Evidence map›Paper›PMID 31470127›Full record

ArticleNeuroImage2020

Sex-biased trajectories of amygdalo-hippocampal morphology change over human development.

Ari M Fish, Ajay Nadig, Jakob Seidlitz, Paul K Reardon, Catherine Mankiw, Cassidy L McDermott, Jonathan D Blumenthal, Liv S Clasen, Francois Lalonde, Jason P Lerch and 3 more

Open access · hybridAbstract read
In one paragraph

Article in NeuroImage, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Cognitive-Affective Social Processing and Emotion Regulation (CASPER) model.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  6. Review
  7. Article
  8. Fractionation of sex differences in human cortical anatomy.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
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  18. Article
  19. Article
  20. Prenatal metal mixtures and sex-specific infant negative affectivity.Environmental epidemiology (Philadelphia, Pa.) · 2021
    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

13 authors at 4 institutions in 2 countries.

Ari M FishDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Ajay NadigDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Jakob SeidlitzDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Paul K ReardonDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Catherine MankiwDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Cassidy L McDermottDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Jonathan D BlumenthalDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Liv S ClasenDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Francois LalondeDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA.
Jason P LerchDepartment of Medical Biophysics, University of Toronto, Toronto, ON, M5T 1R8, Canada; Neurosciences and Mental Health, the Hospital for Sick Children, Toronto, ON, M5T 3H7, Canada.
M Mallar ChakravartyCerebral Imaging Centre, Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada, H3A OG4; Departments of Psychiatry and Biological and Biomedical Engineering, McGill University, Montreal, QC, H3A OG4, Canada.
Russell T ShinoharaDepartment of Biostatistics, Epidemiology, and Informatics, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Armin RaznahanDevelopmental Neurogenomics Unit, Human Genetics Branch, National Institute of Mental Health, Bethesda, MD, 20892, USA. Electronic address: raznahana@mail.nih.gov.
National Institute of Mental Health · USDouglas Mental Health University Institute · CAHospital for Sick Children · CAUniversity of Pennsylvania · US

Funding

Section on Developmental NeurogenomicsZIAMH002949 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI RAZNAHAN, ARMIN · 2016 to 2025
$30.0M
Intramural NIH HHS ZIA MH002949
6 · The paper itself

Abstract

The amygdala and hippocampus are two adjacent allocortical structures implicated in sex-biased and developmentally-emergent psychopathology. However, the spatiotemporal dynamics of amygdalo-hippocampal development remain poorly understood in healthy humans. The current study defined trajectories of volume and shape change for the amygdala and hippocampus by applying a multi-atlas segmentation pipeline (MAGeT-Brain) and semi-parametric mixed-effects spline modeling to 1,529 longitudinally-acquired structural MRI brain scans from a large, single-center cohort of 792 youth (403 males, 389 females) between the ages of 5 and 25 years old. We found that amygdala and hippocampus volumes both follow curvilinear and sexually dimorphic growth trajectories. These sex-biases were particularly striking in the amygdala: males showed a significantly later and slower adolescent deceleration in volume expansion (at age 20 years) than females (age 13 years). Shape analysis localized significant hot-spots of sex-biased anatomical development in sub-regional territories overlying rostral and caudal extremes of the CA1/2 in the hippocampus, and the centromedial nuclear group of the amygdala. In both sexes, principal components analysis revealed close integration of amygdala and hippocampus shape change along two main topographically-organized axes - low vs. high areal expansion, and early vs. late growth deceleration. These results (i) bring greater resolution to our spatiotemporal understanding of amygdalo-hippocampal development in healthy males and females, and (ii) uncover focal sex-differences in the structural maturation of the brain components that may contribute to differences in behavior and psychopathology that emerge during adolescence.

Indexed as

AmygdalaHippocampusSex CharacteristicsAdolescentAdultAtlases as TopicChildChild, PreschoolFemaleHuman DevelopmentHumansLongitudinal StudiesMaleNeuroimagingYoung Adult

Identifiers

PMID31470127
PMCPMC7485527
OpenAlexW2970012504

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.