Pons Mònica, Santos Begoña, Simón-Talero Macarena, Ventura-Cots Meritxell, Riveiro-Barciela Mar, Esteban Rafael, Augustin Salvador, Genescà Joan
Liver Unit, Department of Internal Medicine, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain.
Liver Unit, Department of Internal Medicine, Hospital Universitari Vall d'Hebron, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain.
Therap Adv Gastroenterol. 2017 Aug;10(8):619-629. doi: 10.1177/1756283X17715198. Epub 2017 Jun 27.
We aimed to investigate the early changes in liver and spleen stiffness measurement (LSM, SSM) in hepatitis C virus (HCV) patients with compensated advanced chronic liver disease (cACLD) treated with new antivirals (DAA) to elucidate factors determining the initial change in stiffness and its implications for the long-term follow up of HCV-cured patients.
A total of 41 patients with cACLD who started DAA therapy underwent LSM and SSM at baseline, week 4, end of treatment (EOT), 24 and 48 weeks of follow up using transient elastography.
LSM improved rapidly during the first 4 weeks of treatment (baseline: 20.8kPa; week 4: 17.5kPa, = 0.002), with no significant changes between week 4 and EOT (18.3kPa, = 0.444) and between EOT and 48-week follow up (14.3kPa, = 0.148). Likewise, SSM improved rapidly (baseline: 45.7kPa; week 4: 33.8kPa, = 0.047), with no significant changes between week 4 and EOT (30.8kPa, = 0.153) and between EOT and 48-week follow up (31.2kPa, = 0.317). A higher decrease in LSM was observed in patients with baseline ALT ⩾ twofold upper limit normal (2 × ULN) than in those with ALT < 2 × ULN (-5.7kPa -1.6kPa). Patients who presented a decrease in LSM ⩾ 10% during treatment compared with those with LSM < 10% decrease, showed lower SSM values, higher platelet counts and lower bilirubin levels at 24-week follow up. Those with decrease in SSM ⩾ 10%, presented a higher increase in platelets than those with SSM < 10% change ( = 0.015).
LSM and SSM decrease very rapidly during DAA treatment in cACLD patients suggesting that it most probably reflects a reduction in inflammation rather than in fibrosis. cACLD patients should be maintained under surveillance independently of stiffness changes, because advanced fibrosis can still be present.
我们旨在研究接受新型抗病毒药物(直接抗病毒药物,DAA)治疗的代偿期晚期慢性肝病(cACLD)丙型肝炎病毒(HCV)患者肝脏和脾脏硬度测量值(LSM,SSM)的早期变化,以阐明决定硬度初始变化的因素及其对HCV治愈患者长期随访的意义。
共有41例开始DAA治疗的cACLD患者在基线、第4周、治疗结束(EOT)、随访24周和48周时使用瞬时弹性成像进行LSM和SSM检测。
治疗的前4周LSM迅速改善(基线:20.8kPa;第4周:17.5kPa,P = 0.002),第4周与EOT之间(18.3kPa,P = 0.444)以及EOT与48周随访之间(14.3kPa,P = 0.148)无显著变化。同样,SSM迅速改善(基线:45.7kPa;第4周:33.8kPa,P = 0.047),第4周与EOT之间(30.8kPa,P = 0.153)以及EOT与48周随访之间(31.2kPa,P = 0.317)无显著变化。基线ALT⩾正常上限两倍(2×ULN)的患者LSM下降幅度高于ALT < 2×ULN的患者(-5.7kPa对-1.6kPa)。与LSM下降<10%的患者相比,治疗期间LSM下降⩾10%的患者在24周随访时SSM值更低、血小板计数更高且胆红素水平更低。SSM下降⩾10%的患者血小板增加幅度高于SSM变化<10%的患者(P = 0.015)。
cACLD患者在DAA治疗期间LSM和SSM迅速下降,这表明其很可能反映的是炎症减轻而非纤维化减轻。cACLD患者应独立于硬度变化进行监测,因为仍可能存在晚期纤维化。