Impact of hepatitis C virus genotype-4 eradication following direct acting antivirals on liver stiffness measurement.

IF 2.6 Q2 GASTROENTEROLOGY & HEPATOLOGY
Hepatic Medicine : Evidence and Research Pub Date : 2017-10-06 eCollection Date: 2017-01-01 DOI:10.2147/HMER.S142600
Mohammed Tag-Adeen, Ahlam Mohamed Sabra, Yuko Akazawa, Ken Ohnita, Kazuhiko Nakao
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引用次数: 23

Abstract

Background: Liver fibrosis is the most important prognostic factor in chronic hepatitis C virus (HCV) patients, and Egypt shows the highest worldwide HCV prevalence with genotype-4 pre-dominance. The aim of this study was to investigate the degree of liver stiffness measurement (LSM) improvement after successful HCV eradication.

Patients and methods: The study included 84 chronic HCV Egyptian patients, and was conducted at Qena University Hospital from November 1, 2015 till October 31, 2016. LSM was obtained by FibroScan® before starting direct acting antiviral (DAA) treatment and after achieving sustained virologic response-24 (SVR-24). Based on baseline LSM, patients were stratified into F0-F1, F2, F3 and F4 groups (METAVIR). LSM and laboratory data after achieving SVR-24 was compared with that before starting therapy in each fibrosis group (F0-F4), p-value <0.05 was statistically significant.

Results: Following DAA treatment, 80 patients achieved SVR-24; of these, 50 were males (62.5%), mean age: 54.2±7.6 years, and mean body mass index: 28.6±2.2 kg/m2. Mean baseline LSM dropped from 15.6±10.8 to 12.1±8.7 kPa post-SVR; the maximum change of -5.8 occurred in F4 versus -2.79, -1.28 and +0.08 in F3, F2 and F0-F1 respectively (p<0.0001). At baseline, 41 patients were in the F4 group; only 16 (39%) regressed to non-cirrhotic range (<12.5 kPa), while 25 (61%) were still cirrhotic despite achieving SVR-24 (p<0.0001). Patients who achieved LSM improvement (n=64) have had significantly higher baseline aspartate transferase (AST) and alanine transaminase (ALT). Also, those patients showed significant improvement in AST, AST/platelets ratio index (APRI) and fibrosis-4 index (Fib-4) after achieving SVR; 91% showed AST improvement (p=0.01) and APRI improvement (p=0.01) and 81% showed Fib-4 improvement (p=0.04). Females, diabetics, patients with S3 steatosis and patients older than 50 years showed less LSM improvements than their counterparts. Baseline LSM ≥9 kPa, bilirubin ≥1 mg/dl, ALT ≥36 U/L and AST ≥31 U/L were significant predictors for LSM improvement.

Conclusion: Successful HCV genotype-4 eradication results in significant LSM improvement; the best improvement occurs in F4 patients. But as the majority of cirrhotics are still at risk for liver decompensation and hepatocellular carcinoma development despite achieving SVR-24, early detection and treatment are highly recommended.

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直接作用抗病毒药物后丙型肝炎病毒基因型4根除对肝脏硬度测量的影响
背景:肝纤维化是慢性丙型肝炎病毒(HCV)患者最重要的预后因素,埃及是全球HCV患病率最高的国家,且基因型为4型优势。本研究的目的是调查成功根除HCV后肝脏硬度测量(LSM)的改善程度。患者和方法:该研究纳入了84例埃及慢性HCV患者,于2015年11月1日至2016年10月31日在Qena大学医院进行。LSM是在开始直接作用抗病毒(DAA)治疗前和达到持续病毒学应答-24 (SVR-24)后通过FibroScan®获得的。根据基线LSM,将患者分为F0-F1、F2、F3和F4组(METAVIR)。比较各纤维化组(F0-F4)开始治疗前与达到SVR-24后的LSM及实验室数据,p值结果:经DAA治疗后,80例患者达到SVR-24;其中男性50例(62.5%),平均年龄54.2±7.6岁,平均体重指数28.6±2.2 kg/m2。svr后平均基线LSM由15.6±10.8 kPa降至12.1±8.7 kPa;F3、F2和F0-F1的最大变化分别为-2.79、-1.28和+0.08 (ppp=0.01), APRI改善(p=0.01), 81%的患者Fib-4改善(p=0.04)。女性、糖尿病患者、S3脂肪变性患者和年龄大于50岁的患者相比,LSM的改善更少。基线LSM≥9 kPa、胆红素≥1 mg/dl、ALT≥36 U/L、AST≥31 U/L是LSM改善的显著预测因子。结论:成功根除HCV基因4型可显著改善LSM;F4型患者改善最好。但是,尽管达到了SVR-24,但大多数肝硬化患者仍存在肝脏失代偿和肝细胞癌发展的风险,因此强烈建议早期发现和治疗。
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来源期刊
Hepatic Medicine : Evidence and Research
Hepatic Medicine : Evidence and Research GASTROENTEROLOGY & HEPATOLOGY-
自引率
0.00%
发文量
15
审稿时长
16 weeks
期刊介绍: Hepatic Medicine: Evidence and Research is an international, peer-reviewed, open access, online journal. Publishing original research, reports, editorials, reviews and commentaries on all aspects of adult and pediatric hepatology in the clinic and laboratory including the following topics: Pathology, pathophysiology of hepatic disease Investigation and treatment of hepatic disease Pharmacology of drugs used for the treatment of hepatic disease Although the main focus of the journal is to publish research and clinical results in humans; preclinical, animal and in vitro studies will be published where they will shed light on disease processes and potential new therapies. Issues of patient safety and quality of care will also be considered. As of 1st April 2019, Hepatic Medicine: Evidence and Research will no longer consider meta-analyses for publication.
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