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Record W4396217735 · doi:10.1001/jamaneurol.2024.0991

Downstream Biomarker Effects of Gantenerumab or Solanezumab in Dominantly Inherited Alzheimer Disease

2024· letter· en· W4396217735 on OpenAlexafffund
Olivia Wagemann, Haiyan Liu, Guoqiao Wang, Xinyu Shi, Tobias Bittner, Marzia A. Scelsi, Martin R. Farlow, David B. Clifford, Charlene Supnet, Anna Santacruz, Andrew J. Aschenbrenner, Jason Hassenstab, Tammie L.S. Benzinger, Brian A. Gordon, Kelley A. Coalier, Carlos Cruchaga, Laura Ibáñez, Richard J. Perrin, Chengjie Xiong, Yan Li, John C. Morris, James J. Lah, Sarah Berman, Erik D. Roberson, Christopher H. van Dyck, Douglas Galasko, Serge Gauthier, Ging‐Yuek Robin Hsiung, William S. Brooks, Jérémie Pariente, Catherine J. Mummery, Gregory S. Day, John M. Ringman, Patricio Chrem Méndez, Peter St George‐Hyslop, Nick C. Fox, Kazushi Suzuki, Hamid Okhravi, Jasmeer P. Chhatwal, Johannes Levin, Mathias Jucker, John R. Sims, Karen C. Holdridge, Nicholas K. Proctor, R. Yaari, Scott W. Andersen, Michele Mancini, Jorge J. Llibre‐Guerra, Randall J. Bateman, Eric McDade, Alisha Daniels, Laura Courtney, Xu Xiong, Ruijin Lu, Emily Gremminger, Erin Franklin, Gina Jerome, Elizabeth Herries, Jennifer L. Stauber, Bryce Baker, Matthew Minton, Alison Goate, Alan E. Renton, Danielle M. Picarello, Russ C. Hornbeck, Allison Chen, Charles D. Chen, Shaney Flores, Nelly Joseph‐Mathurin, Steve Jarman, Kelley Jackson, Sarah Keefe, Deborah Koudelis, Parinaz Massoumzadeh, Austin McCullough, Nicole S. McKay, Joyce Nicklaus, Christine Pulizos, Qīng Wáng, Edita Sabaredzovic, Hunter Smith, Jalen Scott, Ashlee Simmons, Jacqueline Rizzo, Jennifer A. Smith, Sarah H. Stout, Celeste M. Karch, Jacob Marsh, David M. Holtzman, Nicolas R. Barthélemy, Jinbin Xu, James M. Noble, Snežana Ikonomović, Neelesh K. Nadkarni, Neill R. Graff‐Radford, Takeshi Ikeuchi, Kensaku Kasuga, Yoshiki Niimi, Edward D. Huey, Stephen Salloway, Peter R. Schofield, Jacob Bechara, Ralph N. Martins, David M. Cash, Natalie S. Ryan, Christoph Laske, Anna Hofmann, Elke Kuder-Buletta, Susanne Gräber‐Sultan, Ulrike Obermueller, Yvonne Roedenbeck, Jonathan Vöglein, Jae‐Hong Lee, Jee Hoon Roh, Raquel Sánchez‐Valle, Pedro Rosa‐Neto, Ricardo Allegri, Ezequiel Surace, Silvia Vázquez, Francisco Lopera, Yudy Milena Leon, Laura Ramírez, David Aguillón, Allan I. Levey, Erik C. B. Johnson, Nicholas T. Seyfried, Anne M. Fagan, Hiroshi Mori, Colin L. Masters

Bibliographic record

VenueJAMA Neurology · 2024
Typeletter
Languageen
FieldMedicine
TopicAlzheimer's disease research and treatments
Canadian institutionsUniversity of British ColumbiaMcGill University
FundersNational Institute of Mental HealthNational Institute on AgingNovo Nordisk CanadaGenentechNational Institutes of HealthDeutsches Zentrum für Neurodegenerative ErkrankungenNovo NordiskEisaiBrightFocus FoundationEli Lilly and CompanyAlzheimer's Research TrustGood Ventures FoundationCentene CorporationSeagenAvid RadiopharmaceuticalsAtara BiotherapeuticsGHR FoundationCanadian Institutes of Health ResearchFoundation for Barnes-Jewish HospitalProthenaNational Center for Advancing Translational SciencesTeva Pharmaceutical IndustriesCure Alzheimer's FundWashington University in St. LouisF. Hoffmann-La RocheBayer VitalCoins for Alzheimer's Research TrustBristol-Myers SquibbEisai CanadaKorea Health Industry Development InstituteBiogenTauRx PharmaceuticalsAlzheimer's AssociationSanofiFoundation for the National Institutes of Health
KeywordsBiomarkerNeurograninMedicineInternal medicineOncologyPlaceboPharmacologyAlzheimer's diseaseNeurodegenerationCerebrospinal fluidGastroenterologyPathologyChemistryDiseaseBiochemistry

Abstract

fetched live from OpenAlex

Importance: Effects of antiamyloid agents, targeting either fibrillar or soluble monomeric amyloid peptides, on downstream biomarkers in cerebrospinal fluid (CSF) and plasma are largely unknown in dominantly inherited Alzheimer disease (DIAD). Objective: To investigate longitudinal biomarker changes of synaptic dysfunction, neuroinflammation, and neurodegeneration in individuals with DIAD who are receiving antiamyloid treatment. Design, Setting, and Participants: From 2012 to 2019, the Dominantly Inherited Alzheimer Network Trial Unit (DIAN-TU-001) study, a double-blind, placebo-controlled, randomized clinical trial, investigated gantenerumab and solanezumab in DIAD. Carriers of gene variants were assigned 3:1 to either drug or placebo. The present analysis was conducted from April to June 2023. DIAN-TU-001 spans 25 study sites in 7 countries. Biofluids and neuroimaging from carriers of DIAD gene variants in the gantenerumab, solanezumab, and placebo groups were analyzed. Interventions: In 2016, initial dosing of gantenerumab, 225 mg (subcutaneously every 4 weeks) was increased every 8 weeks up to 1200 mg. In 2017, initial dosing of solanezumab, 400 mg (intravenously every 4 weeks) was increased up to 1600 mg every 4 weeks. Main Outcomes and Measures: Longitudinal changes in CSF levels of neurogranin, soluble triggering receptor expressed on myeloid cells 2 (sTREM2), chitinase 3-like 1 protein (YKL-40), glial fibrillary acidic protein (GFAP), neurofilament light protein (NfL), and plasma levels of GFAP and NfL. Results: Of 236 eligible participants screened, 43 were excluded. A total of 142 participants (mean [SD] age, 44 [10] years; 72 female [51%]) were included in the study (gantenerumab, 52 [37%]; solanezumab, 50 [35%]; placebo, 40 [28%]). Relative to placebo, gantenerumab significantly reduced CSF neurogranin level at year 4 (mean [SD] β = -242.43 [48.04] pg/mL; P < .001); reduced plasma GFAP level at year 1 (mean [SD] β = -0.02 [0.01] ng/mL; P = .02), year 2 (mean [SD] β = -0.03 [0.01] ng/mL; P = .002), and year 4 (mean [SD] β = -0.06 [0.02] ng/mL; P < .001); and increased CSF sTREM2 level at year 2 (mean [SD] β = 1.12 [0.43] ng/mL; P = .01) and year 4 (mean [SD] β = 1.06 [0.52] ng/mL; P = .04). Solanezumab significantly increased CSF NfL (log) at year 4 (mean [SD] β = 0.14 [0.06]; P = .02). Correlation analysis for rates of change found stronger correlations between CSF markers and fluid markers with Pittsburgh compound B positron emission tomography for solanezumab and placebo. Conclusions and Relevance: This randomized clinical trial supports the importance of fibrillar amyloid reduction in multiple AD-related processes of neuroinflammation and neurodegeneration in CSF and plasma in DIAD. Additional studies of antiaggregated amyloid therapies in sporadic AD and DIAD are needed to determine the utility of nonamyloid biomarkers in determining disease modification. Trial Registration: ClinicalTrials.gov Identifier: NCT04623242.

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)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Research integrity
Consensus categoriesResearch integrity
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Commentary · Consensus signal: none
Teacher disagreement score0.393
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.003
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 head0.028
GPT teacher head0.308
Teacher spread0.280 · 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; both teacher heads agree on what is shown here.

Study designNot applicable
Domainnot available
GenreCommentary

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

Citations28
Published2024
Admission routes2
Has abstractyes

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