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接受直接抗病毒药物治疗的丙型肝炎患者非侵入性纤维化指数值迅速下降。

Rapid decline of noninvasive fibrosis index values in patients with hepatitis C receiving treatment with direct-acting antiviral agents.

作者信息

Hsu Wei-Fan, Lai Hsueh-Chou, Su Wen-Pang, Lin Chia-Hsin, Chuang Po-Heng, Chen Sheng-Hung, Chen Hung-Yao, Wang Hung-Wei, Huang Guan-Tarn, Peng Cheng-Yuan

机构信息

Division of Hepatogastroenterology, Department of Internal Medicine, China Medical University Hospital, No. 2, Yuh-Der Road, 40447, Taichung, Taiwan.

Graduate Institute of Biomedical Science, China Medical University, 40442, Taichung, Taiwan.

出版信息

BMC Gastroenterol. 2019 Apr 27;19(1):63. doi: 10.1186/s12876-019-0973-5.

DOI:10.1186/s12876-019-0973-5
PMID:31029101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6486982/
Abstract

BACKGROUND

Studies on temporal changes in noninvasive fibrosis indices and liver stiffness measurement (LSM) in patients with chronic hepatitis C (CHC) treated with direct-acting antiviral agents (DAAs) are limited.

METHODS

We retrospectively enrolled consecutive patients with CHC who had received DAAs.

RESULTS

In total, we recruited 395 consecutive patients, of which 388 (98.2%) achieved a sustained virologic response (SVR) at 12 weeks after therapy. In patients who received DAA therapy and achieved SVR 12 weeks after therapy (n = 388), the median aspartate aminotransferase/platelet ratio index (APRI) value decreased from 1.19 (0.62-2.44) at baseline to 0.50 (0.32-0.95), 0.51 (0.31-0.92), 0.48 (0.31-0.88), and 0.52 (0.33-0.92) at week 2, week 4, end of therapy, and PW12, respectively (all P < 0.001). The median FIB-4 value decreased from 2.88 (1.56-5.60) at baseline to 2.10 (1.30-3.65), 2.15 (1.30-3.65), 2.11 (1.37-3.76), and 2.22 (1.45-3.82) at week 2, week 4, end of therapy, and PW12, respectively (all P < 0.001). The median alanine aminotransferase level significantly decreased from week 2 until PW12 (all P < 0.001). The platelet count significantly increased from 2 weeks after DAA therapy initiation until PW12 (all P < 0.001); however, the magnitude of changes in the platelet count was low. In patients with paired LSMs obtained using acoustic radiation force impulse elastography at baseline and PW12 (n = 199), the median LSM decreased from 1.78 (1.25-2.30) m/s at baseline to 1.38 (1.14-1.88) m/s at PW12 (P < 0.001).

CONCLUSIONS

Noninvasive fibrosis indices, namely APRI and FIB-4, exhibited a rapid and sustained decline from week 2 until PW12 in patients with CHC who achieved SVR to DAA therapy. The rapid decline in APRI and FIB-4 values might mainly result from improvement in necroinflammation.

摘要

背景

关于接受直接作用抗病毒药物(DAA)治疗的慢性丙型肝炎(CHC)患者非侵入性纤维化指标和肝脏硬度测量(LSM)的时间变化研究有限。

方法

我们回顾性纳入了连续接受DAA治疗的CHC患者。

结果

总共,我们连续招募了395例患者,其中388例(98.2%)在治疗后12周实现了持续病毒学应答(SVR)。在接受DAA治疗并在治疗后12周实现SVR的患者(n = 388)中,天冬氨酸氨基转移酶/血小板比率指数(APRI)的中位数从基线时的1.19(0.62 - 2.44)分别降至治疗第2周时的0.50(0.32 - 0.95)、第4周时的0.51(0.31 - 0.92)、治疗结束时的0.48(0.31 - 0.88)以及治疗后12周时的0.52(0.33 - 0.92)(所有P < 0.001)。FIB - 4的中位数从基线时的2.88(1.56 - 5.60)分别降至治疗第2周时的2.10(1.30 - 3.65)、第4周时的2.15(1.30 - 3.65)、治疗结束时的2.11(1.37 - 3.76)以及治疗后12周时的2.22(1.45 - 3.82)(所有P < 0.001)。丙氨酸氨基转移酶水平从中治疗第2周直到治疗后12周显著下降(所有P < 0.001)。血小板计数从开始DAA治疗后2周直到治疗后12周显著增加(所有P < 0.001);然而,血小板计数的变化幅度较小。在基线和治疗后12周使用声辐射力脉冲弹性成像获得配对LSM的患者(n = 199)中,LSM的中位数从基线时的1.78(1.25 - 2.30)m/s降至治疗后12周时的1.38(1.14 - 1.88)m/s(P < 0.001)。

结论

在接受DAA治疗实现SVR的CHC患者中,非侵入性纤维化指标APRI和FIB - 4从治疗第2周直到治疗后12周呈现快速且持续的下降。APRI和FIB - 4值的快速下降可能主要源于坏死性炎症的改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/ed2165c1cb03/12876_2019_973_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/8ec2dc1212f0/12876_2019_973_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/886ce78f002e/12876_2019_973_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/1af413475a73/12876_2019_973_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/ed2165c1cb03/12876_2019_973_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/8ec2dc1212f0/12876_2019_973_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/886ce78f002e/12876_2019_973_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/1af413475a73/12876_2019_973_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7589/6486982/ed2165c1cb03/12876_2019_973_Fig4_HTML.jpg

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