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Record W4210642195 · doi:10.1002/alz.054475

Despite heightened risk of cognitive decline, no evidence of local atrophy in people with subjective cognitive decline compared to normal controls in ADNI

2021· article· en· W4210642195 on OpenAlexaff
Cassandra Morrison, Mahsa Dadar, Neda Shafiee, D. Louis Collins

Bibliographic record

VenueAlzheimer s & Dementia · 2021
Typearticle
Languageen
FieldMedicine
TopicDementia and Cognitive Impairment Research
Canadian institutionsMcGill UniversityUniversité LavalMontreal Neurological Institute and Hospital
Fundersnot available
KeywordsEntorhinal cortexAtrophyAlzheimer's Disease Neuroimaging InitiativeCognitive declineNeuroimagingMedicineCognitionInternal medicineDementiaHippocampusBrain sizeNeurodegenerationPsychologyNeuroscienceCardiologyMagnetic resonance imagingDiseaseRadiology

Abstract

fetched live from OpenAlex

Abstract Background People with subjective cognitive decline (SCD) are at increased risk for developing Alzheimer’s disease (AD). SCD may thus be a very early clinical manifestations of AD. However, identifying which individuals with SCD will develop AD is difficult with current biomarker techniques. To predict whether someone with SCD will progress to AD, it is necessary to determine whether people with SCD display neurodegeneration in brain regions associated with AD. Method We included 1769 baseline and follow‐up MRI scans for 447 participants (177 normal controls, NC; 100 SCD; and 170 early mild cognitive impairment, eMCI) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). All scans were pre‐processed through a previously validated pipeline. Deformation‐based morphometry (DBM) was performed to examine the pattern of volumetric change over time. An atlas‐based approach was also used to examine mean volume differences for regions of interest (ROIs; lateral ventricles, entorhinal cortex, and amygdala from CerebrA atlas (Manera et al., 2020)) estimated by integrating the Jacobian of the deformation field within the ROI. A previously validated MRI analysis method (SNIPE) was used to determine volume and grading of the hippocampus (Coupe et al., 2012). We applied a linear mixed effects model for all analysis (volume ∼Diagnostic Group +Age +Sex +Amyloid Positivity +APOE e4 +Education +1|ID). Result Longitudinal volume analysis showed slight atrophy in eMCI compared to NC and SCD. ROI analysis revealed that eMCI had smaller volumes than SCD and NC in the amygdala (NC & SCD: p<.001) and entorhinal cortex (NC: p<.001; SCD: p=.01), and larger lateral ventricles (NC & SCD: p=.01). SNIPE volume and grading analysis revealed that eMCI hippocampal volume differed from both NC and SCD (p<.001). SCD and NC did not differ in any of the analyses. With respect to demographics, people with SCD had 2 years more education (p<0.001) than eMCI and NC. Conclusion The structural differences observed in eMCI may act as an early biomarker for AD. Although SCD participants’ brain volumes significantly differed from eMCI, they did not differ from NC. However, lack of SCD:NC differences may be due to confounds (e.g., greater education in SCD) within the sample.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.014
Threshold uncertainty score0.027

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.021
GPT teacher head0.313
Teacher spread0.293 · 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 source (direct Gemma or distilled Codex), 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

Citations0
Published2021
Admission routes1
Has abstractyes

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