Puri P, Sharma P K, Lolusare A, Sashindran V K, Shrivastava S, Nagpal A K
Department of Internal Medicine, Armed Forces Medical College, Pune 411040, India.
Department of Gastroenterology, Army Hospital (R&R), New Delhi 110010, India.
J Clin Exp Hepatol. 2017 Mar;7(1):1-8. doi: 10.1016/j.jceh.2016.12.002. Epub 2016 Dec 29.
While highly active anti-retroviral therapy (HAART) has improved survival of HIV-infected patients, there is increasing liver disease and progressive Hepatitis B Virus (HBV) and Hepatitis C Virus (HCV) related liver disease.
To study the liver function tests (LFT) and HBV and HCV co-infection in HIV-infected patients.
All HIV-positive patients presenting to a tertiary level hospital from April 2009 to April 2011 were evaluated. Baseline LFT, CD4/CD8 counts, ultrasound abdomen, HBsAg, IgG anti-HBc, HBVDNA, Anti-HCV and HCVRNA were done in all patients. LFT was repeated monthly or more frequently with anti-tubercular therapy (ATT)/HAART.
Abnormal LFT were seen in 143/320 (44.6%) HIV-infected patients ( = 320; M-282, F-38; mean age-35.4 ± 7.3 years). Baseline LFT was abnormal in 48 (15%) [hepatotropic viruses-19, alcohol-24, NAFLD-1, disseminated TB-1, idiopathic-03). Subsequent LFT derangement developed in 95/272 (34.9%). In the majority, the LFT abnormality was mild (119/143-83.2%) and multi-factorial [HAART 132 (76.4%), alcohol 69 (48.2%), ATT 31 (21.7%), HBV 16 (11.2%), HCV 15 (10.4%)]. Using multivariate analysis, abnormal LFT were associated with HAART (OR, 5.92; 95%CI, 2.83-12.37), ATT (OR, 2.06; 95%CI, 1.06-3.99) or HCV infection (OR, 2.54; 95%CI, 1.03-6.26). Significant hepatotoxicity requiring drug modification was seen in only 7 cases. HBV, HCV and HBV + HCV co-infection were seen in 37 (11.6%), 28 (8.8%) and 2 (0.6%) respectively. Occult co-infections were rare [HBV-1 (0.3%); HCV-3 (0.9%)].
While LFT abnormalities in HIV are common, they are usually mild and multifactorial. HBV and HCV co-infections were seen in 11.6% and 8.8%, respectively. Occult HBV and HCV infections were rare.
虽然高效抗逆转录病毒疗法(HAART)提高了HIV感染患者的生存率,但肝脏疾病以及与乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)相关的进行性肝病却日益增多。
研究HIV感染患者的肝功能检查(LFT)以及HBV和HCV合并感染情况。
对2009年4月至2011年4月在一家三级医院就诊的所有HIV阳性患者进行评估。对所有患者进行了基线LFT、CD4/CD8计数、腹部超声、HBsAg、IgG抗-HBc、HBVDNA、抗-HCV和HCVRNA检测。在接受抗结核治疗(ATT)/HAART期间,每月或更频繁地重复进行LFT检测。
在320例HIV感染患者中,有143例(44.6%)出现LFT异常(n = 320;男性282例,女性38例;平均年龄35.4±7.3岁)。48例(15%)患者基线LFT异常[嗜肝病毒感染19例,酒精性肝病24例,非酒精性脂肪性肝病1例,播散性结核病1例,特发性肝病3例]。在272例患者中,有95例(34.9%)随后出现LFT紊乱。大多数情况下,LFT异常为轻度(119/143,83.2%)且由多种因素导致[HAART 132例(76.4%),酒精性肝病69例(48.2%),ATT 31例(21.7%),HBV 16例(11.2%),HCV 15例(10.4%)]。多因素分析显示,LFT异常与HAART(比值比,5.92;95%置信区间,2.83 - 12.37)、ATT(比值比,2.06;95%置信区间,1.06 - 3.99)或HCV感染(比值比,2.5