Your browser doesn't support javascript.
loading
Effects of Tumor Necrosis Factor Antagonists in Patients With Primary Sclerosing Cholangitis.
Hedin, Charlotte Rose Hawkey; Sado, Gina; Ndegwa, Nelson; Lytvyak, Ellina; Mason, Andrew; Montano-Loza, Aldo; Gerussi, Alessio; Saffioti, Francesca; Thorburn, Douglas; Nilsson, Emma; Larsson, Geir; Moum, Bjørn A; van Munster, Kim N; Ponsioen, Cyriel Y; Levy, Cynthia; Nogueira, Nicholas F; Bowlus, Christopher L; Gotlieb, Neta; Shibolet, Oren; Lynch, Kate D; Chapman, Roger W; Rupp, Christian; Vesterhus, Mette; Jørgensen, Kristin K; Rorsman, Fredrik; Schramm, Christoph; Sabino, João; Vermeire, Severine; Zago, Alessandra; Cazzagon, Nora; Marschall, Hanns-Ulrich; Ytting, Henriette; Ben Belkacem, Karima; Chazouilleres, Olivier; Almer, Sven; Bergquist, Annika.
Afiliação
  • Hedin CRH; Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden; Division of Gastroenterology, Medical Unit Gastroenterology, Dermatovenereology and Rheumatology, Karolinska University Hospital, Stockholm, Sweden; European Reference Network on Hepatological Diseases. Electronic address: Charl
  • Sado G; Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden; European Reference Network on Hepatological Diseases.
  • Ndegwa N; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Lytvyak E; Katz Group Centre for Pharmacy and Health Research, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
  • Mason A; Katz Group Centre for Pharmacy and Health Research, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
  • Montano-Loza A; Katz Group Centre for Pharmacy and Health Research, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
  • Gerussi A; Sheila Sherlock Liver Center, Royal Free London National Health Service Foundation Trust, Institute for Liver and Digestive Health, University College of London, London, United Kingdom; Internal Medicine Unit, Department of Medicine, University of Udine, Udine, Italy; European Reference Network on H
  • Saffioti F; Sheila Sherlock Liver Center, Royal Free London National Health Service Foundation Trust, Institute for Liver and Digestive Health, University College of London, London, United Kingdom; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy; European Reference Networ
  • Thorburn D; Sheila Sherlock Liver Center, Royal Free London National Health Service Foundation Trust, Institute for Liver and Digestive Health, University College of London, London, United Kingdom; European Reference Network on Hepatological Diseases.
  • Nilsson E; Gastroenterology Clinic, Skåne University Hospital, Lund University, Lund, Sweden.
  • Larsson G; Dept. of Gastroenterology and Hepatology, Clinics of Medicine, Oslo University Hospital, Ullevål, Oslo, Norway; European Reference Network on Hepatological Diseases.
  • Moum BA; Dept. of Gastroenterology and Hepatology, Clinics of Medicine, Oslo University Hospital, Ullevål, Oslo, Norway; European Reference Network on Hepatological Diseases.
  • van Munster KN; Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, The Netherlands; European Reference Network on Hepatological Diseases.
  • Ponsioen CY; Department of Gastroenterology and Hepatology, Academic Medical Center, Amsterdam, The Netherlands; European Reference Network on Hepatological Diseases.
  • Levy C; Division of Hepatology, Miller School of Medicine, Miami, Florida.
  • Nogueira NF; Schiff Center for Liver Diseases, University of Miami, Miami, Florida.
  • Bowlus CL; Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of California Davis, Sacramento, California.
  • Gotlieb N; Department of Gastroenterology and Hepatology, Tel Aviv Sourasky Medical Center, Tel Aviv University, Tel Aviv, Israel.
  • Shibolet O; Department of Gastroenterology and Hepatology, Tel Aviv Sourasky Medical Center, Tel Aviv University, Tel Aviv, Israel.
  • Lynch KD; Translational Gastroenterology Unit, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Chapman RW; Translational Gastroenterology Unit, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Rupp C; Department of Internal Medicine IV, University Hospital Heidelberg, Heidelberg, Germany.
  • Vesterhus M; Department of Medicine, Haraldsplass Deaconess Hospital, Bergen, Norway.
  • Jørgensen KK; Department of Gastroenterology, Akershus University Hospital, Lørenskog, Norway.
  • Rorsman F; Department of Medical Sciences, Gastroenterology Research Group, University Hospital, Uppsala, Sweden.
  • Schramm C; Martin Zeitz Center for Rare Diseases, First Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany; European Reference Network on Hepatological Diseases.
  • Sabino J; Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Leuven, Belgium; European Reference Network on Hepatological Diseases.
  • Vermeire S; Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Leuven, Belgium; European Reference Network on Hepatological Diseases.
  • Zago A; Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy; European Reference Network on Hepatological Diseases.
  • Cazzagon N; Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy; European Reference Network on Hepatological Diseases.
  • Marschall HU; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University Hospital, Gothenburg, Sweden; European Reference Network on Hepatological Diseases.
  • Ytting H; Department of Medical Gastroenterology, Hvidovre Hospital, Department of Hepatology Rigshospitalet, Copenhagen, Denmark; European Reference Network on Hepatological Diseases.
  • Ben Belkacem K; Hepatology Department, French Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, French Network for Rare Liver Diseases in Adults and Children, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Centre de Recherche Saint-Antoine (CRSA), Sorbonne University, Pa
  • Chazouilleres O; Hepatology Department, French Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, French Network for Rare Liver Diseases in Adults and Children, Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris, Centre de Recherche Saint-Antoine (CRSA), Sorbonne University, Pa
  • Almer S; Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden; European Reference Network on Hepatological Diseases.
  • Bergquist A; Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden; European Reference Network on Hepatological Diseases.
Clin Gastroenterol Hepatol ; 18(10): 2295-2304.e2, 2020 09.
Article em En | MEDLINE | ID: mdl-32068151
ABSTRACT
BACKGROUND &

AIMS:

Few patients with primary sclerosing cholangitis (PSC) and inflammatory bowel diseases (IBDs) are exposed to tumor necrosis factor (TNF) antagonists because of the often mild symptoms of IBD. We assessed the effects of anti-TNF agents on liver function in patients with PSC and IBD, and their efficacy in treatment of IBD.

METHODS:

We performed a retrospective analysis of 141 patients with PSC and IBD receiving treatment with anti-TNF agents (infliximab or adalimumab) at 20 sites (mostly tertiary-care centers) in Europe and North America. We collected data on the serum level of alkaline phosphatase (ALP). IBD response was defined as either endoscopic response or, if no endoscopic data were available, clinical response, as determined by the treating clinician or measurements of fecal calprotectin. Remission was defined more stringently as endoscopic mucosal healing. We used linear regression analysis to identify factors associated significantly with level of ALP during anti-TNF therapy.

RESULTS:

Anti-TNF treatment produced a response of IBD in 48% of patients and remission of IBD in 23%. There was no difference in PSC symptom frequency before or after drug exposure. The most common reasons for anti-TNF discontinuation were primary nonresponse of IBD (17%) and side effects (18%). At 3 months, infliximab-treated patients had a median reduction in serum level of ALP of 4% (interquartile range, reduction of 25% to increase of 19%) compared with a median 15% reduction in ALP in adalimumab-treated patients (interquartile range, reduction of 29% to reduction of 4%; P = .035). Factors associated with lower ALP were normal ALP at baseline (P < .01), treatment with adalimumab (P = .090), and treatment in Europe (P = .083).

CONCLUSIONS:

In a retrospective analysis of 141 patients with PSC and IBD, anti-TNF agents were moderately effective and were not associated with exacerbation of PSC symptoms or specific side effects. Prospective studies are needed to investigate the association between use of adalimumab and reduced serum levels of ALP further.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colangite Esclerosante / Doenças Inflamatórias Intestinais Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colangite Esclerosante / Doenças Inflamatórias Intestinais Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article