Evidence map›Paper›PMID 32641180›Full record

ArticleInternational psychogeriatrics2024

Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.

D C Steffens, M E Garrett, K L Soldano, D R McQuoid, A E Ashley-Koch, G G Potter

Open access · diamondAbstract read
In one paragraph

Article in International psychogeriatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genome-wide association studies identify novel loci in rapidly progressive Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  5. Article
  6. Article
  7. Neurobiological Highlights of Cognitive Impairment in Psychiatric Disorders.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Pathomechanisms of Vascular Depression in Older Adults.International journal of molecular sciences · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

D C SteffensDepartment of Psychiatry, University of Connecticut School of Medicine, Farmington, CT, USA.
M E GarrettDepartment of Medicine, Duke University Medicine Center, Durham, NC, USA.
K L SoldanoDepartment of Medicine, Duke University Medicine Center, Durham, NC, USA.
D R McQuoidDepartment of Psychiatry, Duke University Medicine Center, Durham, NC, USA.
A E Ashley-KochDepartment of Medicine, Duke University Medicine Center, Durham, NC, USA.
G G PotterDepartment of Psychiatry, Duke University Medicine Center, Durham, NC, USA.
Duke University · USUniversity of Connecticut · US

Funding

Phenotype Predictors of Cognitive Outcomes in Geriatric DepressionR01MH108578 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI STEFFENS, DAVID C. · 2016 to 2025
$5.5M
NIMH NIH HHS R01 MH108578
6 · The paper itself

Abstract

objectiveThis study sought to conduct a comprehensive search for genetic risk of cognitive decline in the context of geriatric depression.

designA genome-wide association study (GWAS) analysis in the Neurocognitive Outcomes of Depression in the Elderly (NCODE) study.

settingLongitudinal, naturalistic follow-up study.

participantsOlder depressed adults, both outpatients and inpatients, receiving care at an academic medical center. MEASUREMENTS: The Consortium to Establish a Registry for Alzheimer's Disease (CERAD) neuropsychological battery was administered to the study participants at baseline and a minimum of twice within a subsequent 3-year period in order to measure cognitive decline. A GWAS analysis was conducted to identify genetic variation that is associated with baseline and change in the CERAD Total Score (CERAD-TS) in NCODE.

resultsThe GWAS of baseline CERAD-TS revealed a significant association with an intergenic single-nucleotide polymorphism (SNP) on chromosome 6, rs17662598, that surpassed adjustment for multiple testing (

conclusionsOur GWAS of cognitive function and decline among individuals with late-life depression (LLD) has identified promising candidate genes that, upon replication in other cohorts of LLD, may be potential biomarkers for cognitive decline and suggests DHA supplementation as a possible therapy of interest.

Indexed as

Cognitive DysfunctionGenome-Wide Association StudyNeuropsychological TestsPolymorphism, Single NucleotideAgedAged, 80 and overDepressionFemaleFollow-Up StudiesGenetic LociGenetic Predisposition to DiseaseHumansLongitudinal StudiesMaleaffective disordersdementiagenes

Identifiers

PMID32641180
PMCPMC7794099
OpenAlexW3041797608

What OpenQuestion holds

Textmetadata
LicenceTDM
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.