Gut Liver. 2020;14(2):225-231.
Long-term Nucleotide Analogue Treatment Has Higher Levels of Renal Toxicities than Does Entecavir in Patients with Chronic Hepatitis B.
제1저자 조영윤 · 교신저자 김윤준
소속 (2)
- Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
- Department of Internal Medicine, Chung-Ang University Hospital, Seoul, Korea.
Abstract
BACKGROUND/AIMS Renal toxicity is a concern in patients with chronic hepatitis B taking nucleotide analogues, such as adefovir (ADV) and tenofovir disoproxil fumarate (TDF). We sought to determine the long-term renal effects of nucleotide analogue treatment versus entecavir (ETV) treatment.
METHODS In this retrospective single-center study, we selected 87 patients who were treated with ADV and subsequently with TDF from June 2008 to December 2013. ETV-treated patients were matched by treatment duration. We analyzed the creatinine increase over 0.5 mg/dL, glomerular filtration rate (GFR) decrease over 25%, phosphorus decrease under 2.0 mg/dL, and dose reduction of antiviral agents.
RESULTS The median follow-up period was 60.0 months for both groups. The incidence of liver cirrhosis was higher in the ADV-TDF group than in the ETV group (32.2% vs 74.7%, p<0.01). Creatinine increased in both groups during follow-up, but the difference was not significant (5.7% and 2.3%, p=0.44). In addition, GFR decreased more often in the ADV-TDF group than in the ETV group (31.0% and 14.9%, p=0.01). After multivariate Cox regression analysis, ADV-TDF treatment was significantly associated with a GFR decrease over 25% (hazard ratio, 2.10; 95% confidence interval, 1.08 to 4.10; p=0.03) after adjusting for the baseline GFR decrease.
CONCLUSIONS Patients taking nucleotide analogues had a significantly higher number of renal events than did those taking ETV. Clinicians should be aware of the development of renal toxicity in this patient population. Further long-term studies are warranted.
Keywords
Antiviral agentsGuanineHepatitis B, chronicKidney diseases
Figures
그림 출처: PubMed Central 공개 논문 (PMC7096224)
Conflict of interest statement
CONFLICTS OF INTEREST. J.H.Y. has received a research grant from Bayer HealthCare Pharmaceuticals; Y.J.K. has received research grants from Bristol-Myers Squibb, Roche, JW CreaGene, Bukwang Pharmaceuticals, Handok Pharmaceuticals, Hanmi Pharmaceuticals, Yuhan Pharmaceuticals, and Pharmaking, and has received lecture fees from Bayer HealthCare Pharmaceuticals, Gilead Science, MSD Korea, Yuhan Pharmaceuticals, Samil Pharmaceuticals, CJ Pharmaceuticals, Bukwang Pharmaceuticals, and Handok Pharmaceuticals; and S.J.Y. has received a lecture fee from Bayer HealthCare Pharmaceuticals. The other authors declare that they have no conflicting interests.
그 밖의 정보
- 출판 형태
- Evaluation Study, Journal Article
- 저널
- Gut and liver · eISSN 2005-1212
- MeSH
- Adenine / adverse effects / analogs & derivatives · Adult · Aged · Antiviral Agents / adverse effects · Chemical and Drug Induced Liver Injury / epidemiology / etiology · Female · Glomerular Filtration Rate · Guanine / adverse effects / analogs & derivatives · Hepatitis B virus* · Hepatitis B, Chronic / drug therapy · Humans · Incidence · Male · Middle Aged · Nucleotides / adverse effects · Organophosphonates / adverse effects · Proportional Hazards Models · Retrospective Studies · Tenofovir / adverse effects · Time Factors · Treatment Outcome
- Substances
- Antiviral Agents · Nucleotides · Organophosphonates · entecavir · Guanine · adefovir · Tenofovir · Adenine
- 참고문헌
- 25편