Evidence map›Paper›PMID 37881160›Full record

SynthesisHippocampus2023

Age-related differences in hippocampal subfield volumes across the human lifespan: A meta-analysis.

Roya Homayouni, Kelsey L Canada, Samaah Saifullah, Da' Jonae Foster, Charlotte Thill, Naftali Raz, Ana M Daugherty, Noa Ofen

Abstract readMeta-Analysis
In one paragraph

Synthesis in Hippocampus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Pattern separation and pattern completion in early childhood.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Review
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

8 authors.

Roya HomayouniInstitute of Gerontology, Wayne State University, Detroit, Michigan, USA.
Kelsey L CanadaInstitute of Gerontology, Wayne State University, Detroit, Michigan, USA.ORCID 0000-0002-0366-1555
Samaah SaifullahSchool of Medicine, Wayne State University, Detroit, Michigan, USA.
Da' Jonae FosterDepartment of Psychology, Wayne State University, Detroit, Michigan, USA.
Charlotte ThillSchool of Medicine, Wayne State University, Detroit, Michigan, USA.
Naftali RazDepartment of Psychology, Stony Brook University, Stony Brook, New York, USA.
Ana M DaughertyInstitute of Gerontology, Wayne State University, Detroit, Michigan, USA.
Noa OfenInstitute of Gerontology, Wayne State University, Detroit, Michigan, USA.ORCID 0000-0003-3927-8408

Funding

DEVELOPMENT OF MEMORY NETWORKS IN CHILDRENR01MH107512 · NIMH · WAYNE STATE UNIVERSITY · PI Noa Ofen · 2016 to 2026
$5.0M
NEURAL CORRELATES OF AGE-RELATED DIFFERENCES IN MEMORYR01AG011230 · NIA · WAYNE STATE UNIVERSITY · PI DAUGHERTY, ANA MARIE, RAZ, NAFTALI · 1993 to 2020
$4.8M
An integrative multisite study of the influence of socioeconomic disparities on hippocampal subfields developmental trajectoriesF32HD108960 · NICHD · WAYNE STATE UNIVERSITY · PI CANADA, KELSEY LEIGH · 2022 to 2024
$224k
NIA NIH HHS R01 AG011230NICHD NIH HHS F32 HD108960NIH HHS F32-HD108960NIH HHS R01-AG011230NIH HHS R01-MH107512NIMH NIH HHS R01 MH107512
6 · The paper itself

Abstract

The human hippocampus (Hc) is critical for memory function across the lifespan. It is comprised of cytoarchitectonically distinct subfields: dentate gyrus (DG), cornu ammonis sectors (CA) 1-4, and subiculum, each of which may be differentially susceptible to neurodevelopmental and neurodegenerative mechanisms. Identifying age-related differences in Hc subfield volumes can provide insights into neural mechanisms of memory function across the lifespan. Limited evidence suggests that DG and CA3 volumes differ across development while other regions remain relatively stable, and studies of adulthood implicate a downward trend in all subfield volumes with prominent age effects on CA1. Due to differences in methods and limited sampling for any single study, the magnitude of age effects on Hc subfield volumes and their probable lifespan trajectories remain unclear. Here, we conducted a meta-analysis on cross-sectional studies (n = 48,278 participants, ages = 4-94 years) to examine the association between age and Hc subfield volumes in development (n = 11 studies), adulthood (n = 30 studies), and a combined lifespan sample (n = 41 studies) while adjusting estimates for sample sizes. In development, age was positively associated with DG and CA3-4 volumes, whereas in adulthood a negative association was observed with all subfield volumes. Notably, the observed age effects were not different across subfield volumes within each age group. All subfield volumes showed a nonlinear age pattern across the lifespan with DG and CA3-4 volumes showing a more distinct age trajectory as compared to the other subfields. Lastly, among all the study-level variables, only female percentage of the study sample moderated the age effect on CA1 volume: a higher female-to-male ratio in the study sample was linked to the greater negative association between age and CA1 volume. These results document that Hc subfield volumes differ as a function of age offering broader implications for constructing theoretical models of lifespan memory development.

Indexed as

HippocampusLongevityCross-Sectional StudiesFemaleHumansMagnetic Resonance ImagingMaleadultschildrenepisodic memoryhippocampusMRIstructural development

Identifiers

PMID37881160
PMCPMC10841547

What OpenQuestion holds

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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.