Brescini Lucia, Orsetti Elena, Gesuita Rosaria, Piraccini Francesca, Marchionni Elisa, Staffolani Silvia, Castelli Pamela, Drenaggi Davide, Barchiesi Francesco
Department of Biomedical Sciences and Public Health, Clinical Infectious Diseases, Polytechnic University of Marche, Ancona, Italy.
Centre for Epidemiology and Biostatistics, Polytechnic University of Marche, Ancona, Italy.
Hepat Mon. 2014 Aug 5;14(8):e15426. doi: 10.5812/hepatmon.15426. eCollection 2014 Aug.
Due to the high efficacy of combination antiretroviral therapy (cART), the number of patients living with HIV is increasing. Chronic HCV infection has become a leading cause of non-AIDS related morbidity and mortality in patients with HIV infection.
The aim of this cross-sectional study was to identify factors associated with liver fibrosis (LF) in patients with HIV monoinfection and HIV-HCV coinfection.
We analyzed LF by transient elastometry ([TE], Fibroscan) in three groups of patients (HIV, HIV-HCV and HCV) followed at the Infectious Diseases Department of University of Ancona, Italy, between October 2009 and November 2012.
In total, 354 adults including 98 HIV, 70 HIV-HCV and 186 HCV patients were studied. HIV-HCV patients had a longer duration of HIV (P < 0.006) and HCV (P < 0.001) infections. Additionally, they were receiving cART therapy for a longer period (P < 0.001); they had higher prevalence of lipodystrophy (P < 0.001) and higher HCV load (P = 0.004). LF was significantly more pronounced in HCV and HIV-HCV compared to HIV patients (P < 0.001). A total of 13.3%, 39.2% and 51.4% of HIV, HCV and HIV-HCV, respectively, showed a LF ≥ F2. Additionally, a severe LF (F = 4) was significantly more frequent among HIV-HCV compared to other groups. A longer exposure to didanosine, stavudine, lopinavir/ritonavir and fosamprenavir resulted in increased LF by univariate analysis (P ranging from < 0.001 to 0.007). By logistic regression analysis, the only variables significantly associated with increased LF were HCV coinfection, older age, and high AST values (P ranging from < 0.001 to 0.036).
HCV coinfection, older age and AST were associated with LF in patients with HIV infection.
由于联合抗逆转录病毒疗法(cART)疗效显著,感染艾滋病毒的患者数量不断增加。慢性丙型肝炎病毒(HCV)感染已成为艾滋病毒感染者非艾滋病相关发病和死亡的主要原因。
本横断面研究旨在确定单纯感染艾滋病毒和合并感染艾滋病毒与丙型肝炎病毒的患者中与肝纤维化(LF)相关的因素。
2009年10月至2012年11月期间,我们在意大利安科纳大学传染病科对三组患者(艾滋病毒组、艾滋病毒与丙型肝炎病毒合并感染组和丙型肝炎病毒组)采用瞬时弹性成像([TE],Fibroscan)分析肝纤维化情况。
共研究了354名成年人,其中包括98名艾滋病毒患者、70名艾滋病毒与丙型肝炎病毒合并感染患者和186名丙型肝炎病毒患者。艾滋病毒与丙型肝炎病毒合并感染患者的艾滋病毒感染时间(P < 0.006)和丙型肝炎病毒感染时间(P < 0.001)更长。此外,他们接受cART治疗的时间更长(P < 0.001);脂肪代谢障碍患病率更高(P < 0.001),丙型肝炎病毒载量更高(P = 0.004)。与艾滋病毒患者相比,丙型肝炎病毒组和艾滋病毒与丙型肝炎病毒合并感染组的肝纤维化明显更严重(P < 0.001)。艾滋病毒组、丙型肝炎病毒组和艾滋病毒与丙型肝炎病毒合并感染组分别有13.3%、39.2%和51.4%的患者肝纤维化≥F2。此外,与其他组相比,艾滋病毒与丙型肝炎病毒合并感染组中严重肝纤维化(F = 4)的发生率明显更高。单因素分析显示,更长时间使用去羟肌苷、司他夫定、洛匹那韦/利托那韦和福沙普那韦会导致肝纤维化增加(P值范围为< 0.001至0.007)。通过逻辑回归分析,与肝纤维化增加显著相关的唯一变量是丙型肝炎病毒合并感染、年龄较大和天冬氨酸转氨酶(AST)值较高(P值范围为< 0.001至0.036)。
丙型肝炎病毒合并感染、年龄较大和AST与艾滋病毒感染患者的肝纤维化有关。