§
Proteomics involves the
identification of unknown proteins following their separation. The application
of proteomics to Alzheimer disease (AD), is a very new and emerging technology.
Differences in protein expression and post-translational modification (mostly
oxidative modification) of proteins from AD brain and peripheral tissue, as
well as in brain from rodent models of AD, have yielded insights into potential
molecular mechanisms of neurodegeneration in AD. Further work in this area
hopefully will bring new insights about the pathology, biochemistry, and physiology
of AD are beginning to.[i]
Europe and the Fifth Framework Program for Alzheimer disease
Alzheimer disease is an important topic of
the key action on "The aging population and disabilities" of the
European Union's Fifth
Framework Programme. The European commission recognizes the impact of AD on
individuals and society and the urgent need for treatments that can prevent,
arrest and reverse degeneration and death of neurons. The multidisciplinary
projects launched with EU support set a prerequisite in the understanding of
the fundamental molecular and cellular mechanisms of AD and the development of
diagnostic tools that may identify patients at an early pre-symptomatic stage.
Furthermore a consortium of 21 of the most experienced AD laboratories from
Europe and beyond are to carry our research projects integrating data from
studies with tissue cultures and genetically modified animals into a clinical
investigations of demented patients. A broad array of bio-technological methods
is also to be used. Results of these studies will lead to diagnostic screening
strategies combing genetic, pathophysiological and biomarker information. Annex
6.11.2 is the records of the current fifth framework research projects
related to AD.[ii]
Six EU-funded projects were launched in
2000 with a total EU support of € 2 million over 3 years. The ultimate aim of
the projects is to diagnose, prevent, delay the onset or treat Alzheimer
disease.[iii]
§
Five of the 6 projects seek to
understand the mechanisms involved in neurodegeneration and complement each
other by studying various aspects of these mechanisms. All aim at identifying
and testing potential therapeutic strategies, for instance anti-inflammatory
drugs.
§
Two pharmaceutical industries
are already involved as partners in two projects and others will be involved in
others when new potential therapeutic targets are identified.
§
One project focuses on the
needed improvement of cost-effective early diagnosis of dementia and on the
differential diagnosis among the various types of dementia. Differentiating Alzheimer
disease from other dementias is indeed important, since some of the latter can
be treated. This project will essentially try and define widely available
diagnostic procedures, by comparison to positron emission tomography (PET), a
little available and expensive non-invasive metabolic imaging technique.
[i] Butterfield DA, Boyd-Kimball D, Castegna
A. Proteomics in Alzheimer's
disease: insights into potential mechanisms of neurodegeneration. J Neurochem. 2003
Sep;86(6):1313-27.
[ii]http://dbs.cordis.lu/fepcgi/srchidadb?CALLER=PROJ_FP5&QZ_WEBSRCH=alzheimer%27s+disease&USR_SORT=EP_PGA_A+CHAR+ASC. The fifth framework Program. The European
Commission Community Research. 1998-2002. Last accessed May 30, 2004.
[iii] http://europa.eu.int/comm/research/press/2000/pr2109-alz-en.html.
Progress against Alzheimer’s Disease. Press Release Brussels, 21 September
2000. EUROPA. Last accessed May 30, 2004.
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