Polygenic pathways shape white matter vulnerability to Alzheimer’s disease-related pathophysiological changes

Pathway-specific genetic vulnerability to AD is associated with alterations in WM tracts both directly and by moderating the effects of AD-related pathophysiological changes. AD-associated genetic risk should be integrated into the AD diagnostic framework to enable targeted screening and intervention for future preclinical trials aimed at specific biological pathways.

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Publication Details

Journal
Alzheimer s Research & Therapy
Published
2025-11-10
DOI
https://doi.org/10.1186/s13195-025-01888-3
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Polygenic pathways shape white matter vulnerability to Alzheimer’s disease-related pathophysiological changes

Emma S. Luckett, Lyduine E. Collij, Joanna Marguerite Wardlaw, Tiago Gil Oliveira et al.
Alzheimer s Research & Therapy
Amyotrophic Lateral Sclerosis Research
article

Polygenic pathways shape white matter vulnerability to Alzheimer’s disease-related pathophysiological changes

Emma S. Luckett, Lyduine E. Collij, Joanna Marguerite Wardlaw, Tiago Gil Oliveira, Luca Roccatagliata, Luigi Lorenzini, Mario Tranfa, Giuseppe Pontillo, Craig Ritchie, Henk J. M. M. Mutsaerts, Pierre Payoux, Henne Holstege, Pablo Martínez‐Lage, Marcel Reinders, Adam Waldman, Gemma Salvadó, Frederik Barkhof, Juan Domingo Gispert, André Altmann, Matteo Pardini, Alle Meije Wink, Arturo Brunetti, Leonard Pieperhoff, Niccoló Tesi, Natalia Vilor-Tejedor
article en

Abstract

Pathway-specific genetic vulnerability to AD is associated with alterations in WM tracts both directly and by moderating the effects of AD-related pathophysiological changes. AD-associated genetic risk should be integrated into the AD diagnostic framework to enable targeted screening and intervention for future preclinical trials aimed at specific biological pathways.

Alzheimer s Research & TherapyVol. 17(1)
Allen Institute for Brain Science (US), Université Toulouse III - Paul Sabatier (FR), Radboud University Nijmegen (NL), Inserm (FR), Queen Mary University of London (GB), Université Fédérale de Toulouse Midi-Pyrénées (FR), Malmö University (SE), Lund University (SE), Western General Hospital (GB), Vlaams Instituut voor Biotechnologie (BE), Radboud University Medical Center (NL), Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES), Center for Human Genetics (US), Pasqual Maragall Foundation (ES), Amsterdam Neuroscience (NL), Federico II University Hospital (IT), Public Health Scotland (GB), UK Dementia Research Institute (GB), Spanish National Centre for Cardiovascular Research (ES), Hospital Del Mar (ES), Centre for Genomic Regulation (ES), Hospital Braga (PT), Ospedale Policlinico San Martino (IT), National Hospital for Neurology and Neurosurgery (GB), Amsterdam University Medical Centers (NL), Fundacion CITA Alzheimer (ES), Hôpital Paule de Viguier (FR), VIB-KU Leuven Center for Brain & Disease Research (BE), University College London (GB), Imperial College London (GB), University of Naples Federico II (IT), University of Genoa (IT), Delft University of Technology (NL), University of Edinburgh (GB), KU Leuven (BE), University of Minho (PT)
EU Joint Programme – Neurodegenerative Disease Research, European Federation of Pharmaceutical Industries and Associations, Rijksdienst voor Ondernemend Nederland, Alzheimer's Society, British Heart Foundation, European Commission, Fondation Leducq, ZonMw, Ministerio de Ciencia e Innovación, Alzheimer Nederland, UK Dementia Research Institute, Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona, Medical Research Council, Eurostars
Openalex Percentile: Top 53%
Amyotrophic Lateral Sclerosis Research
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