首页> 美国卫生研究院文献>other >Incidence and Risk Factors for Incomplete HBV DNA Suppression in HIV/HBV-Coinfected Patients Initiating Tenofovir-Based Therapy
【2h】

Incidence and Risk Factors for Incomplete HBV DNA Suppression in HIV/HBV-Coinfected Patients Initiating Tenofovir-Based Therapy

机译:在开始使用替诺福韦治疗的HIV / HBV合并感染患者中HBV DNA抑制不完全的发生率和危险因素

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Suppression of hepatitis B virus (HBV) DNA to undetectable levels is an important goal for HIV/HBV-coinfected patients receiving anti-HBV-active antiretroviral therapy (ART), and current guidelines recommend that this outcome should be reached by one year of treatment. However, the proportion of patients that fail to achieve an undetectable HBV DNA at this time point and its determinants remain unknown in clinical practice. The objective of this study was to determine the incidence and risk factors for incomplete HBV suppression following one year of tenofovir-based ART. We performed a cohort study among tenofovir-treated HIV/HBV-coinfected patients. Patients had HBV viremia, initiated tenofovir-based ART, and had HBV DNA measured at one year of therapy. The primary outcome was incomplete HBV suppression (HBV DNA ≥2.6 log IU/mL) at one year. Logistic regression determined odds ratio (ORs) of incomplete HBV suppression for risk factors of interest. Among 133 patients, 54% (95% CI, 46%–63%) had incomplete HBV suppression at one year. Incomplete suppression was associated with higher baseline HBV DNA (OR, 1.46 per log IU/mL increase; 95% CI, 1.1–1.94) and detectable HIV viremia at one year (OR, 2.52; 95% CI, 1.19–5.32). Among 66 patients with suppressed HIV RNA at one year, 28 (42%) failed to achieve an undetectable HBV DNA. Failure to suppress HBV DNA by one year occurred in a sizeable proportion of tenofovir-treated HIV/HBV-coinfected patients. Higher HBV DNA and detectable HIV viremia were risk factors for incomplete HBV suppression.
机译:将乙型肝炎病毒(HBV)DNA抑制到无法检测的水平是接受抗HBV活性抗逆转录病毒疗法(ART)的HIV / HBV感染患者的重要目标,目前的指南建议应在治疗一年后达到这一结果。然而,在这一时间点未能获得无法检测到的HBV DNA的患者比例及其决定因素在临床实践中仍然未知。这项研究的目的是确定使用替诺福韦治疗一年后,HBV抑制不完全的发生率和危险因素。我们对替诺福韦治疗的HIV / HBV合并感染患者进行了一项队列研究。患者患有HBV病毒血症,开始使用基于替诺福韦的抗逆转录病毒疗法,并在治疗一年后测量了HBV DNA。主要结果是一年后HBV抑制不完全(HBV DNA≥2.6log IU / mL)。 Logistic回归确定感兴趣的危险因素对HBV抑制不完全的优势比(OR)。在133例患者中,有54%(95%CI,46%–63%)在一年内HBV抑制不完全。抑制不完全与基线HBV DNA较高(OR,每log IU / mL增加1.46; 95%CI,1.1–1.94)和一年内可检测到的HIV病毒血症相关(OR,2.52; 95%CI,1.15-5.32)。在一年中有66例HIV RNA抑制的患者中,有28例(42%)未能检测到HBV DNA。替诺福韦治疗的HIV / HBV合并感染的患者中有相当大的比例未能在一年内抑制HBV DNA。较高的HBV DNA和可检测的HIV病毒血症是HBV抑制不完全的危险因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号