Evidence map›Paper›PMID 25754080›Full record

ArticleMolecular psychiatry2016

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.

T-K Clarke, M K Lupton, A M Fernandez-Pujals, J Starr, G Davies, S Cox, A Pattie, D C Liewald, L S Hall, D J MacIntyre and 13 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

96 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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36 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

23 authors.

T-K ClarkeDivision of Psychiatry, University of Edinburgh, Edinburgh, UK.
M K LuptonQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
A M Fernandez-PujalsDivision of Psychiatry, University of Edinburgh, Edinburgh, UK.
J StarrCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
G DaviesCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
S CoxCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
A PattieCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
D C LiewaldCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
L S HallDivision of Psychiatry, University of Edinburgh, Edinburgh, UK.
D J MacIntyreDivision of Psychiatry, University of Edinburgh, Edinburgh, UK.
B H SmithDivision of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.
L J HockingDivision of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.
S PadmanabhanInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
P A ThomsonCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
C HaywardMedical Genetics Section, Molecular Medicine Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
N K HansellQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
G W MontgomeryQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
S E MedlandQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
N G MartinQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
M J WrightQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
D J PorteousCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
I J DearyCentre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK.
A M McIntoshDivision of Psychiatry, University of Edinburgh, Edinburgh, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/F019394/1Chief Scientist Office CZB/4/505Chief Scientist Office CZD/16/6Chief Scientist Office CZD/16/6/4Chief Scientist Office ETM/55Chief Scientist Office HR03006Medical Research Council G0700704Medical Research Council MC_PC_U127561128Medical Research Council MR/K026992/1Wellcome Trust 104036Wellcome Trust 104036/Z/14/Z
6 · The paper itself

Abstract

Cognitive impairment is common among individuals diagnosed with autism spectrum disorder (ASD) and attention-deficit hyperactivity disorder (ADHD). It has been suggested that some aspects of intelligence are preserved or even superior in people with ASD compared with controls, but consistent evidence is lacking. Few studies have examined the genetic overlap between cognitive ability and ASD/ADHD. The aim of this study was to examine the polygenic overlap between ASD/ADHD and cognitive ability in individuals from the general population. Polygenic risk for ADHD and ASD was calculated from genome-wide association studies of ASD and ADHD conducted by the Psychiatric Genetics Consortium. Risk scores were created in three independent cohorts: Generation Scotland Scottish Family Health Study (GS:SFHS) (n=9863), the Lothian Birth Cohorts 1936 and 1921 (n=1522), and the Brisbane Adolescent Twin Sample (BATS) (n=921). We report that polygenic risk for ASD is positively correlated with general cognitive ability (beta=0.07, P=6 × 10(-7), r(2)=0.003), logical memory and verbal intelligence in GS:SFHS. This was replicated in BATS as a positive association with full-scale intelligent quotient (IQ) (beta=0.07, P=0.03, r(2)=0.005). We did not find consistent evidence that polygenic risk for ADHD was associated with cognitive function; however, a negative correlation with IQ at age 11 years (beta=-0.08, Z=-3.3, P=0.001) was observed in the Lothian Birth Cohorts. These findings are in individuals from the general population, suggesting that the relationship between genetic risk for ASD and intelligence is partly independent of clinical state. These data suggest that common genetic variation relevant for ASD influences general cognitive ability.

Indexed as

AdolescentAdultAttention Deficit Disorder with HyperactivityAutism Spectrum DisorderCognition DisordersCohort StudiesDatabases, FactualFamily HealthFemaleGenome-Wide Association StudyHumansIntelligence TestsLinear ModelsMaleMultifactorial InheritancePolymorphism, Single Nucleotide

Identifiers

PMID25754080
PMCPMC4759203

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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.