Evidence map›Paper›PMID 34799595›Full record

ArticleScientific reports2021

Large-scale genetic investigation reveals genetic liability to multiple complex traits influencing a higher risk of ADHD.

Luis M García-Marín, Adrián I Campos, Gabriel Cuéllar-Partida, Sarah E Medland, Scott H Kollins, Miguel E Rentería

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-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

12 citing papers in PubMed, 22 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

6 authors at 3 institutions in 2 countries.

Luis M García-MarínDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. luis.garciamarin@qimrberghofer.edu.au.
Adrián I CamposDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Gabriel Cuéllar-PartidaThe University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD, Australia.
Sarah E MedlandDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Scott H KollinsDepartment of Psychiatry & Behavioral Sciences, School of Medicine, Duke University, Durham, NC, USA.
Miguel E RenteríaDepartment of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. miguel.renteria@qimrberghofer.edu.au.
University of Queensland · AUQIMR Berghofer Medical Research Institute · AUDuke University · US

Funding

National Health and Medical Research Council APP1102821National Health and Medical Research Council APP1158125
6 · The paper itself

Abstract

Attention Deficit-Hyperactivity Disorder (ADHD) is a complex psychiatric and neurodevelopmental disorder that develops during childhood and spans into adulthood. ADHD's aetiology is complex, and evidence about its cause and risk factors is limited. We leveraged genetic data from genome-wide association studies (GWAS) and performed latent causal variable analyses using a hypothesis-free approach to infer causal associations between 1387 complex traits and ADHD. We identified 37 inferred potential causal associations with ADHD risk. Our results reveal that genetic variants associated with iron deficiency anemia (ICD10), obesity, type 2 diabetes, synovitis and tenosynovitis (ICD10), polyarthritis (ICD10), neck or shoulder pain, and substance use in adults display partial genetic causality on ADHD risk in children. Genetic variants associated with ADHD have a partial genetic causality increasing the risk for chronic obstructive pulmonary disease and carpal tunnel syndrome. Protective factors for ADHD risk included genetic variants associated with the likelihood of participating in socially supportive and interactive activities. Our results show that genetic liability to multiple complex traits influences a higher risk for ADHD, highlighting the potential role of cardiometabolic phenotypes and physical pain in ADHD's aetiology. These findings have the potential to inform future clinical studies and development of interventions.

Indexed as

Genetic Predisposition to DiseaseAttention Deficit Disorder with HyperactivityChildDatabases, FactualGenetic Association StudiesGenetic LinkageGenetic VariationGenome-Wide Association StudyGenomicsHumansMultifactorial InheritanceObesityPhenotypeRiskSubstance-Related Disorders

Identifiers

PMID34799595
PMCPMC8604995
OpenAlexW3214207620

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.