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Record W4406033262 · doi:10.1186/s13195-024-01659-6

Integrative multiomics reveals common endotypes across PSEN1, PSEN2, and APP mutations in familial Alzheimer’s disease

2025· article· en· W4406033262 on OpenAlexfundno aff
Phoebe Valdes, Andrew B. Caldwell, Qing Liu, Michael Q. Fitzgerald, Srinivasan Ramachandran, Celeste M. Karch, Sarah Adams, Ricardo Allegri, Aki Araki, Nicolas R. Barthélemy, Randall J. Bateman, Jacob Bechara, Tammie L.S. Benzinger, Sarah Berman, Courtney Bodge, Susan E. Brandon, W. K. Brooks, Jared R. Brosch, Jill Buck, Virginia Buckles, Kathleen Carter, Lisa Cash, Charlie Chen, Jasmeer P. Chhatwal, Patricio Chrem Méndez, Jasmin Chua, Helena Chui, Laura Courtney, Carlos Cruchaga, Gregory S. Day, Chrismary DeLaCruz, Darcy Denner, Anna Diffenbacher, Aylin Dincer, Tamara Donahue, J. Maxwell Douglas, Duc M. Duong, Noelia Egido, Bianca Esposito, Anne M. Fagan, Marty Farlow, Becca Feldman, Colleen Fitzpatrick, Shaney Flores, Nick C. Fox, Erin Franklin, Nelly Joseph‐Mathurin, Hisako Fujii, Samantha L. Gardener, Bernardino Ghetti, Alison Goate, Sarah B. Goldberg, Jill Goldman, Alyssa Gonzalez, Brian Gordon, Susanne Gräber‐Sultan, Neill R. Graff‐Radford, Morgan Graham, Julia Gray, Emily Gremminger, Miguel L. Grilo, Alex Groves, Christian Haass, Lisa M. Häsler, Jason Hassenstab, Cortaiga Hellm, Elizabeth Herries, Laura Hoechst-Swisher, Anna Hofmann, David M. Holtzman, Russ C. Hornbeck, Yakushev Igor, Ryoko Ihara, Takeshi Ikeuchi, Snežana Ikonomović, Kenji Ishii, Clifford R. Jack, Gina Jerome, Erik C. B. Johnson, Mathias Jucker, Stephan Käser, Kensaku Kasuga, Sarah Keefe, William E. Klunk, Robert A. Koeppe, Deb Koudelis, Elke Kuder-Buletta, Christoph Laske, Allan I. Levey, Johannes Levin, Yan Li, Oscar L. López, Jacob Marsh, Ralph N. Martins, Neal Scott Mason, Colin L. Masters, Kwasi G. Mawuenyega, Austin McCullough, Eric McDade, Arlene Mejia, Estrella Morenas‐Rodríguez, John Morris, James M. Mountz, Cath Mummery, Neelesh K. Nadkarni, Akemi Nagamatsu, Katie Neimeyer, Yoshiki Niimi, James M. Noble, Joanne Norton, Brigitte Nuscher, Ulricke Obermüller, Antoinette O’Connor, Riddhi Patira, Richard J. Perrin, Lingyan Ping, Oliver Preische, Alan E. Renton, John M. Ringman, Stephen Salloway, Peter Schofield, Michio Senda, Nicholas T. Seyfried, Kristine Shady, Hiroyuki Shimada, Wendy Sigurdson, Jennifer A. Smith, Lori Smith, Beth E. Snitz, Hamid R. Sohrabi, Sochenda Stephens, Kevin Taddei, Sarah Thompson, Jonathan Vöglein, Peter Wang, Qing Wang, Elise A. Weamer, Chengjie Xiong, Jinbin Xu, Xu Xiong, Douglas Galasko, Shauna H. Yuan, Steven L. Wagner, Shankar Subramaniam

Bibliographic record

VenueAlzheimer s Research & Therapy · 2025
Typearticle
Languageen
FieldMedicine
TopicAlzheimer's disease research and treatments
Canadian institutionsnot available
FundersEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentNational Institute of Diabetes and Digestive and Kidney DiseasesInstituto de Salud Carlos IIIFonds de Recherche du Québec - SantéNational Institutes of HealthDeutsches Zentrum für Neurodegenerative ErkrankungenNational Institute of Neurological Disorders and StrokeKorea Health Industry Development InstituteJapan Agency for Medical Research and DevelopmentUniversity of California, San DiegoFondation Brain CanadaFleniEuropean Molecular Biology LaboratoryNational Institute on AgingAlzheimer's AssociationNational Heart, Lung, and Blood InstituteCure Alzheimer's FundNational Cancer InstituteEidgenössische Technische Hochschule ZürichU.S. National Library of MedicineU.S. Department of Veterans AffairsCanadian Institutes of Health ResearchNational Science Foundation
KeywordsPSEN1DiseasePresenilinMedicineDementiaBioinformaticsAlzheimer's diseaseNeurologyMutationNeurodegenerationNeuroscienceGeneticsBiologyGenePsychiatryPathology

Abstract

fetched live from OpenAlex

Abstract Background PSEN1, PSEN2, and APP mutations cause Alzheimer’s disease (AD) with an early age at onset (AAO) and progressive cognitive decline. PSEN1 mutations are more common and generally have an earlier AAO; however, certain PSEN1 mutations cause a later AAO, similar to those observed in PSEN2 and APP . Methods We examined whether common disease endotypes exist across these mutations with a later AAO (~ 55 years) using hiPSC-derived neurons from familial Alzheimer’s disease (FAD) patients harboring mutations in PSEN1 A79V , PSEN2 N141I , and APP V717I and mechanistically characterized by integrating RNA-seq and ATAC-seq. Results We identified common disease endotypes, such as dedifferentiation, dysregulation of synaptic signaling, repression of mitochondrial function and metabolism, and inflammation. We ascertained the master transcriptional regulators associated with these endotypes, including REST, ASCL1, and ZIC family members (activation), and NRF1 (repression). Conclusions FAD mutations share common regulatory changes within endotypes with varying severity, resulting in reversion to a less-differentiated state. The regulatory mechanisms described offer potential targets for therapeutic interventions.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.453
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.001
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.094
GPT teacher head0.451
Teacher spread0.357 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations14
Published2025
Admission routes1
Has abstractyes

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