Background 11/8/2011. Disclosure. Hereditary Periodic Fever Syndromes Mutations in Idiopathic Acute Recurrent Pericarditis.

Similar documents
Acute Pericarditis as the First Manifestation of Familial Mediterranean Fever: A Possible Relationship with Idiopathic Recurrent Pericarditis

FAMILIAL MEDITERRANEAN FEVER (FMF) RAKAN TELFAH not MD, not PHD

The role of E148Q in FMF. Elon Pras Institute of Human Genetics Sheba Medical Center

RISK OF FMF DEVELOPMENT AMONG HETEROZYGOUS PATIENTS IN ARMENIAN POPULATION

Περικαρδίτιδα στην καρδιακή ανεπάρκεια

Umbrella study design in patients with Hereditary Periodic Fevers, an orphan autoimmune disease. Karine Lheritier 15 June 2016 PSI Immunology meeting

YES NO UNKNOWN. Stage I: Rule-Out Dashboard Secondary Findings in Adults ACTIONABILITY PENETRANCE SIGNIFICANCE/BURDEN OF DISEASE NEXT STEPS

hereditary periodic fever periodic fever syndrome recurrent fever familial Mediterranean FMF autoinflammatory syndrome T 1 Tsutomu Oh-ishi

Research trial protocol.

Pericarditis in a Swiss regional hospital

Pericarditis. Marquette University. James F. Ginter Aurora Cardiovascular Services

Colchicine has been used for hundreds of years as an. Pericardial Disease

Even if rarely indicated, recurrent pericarditis often is

Pericardial Disease. Indicators of Poor Prognosis of Acute Pericarditis

Familial Mediterranean Fever. By:Ismaeel Qattam

TNF Receptor Associated Periodic Syndrome (TRAPS)

Policy Number: PHA044 Effective Date: March 1, 2019

Proceedings of the World Small Animal Veterinary Association Sydney, Australia 2007

, David Stultz, MD. Journal Club. David Stultz, MD Cardiology Fellow, PGY 6 November 3, 2005

Familial Mediterranean Fever. For. Professor Brutlag BIO84 16 March 2011

Νόσοι του περικαρδίου. Γεώργιος Λάζαρος Α Πανεπιστημιακή Καρδιολογική Κλινική Ιπποκράτειο Γ.Ν. Αθηνών

The rise and fall of FMF research Fifty years of publications

Policy Number: CS2019D0066C Effective Date: March 1, 2019

Familial Mediterranean Fever in a Sample of Iraqi Patients

Pericardial Diseases 2015 Update

Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations

The factors considered as trigger for the attacks in patients with familial Mediterranean fever

SYSTEMIC JUVENILE IDIOPATHIC ARTHRITIS DRUG

E148Q as A Familial Mediterranean Fever-Causing Mutation: A Clinical-Based Study R A Jarjour ABSTRACT

Colchicine for Post-operative Pericardial Diseases

Introduction. Keywords: AA amyloidosis; TNFRSF1A; MEFV; NALP3; periodic fever

Coverage Criteria: Express Scripts, Inc. monograph dated 12/15/ months or as otherwise noted by indication

Pedido de acesso a dados do Registo Nacional de Doentes Reumáticos (Reuma.pt) da Sociedade Portuguesa de Reumatologia

Diagnosis delay in familial Mediterranean fever (FMF): Social and gender gaps disclosed

Familial Mediterranean Fever

Clinical Study Serum Amyloid A Level in Egyptian Children with Familial Mediterranean Fever

recurrent febrile syndromes what a rheumatologist needs to know

Familial Mediterranean Fever

Fever in Lupus. 21 st April 2014

Acute Pericarditis. clinical practice. The Clinical Problem. Martin M. LeWinter, M.D.

LUPUS CAN DO EVERYTHING, BUT NOT EVERYTHING IS LUPUS LUPUS 101 SLE SUBSETS AUTOIMMUNE DISEASE 11/4/2013 HOWARD HAUPTMAN, MD IDIOPATHIC DISCOID LUPUS

This is an author produced version of Colchicine for children with pericarditis: systematic review of clinical studies.

Familial Cold Autoinflammatory Syndrome

Disclosures. Learning Objectives. Periodic Fever Syndromes. Innate Immune System. Our Immune System

Evaluation of Restless Legs syndrome and growing pains in children with familial Mediterranean fever

Pericardial diseases

Case report. Yasutsugu Fukushima, 1 Kazuki Obara, 1 Hirokuni Hirata, 1 Kumiya Sugiyama, 1 Takeshi Fukuda 1 and Kazuhiko Takabe 2

Cigna Drug and Biologic Coverage Policy

Familial Mediterranean fever

Successful treatment with infliximab and low-dose methotrexate in a Japanese patient with familial Mediterranean fever

TOCILIZUMAB FOR DIFFICULT TO TREAT IDIOPATHIC RETROPERITONEAL FIBROSIS. A PILOT TRIAL

Pediatric rheumatology review. New interest in an old disease: Familial Mediterranean fever

F amilial Mediterranean fever (FMF) is an autosomal

EuroTRAPS, a consortium for new therapeutic models in TNF receptor Associated Periodic Syndrome and hereditary recurrent fevers

F amilial Mediterranean fever (FMF) is an autosomal

Myocarditis and Pericarditis

Efficacy and Safety of Rituximab in the Treatment of Rheumatoid Arthritis and ANCA-associated Vasculitis

Cases from the Clinic Maryland ACP Meeting January 30, 2016

Idiopathic inflammatory myopathies

Mevalonate Kinase Deficiency (MKD), or Hyper IGD Syndrome

Misdiagnosis of familial Mediterranean fever in patients with Anderson Fabry disease

Review New insights in the pathogenesis and therapy of idiopathic recurrent pericarditis in children

This is a refereed journal and all articles are professionally screened and reviewed

THE PERICARDIUM: LOOKING OUTSIDE THE HEART

Vasculitis local: systemic

Πνευμονική υπέρταση και περικαρδιακή συλλογή. Τρόποι αντιμετώπισης

Gastrointestinal evaluation in colchicine-treated familial Mediterranean fever patients with chronic abdominal pain: Cases series

A Case of Impending Cardiac Tamponade Caused by Effusive Constrictive Pericarditis

Fever of unknown origin

Arcalyst (rilonacept)

Blau's Disease / Juvenile Sarcoidosis

High Impact Rheumatology

Colchicine-free remission in familial Mediterranean fever: featuring a unique subset of the disease-a case control study

Pericardial disease. Se-Jung Yoon Cardiology division NHIS Ilsan hospital

Rheumatoid Arthritis. Manish Relan, MD FACP RhMSUS Arthritis & Rheumatology Care Center. Jacksonville, FL (904)

Development of SLE among Possible SLE Patients Seen in Consultation: Long-Term Follow-Up. Disclosures. Background. Evidence-Based Medicine.

Pleural Effusion. Exudative pleural effusion - Involve an increase in capillary permeability and impaired pleural fluid resorption

(1) Les Grands Prés, Villeneuve-Saint Denis. France for the French Society of Cardiology.

Membranous nephropathy. By Mohammed Kamal Nassar, MD Lecturer of Nephrology Mansoura University

Vasculitis local: systemic

Adult-Onset Familial Mediterranean Fever in Northwestern Iran; Clinical Feature and Treatment Outcome

New Evidence reports on presentations given at ACR Improving Radiographic, Clinical, and Patient-Reported Outcomes with Rituximab

Reporting Autoimmune Diseases in Hematopoietic Stem Cell Transplantation

Advance Access publication 1 November 2005 Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes

How 5 Diseases Became One. Moez Tajdin R3 McGill University

Integrative Clinical Hemodyamics

Autoantibodies in the Idiopathic Inflammatory Myopathies

For more information about how to cite these materials visit

Objectives. Highlight typical feature of TB pericarditis. How to make a diagnosis. How to treat TB pericarditis

Long-term exposure to Myozyme results in a decrease of anti-drug antibodies in lateonset Pompe disease patients

Rheumatic heart disease

Adult-onset Still s disease a polygenic autoinflammatory disease

Efficacy and safety of colchicine for pericarditis prevention. Systematic review and meta-analysis

City, University of London Institutional Repository

Autoimmunity and autoinflammation

Centre for Arab Genomic Studies A Division of Sheikh Hamdan Award for Medical Sciences

MEDICAL POLICY I. POLICY POLICY TITLE POLICY NUMBER CANAKINUMAB (ILARIS ) MP-2.147

Case 5 15-year-old male

Carditis: Inside and Out. Derek Brown, MD SAUSHEC Military EMS & Disaster Medicine Fellow

Transcription:

Mutations in Idiopathic Acute Recurrent Pericarditis Disclosure I have no relevant financial relationships to disclose Guillaume Geri, Pierre Hausfater, Catherine Dodé, Zahir Amoura, Jean-Charles Piette, Nathalie Costedoat-Chalumeau, Patrice Cacoub Internal Medicine Department, CNRS UMR 7087, Pierre & Marie Curie University National Reference Center for Autoimmune Diseases La Pitié-Salpêtrière Hospital, Paris, FRANCE References Imazio M, Bobbio M, Cecchi E, Demarie D, Demichelis B, Pomari F, et al. Colchicinee in addition to conventional therapy for acute pericarditis: results of the Colchicine for acute PEricarditis (COPE) trial. Circulation 2005;112(13):2012-6. Background Dode C, Pecheux C, Cazeneuve C, Cattan D, Dervichian M, Goossens M, et al. Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean fever. Am J Med Genet 2000;92(4):241-6. Dode C, Papo T, Fieschi C, Pecheux C, Dion E, Picard F, et al. A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family. Arthritis Rheum 2000;43(7):1535-42. Acute Pericarditis Chest pain, fever, brief course, benign Isolated or part of a more systemic disease Numerous causes Infectious diseases (6-8%)» Tuberculosis (4%)» Pyogenic infection (2%)» Fungal and parasitic infections (rare) Auto-immune diseases (3-5%) Cardiac surgery or myocardial infarction (5-10%) Malignant diseases (5-10%) Idiopathic 70-90% Determined etiology Acute Pericarditis Idiopathic Natural History of Acute Pericarditis Short-term Right Heart Failure <2% Complete recovery Mid-term Chronic pericardial effusion Long-term Recurrence 20-40% Constrictive Pericarditis <2% Lange RA, New Engl J Med 2005 Troughton RW, Lancet 2004 Geri G, Rev Med Int 2010 1

Recurrences of fever lasting from a few days to a few weeks Symptom-free intervals of variable duration Diagnosis should be discussed if : Attacks with a predictable course and a similar set of symptoms Family history Imazio M, 2007 Familial Mediterranean Fever (FMF) The most prevalent periodic fever syndrome Predominantly affects people from the Mediterranean basin Short attacks of serositis (peritonitis, pleuritis, arthritis) & fever Autosomal recessive disease Treatment: colchicine TNF receptor-associated periodic syndrome (TRAPS) Recurrent attacks of fever, myalgia & painful skin erythema Autosomal dominant inheritance Response to high doses prednisone... and TNF alpha-blockers Others HPFS Hyper IgD syndrome Familial cold urticaria and Muckle-Wells syndrome Idiopathic Recurrent Acute Pericarditis (IRAP) Periodic recurrences Symptom-free intervals Family history No auto-immune process Great efficacy of colchicine Hereditary Periodic Fever Syndromes (HPFS) Drenth JPH, New Engl J Med 2001 Idiopathic Recurrent Pericarditis and Hereditary Periodic Fever Syndromes - Litterature data Pericarditis may be the sole manifestation of FMF 2 cases (Tauber T, 1995) Idiopathic recurrent acute pericarditis : FMF in a cohort of Caucasian patients. 0/23 Italian patients with mutation (Brucato A, 2005) Idiopathic recurrent pericarditis refractory to colchicine treatment may reveal TRAPS syndrome 4/30 (13.3%) patients with mutation (Cantarini L, 2009) Imazio M et al. Ann Intern Med 2011 2

Aims Idiopathic Recurrent Pericarditis and Aims 1. To search for the presence of HPFS gene in a large cohort of patients presenting with recurrent pericarditis 2. To analyze the impact of HPFS gene in patients with IRAP on: Sentivitity to treatments, i.e. NSAIDs, colchicine Mid- and long-term outcome, i.e. pericarditis relapses Treatment withdrawal, i.e. steroids Methods Retrospective study: 1990 2010 Pitié Salpêtrière Hospital (tertiary university) Recurrent pericarditis Systematic check-up Methods - 1 - Acute Pericarditis Chest pain and fever Increased inflammatory biomarkers Blood cultures ± pericardial effusion Mycobacteriological searching Recurrent Acute pericarditis HIV serology 2 acute events ANA, dsdna Ab, ANCA, RF, C3 & C4 complement Body CT-scan Pericardial fluid analysis Methods - 2 - Epidemiologic and clinical features Inflammatory biomarkers C-reactive protein (+ if > 20mg/L) Fibrinogen (+ if > 5g/L) Treatment Aspirin and non steroidal anti-inflammatory drugs Corticosteroids & immunosuppressants Colchicine Outcome : pericarditis relapse Delay, number Methods Gene Mutations of Hereditary Periodic Fever Syndrome Genomic DNA isolated from patients peripheral blood leucocytes Mutations: MFEV gene M680I, M694V, M694I, V726A, E148Q TNFRSF1A gene 3

Results Hereditary Periodic Fever Syndrome Mutations in Idiopathic Recurrent Pericarditis The presence of one HPFS gene mutation was found in 14/53 (26.4%) recurrent pericarditis. MFEV gene mutation in 7/53 (13.2%) IRAP patients TNRFS1A gene mutation in 7/53 (13.2%) IRAP patients Hereditary Periodic Fever Syndrome Mutations in Idiopathic Recurrent Pericarditis Hereditary Periodic Fever Syndrome Mutations in Idiopathic Recurrent Pericarditis HPFS gene mutation 14/53 (26.4%) in IRAP MFEV gene (13.2%) Heterozygous M694V: 2 patients Heterozygous M694I: 2 patients Heterozygous E148Q: 3 patients TNRFS1A gene (13.2%) Heterozygous R92Q: 4 patients Homozygous R92Q: 1 patient Heterozygous P46L: 2 patients HPFS gene mutation 14/53 (26.4%) in IRAP MFEV gene (13.2%) vs. < 1% in healthy controls Heterozygous M694V: 2 patients Heterozygous M694I: 2 patients Heterozygous E148Q: 3 patients TNRFS1A gene (13.2%) vs. 1-4% in healthy controls Heterozygous R92Q: 4 patients Homozygous R92Q: 1 patient Heterozygous P46L: 2 patients Epidemiologic Features All patients N= 53 Median age, 36.5 (Q1,Q3),y (24,53) Gender, M/F (%) 32/21 (60.4) HPFS N= 14 45.5 (24,57.8) No HPFS N= 39 33 (23,52.3) P 0.30 9/5 (64.3) 23/16 (59.0) 1 Ethnic origin 0.25 - European 41 (87.2) 11 (78.6) 30 (83.3) - North Africa 5 (10.6) 2 (14.3) 3 (8.3) - Others 1 (2.1) 1 (7.1) 0 (0) - NA 6 0 6 HPFS: hereditary periodic fever syndrome Clinical Features All patients N= 53 HPFS N= 14 No HPFS N= 39 Extracardiac features 36 (67.9) 10 (71.4) 26 (66.7) 1 - Pleural effusion 9 (16.9) 2 (14.3) 7 (17.9) - Arthralgia 7 (13.2) 1 (7.1) 6 (15.4) Time between 2 events, months 3 (1-6) 2.5 (1.8-4) 5 (2-12) 0.19 Increased inflammatory biomarkers, n (%) 36 (67.9) 11 (78.6) 25 (64.1) 0.51 HPFS: hereditary periodic fever syndrome P 4

Treatment of Recurrent Pericarditis & HPFS Mutation Pericarditis Relapse according to HPFS Mutation All patients N= 53 HPFS N= 14 No HPFS N= 39 P Median follow-up, y 2 (1-4) 4 (1-6.5) 2 (1-4) NS Corticosteroids withdrawal 5 out of 7 patients 3/4 with HPFS mutation 2/3 w/o HPFS mutation Relapses under colchicine, n (%) Median time before relapse, months Relapse at colchicine withdrawal, n (%) 18 (34.0) 4 (28.6) No 14 HPFS (36.0) mutation NS HPFS mutation + 7.5 (1.5-16.5) 6 (4-27) 9 (1-12) NS 8 (15.1) 4 (28.6) 4 (10.3) 0.19 HPFS: Hereditary Periodic Fever Syndrome HPFS: hereditary periodic fever syndrome Conclusion Mutations of hereditary periodic fever syndromes are frequently found in patients with idiopathic recurrent pericarditis (26.4%). Such should be searched for in patients presenting with IRAP. The impact of the presence of HPFS gene mutation on more specific therapeutic strategy in IRAP patients will need further studies. Evolution of Recurrent Acute Pericarditis Lotrionte. Am J Cardiol. 2010 N=84 patients, fu 24 months 5

Imazio M et al. Ann Intern Med 2011 6