Evidence map›Paper›PMID 39979475›Full record

ArticleMolecular psychiatry2025

Genetic architectures of childhood maltreatment and causal influence of childhood maltreatment on health outcomes in adulthood.

Tzu-Ting Chen, Chia-Yen Chen, Chao-Yu Liu, Jiwoo Lee, Andrea Ganna, Yen-Chen Anne Feng, Yen-Feng Lin

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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Mapping the genetic landscape of suicide risk: Insights from genomic SEM.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    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

7 authors.

Tzu-Ting Chen *Center for Neuropsychiatric Research, National Health Research Institutes, Miaoli, Taiwan.
Chia-Yen Chen *Biogen, Cambridge, MA, USA.ORCID 0000-0001-9548-5597
Chao-Yu LiuDepartment of Psychiatry, School of Medicine, Yale University, New Haven, CT, USA.
Jiwoo LeeBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0003-0555-585X
Andrea GannaBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID 0000-0002-8147-240X
Yen-Chen Anne FengInstitute of Health Data Analytics and Statistics, College of Public Health, National Taiwan University, Taipei, Taiwan.ORCID 0000-0003-2116-3645
Yen-Feng LinCenter for Neuropsychiatric Research, National Health Research Institutes, Miaoli, Taiwan. yflin@nhri.edu.tw.ORCID 0000-0003-3017-6026

Funding

Ministry of Education (Ministry of Education, Republic of China (Taiwan)) NTU-112V1020-2,NTU-112L9004Ministry of Science and Technology, Taiwan (Ministry of Science and Technology of Taiwan) MOST 109-2314-B-400-017 and 110-2314-B-400-028-MY3National Health Research Institutes (NHRI) NP-111, 112, 113-PP-09NTU | College of Medicine, National Taiwan University (College of Medicine, National Taiwan University) NTU-112L7404
6 · The paper itself

Abstract

Childhood maltreatment is increasingly recognized as a pivotal risk factor for adverse health outcomes. However, comprehensive analyses of its long-term impact are scarce. This study aims to fill this gap by examining the genetic architectures of childhood maltreatment and its influence on adult health and socioeconomic outcomes. Utilizing data from the UK Biobank (N = 129,017), we conducted sex-combined and sex-stratified genome-wide association studies to identify genomic loci associated with five childhood maltreatment subtypes. We then performed genetic correlation and Mendelian randomization (MR) analyses to assess the effects of childhood maltreatment on high-burden diseases, healthcare costs, lifespan, and educational attainment. We identified several novel loci for childhood maltreatment, including one locus for sexual abuse in sex-combined analysis, one novel locus for sexual abuse in males, one locus for emotional neglect in females, and one locus for sexual abuse in females. The pairwise genetic correlations between subtypes of childhood maltreatment were moderate to high, and similar patterns of genetic correlations between childhood maltreatment subtypes were observed in males and females. Childhood maltreatment was genetically correlated with ten out of 16 high-burden diseases significantly after multiple testing correction. Moreover, MR analyses suggest childhood maltreatment may increase the risk of age-related and other hearing loss, low back pain, major depressive disorder, and migraine in adulthood, and reduce the lifespan. Our study elucidates the genetic architecture of specific childhood maltreatment subtypes and the influence of childhood maltreatment on health outcomes in adulthood, highlighting the enduring influence of childhood maltreatment on lifelong health consequences. It is important to develop prevention strategies to lower the incidence of childhood maltreatment and provide support and care for victims of childhood maltreatment for better long-term health outcomes in the population.

Indexed as

Adult Survivors of Child AbuseChild AbuseAdultAgedChildFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisMiddle AgedPolymorphism, Single NucleotideRisk FactorsUnited Kingdom

Identifiers

PMID39979475
PMCPMC12240850

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