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Overview
Persons (6)
MITOCIRCLE - Mitochondrial diseases: From bedside to genome to bedside
Time period:
2005-01-01 - 2007-12-31
Instrument:
Specific Targeted Research Project (STREP)
Call:
FP6-2003-LIFESCIHEALTH-I
The aim of MITOCIRCLE is to optimise efficient and accurate diagnosis throughout the EU and thereby establish best practice for the clinical investigation and management of patients and families with mitochondrial disease. Mitochondrial disorders are often fatal multisystem disorders, associated with abnormalities of the terminal component of mitochondrial energy metabolism, i.e. oxidative phosphorylation (OXPHOS). Defects of the respiratory chain are the biochemical hallmarks of human mitochondrial disease. Because of its dual genetic control, defects in OXPHOS can be due to mutations in either the mitochondrial or nuclear DNA. Although OXPHOS disorders have comon characteristics as a group there is considerable clinical variability among patients, even in those having the same genetic defect. As a result each centre has acces to only relatively small numbers of patients in each disease category, making it difficult for individual centres to develop consensus guidelines for the investigation of mitochondrial diseases. There are currently no clinical or laboratory guidelines for the investigation of suspected mitochondrial disease, resulting in considerable variability in the standard and accuracy of investigation throughout the EU. Developing consensus guidelines with a broad relevance for all suspected patients is a matter of some urgency to ensure rapid and accurate diagnosis of mitochondrial disorders in each member state. This will only be possible through the concerted action of the principal European centres with expertise in both clinical and laboratory aspects. This forms the focus of this proposal - to take advances made in the laboratory back to the clinic and thereby improve the management of patient and families with mitochondrial disease. This will pave the way for futute treatment trials.
Principal investigators
Scientific co-ordinator:
Bert Smeets
(
UNIVERSITEIT MAASTRICHT
)
Other principal investigators:
Valeria Tiranti
(
FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA
)
Patrick Francis Chinnery
(
UNIVERSITY OF NEWCASTLE UPON TYNE
)
Lambertus van den Heuvel
(
STICHTING KATHOLIEKE UNIVERSITEIT
)
Agnes Rötig
(
INSERM - Institut national de la sante et de la recherche medicale
)
Alan Chan
(
PAMGENE INTERNATIONAL BV
)
Related Areas
Development of new diagnostics
Keywords
Congenital Abnormality
abnormalities
Administration
Ambulatory Care Facilities
Association
Cell Nucleus
Clinical Investigators
Diagnosis
Disease
DNA
Efficiency
Energy Metabolism
European Union
Family
Gene Expression Regulation
Genome
Hereditary Diseases
Laboratory
Mitochondria
Mutation
Persons
Oxidative Phosphorylation
Patients
Research Personnel
standards
therapy
Relatives
Homo sapiens
Treatment
Respiratory Chain
Guidelines as Topic
PAVe protocol 1
Ensure
guidelines
defects
Consensus
Forms
Mitochondrial Diseases
Population Group
Countries
Netherlands
Italy
United Kingdom
France
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Last updated on 2011-08-18 at 19:12
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