Evidence map›Paper›PMID 28079061›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2017

Progressive Decline in Hippocampal CA1 Volume in Individuals at Ultra-High-Risk for Psychosis Who Do Not Remit: Findings from the Longitudinal Youth at Risk Study.

New Fei Ho, Daphne J Holt, Mike Cheung, Juan Eugenio Iglesias, Alex Goh, Mingyuan Wang, Joseph Kw Lim, Joshua de Souza, Joann S Poh, Yuen Mei See and 5 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
6.7field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 83 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Effects of diazepam on hippocampal blood flow in people at clinical high risk for psychosis.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Trial
  5. Oxytocin modulates hippocampal perfusion in people at clinical high risk for psychosis.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Trial
  6. Synergistic pathways to psychosis: understanding developmental risk and resilience factors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 3 countries.

New Fei HoInstitute of Mental Health, Singapore, Singapore.ORCID http://orcid.org/0000-0002-0456-3391
Daphne J HoltDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Mike CheungDepartment of Psychology, National University of Singapore, Singapore, Singapore.
Juan Eugenio IglesiasUniversity College London, London, UK.
Alex GohInstitute of Mental Health, Singapore, Singapore.
Mingyuan WangInstitute of Mental Health, Singapore, Singapore.
Joseph Kw LimNeuroscience and Behavioral Disorders Program, Center for Cognitive Neuroscience, Duke-National University of Singapore Graduate Medical School, Singapore, Singapore.
Joshua de SouzaNeuroscience and Behavioral Disorders Program, Center for Cognitive Neuroscience, Duke-National University of Singapore Graduate Medical School, Singapore, Singapore.
Joann S PohNeuroscience and Behavioral Disorders Program, Center for Cognitive Neuroscience, Duke-National University of Singapore Graduate Medical School, Singapore, Singapore.ORCID http://orcid.org/0000-0002-4484-9028
Yuen Mei SeeInstitute of Mental Health, Singapore, Singapore.
Alison R AdcockCenter for Cognitive Neuroscience, Duke University, Durham, NC, USA.
Stephen J WoodSchool of Psychology, University of Birmingham, Birmingham, UK.
Michael Wl CheeNeuroscience and Behavioral Disorders Program, Center for Cognitive Neuroscience, Duke-National University of Singapore Graduate Medical School, Singapore, Singapore.ORCID http://orcid.org/0000-0002-6087-0548
Jimmy LeeInstitute of Mental Health, Singapore, Singapore.ORCID http://orcid.org/0000-0002-7724-7445
Juan ZhouNeuroscience and Behavioral Disorders Program, Center for Cognitive Neuroscience, Duke-National University of Singapore Graduate Medical School, Singapore, Singapore.
National University of Singapore · SGInstitute of Mental Health · SGDuke University · USHarvard University · USUniversity College London · GBUniversity of Birmingham · GB

Funding

The neural basis of deficits in acquisition and extinction of fear in schizophrenR01MH095904 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI HOLT, DAPHNE J · 2012 to 2016
$2.7M
NIMH NIH HHS R01 MH095904
6 · The paper itself

Abstract

Most individuals identified as ultra-high-risk (UHR) for psychosis do not develop frank psychosis. They continue to exhibit subthreshold symptoms, or go on to fully remit. Prior work has shown that the volume of CA1, a subfield of the hippocampus, is selectively reduced in the early stages of schizophrenia. Here we aimed to determine whether patterns of volume change of CA1 are different in UHR individuals who do or do not achieve symptomatic remission. Structural MRI scans were acquired at baseline and at 1-2 follow-up time points (at 12-month intervals) from 147 UHR and healthy control subjects. An automated method (based on an ex vivo atlas of ultra-high-resolution hippocampal tissue) was used to delineate the hippocampal subfields. Over time, a greater decline in bilateral CA1 subfield volumes was found in the subgroup of UHR subjects whose subthreshold symptoms persisted (n=40) and also those who developed clinical psychosis (n=12), compared with UHR subjects who remitted (n=41) and healthy controls (n=54). No baseline differences in volumes of the overall hippocampus or its subfields were found among the groups. Moreover, the rate of volume decline of CA1, but not of other hippocampal subfields, in the non-remitters was associated with increasing symptom severity over time. Thus, these findings indicate that there is deterioration of CA1 volume in persistently symptomatic UHR individuals in proportion to symptomatic progression.

Indexed as

Disease ProgressionProdromal SymptomsAdolescentAdultCA1 Region, HippocampalFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMalePsychotic DisordersRiskSeverity of Illness IndexYoung Adult

Identifiers

PMID28079061
PMCPMC5437892
OpenAlexW2572030788

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.