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ADAPTED SIGNED

Alzheimers Disease Apolipoprotein Pathology for Treatment Elucidation and Development - Sofia ref.: 115975

Total Cost €

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EC-Contrib. €

0

Partnership

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 ADAPTED project word cloud

Explore the words cloud of the ADAPTED project. It provides you a very rough idea of what is the project "ADAPTED" about.

diagnostics    utility    ad       proof    cohorts    backbone    phenotype    leverage    uncover    capacity    genotypes    longitudinal    culture    extreme    human    pleiotropic    modulation    validation    astrocyte    gene    co    biomarkers    attenuate    omics    earliest    endocytosis    free    back    rising    biology    endothelium    differentiate    models    vision    macrophage    cohort    quantitative    proposes    focussed    largely    cells    seminal    hypothesis    unknown    immune    signalling    vasculature    risk    temporal    predictive    homeostasis    lines    identification    marker    effort    tide       suffering    treatment    metabolism    brain    chip    load    fundamental    rigorous    generate    25    homozygote    illuminate    embark    stages    form    blood    mci    neuron    dating    dimension    series    stem    organ    assays    mechanisms    bespoke    clinical    progression    combination    apoe    proteomics    editing    create    combined    ipsc    pluripotent    performed    signatures       acts    influence    experiments    validating    lipid    demands    complexity    data    consistency    broad    follow    diagnostic    harmonised    therapies    biological   

Project "ADAPTED" data sheet

The following table provides information about the project.

Coordinator
FUNDACIO ACE 

Organization address
address: MARQUES DE SENTMENAT 57
city: BARCELONA
postcode: 8014
website: n.a.

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Spain [ES]
 Project website https://imi-adapted.eu
 Total cost 6˙796˙740 €
 EC max contribution 3˙510˙000 € (52%)
 Programme 1. H2020-EU.3.1.7. (Innovative Medicines Initiative 2 (IMI2))
 Code Call H2020-JTI-IMI2-2015-05-two-stage
 Funding Scheme IMI2-RIA
 Starting year 2016
 Duration (year-month-day) from 2016-10-01   to  2020-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO ACE ES (BARCELONA) coordinator 333˙757.00
2    AGENCIA ESTATAL CONSEJO SUPERIOR DEINVESTIGACIONES CIENTIFICAS ES (MADRID) participant 688˙476.00
3    UNIVERSITEIT LEIDEN NL (LEIDEN) participant 470˙677.00
4    UNIVERSITATSKLINIKUM BONN DE (BONN) participant 429˙850.00
5    ERASMUS UNIVERSITAIR MEDISCH CENTRUM ROTTERDAM NL (ROTTERDAM) participant 420˙500.00
6    MIMETAS BV NL (Leiden) participant 305˙102.00
7    CAEBI BIOINFORMATICA SOCIEDAD LIMITADA ES (SEVILLA) participant 282˙062.00
8    KLINIKUM DER UNIVERSITAET ZU KOELN DE (KOELN) participant 244˙812.00
9    DC BIOSCEINCES LTD UK (DUNDEE) participant 186˙514.00
10    MODUS RESEARCH AND INNOVATION LIMITED UK (EDINBURGH) participant 110˙337.00
11    KITE INNOVATION (EUROPE) LIMITED UK (HUDDERSFIELD) participant 37˙912.00
12    ABBVIE DEUTSCHLAND GMBH & CO KG DE (WIESBADEN) participant 0.00
13    BIOGEN IDEC LIMITED UK (MAIDENHEAD) participant 0.00
14    JANSSEN PHARMACEUTICA NV BE (BEERSE) participant 0.00

Map

 Project objective

APOEɛ4 has long been known as a risk factor of LOAD, yet the biological mechanisms through which it acts remain largely unknown and affect both the vasculature and the brain. This complexity and pleiotropic influence demands an integrated hypothesis-free approach to embark on a fundamental study of the gene, the phenotype and modulation by other risk factors. ADAPTED proposes to leverage extreme genotypes from consortium cohorts dating back more than 25 years to generate, and use existing, lines of human induced pluripotent stem cells (iPSC). These cells, with blood cells, will form the backbone of the research programme. We will differentiate them to the most relevant cells for APOE and AD studies and with gene editing create bespoke homozygote ɛ3 and ɛ2 cells for a highly focussed effort on APOE biology. A series of experiments including neuron-astrocyte and macrophage-endothelium co-culture and Organ on a Chip models combined with state-of-the-art omics including quantitative proteomics assays will generate data for rigorous integrated analysis to uncover new signalling pathways related to APOE. Lipid homeostasis, endocytosis, metabolism and immune systems pathways will be investigated in a broad approach. The findings are expected to lead to identification of new treatment approaches and blood based AD signatures with a temporal dimension from the earliest stages of risk identification and progression through MCI to AD. Testing and validation of biomarkers will be performed by examining their influence and predictive capacity in a longitudinal ADAPTED cohort harmonised using a combination of approaches for marker and diagnostic consistency. The impact of this work can be expected to include seminal new finding to illuminate the research path towards new diagnostics and therapies to attenuate the rising tide of suffering from AD. The vision is a follow on with clinical proof of concept validating utility of the results within two years of the end of ADAPTED.

 Deliverables

List of deliverables.
Definition of cognitive composite scores to evaluate rate of disease progression based on cognitive function decline in the ADAPTED cohorts Websites, patent fillings, videos etc. 2020-04-08 21:10:07

Take a look to the deliverables list in detail:  detailed list of ADAPTED deliverables.

 Publications

year authors and title journal last update
List of publications.
2018 Michael Peitz, Tamara Bechler, Catrin Cornelia Thiele, Monika Veltel, Melanie Bloschies, Klaus Fliessbach, Alfredo Ramirez, Oliver Brüstle
Blood-derived integration-free iPS cell line UKBi011-A from a diagnosed male Alzheimer\'s disease patient with APOE ɛ4/ɛ4 genotype
published pages: 250-253, ISSN: 1873-5061, DOI: 10.1016/j.scr.2018.04.011
Stem Cell Research 29 2020-04-08
2018 Sven J. van der Lee, Charlotte E. Teunissen, René Pool, Martin J. Shipley, Alexander Teumer, Vincent Chouraki, Debora Melo van Lent, Juho Tynkkynen, Krista Fischer, Jussi Hernesniemi, Toomas Haller, Archana Singh-Manoux, Aswin Verhoeven, Gonneke Willemsen, Francisca A. de Leeuw, Holger Wagner, Jenny van Dongen, Johannes Hertel, Kathrin Budde, Ko Willems van Dijk, Leonie Weinhold, M. Arfan Ikram, Maik Pietzner, Markus Perola, Michael Wagner, Nele Friedrich, P. Eline Slagboom, Philip Scheltens, Qiong Yang, Robert E. Gertzen, Sarah Egert, Shuo Li, Thomas Hankemeier, Catharina E.M. van Beijsterveldt, Ramachandran S. Vasan, Wolfgang Maier, Carel F.W. Peeters, Hans Jörgen Grabe, Alfredo Ramirez, Sudha Seshadri, Andres Metspalu, Mika Kivimäki, Veikko Salomaa, Ayşe Demirkan, Dorret I. Boomsma, Wiesje M. van der Flier, Najaf Amin, Cornelia M. van Duijn
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies
published pages: , ISSN: 1552-5260, DOI: 10.1016/j.jalz.2017.11.012
Alzheimer\'s & Dementia 2020-04-08
2018 Nienke R. Wevers, Dhanesh G. Kasi, Taylor Gray, Karlijn J. Wilschut, Benjamin Smith, Remko van Vught, Fumitaka Shimizu, Yasuteru Sano, Takashi Kanda, Graham Marsh, Sebastiaan J. Trietsch, Paul Vulto, Henriëtte L. Lanz, Birgit Obermeier
A perfused human blood–brain barrier on-a-chip for high-throughput assessment of barrier function and antibody transport
published pages: , ISSN: 2045-8118, DOI: 10.1186/s12987-018-0108-3
Fluids and Barriers of the CNS 15/1 2020-04-08

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The information about "ADAPTED" are provided by the European Opendata Portal: CORDIS opendata.

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