Prevalence, associated factors, and viral load dynamics of hepatitis B virus infection among HIV patients in three healthcare facilities of South Kivu province, eastern Democratic Republic of Congo : Chronic hepatitis B virus among HIV patients in South Kivu province.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Parvine Basimane Bisimwa, Jean Paulin Mbo Mukonkole, Giscard Wilfried Koyaweda, Cadeau Mugisho Matabishi, Théophile Mitima Kashosi, Omari Mukanga, Denis Mukwege Mukengere, Jean Bisimwa Nachega, Narcisse Patrice Joseph Komas
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引用次数: 0

Abstract

Background: Hepatitis B virus (HBV) significantly impacts public health, particularly among individuals with Human Immunodeficiency Virus (HIV). Co-infection can worsen HBV progression and increase chronic liver disease risks. This study assessed HBV marker frequency, viral load (VL), and associated factors in HIV patients in South Kivu province (Democratic Republic of Congo) to understand the health implications of HBV-HIV co-infection.

Methods: This cross-sectional study, from July 1, 2019, to July 30, 2021, included 864 HIV patients aged 18 to 70 years from General Referral Hospital of Panzi (GRH Panzi), Regional Military Hospital of Bukavu (RMH Bukavu), and Fomulac Hospital. Participants, on antiretroviral therapy, ART (TDF/3TC/DTG or AZT/3TC/LPV/r combinations) or newly diagnosed, consented for blood testing for hepatitis B using enzyme-linked immunosorbent assay (ELISA) and VLs using GeneXpert. Data were analyzed with Stata SE 14.0.

Results: The study found 8.0% HBsAg positivity among HIV patients in South Kivu, with 41.3% and 14.1% showing Anti-HBc and Anti-HBs, respectively. HBsAg positivity was linked to male gender (AOR = 2.96; p = 0.007), rural origin (AOR = 4.32; p = 0.014), treatment at Fomulac Hospital (AOR = 4.87; p = 0.002), marital status (AOR = 4.55; p = 0.036), lower education (AOR = 57.25; p = 0.002), jaundice history (AOR = 3.98; p = 0.021), and < 5 years of unprotected sex (AOR = 10.96; p = 0.002). The HIV VL average was 3.26 ± 3.57 log10 copies/ml, with no significant difference between HIV-only and co-infected individuals (p = 0.6642). In total, 448 (58.0%) participants on ART had undetectable HIV VLs. For HBV, 43.5% had undetectable, 49.3% low, and 7.2% high VLs. A correlation existed between HIV and HBV VLs; undetectable HIV corresponded to undetectable HBV in 62.5%, and high HIV VLs to high HBV in 50.0%.

Conclusion: High HBV co-infection rates in HIV-positive individuals in South Kivu necessitate regular HBV monitoring including prevention, screening, and vaccination strategies in HIV care. Despite ART managing both infections effectively, further research on HBV-related outcomes is essential for improving co-infected patient care.

刚果民主共和国东部南基伍省三个卫生保健设施中艾滋病毒患者中乙型肝炎病毒感染的流行、相关因素和病毒载量动态:南基伍省艾滋病毒患者中的慢性乙型肝炎病毒。
背景:乙型肝炎病毒(HBV)显著影响公众健康,特别是在人类免疫缺陷病毒(HIV)感染者中。合并感染可使HBV恶化并增加慢性肝病的风险。本研究评估了南基伍省(刚果民主共和国)HIV患者的HBV标记物频率、病毒载量(VL)和相关因素,以了解HBV-HIV合并感染对健康的影响。方法:本横断面研究于2019年7月1日至2021年7月30日期间,纳入了来自Panzi综合转诊医院(GRH Panzi),布卡武地区军事医院(RMH Bukavu)和福马拉克医院的864名18至70岁的HIV患者。接受抗逆转录病毒治疗、抗逆转录病毒治疗(TDF/3TC/DTG或AZT/3TC/LPV/r组合)或新诊断的参与者同意使用酶联免疫吸附试验(ELISA)和使用GeneXpert的VLs进行乙型肝炎血液检测。数据采用Stata SE 14.0进行分析。结果:研究发现南基伍省HIV患者中HBsAg阳性率为8.0%,其中41.3%和14.1%分别显示抗- hbc和抗- hbs。HBsAg阳性与男性相关(AOR = 2.96;p = 0.007),农村出身(AOR = 4.32;p = 0.014),在福马拉克医院治疗(AOR = 4.87;p = 0.002)、婚姻状况(AOR = 4.55;p = 0.036),较低学历(AOR = 57.25;p = 0.002)、黄疸史(AOR = 3.98;p = 0.021)和10拷贝/ml,在单独感染hiv和合并感染hiv的个体之间无显著差异(p = 0.6642)。总共有448名(58.0%)接受抗逆转录病毒治疗的参与者检测不到HIV病毒载量。对于HBV, 43.5%的VLs检测不到,49.3%的VLs低,7.2%的VLs高。HIV与HBV VLs存在相关性;62.5%的HIV检测不到对应HBV检测不到,50.0%的HIV高VLs对应HBV检测不到。结论:南基伍省HIV阳性个体HBV合并感染率高,需要定期监测HBV,包括HIV护理中的预防、筛查和疫苗接种策略。尽管抗逆转录病毒治疗有效地控制了两种感染,但进一步研究hbv相关结果对于改善合并感染患者的护理至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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