Oyaro Micah, Wylie John, Chen Chien-Yu, Ondondo Raphael O, Kramvis Anna
Immunology Unit, Department of Human Pathology, University of Nairobi, Kenya.
Department of Medical Microbiology, University of Manitoba, Canada.
South Afr J HIV Med. 2018 Mar 27;19(1):737. doi: 10.4102/sajhivmed.v19i1.737. eCollection 2018.
Drug users act as reservoirs and transmission channels for hepatitis B virus (HBV), hepatitis C virus (HCV) and human immunodeficiency virus (HIV) infections to the general population worldwide. Periodic epidemiological studies to monitor the prevalence and genetic diversity of these infections to inform on interventions are limited.
The objective of this study was to determine the predictors of HIV infection and genetic diversity of HBV and HCV among drug users in Kenya.
A cross-sectional study on previous drug use history among drug users was conducted in three Kenyan cities using a respondent-driven sampling method between January 2011 and September 2012. Blood samples were collected and analysed for the presence of HBV, HCV and HIV serological markers and to determine the genotypes of HBV and HCV.
The overall prevalence of HBV, HCV and HIV among drug users was 4.3%, 6.5% and 11.1%, respectively, with evidence of HBV/HIV, HCV/HIV and HBV/HCV/HIV co-infections. The HBV circulating genotypes were A1 (69%) and D6 (19%), whereas HCV genotypes were 1a (72%) and 4a (22%). Injection drug use was a significant predictor of HIV/HCV infections. Younger age (30 years; aOR (adjusted odds ratio) = 0.50, 95% CI (confidence interval): 0.33-0.76; < 0.001) and early sexual debut (aOR = 0.54, 95% CI: 0.40-0.82; < 0.05) were negatively associated with detection of any of the three infections. Injecting drug use was positively associated with HCV infection (aOR = 5.37, 95% CI: 2.61-11.06; < 0.001).
This high level of genetic diversity exhibited by HBV and HCV isolates requires urgent implementation of harm reduction strategies and continuous monitoring for effective management of the patients.
吸毒者是全球范围内乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)和人类免疫缺陷病毒(HIV)感染向普通人群传播的储存库和传播渠道。用于监测这些感染的流行率和基因多样性以指导干预措施的定期流行病学研究有限。
本研究的目的是确定肯尼亚吸毒者中HIV感染的预测因素以及HBV和HCV的基因多样性。
2011年1月至2012年9月期间,在肯尼亚的三个城市采用应答者驱动抽样方法,对吸毒者既往吸毒史进行了横断面研究。采集血样并分析HBV、HCV和HIV血清学标志物的存在情况,以确定HBV和HCV的基因型。
吸毒者中HBV、HCV和HIV的总体流行率分别为4.3%、6.5%和11.1%,存在HBV/HIV、HCV/HIV和HBV/HCV/HIV合并感染的证据。HBV流行基因型为A1(69%)和D6(19%),而HCV基因型为1a(72%)和4a(22%)。注射吸毒是HIV/HCV感染的重要预测因素。年龄较小(≤30岁;调整优势比(aOR)=0.50,95%置信区间(CI):0.33 - 0.76;P<0.001)和初次性行为较早(aOR = 0.54,95%CI:0.40 - 0.82;P<0.05)与这三种感染中任何一种的检测呈负相关。注射吸毒与HCV感染呈正相关(aOR = 5.37,95%CI:2.61 - 11.06;P<0.001)。
HBV和HCV分离株表现出的这种高度基因多样性需要紧急实施减少伤害策略并持续监测,以便对患者进行有效管理。