Evidence map›Paper›PMID 40247129›Full record

ArticleMolecular psychiatry2025

The moderation of genetic risk for ten major psychiatric and substance use disorders by the genetic aptitude for educational attainment.

Kenneth S Kendler, Henrik Ohlsson, Jan Sundquist, Kristina Sundquist

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Kenneth S KendlerVirginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA. Kenneth.Kendler@vcuhealth.org.ORCID 0000-0001-8689-6570
Henrik OhlssonCenter for Primary Health Care Research, Department of Clinical Sciences, Lund University, Malmö, Sweden.
Jan SundquistCenter for Primary Health Care Research, Department of Clinical Sciences, Lund University, Malmö, Sweden.ORCID 0000-0001-7228-5015
Kristina SundquistCenter for Primary Health Care Research, Department of Clinical Sciences, Lund University, Malmö, Sweden.

Funding

Identifying the genetic causes of depression in a deeply phenotyped population from South KoreaU01MH126798 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHN, YONG MIN, FLINT, JONATHAN · 2021 to 2025
$8.9M
Genetic, Social, and Developmental Epidemiology of Drug Use DisordersR01DA030005 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI KENNETH SEEDMAN KENDLER, JAN O SUNDQUIST · 2010 to 2026
$7.6M
Social, Developmental and Genetic Epidemiology of Alcohol Use DisordersR01AA023534 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI KENDLER, KENNETH SEEDMAN, SUNDQUIST, KRISTINA · 2015 to 2023
$4.0M
NIAAA NIH HHS R01 AA023534NIDA NIH HHS R01 DA030005NIMH NIH HHS U01 MH126798U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) U01MH126798U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) R01AA023534U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) R01DA030005Vetenskapsrådet (Swedish Research Council) 2020-01175Vetenskapsrådet (Swedish Research Council) 2021-06467
6 · The paper itself

Abstract

We seek to clarify the impact of the Genetic Aptitude for Educational Attainment (GAEA) on risk for 10 psychiatric disorders divided into 4 groups: Internalizing, Externalizing, Eating/Compulsive and Psychotic. Educational attainment and psychiatric and substance use disorder information were obtained from national Swedish registries. GAEA and disorder-specific family genetic risk score (FGRS) were calculated from extended pedigrees. In males, information on IQ and resilience was obtained from the Swedish conscript registry. Affected individuals were born in Sweden from 1973-1995 to Swedish born parents. Controlling for disorder specific FGRS, GAEA were negatively and substantially associated with risk for externalizing and internalizing disorders, minimally associated with psychotic disorder risk and positively and modestly associated with risk for eating/compulsive disorders. While the majority of GAEA effect on risk for externalizing disorders was mediated through impact on IQ, for internalizing disorders, mediation was largely through resilience. For externalizing and internalizing disorders, interactions between GAEA and disorder specific FGRS were robust and negative - the slope of disorder risk with increasing genetic liability was steepest in those with low GAEA. For eating disorders, interactions were modest and positive -the slope of risk with increasing genetic liability being steepest in individuals with high GAEA. We found that the impact of GAEA on risk for psychiatric and substance can be substantial and varies widely across disorders in magnitude, direction, and mediation. GAEA also often interacts, sometimes robustly, with disorder specific genetic risk factors. Comprehensive risk models for psychiatric disorders should consider the inclusion of GAEA.

Indexed as

Mental DisordersSubstance-Related DisordersAdolescentAdultAptitudeEducational StatusFemaleGenetic Predisposition to DiseaseHumansIntelligenceMaleMiddle AgedRegistriesRisk FactorsSwedenYoung Adult

Identifiers

PMID40247129
PMCPMC12185330

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.