Kapogiannis Bill G, Leister Erin, Siberry George K, Van Dyke Russell B, Rudy Bret, Flynn Patricia, Williams Paige L
aMaternal and Pediatric Infectious Disease Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland bCenter for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, Massachusetts cTulane University Health Sciences Center, New Orleans, Louisiana dNew York University, New York, New York eSt. Jude Children's Research Hospital, Memphis, Tennessee, USA.
AIDS. 2016 Mar 27;30(6):889-98. doi: 10.1097/QAD.0000000000001003.
To longitudinally characterize noninvasive markers of liver disease in HIV-infected youth.
HIV infection, without viral hepatitis coinfection, may contribute to liver disease. Noninvasive markers of liver disease [FIB-4 (Fibrosis-4) and APRI (aspartate aminotransferase-to-platelet ratio index)] have been evaluated in adults with concomitant HIV and hepatitis C, but are less studied in children.
In prospective cohorts of HIV-infected and HIV-uninfected youth, we used linear regression models to compare log-transformed FIB-4 and APRI measures by HIV status based on a single visit at ages 15-20 years. We also longitudinally modeled trends in these measures in HIV-infected youth with two or more visits to compare those with behavioral vs. perinatal HIV infection (PHIV) using mixed effect linear regression, adjusting for age, sex, body mass index, and race/ethnicity.
Of 1785 participants, 41% were men, 57% black non-Hispanic, and 27% Hispanic. More HIV-infected than uninfected youth had an APRI score more than 0.5 (13 vs. 3%, P < 0.001). Among 1307 HIV-infected participants with longitudinal measures, FIB-4 scores increased 6% per year (P < 0.001) among all HIV-infected youth, whereas APRI scores increased 2% per year (P = 0.007) only among PHIV youth. The incidence rates (95% confidence interval) of progression of APRI to more than 0.5 and more than 1.5 were 7.5 (6.5-8.7) and 1.4 (1.0-1.9) cases per 100 person-years of follow-up, respectively. The incidence of progression of FIB-4 to more than 1.5 and more than 3.25 were 1.6 (1.2-2.2) and 0.3 (0.2-0.6) cases per 100 person-years, respectively.
APRI and FIB-4 scores were higher among HIV-infected youth. Progression to scores suggesting subclinical fibrosis or worse was common.
纵向描述感染HIV的青少年肝病的非侵入性标志物。
未合并病毒性肝炎感染的HIV感染可能导致肝病。已在合并HIV和丙型肝炎的成人中评估了肝病的非侵入性标志物[FIB-4(纤维化-4)和APRI(天冬氨酸转氨酶与血小板比值指数)],但在儿童中的研究较少。
在感染HIV和未感染HIV的青少年前瞻性队列中,我们使用线性回归模型,根据15至20岁时的单次就诊情况,按HIV感染状态比较经对数转换的FIB-4和APRI测量值。我们还对有两次或更多次就诊的感染HIV的青少年中这些测量值的纵向趋势进行建模,使用混合效应线性回归比较行为感染HIV与围产期HIV感染(PHIV)的青少年,并对年龄、性别、体重指数和种族/民族进行调整。
在1785名参与者中,41%为男性,57%为非西班牙裔黑人,27%为西班牙裔。APRI评分大于0.5的感染HIV的青少年比未感染HIV的青少年更多(13%对3%,P<0.001)。在1307名有纵向测量值的感染HIV的参与者中,所有感染HIV的青少年中FIB-4评分每年增加6%(P<0.001),而仅在围产期感染HIV的青少年中APRI评分每年增加2%(P=0.007)。APRI进展至大于0.5和大于1.5的发生率(95%置信区间)分别为每100人年随访7.5(6.5 - 8.�)例和1.4(1.0 - 1.9)例。FIB-4进展至大于1.5和大于3.25的发生率分别为每100人年1.6(1.2 - 2.2)例和0.3(0.2 - 0.6)例。
感染HIV的青少年中APRI和FIB-4评分更高。进展至提示亚临床纤维化或更严重程度的评分很常见。