MétaCan
Menu
Back to cohort
Record W4379377132 · doi:10.1002/alz.13316

Rare neurovascular genetic and imaging markers across neurodegenerative diseases

2023· article· en· W4379377132 on OpenAlexaffabout
Allison A. Dilliott, Stephanie Berberian, Kelly M. Sunderland, Malcolm A. Binns, Julia Zimmer, Miracle Ozzoude, Christopher J.M. Scott, Fuqiang Gao, Anthony E. Lang, David P. Breen, Maria Carmela Tartaglia, Brian Tan, Richard H. Swartz, Ekaterina Rogaeva, Michael Borrie, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, Morris Freedman, Sanjeev Kumar, Stephen Pasternak, Bruce G. Pollock, Tarek K. Rajji, David F. Tang‐Wai, Agessandro Abrahão, John Turnbull, Lorne Zinman, Leanne K. Casaubon, Dar Dowlatshahi, Ayman Hassan, Jennifer Mandzia, Demetrios J. Sahlas, Gustavo Saposnik, David A. Grimes, Connie Marras, Thomas Steeves, Mario Masellis, Sali M.K. Farhan, Robert Bartha, Sean Symons, Robert A. Hegele, Sandra E. Black, Joel Ramirez

Bibliographic record

VenueAlzheimer s & Dementia · 2023
Typearticle
Languageen
FieldMedicine
TopicCerebrovascular and genetic disorders
Canadian institutionsHealth Sciences CentreThunder Bay Regional Research InstituteMcMaster UniversityHamilton Health SciencesCentre for Addiction and Mental HealthOttawa HospitalBruyèreSt. Joseph’s Healthcare HamiltonHeart and Stroke FoundationSt Joseph's Health CarePublic Health OntarioSt Joseph's Health CentreToronto Western HospitalUniversity Health NetworkOccupational Cancer Research CentreSinai Health SystemBaycrest HospitalOntario Brain InstituteSt. Michael's HospitalSunnybrook Health Science CentreUniversity of OttawaMcGill UniversityToronto Dementia Research AllianceWestern UniversityUniversity of TorontoMontreal Neurological Institute and Hospital
Fundersnot available
KeywordsNeurovascular bundleNeuroimagingDiseaseMedicineMagnetic resonance imagingNeurosciencePathologyBioinformaticsPsychologyPsychiatryBiologyRadiology

Abstract

fetched live from OpenAlex

INTRODUCTION: Cerebral small vessel disease (SVD) is common in patients with cognitive impairment and neurodegenerative diseases such as Alzheimer's and Parkinson's. This study investigated the burden of magnetic resonance imaging (MRI)-based markers of SVD in patients with neurodegenerative diseases as a function of rare genetic variant carrier status. METHODS: The Ontario Neurodegenerative Disease Research Initiative study included 520 participants, recruited from 14 tertiary care centers, diagnosed with various neurodegenerative diseases and determined the carrier status of rare non-synonymous variants in five genes (ABCC6, COL4A1/COL4A2, NOTCH3/HTRA1). RESULTS: NOTCH3/HTRA1 were found to significantly influence SVD neuroimaging outcomes; however, the mechanisms by which these variants contribute to disease progression or worsen clinical correlates are not yet understood. DISCUSSION: Further studies are needed to develop genetic and imaging neurovascular markers to enhance our understanding of their potential contribution to neurodegenerative diseases.

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 categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.366
Threshold uncertainty score0.887

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
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 head0.013
GPT teacher head0.266
Teacher spread0.252 · 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.

The models applied no category: nothing in the taxonomy fit this work.
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

Citations7
Published2023
Admission routes2
Has abstractyes

Explore more

Same venueAlzheimer s & DementiaSame topicCerebrovascular and genetic disordersFrench-language works237,207