Hepatitis B surface antigen quantification as a predictor of seroclearance during treatment in HIV-hepatitis B virus coinfected patients from Sub-Saharan Africa

被引:30
|
作者
Boyd, Anders [1 ]
Maylin, Sarah [2 ,4 ]
Moh, Raoul [5 ]
Mahjoub, Nadia [2 ]
Gabillard, Delphine [7 ,8 ]
Eholie, Serge Paul [5 ,6 ,13 ]
Danel, Christine [5 ,7 ]
Anglaret, Xavier [5 ,7 ]
Zoulim, Fabien [9 ,10 ]
Girard, Pierre-Marie [11 ,12 ]
Delaugerre, Constance [2 ,3 ,4 ]
Lacombe, Karine [11 ,12 ]
机构
[1] Inst Pierre Louis Epidemiol & Sante Publ, INSERM, UMR S1136, Paris, France
[2] Hop St Louis, AP HP, Lab Virol, Paris, France
[3] INSERM, U941, Paris, France
[4] Univ Paris Diderot, Paris, France
[5] Treichville Univ Hosp, ANRS Res Site, Programme PAC CI, Abidjan, Cote Ivoire
[6] Treichville Univ, Teaching Hosp, Dept Infect & Trop Dis, Abidjan, Cote Ivoire
[7] INSERM, Epidemiol Biostat, Bordeaux, France
[8] Univ Bordeaux, ISPED, Bordeaux, France
[9] INSERM, Ctr Rech Canc Lyon, Equipe 15, U1052, Lyon, France
[10] INSERM, Ctr Rech Canc Lyon, Equipe 16, U1052, Lyon, France
[11] St Antoine Hosp, Dept Infect & Trop Dis, Paris, France
[12] Univ Paris 06, Sorbonne Univ, Inst Pierre Louis Epidemiol & Sante Publ, UMR S 1136,U897, Paris, France
[13] Univ Felix Houphouet Boigny, Sch Med, Abidjan, Cote Ivoire
关键词
chronic viral hepatitis; HBeAg quantification; HBsAg quantification; immunosuppression; serological endpoints; ANTIRETROVIRAL THERAPY; NATURAL-HISTORY; VIRAL-HEPATITIS; TENOFOVIR; HBV; HBEAG; MANAGEMENT; LAMIVUDINE; MORTALITY; INFECTION;
D O I
10.1111/jgh.13156
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimIn Sub-Saharan Africa, seroclearance of hepatitis B surface antigen (HBsAg) and hepatitis B e antigen (HBeAg), including their quantifiable markers, have rarely been evaluated during long-term antiviral treatment among patients coinfected with HIV and hepatitis B virus (HBV). MethodsIn this prospective cohort study from two randomized-control trials in Cote d'Ivoire, 161 antiretroviral-naive HIV-HBV coinfected patients starting lamivudine (n=76) or tenofovir/emtricitabine (n=85) containing antiretroviral therapy were included. HBV DNA was quantified using an in-house assay (detection limit=12copies/mL) and HBsAg quantification (qHBsAg) using the Elecsys assay. ResultsOverall, 33 (20.5%) patients were HBeAg positive, 121 (75.2%) had detectable HBV DNA, and 92/93 (98.9%) harbored HBV genotype E. Median treatment duration was 35.5months (interquartile range: 24.3-36.4). Among HBeAg-positive patients, cumulative proportion with HBeAg seroclearance was 46.3% (n=14). Overall, cumulative proportion of HBsAg seroclearance was 6.6% (n=10). Lower baseline qHBsAg levels and strong 12-month declines in qHBsAg were significantly associated with HBsAg seroclearance for both HBeAg-negative and HBeAg-positive patients. When taken at certain levels, these determinants provided moderate sensitivity (Se) and specificity (Sp) in predicting HBsAg seroclearance at month 36 (1000IU/mL at baseline, Se=0.80, Sp=0.80; 1.0log(10)IU/mL drop at month 12, Se=0.57, Sp=1.00). Instead, qHBsAg levels 100 or 10IU/mL at month 12 were optimal (both Se=0.90 and Sp=1.00). Detectable HBV-DNA provided fairly high Se and Sp when evaluated at baseline (Se=1.00, Sp=0.80), but not at month 12 (Se=0.80, Sp=0.40). ConclusionsHBsAg seroclearance rates are not common in patients from Sub-Saharan Africa treated with anti-HBV containing antiretroviral therapy. qHBsAg levels at 12months of treatment may accurately predict HBsAg seroclearance.
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收藏
页码:634 / 644
页数:11
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