Non-invasive tests for clinically significant portal hypertension after HCV cure
- PMID: 36063968
- DOI: 10.1016/j.jhep.2022.08.025
Non-invasive tests for clinically significant portal hypertension after HCV cure
Abstract
Background & aims: Non-invasive tests (NITs) for clinically significant portal hypertension (CSPH; hepatic venous pressure gradient [HVPG] ≥10 mmHg) have predominantly been studied in patients with active HCV infection. Investigations after HCV cure are limited and have yielded conflicting results. We conducted a pooled analysis to determine the diagnostic/prognostic utility of liver stiffness measurement (LSM)/platelet count (PLT) in this setting.
Methods: A total of 418 patients with pre-treatment HVPG ≥6 mmHg who achieved sustained virological response (SVR) and underwent post-treatment HVPG measurement were assessed, of whom 324 (HVPG/NIT-cohort) also had paired data on pre-/post-treatment LSM/PLT. The derived LSM/PLT criteria were then validated against the direct endpoint decompensation in 755 patients with compensated advanced chronic liver disease (cACLD) with SVR (cACLD-validation-cohort).
Results: HVPG/NIT-cohort: Among patients with cACLD, the pre-/post-treatment prevalence of CSPH was 80%/54%. The correlation between LSM/HVPG increased from pre- to post-treatment (r = 0.45 vs. 0.60), while that of PLT/HVPG remained unchanged. For given LSM/PLT values, HVPG tended to be lower post- vs. pre-treatment, indicating the need for dedicated algorithms. Combining post-treatment LSM/PLT yielded a high diagnostic accuracy for post-treatment CSPH in cACLD (AUC 0.884; 95% CI 0.843-0.926). Post-treatment LSM <12 kPa & PLT >150 G/L excluded CSPH (sensitivity: 99.2%), while LSM ≥25 kPa was highly specific for CSPH (93.6%). cACLD-validation-cohort: the 3-year decompensation risk was 0% in the 42.5% of patients who met the LSM <12 kPa & PLT >150 G/L criteria. In patients with post-treatment LSM ≥25 kPa (prevalence: 16.8%), the 3-year decompensation risk was 9.6%, while it was 1.3% in those meeting none of the above criteria (prevalence: 40.7%).
Conclusions: NITs can estimate the probability of CSPH after HCV cure and predict clinical outcomes. Patients with cACLD but LSM <12 kPa & PLT>150 G/L may be discharged from portal hypertension surveillance if no co-factors are present, while patients with LSM ≥25 kPa require surveillance/treatment.
Lay summary: Measurement of liver stiffness by a specific ultrasound device and platelet count (a simple blood test) are broadly used for the non-invasive diagnosis of increased blood pressure in the veins leading to the liver, which drives the development of complications in patients with advanced liver disease. The results of our pooled analysis refute previous concerns that these tests are less accurate after the cure of hepatitis C virus (HCV) infection. We have developed diagnostic criteria that facilitate personalized management after HCV cure and allow for a de-escalation of care in a high proportion of patients, thereby decreasing disease burden.
Keywords: CSPH; HVPG; LSM; NIT; SVR; aetiological cure; chronic hepatitis C; hepatic venous pressure gradient; liver stiffness measurement; platelet count; sustained virologic response; transient elastography.
Copyright © 2022 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
Conflict of interest statement
Conflict of interest G.S. received travel support from Gilead. S.L. received grant support from Gilead and served as a speaker and/or consultant and/or advisory board member for AbbVie, Gilead, and MSD. E.L.M. received grant support from Novartis. A.B. has nothing to disclose. E.A. has nothing to disclose. E.L. has nothing to disclose. L.T. served as a speaker and/or consultant and/or advisory board member for AbbVie, Gilead, Bayern, Janssen, and W. L. Gore & Associates, and received travel support from AbbVie, MSD, and Gilead. P.S. served as a consultant for PharmaIN. E.M. has nothing to disclose. L.E. has nothing to disclose. C.D. has nothing to disclose. L.I.-M. has nothing to disclose. A.P. has nothing to disclose. J.I.F. has nothing to disclose. M.A. has nothing to disclose. A.Z. has nothing to disclose. A.C. has nothing to disclose. H.H.-E. has nothing to disclose. I.S.L.S. has nothing to disclose. J.J. has nothing to disclose. H.Y. served as a speaker and/or consultant and/or advisory board member for AbbVie, Gilead, Otuka, Asuka, and MSD. S.M.F. has nothing to disclose. E.A.T. served as a speaker and/or consultant and/or advisory board member for Intercept, Gilead, Pfizer, NovoNordisk and Orphalan. F.P.R. served as a speaker and/or consultant and/or advisory board member for AbbVie, Biotest, Gilead, and MSD, and received travel support from AbbVie, Biotest, and Gilead. G.C. has nothing to disclose. X.F. served as a speaker and/or consultant for AbbVie and Gilead. R.B. served as a speaker and/or consultant and/or advisory board member for AbbVie, Gilead, and Janssen. C.V. has nothing to disclose. V.H.-G. served as a speaker and/or consultant and/or advisory board member for W. L. Gore & Associates. T.R. served as a speaker and/or consultant and/or advisory board member for AbbVie, Bayer, Boehringer Ingelheim, Gilead, Intercept, MSD, Siemens, and W. L. Gore & Associates and received grants/research support from AbbVie, Boehringer Ingelheim, Gilead, MSD, Philips, and W. L. Gore & Associates as well as travel support from Boehringer Ingelheim and Gilead. J.B. served as a lecturer or consultant for W. L. Gore & Associates, Actelion and Surrozen, and received grants from the ‘Siftung für Leberkrankheiten Bern’. J.C.G.-P. served as a speaker and/or consultant and/or advisory board member for Cook and W. L. Gore & Associates and received grants/research support from Conatus, Exalenz, Novartis, and Theravance. M.M. served as a speaker and/or consultant and/or advisory board member for AbbVie, Bristol-Myers Squibb, Gilead, Collective Acumen, and W. L. Gore & Associates and received travel support from AbbVie, Bristol-Myers Squibb, and Gilead. Please refer to the accompanying ICMJE disclosure forms for further details.
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