TY - JOUR
T1 - Genetically determined Alzheimer's disease research advances
T2 - The Down Syndrome & Autosomal Dominant Alzheimer's Disease 2024 Conference
AU - DSAD-ADAD conference group
AU - Falgàs, Neus
AU - Maure-Blesa, Lucia
AU - Ances, Beau
AU - Flores-Aguilar, Lisi
AU - Hartley, Sigan
AU - Hassenstab, Jason
AU - Iulita, M. Florencia
AU - Janicki, Matthew
AU - Koenig, Katherine
AU - Lao, Patrick
AU - Levin, Johannes
AU - McDade, Eric
AU - Meijer, Laurent
AU - Rafii, Michael S.
AU - Snyder, Heather M.
AU - Sánchez-Valle, Raquel
AU - Fortea, Juan
AU - Arriola Infante, Jose
AU - Balasa, Mirea
AU - Barroeta, Isabel
AU - Barthelemy R, Nicolas
AU - Bejanin, Alexandre
AU - Benejam, Bessy
AU - Bosch, Beatriz
AU - Bradshaw, Angela
AU - Carmona-Iragui, Maria
AU - Cohen, Ann
AU - Comas Albertí, Aina
AU - Csincsik, Lajos
AU - Cuello, A. Claudio
AU - del Hoyo Soriano, Laura
AU - Dijkstra, Janna
AU - Edwards, Natalie
AU - Giménez, Sandra
AU - Gonzalez-Ortiz, Fernando
AU - Gordon, Brian
AU - Gutiérrez Fernández, Sara
AU - Handen, Benjamin
AU - Jacob, Charlotte
AU - Johnson, Erik
AU - Johansson, Charlotte
AU - Lladó, Albert
AU - Lleó, Alberto
AU - Morabito, Samuel
AU - Morcillo-Nieto, Alejandra O.
AU - Montoliu-Gaya, Laia
AU - Okafor, Michael
AU - Pérez-Millan, Agnes
AU - Potier, Marie Claude
AU - Ringman, John
AU - Rodríguez-Baz, Íñigo
AU - Rubenstein, Eric
AU - Ryan, Natalie S.
AU - Strydom, André
AU - Vaqué-Alcázar, Lidia
AU - Vermunt, Lisa
AU - Videla Toro, Laura
AU - Zaman, Shahid
N1 - Publisher Copyright:
© 2025 The Author(s). Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.
PY - 2025/7
Y1 - 2025/7
N2 - INTRODUCTION: The Down syndrome-associated Alzheimer's disease (DSAD) autosomal dominant Alzheimer's disease (ADAD) 2024 Conference in Barcelona, convened under an Alzheimer's Association International Society to Advance Alzheimer's Research and Treatment (ISTAART) grant through the Down syndrome and Alzheimer's disease (AD) Professional Interest Area (PIA), brought together global researchers to foster collaboration and knowledge exchange between the fields of DSAD and ADAD. METHODS: This article provides a synthesis review of the conference proceedings, summarizing key discussions on biomarkers, natural history models, clinical trials, and ethical considerations in anti-amyloid therapies. RESULTS: A total of 211 attendees from 16 countries joined the meeting. Global researchers presented on disease mechanisms, therapeutic developments, and patient care strategies. Discussions focused on challenges and opportunities unique to DSAD and ADAD. Experts emphasized the urgent need for tailored clinical trials for ADAD and DSAD and debated the safety and efficacy of anti-amyloid treatments. Ethical considerations highlighted equitable access to therapies and the crucial role of patient and caregiver involvement. DISCUSSION: The conference highlighted the importance of inclusive research and collaboration across the genetic forms of AD. Highlights: Biomarker research and natural history models developed in Down syndrome-associated Alzheimer's disease (DSAD) and autosomal dominant Alzheimer's disease (ADAD) enable the prediction of disease progression not only for DSAD and ADAD, but also for sporadic Alzheimer's disease (AD). -Collaboration and knowledge exchange among researchers across these genetic forms of AD will accelerate our understanding of the pathophysiology and advance preventive trials in DSAD and ADAD. -Tailored clinical trials for DSAD are urgently needed to address specific safety and efficacy concerns. -Inclusive research practices are crucial for advancing treatments and understanding of DSAD and ADAD.
AB - INTRODUCTION: The Down syndrome-associated Alzheimer's disease (DSAD) autosomal dominant Alzheimer's disease (ADAD) 2024 Conference in Barcelona, convened under an Alzheimer's Association International Society to Advance Alzheimer's Research and Treatment (ISTAART) grant through the Down syndrome and Alzheimer's disease (AD) Professional Interest Area (PIA), brought together global researchers to foster collaboration and knowledge exchange between the fields of DSAD and ADAD. METHODS: This article provides a synthesis review of the conference proceedings, summarizing key discussions on biomarkers, natural history models, clinical trials, and ethical considerations in anti-amyloid therapies. RESULTS: A total of 211 attendees from 16 countries joined the meeting. Global researchers presented on disease mechanisms, therapeutic developments, and patient care strategies. Discussions focused on challenges and opportunities unique to DSAD and ADAD. Experts emphasized the urgent need for tailored clinical trials for ADAD and DSAD and debated the safety and efficacy of anti-amyloid treatments. Ethical considerations highlighted equitable access to therapies and the crucial role of patient and caregiver involvement. DISCUSSION: The conference highlighted the importance of inclusive research and collaboration across the genetic forms of AD. Highlights: Biomarker research and natural history models developed in Down syndrome-associated Alzheimer's disease (DSAD) and autosomal dominant Alzheimer's disease (ADAD) enable the prediction of disease progression not only for DSAD and ADAD, but also for sporadic Alzheimer's disease (AD). -Collaboration and knowledge exchange among researchers across these genetic forms of AD will accelerate our understanding of the pathophysiology and advance preventive trials in DSAD and ADAD. -Tailored clinical trials for DSAD are urgently needed to address specific safety and efficacy concerns. -Inclusive research practices are crucial for advancing treatments and understanding of DSAD and ADAD.
KW - Autosomal dominant Alzheimer's disease
KW - Biomarkers
KW - Clinical trials
KW - Down syndrome
KW - Neuroimaging
KW - Pathophysiology
UR - https://www.scopus.com/pages/publications/105010489791
U2 - 10.1002/alz.70309
DO - 10.1002/alz.70309
M3 - Review article
C2 - 40604347
AN - SCOPUS:105010489791
SN - 1552-5260
VL - 21
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
IS - 7
M1 - e70309
ER -