Korean J Transplant.  2020 Dec;34(Supple 1):S10. 10.4285/ATW2020.OR-1240.

Renal safety of tenofovir disoproxil fumarate and entecavir in liver transplant patients: a nationwide Korean registry study

Affiliations
  • 1Division of Transplantation, Department of Surgery, Severance Hospital, Seoul, Korea
  • 2Division of Hepatobiliary, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
  • 3Division of Hepatobiliary, Department of Surgery, Seoul National University Hospital, Seoul, Korea
  • 4Division of Transplantation, Department of Surgery, Samsung Medical Center, Seoul, Korea
  • 5Division of Hepatobiliary, Department of Surgery, Pusan National University Yangsan Hospital, Yangsan, Korea
  • 6Division of Hepatobiliary, Department of Surgery, Ajou University School of Medicine, Suwon, Korea
  • 7Division of Hepatobiliary, Department of Surgery, Daegu Catholic University Medical Center, Daegu, Korea
  • 8Division of Hepatobiliary, Department of Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
  • 9Division of Hepatobiliary, Department of Surgery, Korea University College of Medicine, Seoul, Korea

Abstract

Background
Entecavir and tenofovir are currently the first-line drugs in liver transplantation (LT) patients for the prevention of hepatitis B virus recurrence. Despite its proven efficacy, the renal safety of tenofovir in LT patients has not been well defined. We aimed to assess the impact of tenofovir on renal function compared to that of entecavir after LT.
Methods
We analyzed 817 LT patients treated with entecavir (n=366) or tenofovir (n=451) between 2014 and 2017. The estimated glomerular filtration rate (eGFR) was calculated using the Chronic Kidney Disease Epidemiology Collaboration equation. Renal function deterioration was defined as progression of chronic kidney disease stage and ≥20% eGFR decline from 1 month after LT.
Results
Mean eGFR at 1 month after LT was 91.1±22.0 mL/min/1.73 ㎡ for entecavir and 89.1±23.7 mL/min/1.73 ㎡ for tenofovir group (P=0.312). During a median follow-up of 29 months, the cumulative incidence of renal function deterioration was significantly higher in the tenofovir group than in the entecavir group (355.5% vs. 27.1%, P=0.01). Tenofovir (odd ratio [OR], 1.52; 95% confidence interval [CI], 1.11–2.08; P=0.009), old age (OR, 1.45; 95% CI, 1.01–2.09; P=0.044), low body mass index (OR, 2.02; 95% CI, 1.44–2.84; P<0.001), and diabetes mellitus (OR, 1.68; 95% CI, 1.18–2.08; P=0.009) were independent risk factors for renal function deterioration.
Conclusions
The use of tenofovir was significantly associated with renal function deterioration in LT patients. In the setting of LT, tenofovir should be used with caution in high-risk patients and renal function should be carefully monitored.

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