Evidence map›Paper›PMID 36855850›Full record

ArticleBipolar disorders2023

Subfield-specific longitudinal changes of hippocampal volumes in patients with early-stage bipolar disorder.

Bruce Atwood, Walid Yassin, Shi Yu Chan, Mei-Hua Hall

Abstract read
In one paragraph

Article in Bipolar disorders, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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2 · The registry

The trial behind it

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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

3 citing papers in PubMed.

  1. Exposotypes in psychotic disorders.Scientific reports · 2025
    Article
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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

4 authors.

Bruce AtwoodPsychosis Neurobiology Laboratory, McLean Hospital, Belmont, Massachusetts, USA.
Walid YassinPsychosis Neurobiology Laboratory, McLean Hospital, Belmont, Massachusetts, USA.
Shi Yu ChanPsychosis Neurobiology Laboratory, McLean Hospital, Belmont, Massachusetts, USA.
Mei-Hua HallPsychosis Neurobiology Laboratory, McLean Hospital, Belmont, Massachusetts, USA.ORCID 0000-0002-4558-7023

Funding

Neurobiological Markers as Predictors of Later Functional Outcome in First Episode PsychosisR01MH109687 · NIMH · MCLEAN HOSPITAL · PI HALL, MEI-HUA · 2016 to 2021
$2.5M
NIMH NIH HHS R01 MH109687NIMH NIH HHS R01MH109687
6 · The paper itself

Abstract

backgroundThe hippocampus is a heterogeneous structure composed of biologically and functionally distinct subfields. Hippocampal aberrations are proposed to play a fundamental role in the etiology of psychotic symptoms. Bipolar disorder (BPD) has substantial overlap in symptomatology and genetic liability with schizophrenia (SZ), and reduced hippocampal volumes, particularly at the chronic illness stages, are documented in both disorders. Studies of hippocampal subfields in the early stage of BPD are limited and cross-sectional findings to date report no reduction in hippocampal volumes. To our knowledge, there have been no longitudinal studies of BPD evaluating hippocampal volumes in the early phase of illness. We investigated the longitudinal changes in hippocampal regions and subfields in BPD mainly and in early stage of psychosis (ESP) patients more broadly and compared them to those in controls (HC).

methodsBaseline clinical and structural MRI data were acquired from 88 BPD, from a total of 143 ESP patients, and 74 HCs. Of those, 66 participants (23 HC, 43 patients) completed a 12-month follow-up visit. The hippocampus regions and subfields were segmented using Freesurfer automated pipeline.

resultsWe found general baseline deficits in hippocampal volumes among BPD and ESP cohorts. Both cohorts displayed significant increases in the anterior hippocampal region and dentate gyrus compared with controls. Additionally, antipsychotic medications were positively correlated with the posterior region at baseline.

conclusionThese findings highlight brain plasticity in BPD and in ESP patients providing evidence that deviations in hippocampal volumes are adaptive responses to atypical signaling rather than progressive degeneration.

Indexed as

Bipolar DisorderPsychotic DisordersSchizophreniaCross-Sectional StudiesHippocampusHumansMagnetic Resonance ImagingOrgan Sizebipolar disorderearly-stage psychosishippocampus subfield volumeslongitudinal

Identifiers

PMID36855850
PMCPMC10330583

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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 OpenQuestion graph.