Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON)-An International Network on Care and Research for Patients With Neurodegeneration With Brain Iron Accumulation (NBIA).

NBIA TIRCON clinical network movement disorder orphan disease patient registry

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2021
Historique:
received: 15 12 2020
accepted: 28 01 2021
entrez: 11 3 2021
pubmed: 12 3 2021
medline: 12 3 2021
Statut: epublish

Résumé

In order to improve clinical care, coordinate research activities and raise awareness for the ultra-orphan Neurodegeneration with Brain Iron Accumulation (NBIA) disorders, a group of NBIA clinicians and researchers, industry partners and patient advocacies from six European countries, Canada and the US joined forces in 2010 to set-up the collaborative initiative TIRCON (Treat Iron-Related Childhood-Onset Neurodegeneration). As a research project, TIRCON received funding in the 7th Framework Programme (FP7) of the European Union (EU) from 2011 to 2015. After successful and timely completion of the initial FP7 project, funding and donations from industry and patient organizations have sustained the further development of TIRCON's dedicated clinical research infrastructure and its governance architecture, as well as the ongoing efforts undertaken in the NBIA community to establish a network of care. From the beginning, the University Hospital of the Ludwig-Maximilians-University in Munich, Germany has been coordinating the TIRCON initiative. It consists of 8 work packages, of which the first double-blind, placebo-controlled, randomized, multi-site clinical trial in NBIA (deferiprone in PKAN, completed) and a global patient registry and biobank, currently comprising baseline and follow-up data of > 400 NBIA patients have gained particular importance. Here we describe TIRCON's history with all the challenges and achievements in diagnosing and treating NBIA. Today, TIRCON lays the ground for future clinical care and research. In these times, it may also serve as a good example of well-directed governmental funding and fruitful international scientific collaboration.

Identifiants

pubmed: 33692746
doi: 10.3389/fneur.2021.642228
pmc: PMC7937633
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

642228

Informations de copyright

Copyright © 2021 Karin, Büchner, Gauzy, Klucken and Klopstock.

Déclaration de conflit d'intérêts

TK served as coordinating investigator of the FORT trial; received research funding from Retrophin Inc.; served as coordinating investigator of the deferiprone in PKAN randomized and extension trial; received research funding from ApoPharma Inc.; received support from the European Commission 7th Framework Programme (FP7/2007-2013, HEALTH-F2-2011, grant agreement No. 277984, TIRCON) and from the European Reference Network for Rare Neurological Diseases (ERN-RND), co-funded by the European Commission (ERN-RND: 3HP 767231); provided consulting services to CoA Therapeutics and TM3 Therapeutics; received travel support from ApoPharma Inc. BB provided consulting services to Retrophin Inc. and ApoPharma Inc. IK received travel support from ApoPharma Inc. FG received support from the European Commission 7th Framework Programme (FP7/2007-2013, HEALTH-F2-2011, grant agreement No.277984, TIRCON). AK received support from the European Commission 7th Framework Programme (FP7/2007-2013, HEALTH-F2-2011, grant agreement No. 277984, TIRCON); received travel support from Retrophin Inc.

Références

Am J Hum Genet. 2011 Oct 7;89(4):543-50
pubmed: 21981780
Am J Hum Genet. 2008 Nov;83(5):610-5
pubmed: 18950739
Med Care. 2001 Aug;39(8):800-12
pubmed: 11468499
Psychiatry Res. 1989 May;28(2):193-213
pubmed: 2748771
Nat Genet. 2001 Aug;28(4):345-9
pubmed: 11479594
Dev Med Child Neurol. 1999 Jun;41(6):404-11
pubmed: 10400175
Mol Genet Metab. 2017 Mar;120(3):278-287
pubmed: 28034613
Clin Trials. 2019 Aug;16(4):410-418
pubmed: 31055958
Lancet Neurol. 2019 Jul;18(7):631-642
pubmed: 31202468
Ann Clin Transl Neurol. 2020 Aug;7(8):1340-1351
pubmed: 32705819
Parkinsonism Relat Disord. 2014 Jun;20(6):651-4
pubmed: 24661465
Mol Genet Metab. 2019 Dec;128(4):463-469
pubmed: 31540697
Mov Disord. 2017 Nov;32(11):1620-1630
pubmed: 28845923
Mov Disord. 2008 Nov 15;23(15):2129-70
pubmed: 19025984
Mov Disord Clin Pract. 2019 Jan 22;6(2):139-149
pubmed: 30838313
Mov Disord. 2020 Nov 16;:
pubmed: 33200489
Orphanet J Rare Dis. 2012 Sep 17;7:66
pubmed: 22985983
Case Rep Neurol Med. 2017;2017:3247034
pubmed: 28567317
Proc Natl Acad Sci U S A. 2010 Apr 13;107(15):6988-93
pubmed: 20351285
Am J Hum Genet. 2014 Jan 2;94(1):11-22
pubmed: 24360804
Front Neurol. 2020 Sep 10;11:1024
pubmed: 33013674
Am J Hum Genet. 2012 Dec 7;91(6):1144-9
pubmed: 23176820

Auteurs

Ivan Karin (I)

Department of Neurology, Friedrich-Baur-Institute, University Hospital of the Ludwig-Maximilians-University (LMU), Munich, Germany.

Boriana Büchner (B)

Department of Neurology, Friedrich-Baur-Institute, University Hospital of the Ludwig-Maximilians-University (LMU), Munich, Germany.

Florence Gauzy (F)

Office of International Science Cooperation, Bavarian Research Alliance (BayFOR), Munich, Germany.

Angelika Klucken (A)

Hoffnungsbaum e.V., Velbert, Germany.

Thomas Klopstock (T)

Department of Neurology, Friedrich-Baur-Institute, University Hospital of the Ludwig-Maximilians-University (LMU), Munich, Germany.
Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.

Classifications MeSH