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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.

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

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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