Hepatitis B and C viral coinfections and their association with HIV viral load suppression among HIV-1 infected patients on ART at Mekelle hospital, northern Ethiopia

被引:3
|
作者
Teame, Gebrecherkos [1 ]
Gebreyesus, Araya [2 ]
Tsegay, Ephrem [2 ]
Gebretsadik, Mulu [3 ]
Adane, Kelemework [4 ]
机构
[1] Tigray Hlth Res Inst, Mekelle, Ethiopia
[2] Mekelle Univ, Coll Hlth Sci, Dept Microbiol & Immunol, Div Biomed Sci, Mekelle, Ethiopia
[3] Ayder Comprehens Specialized Hosp, Dept Clin Lab, Mekelle, Ethiopia
[4] Addis Ababa Univ, Coll Hlth Sci, Sch Med, Dept Microbiol Immunol & Parasitol, Addis Ababa, Ethiopia
关键词
Antiretroviral therapy; HBV; HCV; HIV; Viral load suppression; HUMAN-IMMUNODEFICIENCY-VIRUS; ACTIVE ANTIRETROVIRAL THERAPY; NATURAL-HISTORY; PREVALENCE; INFECTION; PROGRESSION; MORTALITY; ADHERENCE; RESPONSES; AFRICA;
D O I
10.1186/s12981-022-00479-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Although Ethiopia is endemic to viral hepatitis and HIV, data that could guide population-specific interventions are limited. In this study, we determined the seroprevalence of hepatitis B virus (HBV) and hepatitis C virus (HCV) and assessed their associations with HIV-1 viral load suppression among HIV-1 infected patients on antiretroviral therapy (ART) at Mekelle hospital in northern Ethiopia.Methods: Between February and April 2020, blood samples were collected from 439 participants. Samples were screened for HBsAg and anti-HCV on the immunochromatographic test and confirmed using the Enzyme-Linked Immuno-sorbent assay (Beijing Wantai Co. China). HIV-1 viral load was quantified using reverse transcription-polymerase chain reaction (RT-PCR) on the Abbott platform. Binary and multivariable logistic regression was performed to identify potential predictors.Results: Overall, 10% (44/439) and 3.6% (16/439) of the participants were coinfected with HBV and HCV, respectively. In a multivariate analysis, being illiterate (AOR = 6.57; 95% CI 1.04-41.6), and having a history of sexually transmitted infections (AOR = 4.44; 95% CI 1.31-15.0) and multiple sexual partners (AOR = 29.9; 95% CI 7.82-114.8) were associated with HBV infection. On the other hand, participants with a history of chronic non-communicable diseases (AOR = 10.6, 95% CI 1.61-70.1), and those reporting a history of sexually transmitted infections (AOR = 5.21, 95% CI 1.39-19.5) were more likely to be infected with HCV. In further analysis, HCV infection status was significantly associated with decreased viral load suppression rate (AOR = 7.14; 95% CI 2.18-23.3) whereas no significant association was observed with the HBV infection.Conclusions: The HBV coinfection rate in our study is high and, as per WHO's standard, corresponds to a hyperendemic level. The HCV coinfection rate is also substantially high and urges attention given its influence on the viral load suppression of HIV patients on ART at our study site. Our findings suggest the need to adopt universal screening and vaccination of people with HIV against HBV and screening for HCV at our study site and in Ethiopia at large, which contributes to Ethiopia's progress towards the 2030 global target of reducing the HBV infection.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Association between KIR genotypes and HLA-B alleles on viral load in Southern Brazilian individuals infected by HIV-1 subtypes B and C
    Fernandes-Cardoso, Juliana
    Suffert, Theodoro Armando
    Correa, Maria da Gloria
    Job Jobim, Luiz Fernando
    Jobim, Mariana
    Salim, Patricia Hartstein
    Arruda, Monica Barcelos
    Boullosa, Lidia Theodoro
    Tanuri, Amilcar
    Porto, Luis Cristovao
    Ferreira, Orlando C., Jr.
    HUMAN IMMUNOLOGY, 2016, 77 (10) : 854 - 860
  • [32] Effect of hemodialysis and antiretroviral therapy on plasma viral load in HIV-1 infected hemodialysis patients
    Ahuja, TS
    Niaz, N
    Velasco, A
    Watts, B
    Paar, D
    CLINICAL NEPHROLOGY, 1999, 51 (01) : 40 - 44
  • [33] Rebound of HIV-1 viral load after suppression to very low levels
    Staszewski, S
    Miller, V
    Sabin, C
    Berger, A
    Hill, AM
    Phillips, AN
    AIDS, 1998, 12 (17) : 2360 - 2360
  • [34] Quantification of HIV-1 viral load in the fluid of ranulas in HIV-positive patients
    Syebele, Kabunda
    Buetow, Kurt-W
    Webber, Lynne
    Manda, Samuel O.
    ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 2011, 111 (06): : 715 - 719
  • [35] Correlates of HIV sustained viral suppression in HIV/hepatitis C virus coinfected patients: possible role of the hepatitis C virus sustained viral response
    Bani-Sadr, Firouze
    Loko, Marc-Arthur
    Pambrun, Elodie
    Winnock, Maria
    Carrieri, Patrizia
    Gilbert, Camille
    Duvivier, Claudine
    Bouchaud, Olivier
    Gervais, Anne
    Dabis, Francois
    Salmon, Dominique
    AIDS, 2014, 28 (08) : 1155 - 1160
  • [36] Whole blood versus plasma spots for measurement of HIV-1 viral load in HIV-infected African patients
    Mwaba, P
    Cassol, S
    Nunn, A
    Pilon, R
    Chintu, C
    Janes, M
    Zumla, A
    LANCET, 2003, 362 (9401): : 2067 - 2068
  • [37] Increasing impact of chronic viral hepatitis on hospital admissions and mortality among HIV-infected patients
    Martín-Carbonero, L
    Soriano, V
    Valencia, E
    García-Samaniego, J
    López, M
    González-Lahoz, J
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2001, 17 (16) : 1467 - 1471
  • [38] Suppression of HIV-1 Plasma Viral Load Below Detection Preserves IL-17 Producing T Cells in HIV-1 Infected Children
    Leal, F. E.
    Ndhlovu, L. C.
    Jha, A. R.
    Chapman, J. M.
    Snyder-Cappione, J. E.
    Pagan, M.
    Boland, B. S.
    Norris, P. J.
    Rosenberg, M. G.
    Nixon, D. F.
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2008, 24 : 130 - 131
  • [39] Viral load suppression and HIV-1 drug resistance mutations in persons with HIV on TLD/TAFED in Zambia
    Luwaya, Emmanuel L.
    Mwape, Lackson
    Bwalya, Kaole
    Siakabanze, Chileleko
    Hamooya, Benson M.
    Masenga, Sepiso K.
    PLOS ONE, 2024, 19 (09):
  • [40] Plasma HIV-1 RNA viral load and serum vitamin A and E levels in HIV-1 infected pregnant women
    Phuapradit, W
    Panburana, P
    Jaovisidha, A
    Puchaiwatananon, O
    Chantratita, W
    Bhodhiphala, P
    Pairoj, W
    AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 2000, 40 (01): : 78 - 80