El-Ghandour Ahmed, Youssif Tarek, Ibrahim Wesam, Abdelsattar Hoda Ahmed, Bawady Somia Abd Elhamid, Wagih Mariam, El-Nakeep Sarah
Hepatology and Gastroenterology Unit, Internal Medicine Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Clinical Pathology Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Egypt J Intern Med. 2023;35(1):12. doi: 10.1186/s43162-023-00197-1. Epub 2023 Feb 13.
Hepatitis C is associated with metabolic effects and fatty liver disease. The effect of different direct antivirals on the liver steatosis, and the metabolic profile, still needs to be established. The aim of this study is to determine the effect of achieving the sustained virological response after 12 weeks (SVR-12 weeks) with different combinations of direct antiviral drugs, on the hepatic steatosis, and fibrosis presented by laboratory and transient elastography parameters. Our study population is nondiabetic, chronically infected HCV Egyptian patients and naïve to any form of HCV treatment.
This cohort study was carried on 100 nondiabetic HCV treatment-naïve patients attending the Hepatology Clinic, in the Gastroenterology and Hepatology Department, Ain Shams University, and Kobry El Koba Military Hospital. The patients were divided into four groups according to their treatment regimens as follows: group A: 25 patients who received sofosbuvir (400 mg) and daclatasvir (60 mg) daily for 12 weeks; group B: 25 patients who received sofosbuvir (400 mg) and ledipasvir (90 mg) daily for 12 weeks; group C: 25 patients who received ombitasvir (12.5 mg), paritaprevir (75 mg), and ritonavir (50 mg) daily for 12 weeks; and group D: 25 patients who received sofosbuvir (400 mg) and simeprevir (150 mg) daily for 12 weeks. All patients were subjected to the following investigations: HCV quantitative PCR before and after 12 weeks of treatment, clinical and laboratory metabolic evaluation including alfa-fetoprotein level, thyroid profile assessment, ferritin level, pelvi-abdominal ultrasound, and FibroScan examination.
All patients achieved SVR after 12 weeks. FibroScan median decreased ( < 0.001) from 19.29 ± 6.97 kPa at baseline to 14.15 ± 6.48 kPa at SVR12. NAFLD score median increased from 1.88 (1.49-2.22) at baseline to 2.01 (1.61-2.33) after 12 weeks of treatment. The highest level of NAFLD score was in group C, and the lowest was in group B. The BMI mean decreased from 28.31 ± 1.53 at baseline to 28.07 ± 1.52 at SVR12. HbA1C level mean decreased from 5.73 ± 0.23 at baseline to 5.40 ± 0.24 at SVR12. In addition, liver enzymes, cholesterol, triglycerides, APRI score (AST-platelet ratio index), and HBA1C decreased after 12-week treatment with a statistically significant difference, while the mean LDL increased after 12 weeks of treatment.
DAAs affect the metabolic profile of the treated patients. There is a noticed improvement in the FibroScan, NAFLD score, and lipid profile after achieving the SVR-12 weeks. However, LDL is increased after viral cure, mostly due to viral-host molecular interaction.
丙型肝炎与代谢效应和脂肪性肝病相关。不同直接抗病毒药物对肝脏脂肪变性和代谢谱的影响仍有待确定。本研究的目的是确定使用不同直接抗病毒药物组合治疗12周后实现持续病毒学应答(SVR - 12周)对肝脏脂肪变性和纤维化的影响,通过实验室和瞬时弹性成像参数来体现。我们的研究人群为非糖尿病、慢性感染丙型肝炎病毒的埃及患者,且未接受过任何形式的丙型肝炎治疗。
本队列研究对100例未接受过丙型肝炎治疗的非糖尿病患者进行,这些患者来自艾因夏姆斯大学胃肠病学和肝病学系肝病门诊以及科卜里·埃尔·科巴军事医院。根据治疗方案将患者分为四组:A组:25例患者每天接受索磷布韦(400mg)和达卡他韦(60mg)治疗12周;B组:25例患者每天接受索磷布韦(400mg)和来迪帕司韦(90mg)治疗12周;C组:25例患者每天接受奥比他韦(12.5mg)、帕利哌韦(75mg)和利托那韦(50mg)治疗12周;D组:25例患者每天接受索磷布韦(400mg)和simeprevir(150mg)治疗12周。所有患者均接受以下检查:治疗12周前后的丙型肝炎定量PCR、临床和实验室代谢评估,包括甲胎蛋白水平、甲状腺功能评估、铁蛋白水平、盆腔腹部超声以及FibroScan检查。
所有患者在12周后均实现了SVR。FibroScan中位数从基线时的19.29±6.97kPa降至SVR12时的14.15±6.48kPa(<0.001)。非酒精性脂肪性肝病(NAFLD)评分中位数从基线时的1.88(1.49 - 2.22)增加至治疗12周后的2.01(1.6 + 1 - 2.33)。NAFLD评分最高的是C组,最低的是B组。体重指数(BMI)均值从基线时的28.31±1.53降至SVR12时的28.07±1.52。糖化血红蛋白(HbA1C)水平均值从基线时的5.73±0.23降至SVR12时的5.40±0.24。此外,治疗12周后肝酶、胆固醇、甘油三酯、APRI评分(AST - 血小板比率指数)和HbA1C均下降,差异具有统计学意义,而治疗12周后低密度脂蛋白(LDL)均值升高。
直接抗病毒药物(DAAs)会影响接受治疗患者的代谢谱。在实现SVR - 12周后,FibroScan、NAFLD评分和血脂谱有明显改善。然而,病毒清除后LDL升高,主要是由于病毒与宿主的分子相互作用。