Hepatitis B and renal function: A matched study comparing non-hepatitis B, untreated, treated and cirrhotic hepatitis patients.


Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
04 2019
Historique:
received: 23 04 2018
revised: 17 10 2018
accepted: 26 10 2018
pubmed: 22 11 2018
medline: 19 5 2020
entrez: 22 11 2018
Statut: ppublish

Résumé

Renal impairment is associated with chronic hepatitis B (CHB). To overcome prior study design differences, we used propensity score matching to balance the non-CHB and CHB cohorts and generalized linear modelling (GLM, models using probit and logit linking functions for complex models) to evaluate the effect of CHB, treatment and cirrhosis on renal function. A retrospective cohort (1996-2017) from one U.S. university medical centre. Included patients had ≥12 months of serial creatinine laboratories and a baseline estimated glomerular filtration rate (eGFR, by the Modification of Diet in Renal Disease Study equation) ≥60 mL/min/1.73 m Adjusted mean eGFR was significantly higher for non-CHB vs. untreated CHB patients (eGFR 87.4 vs. 85.6, P= 0.004, n = 580, median follow-up = 82 months). A significant difference in adjusted mean eGFR between untreated vs. entecavir (ETV)-treated CHB patients (eGFR 85.1 vs. 83.5, P= 0.02, n = 340, median follow-up = 70 months) was found among non-cirrhotic CHB. Among treated CHB, there was no difference in adjusted mean eGFR between non-cirrhotic vs. cirrhotic patients (eGFR 77.0 vs. 76.5; P= 0.66, n = 112, median follow-up = 58 months). After PSM and GLM, the significant predictors for worsening renal function were age, hypertension and diabetes mellitus but not CHB, ETV or cirrhosis. However, given small sample size, data regarding the use of ETV in patients with cirrhosis should be interpreted with caution and requires additional investigation.

Sections du résumé

BACKGROUND & AIM
Renal impairment is associated with chronic hepatitis B (CHB). To overcome prior study design differences, we used propensity score matching to balance the non-CHB and CHB cohorts and generalized linear modelling (GLM, models using probit and logit linking functions for complex models) to evaluate the effect of CHB, treatment and cirrhosis on renal function.
METHODS
A retrospective cohort (1996-2017) from one U.S. university medical centre. Included patients had ≥12 months of serial creatinine laboratories and a baseline estimated glomerular filtration rate (eGFR, by the Modification of Diet in Renal Disease Study equation) ≥60 mL/min/1.73 m
RESULTS
Adjusted mean eGFR was significantly higher for non-CHB vs. untreated CHB patients (eGFR 87.4 vs. 85.6, P= 0.004, n = 580, median follow-up = 82 months). A significant difference in adjusted mean eGFR between untreated vs. entecavir (ETV)-treated CHB patients (eGFR 85.1 vs. 83.5, P= 0.02, n = 340, median follow-up = 70 months) was found among non-cirrhotic CHB. Among treated CHB, there was no difference in adjusted mean eGFR between non-cirrhotic vs. cirrhotic patients (eGFR 77.0 vs. 76.5; P= 0.66, n = 112, median follow-up = 58 months).
CONCLUSION
After PSM and GLM, the significant predictors for worsening renal function were age, hypertension and diabetes mellitus but not CHB, ETV or cirrhosis. However, given small sample size, data regarding the use of ETV in patients with cirrhosis should be interpreted with caution and requires additional investigation.

Identifiants

pubmed: 30460749
doi: 10.1111/liv.14009
doi:

Substances chimiques

Antiviral Agents 0
entecavir 5968Y6H45M
Guanine 5Z93L87A1R
Creatinine AYI8EX34EU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

655-666

Informations de copyright

© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Auteurs

Vinh Vu (V)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Sam Trinh (S)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

An Le (A)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Tiffani Johnson (T)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Joseph Hoang (J)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Donghak Jeong (D)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Linda Henry (L)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Scott Barnett (S)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Ramsey Cheung (R)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

Mindie H Nguyen (MH)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Stanford, California.

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Classifications MeSH