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Renal tubular dysfunction during long‐term adefovir or tenofovir therapy in chronic hepatitis B
Author(s) -
Gara N.,
Zhao X.,
Collins M. T.,
Chong W. H.,
Kleiner D. E.,
Jake Liang T.,
Ghany M. G.,
Hoofnagle J. H.
Publication year - 2012
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/j.1365-2036.2012.05093.x
Subject(s) - adefovir , medicine , entecavir , renal function , creatinine , urology , tenofovir , gastroenterology , proteinuria , urinary system , hepatitis b , kidney , chronic hepatitis , endocrinology , lamivudine , virology , virus , human immunodeficiency virus (hiv)
Summary Background Adefovir and tenofovir are nucleotide analogues used as long‐term therapy of chronic hepatitis B. Side effects are few, but prolonged and high‐dose therapy has been associated with proximal renal tubular dysfunction ( RTD ). Aim To assess the incidence of RTD during long‐term nucleotide therapy of chronic hepatitis B. Methods A total of 51 patients being treated at the C linical C enter, N ational I nstitutes of H ealth were studied. Diagnosis of RTD required de novo appearance of at least three of five features: hypophosphataemia, hypouricaemia, serum creatinine elevation, proteinuria or glucosuria. Results Among 51 patients treated for 1–10 (mean 7.4) years with adefovir ( n = 42), tenofovir ( n = 4) or adefovir followed by tenofovir ( n = 5), 7 (14%) developed RTD . Time to onset ranged from 22 to 94 (mean 49) months with an estimated 10‐year cumulative rate of 15%. All seven had low urinary percent maximal tubular reabsorption of phosphate (<82%). Patients with RTD were older (58 vs. 44 years; P = 0.01) and had lower baseline glomerular filtration rates (82 vs. 97 cc/min; P = 0.08) compared to those without; but did not differ in other features. Six patients with RTD were switched to entecavir, all subsequently had improvements in serum phosphate (2.0–3.0 mg/dL), creatinine (1.6–1.1 mg/dL), uric acid (2.7–3.8 mg/dL) and proteinuria. Conclusions Renal tubular dysfunction develops in 15% of patients treated with adefovir or tenofovir for 2–9 years and is partially reversible with change to other antivirals. Monitoring for serum phosphate, creatinine and urinalysis is prudent during long‐term adefovir and tenofovir therapy.