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Novel biomarkers for improving diagnostics, prognostics, and treatments of Alzheimer’s disease

Project description

The road to more accurate diagnostics for Alzheimer’s disease

Alzheimer’s disease (AD) is a challenge in global health, marked by its prevalence and complex diagnostic hurdles. With a pre-symptomatic phase spanning decades, identifying and treating AD early remains elusive. Current clinical diagnostics for AD are suboptimal, leading to ineffective treatments, particularly in primary care settings. As such, there is an urgent need for more accurate diagnostics. In this context, the ERC-funded ADVANCE-AD project aims to revolutionise AD management using novel blood-based biomarkers. Firstly, it will overhaul clinical work-ups for symptomatic patients with scalable, non-invasive tools. Secondly, it will pioneer pre-symptomatic detection algorithms to fast-track effective therapies. By analysing existing trials, ADVANCE-AD aims to evaluate potential treatments, from statins to genetic therapies.

Objective

Alzheimers disease (AD) is the most common cause of dementia and a major global health challenge. AD has a long pre-symptomatic phase spanning several decades. The accuracy of clinical AD diagnostics is mediocre, especially in primary care. This results in suboptimal treatment and care, which is especially problematic in light of emerging anti-amyloid therapies. ADVANCE-AD aims to revolutionize AD diagnostics and prognostics and fast-track the development of new effective therapies by using novel blood-based biomarkers forbeta-amyloid, tau, neurodegeneration and neuroinflammation.
First, my team will transform the clinical work-up of symptomatic AD patients globally by developing scalable, non-invasive and cost-effective diagnostic and prognostic algorithms based on novel blood-based biomarkers and digital tools.
Second, disease-modifying therapies should be initiated already in the pre-symptomatic phase to be very effective. My team will therefore develop cost-effective diagnostic algorithms to identify AD pathology in individuals without cognitive symptoms, and prognostic algorithms to detect those most likely to develop symptoms and thereby benefit from new therapies. These new algorithms will then be used to recruit individuals into a pre-symptomatic trial-ready cohort to efficiently evaluate new anti-AD drugs.
Third, new drug candidates for our trial-ready cohort will be identified using large-scale analyses of the novel AD-related biomarkers in biobanked longitudinal blood samples from already performed randomized placebo-controlled trials. Using this high risk/high-gain approach, we will evaluate if different classes of existing drugs (e.g. statins, GLP-1 agonists, anti-inflammatory agents) can halt development of AD and neurodegeneration. Finally, a novel genetic anti-tau treatment will be evaluated in this trial-ready cohort.
ADVANCE-AD builds on world-leading research and will likely result in breakthroughs in early diagnostics and treatments for AD.

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2022-ADG

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Host institution

LUNDS UNIVERSITET
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 2 500 000,00
Address
Paradisgatan 5c
22100 Lund
Sweden

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Region
Södra Sverige Sydsverige Skåne län
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 2 500 000,00

Beneficiaries (1)

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