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21
LONGITUDINAL REAL-WORLD STUDY ON ESTIMATED
GLOMERULAR FILTRATION RATE (EGFR) CHANGES IN
ENTECAVIR (ETV) VERSUS TENOFOVIR DISOPROXIL
FUMARATE (TDF)-TREATED CHRONIC HEPATITIS B (CHB)
PATIENTS: A REAL-B STUDY
Lung Yi Mak1, Joseph Hoang2, Dae Won Jun3, Chien Hung
Chen4, Cheng-Yuan Peng5, Ming-Lun Yeh6, Sung Eun Kim7,
Jae Yoon Jeong8, Eileen Yoon9, Hyunwoo Oh10, Pei-Chien
Tsai11, Chung-Feng Huang12, Sang Bong Ahn13, Qing Xie14,
Grace Lai-Hung Wong15, Masaru Enomoto16, Huy Trinh17,
Jae-Jun Shim18, Dong Hyun Lee19, Li Liu20, Ritsuzo Kozuka16,
Yong Kyun Cho21, Soung Won Jeong22, Hyoung Su Kim23,
Rui Huang24, Rex Wan-Hin Hui1, Vivien Tsui1, Eiichi Ogawa25,
Chia-Yen Dai12, Jee-Fu Huang26, Ramsey Cheung27, Chao
Wu28, Wan-Long Chuang29, Ming-Lung Yu12, Man Fung Yuen1
and Mindie H. Nguyen30, (1)Medicine, The University of
Hong Kong, (2)Division of Gastroenterology and Hepatology,
Stanford University Medical Center, (3)Hanyang University,
(4)Division of Hepatogastroenterology, Department of Internal
Medicine, Kaohsiung Chang Gung Memorial Hospital, (5)
Division of Hepatology and Gastroenterology, Department
of Internal Medicine, China Medical University Hospital,
(6)Department of Internal Medicine, Kaohsiung Medical
University Hospital, (7)Department of Internal Medicine,
Hallym University Sacred Heart Hospital, (8)Department of
Internal Medicine, Hanyang University College of Medicine,
Guri Hospital, (9)Inje University Sanggye Paik Hospital,
(10)Department of Internal Medicine,, Hanyang University
Hospital, (11)Hepatobiliary Division, Department of Internal
Medicine, Kaohsiung Medical University Hospital, Kaohsiung
Medical University, (12)Hepatobiliary Division, Department
of Internal Medicine, Kaohsiung Medical University Hospital,
Kaohsiung Medical University, Kaohsiung, Taiwan, (13)
Department of Internal Medicine, Eulji University School
of Medicine, (14)Shanghai Jiaotong University School of
Medicine, Ruijin Hospital, China, (15)Department of Medicine
and Therapeutics, Medical Data Analytic Centre (MDAC),
Institute of Digestive Disease, The Chinese University of Hong
Kong, (16)Department of Hepatology, Osaka City University
Graduate School of Medicine, (17)San Jose Gastroenterology,
(18)Department of Internal Medicine, Kyung Hee University
Hospital, (19)Gastroenterology, Good Gang-an Hospital,
(20)Hepatology, The Third Hospital of Kumming City, (21)
Department of Internal Medicine, Sungkyunkwan University
School of Medicine, (22)Department of Internal Medicine,
College of Medicine, Soonchunhyang University, (23)Internal
Medicine, Hallym University Kangdong Sacred Heart Hospital,
(24)Department of Infectious Diseases, Nanjing Drum Tower
Hospital, the Affiliated Hospital of Nanjing University Medical
School, (25)Department of General Internal Medicine, Kyushu
University Hospital, (26)Faculty of Internal Medicine and
Hepatitis Research Center, College of Medicine, and Center
for Cohort Study, Kaohsiung Medical University, Kaohsiung,
Taiwan, (27)Division of Gastroenterology and Hepatology,
Department of Medicine, Stanford University Medical Center
(28)Department of Infectious Diseases, Nanjing Drum Tower
Hospital, (29)Hepatobiliary Division, Department of Internal
Medicine, Kaohsiung Medical University Hospital, Kaohsiung,
Taiwan, (30)Gastroenterology and Hepatology, Stanford
University Medical Center
Background: Decreased renal function is sometimes
observed in CHB patients maintained on long-term oral
antiviral therapy, and it is controversial whether TDF is more
renal toxic than ETV We aimed to compare the longitudinal
eGFR changes of ETV vs TDF patients and to identify factors
associated with eGFR changes
Methods: We performed
a retrospective study of 4983 adult treatment-naïve CHB
patients who were initiated on TDF (n=1790) or ETV
(n=3193) then observed for ≥12 months at 22 centers from
the US, HK, Korea, Taiwan, Japan and Mainland China We
assessed eGFR (mL/min/1 73m2) using the CKD-EPI formula
at baseline and about every 6 months ETV and TDF patients
were balanced via propensity score matching (PSM) on age,
gender, DM, HTN, cirrhosis, baseline eGFR, and follow-up
duration We used multivariable generalized linear modeling
(GLM) to adjust mean eGFR during follow up for cirrhosis,
HTN, and DM, and multivariable Cox regression to identify
factors associated with decreased renal function by at least
one CKD stage as per KDIGO staging (eGFR >90 for stage 1,
60-89 stage 2, 45-59 stage 3a, 30-44 stage 3b, and <30 stage
4/5) .
Results: In the total cohort (mean age 48 9 years, 66 7%
male), DM, HTN, and cirrhosis were respectively present in
13 1%, 21 2%, and 43 9% of the ETV group as compared to
10 7%, 17%, 29 7% for the TDF group (P<0 05) The baseline
eGFR was higher for the TDF vs ETV group (76 9 vs 74 1,
P=0 018) PSM yielded 1406 pairs of ETV or TDF patients
with baseline eGFR ≥60 and 357 pairs for the eGFR<60
group Multivariable GLM analysis of the total (unmatched)
cohort as well as the matched eGFR ≥60 and matched
eGFR <60 cohorts revealed lower adjusted mean eGFRs in
TDF (vs ETV) patients (all P<0 01; Figures 1A-C), though
the mean eGFR difference was small in all comparisons
(1 2-3 1 mL/min/1 73m2). Among PSM eGFR≥60 patients,
the 5-year cumulative incidence of renal impairment were
45 08% for ETV and 49 8% for TDF (P=0 0039; Figure 1D) In
multivariable Cox regression, TDF (HR 1 41), higher baseline
eGFR (HR 0 99), older age (HR 1 02), male (HR 2 16),
presence of DM or HTN (HR 1 4), and higher FIB-4 score
(HR 1 02) were all associated with worsening renal function
by at least one CKD stage Conclusion: TDF was associated
with lower mean eGFR throughout the 5-year on-treatment
follow-up and independently associated with incident renal
impairment, suggesting cautious use especially in those at
high risk for renal injury
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