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Targeting abnormal metabolism in Alzheimer's disease: The Drug Repurposing for Effective Alzheimer's Medicines (DREAM) study
Author(s) -
Desai Rishi J.,
Varma Vijay R.,
Gerhard Tobias,
Segal Jodi,
Mahesri Mufaddal,
Chin Kristyn,
nenmacher Edward,
Gabbeta Avinash,
Mammen Anup M.,
Varma Sudhir,
Horton Daniel B.,
Kim Seoyoung C.,
Schneeweiss Sebastian,
Thambisetty Madhav
Publication year - 2020
Publication title -
alzheimer's and dementia: translational research and clinical interventions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.49
H-Index - 30
ISSN - 2352-8737
DOI - 10.1002/trc2.12095
Subject(s) - medicine , disease , drug repositioning , repurposing , clinical trial , drug development , dementia , alzheimer's disease , galantamine , drug , bioinformatics , donepezil , intensive care medicine , pharmacology , pathology , biology , ecology
Drug discovery for disease‐modifying therapies for Alzheimer's disease and related dementias (ADRD) based on the traditional paradigm of experimental animal models has been disappointing. We describe the rationale and design of the Drug Repurposing for Effective Alzheimer's Medicines (DREAM) study, an innovative multidisciplinary alternative to traditional drug discovery. First, we use a systems biology perspective in the "hypothesis generation" phase to identify metabolic abnormalities that may either precede or interact with the accumulation of ADRD neuropathology, accelerating the expression of clinical symptoms of the disease. Second, in the "hypothesis refinement" phase we propose use of large patient cohorts to test whether drugs approved for other indications that also target metabolic drivers of ADRD pathogenesis might alter the trajectory of the disease. We emphasize key challenges in population‐based pharmacoepidemiologic studies aimed at quantifying the association between medication use and ADRD onset and outline robust causal inference principles to safeguard against common pitfalls. Candidate ADRD treatments emerging from this approach will hold promise as plausible disease‐modifying therapies for evaluation in randomized controlled trials.

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