Evidence map›Paper›PMID 22005930›Full record

SynthesisMolecular psychiatry2012

Genome-wide association study of Alzheimer's disease with psychotic symptoms.

P Hollingworth, R Sweet, R Sims, D Harold, G Russo, R Abraham, A Stretton, N Jones, A Gerrish, J Chapman and 33 more

Open access · greenAbstract readMeta-AnalysisMulticenter Study
In one paragraph

Synthesis in Molecular psychiatry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 6 pooled it
5.8field-weighted citation impact, top 4% 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

69 citing papers in PubMed, 6 syntheses or guidelines pooled it, 132 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  6. Pooled it
  7. Trial
  8. Article
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  11. Connecting genomic and proteomic signatures of amyloid burden in the brain.medRxiv : the preprint server for health sciences · 2024
    Article
  12. Review
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  18. The neural signatures of psychoses in Alzheimer's disease: a neuroimaging genetics approach.European archives of psychiatry and clinical neuroscience · 2023
    Article
  19. Article
  20. Review

9 more citing papers are in PubMed but not listed here.

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

43 authors at 10 institutions in 3 countries.

P HollingworthMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Neurosciences and Mental Health Research Institute, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff, UK.
R Sweet
R Sims
D Harold
G Russo
R Abraham
A Stretton
N Jones
A Gerrish
J Chapman
D Ivanov
V Moskvina
S Lovestone
P Priotsi
M Lupton
C Brayne
M Gill
B Lawlor
A Lynch
D Craig
B McGuinness
J Johnston
C Holmes
G Livingston
N J Bass
H Gurling
A McQuillin
GERAD Consortium
National Institute on Aging Late-Onset Alzheimer's Disease Family Study Group
P Holmans
L Jones
B Devlin
L Klei
M M Barmada
F Y Demirci
S T DeKosky
O L Lopez
P Passmore
M J Owen
M C O'Donovan
R Mayeux
M I Kamboh
J Williams
Cardiff University · GBMedical Research Council · GBUniversity of Pittsburgh · USQueen's University Belfast · GBUniversity College London · GBKing's College London · GBTrinity College Dublin · IEColumbia University · USUniversity of Cambridge · GBUniversity of Southampton · GB

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
Smartphone-Based "Burst" Cognitive AssessmentsP01AG003991 · NIA · WASHINGTON UNIVERSITY · PI JOHN MORRIS · 1985 to 2026
$69.5M
THERAPEUTIC EFFECTS OF INTRA-NASAL INSULIN DETEMIRP50AG005136 · NIA · UNIVERSITY OF WASHINGTON · PI GRABOWSKI, THOMAS J. · 1985 to 2019
$57.2M
WASHINGTON UNIVERSITY ALZHEIMERS DISEASE RESEARCH CENTERP50AG005681 · NIA · WASHINGTON UNIVERSITY · PI FAGAN, ANNE · 1985 to 2019
$52.1M
SUPPLEMENT TO RUSH ALZHEIMERS DISEASE CENTER COREP30AG010161 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI LEURGANS, SUE E. · 1991 to 2020
$49.1M
Satellite Diagnostic and Treatment Clinic CoreP50AG008702 · NIA · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI DE JAGER, PHILIP L · 1989 to 2019
$46.3M
TREATMENT OF DEPRESSION IN ALZHEIMER'S DISEASEP50AG005133 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KAMBOH, M. ILYAS · 1985 to 2019
$43.0M
THE ROLE OF ADVANCED CAA IN ALZHEIMER'S DEMENTIAP50AG005134 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI HYMAN, BRADLEY T. · 1985 to 2018
$42.1M
VASCULAR RISK AND COGNITIVE STATUS IN A LATINO POPULATIONP50AG005142 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BRASKIE, MEREDITH NICOLE · 1985 to 2019
$41.0M
VESICULAR LOCALIZATION AND FUNCTION OF PRESENILIN 1 FRAGMENTP50AG005138 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GROSSMAN, HILLEL · 1985 to 2019
$37.9M
Research Education ComponentP30AG010133 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI SAYKIN, ANDREW J · 1991 to 2020
$37.3M
UPenn ADCC Biomarker CoreP30AG010124 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DETRE, JOHN A · 1991 to 2020
$35.1M
Medical Research Council G0300429Medical Research Council G0800509Medical Research Council G0902227Medical Research Council MC_U123160651Medical Research Council MC_U123160657NHGRI NIH HHS HHSN268200782096CNIA NIH HHS AG027224NIA NIH HHS P01 AG002219NIA NIH HHS P01 AG003991NIA NIH HHS P01AG02219NIA NIH HHS P01AG03991NIA NIH HHS P01AG05138NIA NIH HHS P30 AG008017NIA NIH HHS P30AG008017NIA NIH HHS P30 AG010124NIA NIH HHS P30 AG010133NIA NIH HHS P30AG010133NIA NIH HHS P30 AG010161NIA NIH HHS P30 AG012300NIA NIH HHS P30 AG013846NIA NIH HHS P30AG013846NIA NIH HHS P30 AG013854NIA NIH HHS P30 AG028377NIA NIH HHS P30AG028377NIA NIH HHS P30 AG028383NIA NIH HHS P30AG028383NIA NIH HHS P30AG10124NIA NIH HHS P30AG10161NIA NIH HHS P30AG12300NIA NIH HHS P30AG13854NIA NIH HHS P50 AG005133NIA NIH HHS P50AG005133NIA NIH HHS P50 AG005134NIA NIH HHS P50 AG005136NIA NIH HHS P50 AG005138NIA NIH HHS P50 AG005142NIA NIH HHS P50 AG005681NIA NIH HHS P50 AG008702NIA NIH HHS P50AG016579NIA NIH HHS P50 AG016582NIA NIH HHS P50AG016582NIA NIH HHS P50AG05134NIA NIH HHS P50AG05136NIA NIH HHS P50AG05138NIA NIH HHS P50AG05142NIA NIH HHS P50AG05681NIA NIH HHS P50AG08702NIA NIH HHS P50AG165574NIA NIH HHS R01 AG027224NIA NIH HHS R01AG027224NIA NIH HHS R01 AG030653NIA NIH HHS R01AG030653NIA NIH HHS R01 AG041797NIA NIH HHS U24 AG021886NIA NIH HHS U24AG021886NIA NIH HHS U24 AG026395NIA NIH HHS U24AG026395NIA NIH HHS U24 AG056270NIMH NIH HHS R01 MH057881Wellcome Trust 082604Wellcome Trust 095317
6 · The paper itself

Abstract

Psychotic symptoms occur in ~40% of subjects with Alzheimer's disease (AD) and are associated with more rapid cognitive decline and increased functional deficits. They show heritability up to 61% and have been proposed as a marker for a disease subtype suitable for gene mapping efforts. We undertook a combined analysis of three genome-wide association studies (GWASs) to identify loci that (1) increase susceptibility to an AD and subsequent psychotic symptoms; or (2) modify risk of psychotic symptoms in the presence of neurodegeneration caused by AD. In all, 1299 AD cases with psychosis (AD+P), 735 AD cases without psychosis (AD-P) and 5659 controls were drawn from Genetic and Environmental Risk in AD Consortium 1 (GERAD1), the National Institute on Aging Late-Onset Alzheimer's Disease (NIA-LOAD) family study and the University of Pittsburgh Alzheimer Disease Research Center (ADRC) GWASs. Unobserved genotypes were imputed to provide data on >1.8 million single-nucleotide polymorphisms (SNPs). Analyses in each data set were completed comparing (1) AD+P to AD-P cases, and (2) AD+P cases with controls (GERAD1, ADRC only). Aside from the apolipoprotein E (APOE) locus, the strongest evidence for association was observed in an intergenic region on chromosome 4 (rs753129; 'AD+PvAD-P' P=2.85 × 10(-7); 'AD+PvControls' P=1.11 × 10(-4)). SNPs upstream of SLC2A9 (rs6834555, P=3.0 × 10(-7)) and within VSNL1 (rs4038131, P=5.9 × 10(-7)) showed strongest evidence for association with AD+P when compared with controls. These findings warrant further investigation in larger, appropriately powered samples in which the presence of psychotic symptoms in AD has been well characterized.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseApolipoproteins ECase-Control StudiesChromosomes, Human, Pair 4DNA, IntergenicFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGlucose Transport Proteins, FacilitativeHumansMaleMiddle AgedNeurocalcinPolymorphism, Single NucleotideApolipoproteins EDNA, IntergenicGlucose Transport Proteins, FacilitativeNeurocalcinSLC2A9 protein, humanVSNL1 protein, human

Identifiers

PMID22005930
PMCPMC3272435
OpenAlexW1976385354

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.