Jaquet Antoine, Wandeler Gilles, Nouaman Marcellin, Ekouevi Didier K, Tine Judicaël, Patassi Akouda, Coffie Patrick A, Tanon Aristophane, Seydi Moussa, Attia Alain, Dabis François
INSERM U1219 Bordeaux Population Health Research, ISPED, Université de Bordeaux, Bordeaux, France.
Service de maladies infectieuses et tropicales, CRCF, CHU de Fann, Dakar, Sénégal.
J Int AIDS Soc. 2017 Feb 17;19(1):21424. doi: 10.7448/IAS.20.1.21424.
Liver fibrosis is often the first stage of liver disease in people living with HIV (PLWHIV) in industrialized countries. However, little is known about liver fibrosis and its correlates among PLWHIV in sub-Saharan Africa.
The study was undertaken in three HIV referral clinics in Côte d'Ivoire, Senegal and Togo. Enrolled PLWHIV underwent a non-invasive assessment of liver fibrosis combining liver stiffness measure (LSM) with transient elastography and the aspartate aminotransferase-to-platelet ratio index (APRI). Significant liver fibrosis was defined as LSM ≥7.1 kPa. Patients were screened for alcohol use (alcohol use disorder identification test (AUDIT)-C questionnaire), hepatitis B virus (HBV) antigen, hepatitis Delta virus (HDV) antibody and anti-hepatitis C (HCV) antibody. A logistic regression model was used to identify the factors associated with significant liver fibrosis.
A total of 807 PLWHIV were screened at a median age of 43 years (interquartile range (IQR): 36-50). Their median CD4 count was 393 cells/mm (IQR: 234-563) and 682 (84.5%) were on antiretroviral therapy (ART). The prevalence of significant fibrosis was 5.3% (3.8-6.7). Infections with HBV and HCV were identified in 74 (9.2%) and nine (1.1%) participants. Main factors associated with liver fibrosis were alcohol use (AUDIT-C >6): (odds ratio (OR) = 4.0, confidence interval (CI): 1.2-14.0), (Ref. AUDIT-C <4) and HBV infection (OR = 2.9, CI: 1.2-7.2). Of the 74 patients positively screened for HBV, 50.0% were on a tenofovir-based ART regimen. Overall, 10% of HIV/HBV coinfected patients were detected with a positive HDV antibody with a higher prevalence in patients with a significant liver fibrosis (43.0%) compared to others (6.3%) ( = 0.01).
Considering the WHO recommendations to screen for HBV infection and treat co-infected patients with tenofovir-based ART, screening of alcohol use and brief interventions to prevent alcohol abuse should be implemented in West Africa, especially in HBV/HIV co-infected patients.
在工业化国家,肝纤维化通常是艾滋病病毒感染者(PLWHIV)肝病的第一阶段。然而,关于撒哈拉以南非洲地区PLWHIV的肝纤维化及其相关因素知之甚少。
该研究在科特迪瓦、塞内加尔和多哥的三家艾滋病病毒转诊诊所进行。入组的PLWHIV接受了肝纤维化的无创评估,结合肝脏硬度测量(LSM)与瞬时弹性成像以及天冬氨酸氨基转移酶与血小板比值指数(APRI)。显著肝纤维化定义为LSM≥7.1kPa。对患者进行酒精使用情况筛查(酒精使用障碍识别测试(AUDIT)-C问卷)、乙型肝炎病毒(HBV)抗原、丁型肝炎病毒(HDV)抗体和抗丙型肝炎病毒(HCV)抗体检测。采用逻辑回归模型确定与显著肝纤维化相关的因素。
共筛查了807例PLWHIV,中位年龄为43岁(四分位间距(IQR):36 - 50)。他们的中位CD4细胞计数为393个/mm³(IQR:234 - 563),682例(84.5%)正在接受抗逆转录病毒治疗(ART)。显著纤维化的患病率为5.3%(3.8 - 6.7)。74例(9.2%)参与者检测出HBV感染,9例(1.1%)检测出HCV感染。与肝纤维化相关的主要因素是酒精使用(AUDIT - C>6):(比值比(OR)=4.0,置信区间(CI):1.2 - 14.0),(参照AUDIT - C<4)以及HBV感染(OR = 2.9,CI:1.2 - 7.2)。在74例HBV筛查呈阳性的患者中,50.0%接受基于替诺福韦的ART方案。总体而言,10%的HIV/HBV合并感染患者检测出HDV抗体阳性,与其他患者(6.3%)相比,显著肝纤维化患者中的患病率更高(43.0%)(P = 0.01)。
考虑到世界卫生组织关于筛查HBV感染并用基于替诺福韦的ART治疗合并感染患者的建议,应在西非实施酒精使用筛查以及预防酒精滥用的简短干预措施,尤其是在HBV/HIV合并感染患者中。