Evidence map›Paper›PMID 38238328›Full record

ArticleTranslational psychiatry2024

Investigation of genetic determinants of cognitive change in later life.

Liam Mahedy, Emma L Anderson, Kate Tilling, Zak A Thornton, Andrew R Elmore, Sándor Szalma, Arthur Simen, Meredith Culp, Stephen Zicha, Brian T Harel and 3 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Liam MahedyMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0001-5417-6595
Emma L AndersonMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Kate TillingMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Zak A ThorntonMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Andrew R ElmoreMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0003-0292-447X
Sándor SzalmaTakeda Development Center Americas, Inc., San Diego, CA, USA.ORCID 0000-0001-7591-3902
Arthur SimenTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Meredith CulpTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Stephen ZichaTakeda Development Center Americas, Inc., Cambridge, MA, USA.
Brian T HarelTakeda Development Center Americas, Inc., Cambridge, MA, USA.
George Davey SmithMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0002-1407-8314
Erin N SmithTakeda Development Center Americas, Inc., San Diego, CA, USA.
Lavinia PaternosterMRC Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK. lavinia.paternoster@bristol.ac.uk.ORCID 0000-0003-2514-0889
Takeda (United States) · USUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Bristol · GB

Funding

Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/3Medical Research Council MC_UU_00032/1Medical Research Council MC_UU_00032/2
6 · The paper itself

Abstract

Cognitive decline is a major health concern and identification of genes that may serve as drug targets to slow decline is important to adequately support an aging population. Whilst genetic studies of cross-sectional cognition have been carried out, cognitive change is less well-understood. Here, using data from the TOMMORROW trial, we investigate genetic associations with cognitive change in a cognitively normal older cohort. We conducted a genome-wide association study of trajectories of repeated cognitive measures (using generalised estimating equation (GEE) modelling) and tested associations with polygenic risk scores (PRS) of potential risk factors. We identified two genetic variants associated with change in attention domain scores, rs534221751 (p = 1 × 10

Indexed as

Cognition DisordersCognitive DysfunctionAdaptor Proteins, Signal TransducingAgedCognitionCross-Sectional StudiesGenome-Wide Association StudyHumansNeural Cell Adhesion MoleculesAdaptor Proteins, Signal TransducingCRIPT protein, humanNCAM2 protein, humanNeural Cell Adhesion Molecules

Identifiers

PMID38238328
PMCPMC10796929
OpenAlexW4390976493

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.