Evidence map›Paper›PMID 40054762›Full record

ArticleBiological psychiatry2025

A Cross-Generational Methylomic Signature of Infant Maltreatment in Newborn Rhesus Macaques.

Roy Lardenoije, Michelle N C A Smulders, Elyse L Morin, Brittany R Howell, Dora Guzman, Jerrold S Meyer, Kerry J Ressler, Mar Sánchez, Torsten Klengel

Abstract read
In one paragraph

Article in Biological psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Review
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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

9 authors.

Roy LardenoijeDepartment of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany; McLean Hospital, Harvard Medical School, Boston, Massachusetts.
Michelle N C A SmuldersMcLean Hospital, Harvard Medical School, Boston, Massachusetts; Department of Biomedical Sciences, University of Amsterdam, Amsterdam, the Netherlands.
Elyse L MorinDepartment of Psychiatry & Behavioral Sciences, Emory School of Medicine, Atlanta, Georgia; Emory National Primate Research Center, Emory University, Atlanta, Georgia.
Brittany R HowellDepartment of Psychiatry & Behavioral Sciences, Emory School of Medicine, Atlanta, Georgia; Emory National Primate Research Center, Emory University, Atlanta, Georgia; University of Minnesota, Institute of Child Development, Minneapolis, Minnesota.
Dora GuzmanDepartment of Psychiatry & Behavioral Sciences, Emory School of Medicine, Atlanta, Georgia; Emory National Primate Research Center, Emory University, Atlanta, Georgia.
Jerrold S MeyerDepartment of Psychological and Brain Sciences, University of Massachusetts, Amherst, Massachusetts.
Kerry J ResslerMcLean Hospital, Harvard Medical School, Boston, Massachusetts.
Mar SánchezDepartment of Psychiatry & Behavioral Sciences, Emory School of Medicine, Atlanta, Georgia; Emory National Primate Research Center, Emory University, Atlanta, Georgia.
Torsten KlengelDepartment of Psychiatry and Psychotherapy, University Medical Center Göttingen, Göttingen, Germany; McLean Hospital, Harvard Medical School, Boston, Massachusetts. Electronic address: tklengel@mclean.harvard.edu.

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Project 3: The neurobiology of adverse early care in rhesus infants....P50MH078105 · NIMH · UNIVERSITY OF MINNESOTA · PI FOX, NATHAN A · 2009 to 2013
$9.9M
Early Life Stress, Chronic Drug Use and Neuroplasticity in Nonhuman Primate Models of Cocaine Abuse: Relevance to Treatment StrategiesR01DA052909 · NIDA · EMORY UNIVERSITY · PI Michael A Nader, MAR M SANCHEZ · 2021 to 2026
$4.9M
Early life stress and adolescent cocaine abuse: neurobiological vulnerabilitiesR01DA038588 · NIDA · EMORY UNIVERSITY · PI SANCHEZ, MAR M · 2014 to 2020
$3.5M
Understanding the transgenerational epigenetic effect of maternal psychosocial trauma exposure on infants via lncRNA-sequencingR01HD102974 · NICHD · MCLEAN HOSPITAL · PI KLENGEL, TORSTEN, KOEN , NASTASSJA · 2020 to 2024
$2.9M
Longitudinal DNA methylation in a non-human primate model of early-life stressR21HD088931 · NICHD · MCLEAN HOSPITAL · PI KLENGEL, TORSTEN, RESSLER, KERRY J. · 2017 to 2018
$473k
Effects of Stress and Obesity on Longitudinal Epigenetic ProgrammingR21HD097524 · NICHD · MCLEAN HOSPITAL · PI ETHUN, KELLY F, KLENGEL, TORSTEN · 2019 to 2020
$465k
Quantitation of bioactive molecules using triple quadrupole mass spectrometryS10OD010757 · OD · EMORY UNIVERSITY · PI PRUETT, SARAH TROTMAN · 2012 to 2012
$410k
Neurodevelopmental Correlates of Psychopathology Following Infant MaltreatmentF31MH086203 · NIMH · EMORY UNIVERSITY · PI HOWELL, BRITTANY ROLLINS · 2010 to 2012
$91k
NICHD NIH HHS R01 HD102974NICHD NIH HHS R21 HD088931NICHD NIH HHS R21 HD097524NIDA NIH HHS R01 DA038588NIDA NIH HHS R01 DA052909NIH HHS P51 OD011132NIH HHS S10 OD010757NIMH NIH HHS F31 MH086203NIMH NIH HHS P50 MH078105
6 · The paper itself

Abstract

backgroundEarly-life adversity (ELA) results in detrimental physical and mental health outcomes. The impact of ELA can reverberate across generations, with epigenetic modifications being one of the proposed biological correlates of exposure to ELA. Here, we bridge the translational gap between rodent models and clinical studies by utilizing a nonhuman primate model to study the cross-generational epigenetic and functional footprints of physical maltreatment and neglect.

methodsMethylomic profiling was performed using the Illumina MethylationEPIC array platform, adapted for rhesus macaques. A total of 339,081 individual methylation sites were compared between newborn offspring of maltreated (n = 14, 8 female) and nonmaltreated (n = 12, 5 female) mothers.

resultsWe identified 409 differentially methylated positions (DMPs) and 7 differentially methylated regions associated with the cross-generational impact of infant maltreatment. A subsequent pathway enrichment analysis revealed 78 enriched pathways. Neonatal blood cortisol levels were significantly lower in animals with a maltreated mother (maltreated n = 13, 7 female; control n = 9, 4 female). Of the 409 DMPs, 46 showed an association with blood cortisol levels, 19 of which were found to potentially mediate the association between ancestral infant maltreatment and decreased blood cortisol levels. Finally, 137 of the DMPs were associated with a human trait in the EWAS Atlas, including child abuse and glucocorticoid exposure.

conclusionsThese findings provide deeper insight into the role of epigenetic alterations across generations after environmental insults and how this may impact the development of phenotypic alterations in offspring of individuals exposed to maltreatment.

Indexed as

DNA MethylationEpigenesis, GeneticAnimalsAnimals, NewbornFemaleHydrocortisoneMacaca mulattaMaleHydrocortisoneAncestral experiencesChildhood maltreatmentDNA methylationEarly-life stressEpigeneticsNonhuman primate

Identifiers

PMID40054762
PMCPMC12353506

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