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Combination of fibrates with obeticholic acid is able to normalise biochemical liver tests in patients with difficult-to-treat primary biliary cholangitis

Authors :
Pietro Invernizzi
Dominique Larrey
Thomas Berg
Christine Silvain
Christina Weiler-Normann
Rodolphe Anty
Cervoni Jp
Albert Parés
Cynthia Levy
Olivier Chazouillères
Laurent Lam
Christophe Bureau
Isabelle Rosa-Hezode
Palak J. Trivedi
Christoph Schramm
Nora Cazzagon
Laurent Alric
Vincent Leroy
Alexandra Heurgué
Frederik Nevens
Jérôme Dumortier
Pierre Antoine Soret
Olivier Roux
Marco Carbone
Fabrice Carrat
Pascal Potier
Lena Smets
Christophe Corpechot
Gestionnaire, Hal Sorbonne Université
Centre de Référence des Maladies Rares - Maladies Inflammatoires des Voies Biliaires et Service d’Hépatologie [CHU Saint-Antoine]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Saint-Antoine [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)
Centre de Recherche Saint-Antoine (CRSA)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)
Institut Pierre Louis d'Epidémiologie et de Santé Publique (iPLESP)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)
Service de santé publique [CHU Saint-Antoine]
University Hospitals Leuven [Leuven]
Leipzig University
Università degli Studi di Milano-Bicocca = University of Milano-Bicocca (UNIMIB)
Centre Hospitalier Universitaire [Grenoble] (CHU)
University Hospitals Birmingham [Birmingham, Royaume-Uni]
Azienda Ospedale Università di Padova = Hospital-University of Padua (AOUP)
University Hospital Hamburg-Eppendorf
Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf [Hamburg] (UKE)
Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)
Université Toulouse III - Paul Sabatier (UT3)
Université Fédérale Toulouse Midi-Pyrénées
Centre Hospitalier Intercommunal de Créteil (CHIC)
Centre Hospitalier Universitaire de Reims (CHU Reims)
Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)
Hôpital Edouard Herriot [CHU - HCL]
Hospices Civils de Lyon (HCL)
Centre Hospitalier Régional d'Orléans (CHRO)
Centre de référence des Maladies Vasculaires du Foie [Paris] (FILFOIE)
Hôpital Beaujon [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Centre hospitalier universitaire de Poitiers (CHU Poitiers)
Centre Hospitalier Universitaire de Nice (CHU Nice)
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
University of Miami Leonard M. Miller School of Medicine (UMMSM)
Clinic Barcelona Hospital Universitari
Soret, P
Lam, L
Carrat, F
Smets, L
Berg, T
Carbone, M
Invernizzi, P
Leroy, V
Trivedi, P
Cazzagon, N
Weiler-Normann, C
Alric, L
Rosa-Hezode, I
Heurgue, A
Cervoni, J
Dumortier, J
Potier, P
Roux, O
Silvain, C
Bureau, C
Anty, R
Larrey, D
Levy, C
Pares, A
Schramm, C
Nevens, F
Chazouilleres, O
Corpechot, C
Source :
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2021, 53 (10), pp.1138--1146. ⟨10.1111/apt.16336⟩
Publication Year :
2021
Publisher :
Blackwell Publishing Ltd, 2021.

Abstract

Background: Obeticholic acid (OCA) and fibrates are second-line therapies for patients with primary biliary cholangitis (PBC) with an inadequate response to ursodeoxycholic acid (UDCA). Aim: To know whether OCA and fibrates, administered together in combination with UDCA, have additive beneficial effects in patients with difficult-to-treat PBC. Methods: PBC patients treated for ≥3months with UDCA, OCA and fibrates (bezafibrate or fenofibrate) due to failure of either second-line therapy were included in a multicentre, uncontrolled retrospective cohort study. Changes in biochemical liver tests and pruritus were analysed using a generalised linear mixed-effect model. Results: Among 58 patients included, half received OCA as second-line and fibrates as third-line therapy (Group OCA-Fibrate), while the other half had the inverse therapeutic sequence (Group Fibrate-OCA). The mean duration of triple therapy was 11months (range 3-26). Compared to dual therapy, triple therapy was associated with a significant gain in alkaline phosphatase (ALP) reduction: 22% per first year (95% CI 12%-31%), an effect that was stronger in OCA-Fibrate than in Fibrate-OCA group. Triple therapy was associated with a 3.4 (95% CI 1.4-8.2) odds ratio (OR) of reaching normal ALP and with a significant decrease in gamma-glutamyl transpeptidase (GGT), alanine aminotransferase (ALT), aspartate aminotransferase (AST) and total bilirubin. The ORs of achieving the Paris-2 and Toronto criteria of adequate biochemical response were 6.8 (95% CI 2.8-16.7) and 9.2 (95% CI 3.4-25.1) respectively. Finally, triple therapy significantly improved pruritus in OCA-Fibrate but not in Fibrate-OCA group. Conclusions: Triple therapy with UDCA, OCA and fibrates is able to normalise biochemical liver tests and improve pruritus in patients with difficult-to-treat PBC.

Details

Language :
English
Database :
OpenAIRE
Journal :
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2021, 53 (10), pp.1138--1146. ⟨10.1111/apt.16336⟩
Accession number :
edsair.doi.dedup.....f158862dc3423fdff68f823dc8ca1557
Full Text :
https://doi.org/10.1111/apt.16336⟩