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Record W4406223177 · doi:10.1002/alz.095772

Genome‐Wide Associations of Cognitive Domains and their Correlation with Polygenic Risk Scores for Antidepressant Response in Late‐Life Depression

2024· article· en· W4406223177 on OpenAlexaff
Samar S. M. Elsheikh, Victoria Marshe, Małgorzata Maciukiewicz, Farhana Islam, Xiaoyu Men, Vanessa Goncalves, Daniel Felsky, James L. Kennedy, Benoit H. Mulsant, Charles F. Reynolds, Eric J. Lenze, Daniel J. Müller

Bibliographic record

VenueAlzheimer s & Dementia · 2024
Typearticle
Languageen
FieldPsychology
TopicCognitive Abilities and Testing
Canadian institutionsUniversity of TorontoCentre for Addiction and Mental Health
Fundersnot available
KeywordsPolygenic risk scoreDepression (economics)AntidepressantCorrelationGenome-wide association studyCognitionClinical psychologyMedicinePsychologyPsychiatryBiologyGeneticsGeneSingle-nucleotide polymorphismGenotypeAnxiety

Abstract

fetched live from OpenAlex

Abstract Background Late‐life depression (LLD) often coincides with cognitive decline, impacting antidepressant treatment outcomes. Investigating the genetic profile of cognitive function and its association with antidepressant response in individuals with LLD is crucial. Method In the Incomplete Response in Late‐Life Depression: Getting to Remission (IRL‐GRey) study, 307 older adults with major depressive disorder underwent 12‐week venlafaxine treatment. A genome‐wide association study (GWAS) of five cognitive domains using the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) was conducted. Functional annotations were performed using FUMA. Polygenic risk scores (PRSs) for antidepressant non‐remission and symptom improvement were using PRSice v2. Associations between PRSs and cognitive domains were analyzed, adjusting for age, sex, and genomic principal components. Bonferroni correction and permutation tests were applied to address multiple testing issues. Result Out of the five cognitive domains, significant SNPs were identified for the attention domain (lead SNP rs67854110, beta = ‐9.91, CI = [‐13.12, ‐6.70], P = 4.4e −09 ). Top suggestive genes associated with language showed differential expression in the hypothalamus, cortex, and nucleus accumbens (P bon = 0.001). The language gene set analysis exhibited significant enrichment with the GWAS Catalog set response to cognitive‐behavioral therapy in depression (P = 9.24e −11 ). Additionally, the top SNP associated with delayed memory (rs13087568, beta = ‐8.24, CI = [‐11.36, ‐5.11], P = 4.5e −07 ) was previously linked to depressive symptoms by other studies. Polygenic risk scores (PRS) for non‐remission negatively correlated with attention (P Threshold = 0.0001, N SNPS = 39, OR = 0.105 [0.016, 0.686], P = 0.019), immediate memory (P Threshold = 0.001, N SNPS = 320, OR = 0.074 [0.011, 0.490], P = 0.0072), and delayed memory (P Threshold = 0.01, N SNPS = 2449, OR = 0.107 [0.021, 0.540], P = 0.0074). PRS for symptom improvement showed a positive correlation with delayed memory (PThreshold = 0.001, N SNPS = 385, OR = 5.329 [1.056, 26.885], P = 0.044). However, none of the PRS associations survived the Bonferroni threshold. Conclusion These findings suggest a genetic link between cognitive domains and antidepressant response in LLD, reinforcing previous associations. Understanding genetic contributions to cognitive decline in older adults with depression could aid in early identification and interventions to prevent dementia.

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 categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.061
Threshold uncertainty score0.538

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
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 head0.031
GPT teacher head0.303
Teacher spread0.272 · 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".

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Citations0
Published2024
Admission routes1
Has abstractyes

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