Changing epidemiology and viral interplay of hepatitis B, C and D among injecting drug user-dominant prisoners in Taiwan

Author:

Lu Ming-Ying,Chen Chun-Ting,Shih Yu-Lueng,Tsai Pei-Chien,Hsieh Meng-Hsuan,Huang Chung-Feng,Yeh Ming-Lun,Huang Ching-I,Wang Shu-Chi,Tsai Yi-Shan,Ko Yu-Min,Lin Ching-Chih,Chen Kuan-Yu,Wei Yu-Ju,Hsu Po-Yao,Hsu Cheng-Ting,Jang Tyng-Yuan,Liu Ta-Wei,Liang Po-Cheng,Hsieh Ming-Yen,Lin Zu-Yau,Chen Shinn-Cherng,Huang Jee-Fu,Dai Chia-Yen,Chuang Wan-Long,Yu Ming-Lung,Chang Wen-Yu

Abstract

AbstractThe spreading of viral hepatitis among injecting drug users (IDU) is an emerging public health concern. This study explored the prevalence and the risks of hepatitis B virus (HBV), hepatitis C virus (HCV) and hepatitis D virus (HDV) among IDU-dominant prisoners in Taiwan. HBV surface antigen (HBsAg), antibodies to HCV (anti-HCV) and HDV (anti-HDV), viral load and HCV genotypes were measured in 1137(67.0%) of 1697 prisoners. 89.2% of participants were IDUs and none had HIV infection. The prevalence of HBsAg, anti-HCV, dual HBsAg/anti-HCV, HBsAg/anti-HDV, and triple HBsAg/anti-HCV/anti-HDV was 13.6%, 34.8%, 4.9%, 3.4%, and 2.8%, respectively. HBV viremia rate was significantly lower in HBV/HCV-coinfected than HBV mono-infected subjects (66.1% versus 89.9%, adjusted odds ratio/95% confidence intervals [aOR/CI] = 0.27/0.10–0.73). 47.5% anti-HCV-seropositive subjects (n = 396) were non-viremic, including 23.2% subjects were antivirals-induced. The predominant HCV genotypes were genotype 6(40.9%), 1a(24.0%) and 3(11.1%). HBsAg seropositivity was negatively correlated with HCV viremia among the treatment naïve HCV subjects (44.7% versus 72.4%, aOR/CI = 0.27/0.13–0.58). Anti-HCV seropositivity significantly increased the risk of anti-HDV-seropositivity among HBsAg carriers (57.1% versus 7.1%, aOR/CI = 15.73/6.04–40.96). In conclusion, IUDs remain as reservoirs for multiple hepatitis viruses infection among HIV-uninfected prisoners in Taiwan. HCV infection increased the risk of HDV infection but suppressed HBV replication in HBsAg carriers. An effective strategy is mandatory to control the epidemic in this high-risk group.

Funder

Taiwan Liver Research Foundation

Kaohsiung Medical University

Kaohsiung Medical University Hospital

Center for Cancer Research of Kaohsiung Medical University

Liquid Biopsy and Cohort Research Center of Kaohsiung Medical University

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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