Efficacy and safety of entecavir for hepatitis B virus-associated glomerulonephritis with renal insufficiency.


Journal

Clinical and experimental nephrology
ISSN: 1437-7799
Titre abrégé: Clin Exp Nephrol
Pays: Japan
ID NLM: 9709923

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 17 09 2022
accepted: 13 04 2023
medline: 19 7 2023
pubmed: 28 4 2023
entrez: 28 4 2023
Statut: ppublish

Résumé

HBV-GN is one of the most common secondary kidney diseases in China. Entecavir is a first-line antiviral therapy in patients with HBV-GN. This retrospective study explored whether entecavir is effective and safe for the treatment of HBV-GN with renal insufficiency. We screened patients diagnosed with HBV-GN in The Affiliated Hospital of Qingdao University who had elevated serum creatinine levels. Group 1 (30 patients) was given entecavir as antiviral treatment. Group 2 (28 patients) was treated with ARBs. Changes in renal function and the possible influencing factors were observed, with a mean follow-up duration of 36 months. At the end of follow-up, the elevation in the serum creatinine level and reduction in the eGFR were greater in group 1 than in group 2. The overall renal survival rate, using eGFR < 15 ml/min as the primary renal end point, was 96.7% in group 1 and 67.9% in group 2. Urine protein excretion was decreased in both groups. Treatment with entecavir and the remission of proteinuria were protective factors against renal function impairment, while a lower baseline eGFR was a risk factor for progression to ESRD. Entecavir slows the progression of renal function impairment in HBV-GN and exerts a significant renal protective effect.

Sections du résumé

BACKGROUND BACKGROUND
HBV-GN is one of the most common secondary kidney diseases in China. Entecavir is a first-line antiviral therapy in patients with HBV-GN.
OBJECTIVE OBJECTIVE
This retrospective study explored whether entecavir is effective and safe for the treatment of HBV-GN with renal insufficiency.
METHODS METHODS
We screened patients diagnosed with HBV-GN in The Affiliated Hospital of Qingdao University who had elevated serum creatinine levels. Group 1 (30 patients) was given entecavir as antiviral treatment. Group 2 (28 patients) was treated with ARBs. Changes in renal function and the possible influencing factors were observed, with a mean follow-up duration of 36 months.
RESULTS RESULTS
At the end of follow-up, the elevation in the serum creatinine level and reduction in the eGFR were greater in group 1 than in group 2. The overall renal survival rate, using eGFR < 15 ml/min as the primary renal end point, was 96.7% in group 1 and 67.9% in group 2. Urine protein excretion was decreased in both groups. Treatment with entecavir and the remission of proteinuria were protective factors against renal function impairment, while a lower baseline eGFR was a risk factor for progression to ESRD.
CONCLUSIONS CONCLUSIONS
Entecavir slows the progression of renal function impairment in HBV-GN and exerts a significant renal protective effect.

Identifiants

pubmed: 37115381
doi: 10.1007/s10157-023-02351-z
pii: 10.1007/s10157-023-02351-z
doi:

Substances chimiques

entecavir 5968Y6H45M
Creatinine AYI8EX34EU
Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

680-686

Subventions

Organisme : National Natural Science Foundation of China
ID : 81870494

Informations de copyright

© 2023. The Author(s), under exclusive licence to The Japanese Society of Nephrology.

Références

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Auteurs

Yani Yu (Y)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Lingyu Xu (L)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Ting Xu (T)

Department of Gerontology, The 971th Hospital of PLA, Qingdao, 266071, Shandong, China.

Chengyu Yang (C)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Quandong Bu (Q)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Wei Zhang (W)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Long Zhao (L)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Yan Xu (Y)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China.

Wei Jiang (W)

Department of Nephrology, The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, China. jiangwei866@qdu.edu.cn.

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