Evidence map›Paper›PMID 18848371›Full record

ArticleNeurobiology of aging2010

Polymorphisms in LMNA and near a SERPINA gene cluster are associated with cognitive function in older people.

Christie Cluett, Carol Brayne, Robert Clarke, Grimley Evans, Fiona Matthews, David C Rubinsztein, Felicia Huppert, David J Llewellyn, Neil Rice, William Henley and 3 more

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2010. 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
0.4field-weighted citation impact, top 30% 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, 12 citations in OpenAlex.

  1. Article
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  6. Novel linkage ofInternational journal of cardiology. Heart & vasculature · 2015
    Article
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 4 institutions in 1 country.

Christie CluettPeninsula Medical School, RD&E Wonford Site, Exeter, UK.
Carol Brayne
Robert Clarke
Grimley Evans
Fiona Matthews
David C Rubinsztein
Felicia Huppert
David J Llewellyn
Neil Rice
William Henley
Timothy M Frayling
Anna Murray
David Melzer
Peninsula College of Medicine and Dentistry · GBAddenbrooke's Hospital · GBMRC Biostatistics Unit · GBUniversity of Oxford · GB

Funding

Aging pathways polymorphisms in older personsR01AG024233 · NIA · UNIVERSITY OF CAMBRIDGE · PI MELZER, DAVID · 2004 to 2007
$1.2M
Department of HealthMedical Research Council G9901400Medical Research Council MC_U105292687Medical Research Council MC_U137686857NIA NIH HHS R01 AG024233NIA NIH HHS R01AG24233Wellcome Trust 064354
6 · The paper itself

Abstract

A recent genome-wide association (GWA) study of late-onset Alzheimer's disease (LOAD) identified 15 novel single nucleotide polymorphisms (SNPs) independent of ApoE. We hypothesised that variants associated with LOAD are also associated with poor cognitive function in elderly populations. We measured additive associations between the five most strongly associated LOAD SNPs and grouped Mini Mental State Examination (MMSE) scores. Variants were genotyped in respondents (mean age 79 years) from the Oxford Healthy Ageing project (OHAP) and other sites of the MRC Cognitive Function and Ageing Study (MRC-CFAS). In adjusted ordinal logistic models, two variants were associated with poorer cognitive function: rs11622883 (OR=1.14, 95% CI: 1.01-1.28, p=0.040) and rs505058 (OR=1.29, 95% CI: 1.02-1.64, p=0.036). These SNPs are close to a SERPINA gene cluster and within LMNA, respectively. The mechanisms underlying the associations with cognitive impairment and LOAD require further elucidation, but both genes are interesting candidates for involvement in age-related cognitive impairment.

Indexed as

Polymorphism, GeneticAgedAged, 80 and overAlzheimer DiseaseCausalityCognitionCognition DisordersComorbidityFemaleGenetic Predisposition to DiseaseHumansIncidenceLamin Type ALinkage DisequilibriumMultigene FamilyPolymorphism, Single NucleotideLamin Type ALMNA protein, humanSerpins

Identifiers

PMID18848371
PMCPMC2975102
OpenAlexW2115007439

What OpenQuestion holds

Textmetadata
LicenceTDM
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.