p</jats:italic>&lt;0.001, for detecting the use of ≥3 high-risk medicinal products and an increase in ALT levels from &lt;1 ULN at baseline to &gt;2 ULN, 195 pairs; OR=2.59 (1.48–4.53), <jats:italic>p</jats:italic>&lt;0.001, for detecting the use of ≥3 high-risk medicinal products and an increase in ALT levels from &lt;1 ULN at baseline to &gt;3 ULN, 115 pairs). Certain medicinal products were associated with a significant increase in the risk of ALT rising to levels &gt;2 ULN in patients with baseline levels &lt;1 ULN (remdesivir: OR=4.38 (2.98–6.42), <jats:italic>p</jats:italic>&lt;0.001; olokizumab: OR=7.83 (3.35–18.32), <jats:italic>p</jats:italic>&lt;0.001; and levilimab: OR=3.0 (1.19–7.56), <jats:italic>p</jats:italic>=0.014) and levels &gt;3 ULN in patients with baseline levels &lt;2 ULN (remdesivir: OR=2.0 (1.21–3.30), <jats:italic>p</jats:italic>=0.006; olokizumab: OR=3.94 (2.35–6.62), <jats:italic>p</jats:italic>&lt;0.001; and levilimab: OR=2.67 (1.24–5.74), <jats:italic>p</jats:italic>=0.009).</jats:p><jats:p><jats:bold>CONCLUSIONS.</jats:bold> According to this study, there is a statistically significant association between elevated ALT levels in hospitalised COVID-19 patients and the use of several hepatotoxic medicines. Further studies are required to assess the safety of medicines used to treat COVID-19. It is also necessary to develop methods for the early detection and prevention of DILI.</jats:p>", "author": [ { "ORCID": "https://orcid.org/0000-0002-0258-4092", "affiliation": [ { "name": "Volgograd State Medical University" } ], "authenticated-orcid": true, "family": "Petrov", "given": "V. I.", "sequence": "first" }, { "ORCID": "https://orcid.org/0000-0002-4778-5015", "affiliation": [ { "name": "Volgograd State Medical University" } ], "authenticated-orcid": true, "family": "Ryazanova", "given": "A. Yu.", "sequence": "additional" }, { "ORCID": "https://orcid.org/0000-0002-2578-6228", "affiliation": [ { "name": "Volgograd State Medical University" } ], "authenticated-orcid": true, "family": "Tokareva", "given": "N. 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