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Medicine (Baltimore). 2016;95(21):e3671.

Pretransplant Hepatitis B Viral Infection Increases Risk of Death After Kidney Transplantation: A Multicenter Cohort Study in Korea.

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제1저자 이정환 · 교신저자 이정표

소속 (1)
  1. From the Internal Medicine (JL), Hallym University Hangang Sacred Heart Hospital, Seoul; Internal Medicine (JHC, CDK), Kyungpook National University Hospital, Daegu; Department of Internal Medicine (JSL), Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan; Internal Medicine (DWA, CSL, JPY), Seoul National University Boramae Medical Center; Internal Medicine (CA, YSK), Seoul National University Hospital; Surgery (IMJ), Seoul National University Boramae Medical Center; Surgery (DJH, YHK), Ulsan University Seoul Asan Medical Center, Seoul, Korea.

Abstract

Clinical outcomes in kidney transplant recipients (KTRs) with hepatitis B virus (HBV) have not been thoroughly evaluated. Here, we investigated recent posttransplant clinical outcomes of KTRs with HBV and compared them with KTRs with hepatitis C virus (HCV) and seronegative KTRs.Of 3855 KTRs from April 1999 to December 2011, we enrolled 3482 KTRs who had viral hepatitis serology data; the patients were followed up for 89.1 ± 54.1 months. The numbers of recipients with HBV and HCV were 160 (4.6%) and 55 (1.6%), respectively. We analyzed the clinical outcomes, including overall mortality and graft failure, among patients who had undergone kidney transplantation.Patients with HBV showed poorer survival (P = 0.019; adjusted hazard ratio [HR] = 2.370; 95% confidence interval [CI]: 1.155-4.865) than KTRs without HBV. However, the graft survival of patients with chronic hepatitis B did not differ from that of patients without HBV. Hepatic complications were the primary causes of mortality of KTRs with HBV. Mortality significantly correlated with a higher grade of inflammation (P = 0.002) and with the use of lamivudine or adefovir antiviral treatment (P = 0.016). HBV-positive KTRs treated with the new-generation antiviral agent entecavir showed improved patient survival compared with KTRs receiving lamivudine (log-rank P = 0.050). HCV did not affect patient survival; however, it increased the incidence of graft failure (P = 0.010; adjusted HR = 2.899; 95% CI: 1.289-6.519). KTRs with HCV had an increased incidence of acute rejection (log-rank P = 0.005, crude HR = 2.144; 95% CI: 1.341-3.426; P = 0.001).KTRs with chronic hepatitis B may exhibit poor survival due to post-transplantation hepatic complications. Pretransplant histological liver evaluations and adequate antiviral management with potent nucleoside/nucleotide analogues are needed to improve the survival of KTRs with chronic hepatitis B even when liver function is within the normal range.

Figures

FIGURE 1
FIGURE 1 The annual trend of kidney transplantations and prophylactic antiviral treatment. A, Total kidney transplantations and proportion of kidney transplantation recipients with HBV and HCV. The number of kidney transplantations is continuously increasing. The proportion of kidney transplantation recipients with HBV is larger than that with HCV. B, Among KTRs with HBV, the number of patients who received no prophylactic antiviral treatment continually decreased over time. Prior to 2007, lamivudine was the primary antiviral agent used to treat KTRs with HBV. Since 2008, increasing numbers of patients have been treated with entecavir.
FIGURE 2
FIGURE 2 Patient survival is presented in a Kaplan–Meier survival plot. Kidney transplantation recipients with HBV show poorer overall survival (log-rank P <0.001) than those with HCV or negative hepatitis serology.
FIGURE 3
FIGURE 3 Patient survival among KTRs with HBV. A, Patient survival according to inflammation on liver biopsy. B, Patient survival according to fibrosis on liver biopsy. C, Patient survival according to antiviral treatment. KTRs who exhibited liver inflammation on the liver biopsy showed a tendency toward poorer survival than those without liver inflammation (log-rank, P = 0.070). KTRs who had severe fibrosis or liver cirrhosis showed significantly poorer survival than those without fibrosis (log-rank, P = 0.047). KTRs who were treated with new-generation antiviral agents such as entecavir showed better survival than those who were treated with lamivudine or adefovir (log-rank, P = 0.050). ∗Normal or minimal inflammation in liver biopsy, †above mild inflammation on liver biopsy.
FIGURE 4
FIGURE 4 Graft survival and events free survival of acute rejection. A, Graft survival in patients with HCV was poorer (log-rank P <0.001) than in those with HBV or negative hepatitis serology. B, KTRs with HCV showed a significantly higher incidence of acute rejection (log-rank P = 0.005; crude HR = 2.144 (1.341–3.426), P = 0.001) than KTRs with HBV or seronegativity.

그림 출처: PubMed Central 공개 논문 (PMC4902351)

Conflict of interest statement

The authors have no conflicts of interest to disclose.

그 밖의 정보
출판 형태
Journal Article, Multicenter Study, Observational Study
저널
Medicine · eISSN 1536-5964
MeSH
Adult · Antiviral Agents / therapeutic use · Biopsy · Cohort Studies · Female · Graft Survival · Hepatitis B / complications / drug therapy · Hepatitis C / complications / drug therapy · Humans · Kidney Transplantation / mortality / statistics & numerical data · Male · Middle Aged · Proportional Hazards Models · Renal Insufficiency / complications / surgery · Republic of Korea / epidemiology · Tertiary Care Centers
Substances
Antiviral Agents
참고문헌
43편