TY - JOUR
T1 - Dynamics of liver stiffness measurement and clinical course of primary biliary cholangitis
AU - Global & ERN Rare-Liver PBC Study Groups
AU - Lam, Laurent
AU - Soret, Pierre-Antoine
AU - Lemoinne, Sara
AU - Hansen, Bettina
AU - Hirschfield, Gideon
AU - Gulamhusein, Aliya
AU - Montano-Loza, Aldo J.
AU - Lytvyak, Ellina
AU - Parés, Albert
AU - Olivas, Ignasi
AU - Londono, Maria-Carlota
AU - Rodríguez-Tajes, Sergio
AU - Eaton, John E.
AU - Osman, Karim T.
AU - Schramm, Christoph
AU - Sebode, Marcial
AU - Lohse, Ansgar W.
AU - Dalekos, George
AU - Gatselis, Nikolaos
AU - Nevens, Frederik
AU - Cazzagon, Nora
AU - Zago, Alessandra
AU - Russo, Francesco Paolo
AU - Floreani, Annarosa
AU - Abbas, Nadir
AU - Trivedi, Palak
AU - Thorburn, Douglas
AU - Saffioti, Francesca
AU - Barkai, Laszlo
AU - Roccarina, Davide
AU - Calvaruso, Vicenza
AU - Fichera, Anna
AU - Delamarre, Adèle
AU - Sobenko, Natalia
AU - Villamil, Alejandra Maria
AU - Medina-Morales, Esli
AU - Bonder, Alan
AU - Patwardhan, Vilas
AU - Rigamonti, Cristina
AU - Carbone, Marco
AU - Invernizzi, Pietro
AU - Cristoferi, Laura
AU - van der Meer, Adriaan
AU - de Veer, Rozanne
AU - Zigmond, Ehud
AU - Yehezkel, Eyal
AU - Kremer, Andreas E.
AU - Deibel, Ansgar
AU - Bruns, Tony
AU - Große, Karsten
AU - Wetten, Aaron
AU - Dyson, Jessica Katharine
AU - Jones, David
AU - Levy, Cynthia
AU - Tanaka, Atsushi
AU - Dumortier, Jérôme
AU - Pageaux, Georges-Philippe
AU - de Lédinghen, Victor
AU - Carrat, Fabrice
AU - Chazouillères, Olivier
AU - Corpechot, Christophe
PY - 2024/7/15
Y1 - 2024/7/15
N2 - Background & aims: In primary biliary cholangitis (PBC), static liver stiffness measurement (LSM) has proven prognostic value. However, the added prognostic value of LSM time course in this disease remains uncertain.
Methods: We conducted an international retrospective cohort study among PBC patients treated with ursodeoxycholic acid (UDCA) and followed by vibration-controlled transient elastography (VCTE) between 2003 and 2022. Using joint modeling, the association of LSM trajectory and the incidence of serious clinical events (SCE), defined as cirrhosis complications, liver transplantation (LT) or death, was quantified using the hazard ratio (HR) and its confidence interval (CI).
Results: A total of 6,362 LSMs were performed in 3,078 patients (2,007 on UDCA alone; 13% with cirrhosis), in whom 316 SCE occurred over 14,445 person-years (median follow-up, 4.2 years; incidence rate, 21.9 per 1,000 person-years). LSM progressed in 59% of patients (mean 0.39 kPa/year). After adjusting for prognostic factors at baseline, including LSM, any relative change in LSM was associated with a significant variation in SCE risk (p<0.001). For example, the adjusted HRs (95% CI) associated with a 20% annual variation in LSM were 2.13 (1.89 – 2.45) for the increase and 0.40 (0.33 – 0.46) for the decrease. The association between LSM trajectory and SCE risk persisted regardless of treatment response or duration, when patients with cirrhosis were excluded, and when only death or LT was considered.
Conclusions: Tracking longitudinal changes in LSM using VCTE provides valuable insights into PBC prognosis, offering a robust predictive measure for the risk of SCE. LSM could be used as a clinically relevant surrogate endpoint in PBC clinical trials.
AB - Background & aims: In primary biliary cholangitis (PBC), static liver stiffness measurement (LSM) has proven prognostic value. However, the added prognostic value of LSM time course in this disease remains uncertain.
Methods: We conducted an international retrospective cohort study among PBC patients treated with ursodeoxycholic acid (UDCA) and followed by vibration-controlled transient elastography (VCTE) between 2003 and 2022. Using joint modeling, the association of LSM trajectory and the incidence of serious clinical events (SCE), defined as cirrhosis complications, liver transplantation (LT) or death, was quantified using the hazard ratio (HR) and its confidence interval (CI).
Results: A total of 6,362 LSMs were performed in 3,078 patients (2,007 on UDCA alone; 13% with cirrhosis), in whom 316 SCE occurred over 14,445 person-years (median follow-up, 4.2 years; incidence rate, 21.9 per 1,000 person-years). LSM progressed in 59% of patients (mean 0.39 kPa/year). After adjusting for prognostic factors at baseline, including LSM, any relative change in LSM was associated with a significant variation in SCE risk (p<0.001). For example, the adjusted HRs (95% CI) associated with a 20% annual variation in LSM were 2.13 (1.89 – 2.45) for the increase and 0.40 (0.33 – 0.46) for the decrease. The association between LSM trajectory and SCE risk persisted regardless of treatment response or duration, when patients with cirrhosis were excluded, and when only death or LT was considered.
Conclusions: Tracking longitudinal changes in LSM using VCTE provides valuable insights into PBC prognosis, offering a robust predictive measure for the risk of SCE. LSM could be used as a clinically relevant surrogate endpoint in PBC clinical trials.
KW - PBC
KW - Liver stiffness
KW - Elastography
KW - FibroScan
KW - Time course
KW - Prognosis
U2 - 10.1016/j.cgh.2024.06.035
DO - 10.1016/j.cgh.2024.06.035
M3 - Article
SN - 1542-3565
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
ER -