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http://dx.doi.org/10.5487/TR.2017.33.4.343

Lamivudine Therapy Exacerbates Bilirubinemia in Patients Underlying Severely Advanced Hepatitis  

Choi, Young Hee (College of Pharmacy, Dongguk University_Seoul)
Lee, Chang Ho (Department of Pharmacology, College of Medicine, Hanyang University)
Ko, Myong Suk (Korea Intellectual Property Strategy Agency, Business Cooperation Team)
Han, Hyun Joo (Department of Pharmacy, Seoul National University Hospital)
Kim, Sang Geon (Department of Pharmacy, Seoul National University Hospital)
Publication Information
Toxicological Research / v.33, no.4, 2017 , pp. 343-350 More about this Journal
Abstract
Lamivudine belongs to the set of antiviral agents effective against hepatitis B virus infection. Given case reports on liver injuries after certain antiviral agent treatments, this study examined the effects of lamivudine on alanine aminotransferase (ALT) and total bilirubin (TB) using a medical system database. A total of 1,321 patients taking lamivudine alone or with others were evaluated using laboratory hits in an electronic medical system at Seoul National University Hospital from 2005 through 2011. The patients were grouped according to prior ALT results: G#1, ALT < 40 IU/L; G#2, 40 IU/L ${\leq}$ ALT < 120 IU/L; G#3, 120 IU/L ${\leq}$ ALT < 240 IU/L; and G#4, ALT ${\geq}$ 240 IU/L. In G#1 and G#2 patients, lamivudine or adefovir treatment decreased ALT and TB compared to prior values. In G#3 and G#4 patients with three times the upper limit of normal (ULN) ${\leq}$ ALT < 15 times the ULN, both ALT and TB were decreased after treatment with lamivudine alone, or adefovir following lamivudine therapy, indicating that lamivudine therapy ameliorated liver functions. However, in G#4 patients who experienced severely advanced hepatitis (ALT ${\geq}$ 15 times the ULN, or ${\geq}$ 600 IU/L), lamivudine augmented TBmax ($6.3{\rightarrow}13.3mg/dL$) despite a slight improvement in ALT ($839{\rightarrow}783IU/L$), indicative of exacerbation of bilirubinemia. Patients who used adefovir after lamivudine also showed a high incidence of hyperbilirubinemia when they experienced severely advanced hepatitis. Treatment with adefovir alone did not show the effect. In conclusion, lamivudine may increase the risk of hyperbilirubinemia in patients with severely advanced hepatitis, implying that caution should be exercised when using lamivudine therapy in certain patient populations.
Keywords
Lamivudine; Drug-associated hyperbilirubinemia; Laboratory signal hits; Total bilirubin; ALT;
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1 Jha, A.K., Kuperman, G.J., Teich, J.M., Leape, L., Shea, B., Rittenberg, E., Burdick, E., Seger, D.L., Vander Vliet, M. and Bates, D.W. (1998) Identifying adverse drug events: development of a computer-based monitor and comparison with chart review and stimulated voluntary report. J. Am. Med. Inform. Assoc., 5, 305-314.   DOI
2 Kohn, L.T., Corrgan, J.M. and Donaldson, M.S. (1999) To Err in Human: Building a Safer Health System, National Academy Press, Washington, D.C.
3 Cousins, D. and Baker, M. (2004) The work of the National Patient Safety Agency to improve medication safety. Br. J. Gen. Pract., 54, 331-333.
4 Verhaz, A. (2014) Experience with lamivudine treatment for severe acute hepatitis B. Srp. Arh. Celok. Lek., 142, 703-707.   DOI
5 Lee, Y.H., Kang, U.G. and Park, R.W. (2008) Development of adverse drug event surveillance system using BI technology. Int. J. Contents, 9, 106-113.
6 Rodriguez-Monguio, R., Otero, M.J. and Rovira, J. (2003) Assessing the economic impact of adverse drug effects. Pharmacoeconomics, 21, 623-650.   DOI
7 Tisdale, J.E. and Miller, D.A. (2005) Drug-Induced Diseases. Prevention, Detection and Management, Ameritan Society of Health-System Pharmacist Press, Bethesda, Maryland, p. 1004.
8 Ah, Y.M., Kim, Y.H., Kim, M.-J., Choi, Y.H., Park, K.H., Son, I.J. and Kim, S.G. (2008) Drug-induced hyperbilirubinemia and the clinical influencing factors. Drug Metab. Rev., 40, 511-537.   DOI
9 Kaplowitz, N. (2003) Drug-induced liver disorders: introduction and overview in Drug-Induced Liver Disease (Kaplowitz, N. and Deleve, L.D. Eds.). Marcel Dekker Inc., New York, pp. 150-158.
10 Zimmerman, H.J. (1999) Hepatotoxicity. The Adverse Effects of Drugs and Other Chemicals on the Liver (2nd edition), Lippincott Williams & Wilkins, Philadelphia, pp. 235-249.
11 Li, X., Jie, Y., You, X., Shi, H., Zhang, M., Wu, Y., Lin, G., Li, X., Gao, Z. and Chong, Y. (2015) Optimized combination therapies with adefovir dipivoxil (ADV) and lamivudine, telbivudine, or entecavir may be effective for chronic hepatitis B patients with a suboptimal response to ADV monotherapy. Int. J. Clin. Exp. Med., 8, 21062-21070.
12 Pradeep Kumar, S., Medhi, S., Asim, M., Das, B.C., Gondal, R. and Kar, P. (2011) Evaluation of adefovir & lamivudine in chronic hepatitis B: correlation with HBV viral kinetic, hepatic-necro inflammation & fibrosis. Indian J. Med. Res., 133, 50-56.
13 Wang, G.L., Liu, Y., Qiu, P., Zhou, S.F., Xu, L.F., Wen, P., Wen, J.B. and Xiao, X.Z. (2016) Cost-effectiveness of Lamivudine, Telbivudine, Adefovir Dipivoxil and Entecavir on decompensated hepatitis B virus-related cirrhosis. Eur. Rev. Med. Pharmacol. Sci., 20, 866-872.
14 Korenblat, K.M. and Berk, P.D. (2005) Hyperbilirubinemia in the setting of antiviral therapy. Clin. Gastroenterol. Hepatol., 3, 303-310.   DOI
15 Zhang, C., Ke, W., Liu, L., Gao, Y., Yao, Z., Ye, X., Zhou, S. and Yang, Y. (2016) Cost-effectiveness comparison of lamivudine plus adefovir combination treatment and nucleos(t)ide analog monotherapies in Chinese chronic hepatitis B patients. Drug Des. Devel. Ther., 10, 897-910.
16 Leung, N.W.Y., Lai, C.-L., Chang, T.-T., Guan, R., Lee, C.-M., Ng, K.-Y., Lim, S.-G., Wu, P.C., Dent, J.C., Edmundson, S., Condreay, L.D. and Chien, R.N. (2001) Extended lamivudine treatment in patients with chronic hepatitis B enhances hepatitis B e antigen seroconversion rates: results after 3 years of therapy. Hepatology, 33, 1527-1532.   DOI
17 Perrillo, R., Schiff, E., Yoshida, E., Statler, A., Hirsch, K., Wright, T., Gutfreund, K., Lamy, P. and Murray, A. (2000) Adefovir dipivoxil for the treatment of lamivudine-resistant hepatitis B mutants. Hepatology, 32, 129-134.
18 Wan, Z., Wu, Y., Yi, J., You, S., Liu, H., Sun, Z., Zhu, B., Zang, H., Li, C., Liu, F., Li, D., Mao, Y. and Xin, S. (2015) Combining serum cystatin C with total bilirubin improves short-term mortality prediction in patients with HBV-related acute-on-chronic liver failure. PLoS ONE, 10, e0116968.   DOI
19 Kudo, M., Todo, A., Ikekubo, K., Hino, M., Yonekura, Y., Yamamoto, K. and Torizuka, K. (2014) Functional hepatic imaging with receptor-binding radiopharmaceutical: clinical potential as a measure of functioning hepatocyte mass. Gastroenterol. Jpn., 26, 734-741.
20 Rowland, A., Mackenzie, P.I. and Miners, J.O. (2015) Transporter-mediated uptake of UDP-glucuronic acid by human liver microsomes: assay conditions, kinetics, and inhibition. Drug Metab. Dispos., 43, 147-153.
21 Tsubota, A., Arase, Y., Saitoh, S., Kobayashi, M., Suzuki, Y., Suzuki, F., Chayama, K., Murashima, N., Ikeda, K., Kobayashi, M. and Kumada, H. (2001) Lamivudine therapy for spontaneously occurring severe acute exacerbation in chronic hepatitis B virus infection: a preliminary study. Am. J. Gastroenterol., 96, 557-562.   DOI
22 Pirmohamed, M., James, S., Meakin, S., Green, C., Scott, A.K., Walley, T.J., Farrar, K., Park, B.K. and Breckenridge, A.M. (2004) Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients. BMJ, 329, 15-19.   DOI
23 Lazarous, J., Pomeranz, B. and Corey, P.N. (1998) Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA, 279, 1200-1205.   DOI
24 Mauben, M., Madigan, D., Gerritis, C.M. (2007) The role of data mining in pharmacovigilance. Expert Opin. Drug Saf., 14, 929-948.
25 Liu, C., Ye, J., Jia, H., Zhang, M., Han, H., Chen, F. and Chen, C. (2013) Entecavir and lamivudine therapy for severe acute chronic hepatitis B. Exp. Ther. Med., 5, 545-548.   DOI
26 Peters, M.G., Hann, H.W., Martin, P., Heathcote, E.J., Buggisch, P., Rubin, R., Bourliere, M., Kowdley, K., Trepo, C., Gray, D.F., Sullivan, M., Kleber, K., Ebrahimi, R., Xiong, S. and Brosgart, C.L. (2004) Adefovir dipivoxil alone or in combination with lamivudine in patients with lamivudine-resistant chronic hepatitis B. Gastroenterology, 126, 91-101.   DOI
27 Uglietti, A., Zanaboni, D., Gnarini, M. and Maserati, R. (2013) Emtricitabine/tenofovir in the treatment of HIV infection: current PK/PD evaluation. Expert Opin. Drug Metab. Toxicol., 8, 1305-1314.
28 Andreea, F. and Marius, B. (2009) Adverse drug reactions in clinical practice: a causality assessment of a case of druginduced pancreatitis. J. Gastrointest. Liver Dis., 18, 353-358.
29 Barcena, R., Del Campo, S., Moraleda, G., Casanovas, T., Prieto, M., Buti, M., Moreno, J.M., Cuervas, V., Fraga, E., De la Mata, M., Otero, A., Delgado, M., Loinaz, C., Barrios, C., Dieguez, M.L., Mas, A., Sousa, J.M., Herrero, J.I., Muñoz, R., Avilés, J.F., Gonzalez, A. and Rueda, M. (2005) Study on the efficacy and safety of adefovir dipivoxil treatment in postliver transplant patients with hepatitis B virus infection and lamivudine-resistant hepatitis B virus. Transplant. Proc., 37, 3960-3962.   DOI
30 Ben-Ari, Z., Mor, E. and Tur-Kaspa, R. (2003) Experience with lamivudine therapy for hepatitis B virus infection before and after liver transplantation, and review of the literature. J. Intern. Med., 253, 544-552.   DOI
31 Bonkovsky, H.L., Azar, R., Bird, S., Szabo, G. and Banner, B. (2002) Severe cholestatic hepatitis caused by thiazolidinediones: risks associated with substituting rosiglitazone for troglitazone. Dig. Dis. Sci., 47, 1632-1637.   DOI
32 Brickford, C.L. and Spencer, A.P. (2005) Biliary sludge and hyperbilirubinemia associated with ceftriaxone in an adult: case report and review of the literature. Pharmacotherapy, 25, 1389-1395.   DOI
33 Thompson, P.D., Clarkson, P. and Karas, R.H. (2003) Statinassociated myopathy. JAMA, 289, 1681-1690.   DOI
34 Willens, H.J. (2000) Clopidogrel-induced mixed hepatocellular and cholestatic liver injury. Am. J. Ther., 7, 317-318.   DOI