Evidence map›Paper›PMID 32093799›Full record

ArticleEuropean psychiatry : the journal of the Association of European Psychiatrists2020

Brain structure, IQ, and psychopathology in young offspring of patients with schizophrenia or bipolar disorder.

Neeltje E M van Haren, Nikita Setiaman, Martijn G J C Koevoets, Heleen Baalbergen, Rene S Kahn, Manon H J Hillegers

Open access · goldAbstract read
In one paragraph

Article in European psychiatry : the journal of the Association of European Psychiatrists, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  11. Intracortical Myelin in Youths at Risk for Depression.Biological psychiatry global open science · 2024
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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

6 authors at 2 institutions in 2 countries.

Neeltje E M van HarenDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht, The Netherlands.
Nikita SetiamanDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht, The Netherlands.
Martijn G J C KoevoetsDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht, The Netherlands.ORCID 0000-0002-8347-0379
Heleen BaalbergenDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht, The Netherlands.
Rene S KahnDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht, The Netherlands.
Manon H J HillegersDepartment of Psychiatry, University Medical Center Utrecht Brain Center, Utrecht, The Netherlands.
Erasmus MC · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStudying offspring of schizophrenia (SZo) and bipolar disorder patients (BDo) provides important information on the putative neurodevelopmental trajectories underlying development toward severe mental illnesses. We compared intracranial volume (ICV), as a marker for neurodevelopment, and global and local brain measures between SZo or BDo and control offspring (Co) in relation to IQ and psychopathology.

methodsT1-weighted magnetic resonance imaging (MRI) brain scans were obtained from 146 participants (8-19 years; 40 SZo, 66 BDo, 40 Co). Linear mixed models were applied to compare ICV, global, and local brain measures between groups. To investigate the effect of ICV, IQ (four subtests Wechsler Intelligence Scale for Children/Wechsler Adult Intelligence Scale-III) or presence of psychopathology these variables were each added to the model.

resultsSZo and BDo had significantly lower IQ and more often met criteria for a lifetime psychiatric disorder than Co. ICV was significantly smaller in SZo than in BDo (d = -0.56) and Co (d = -0.59), which was largely independent of IQ (respectively, d = -0.54 and d = -0.35). After ICV correction, the cortex was significantly thinner in SZo than in BDo (d = -0.42) and Co (d = -0.75) and lateral ventricles were larger in BDo than in Co (d = 0.55). Correction for IQ or lifetime psychiatric diagnosis did not change these findings.

conclusionsDespite sharing a lower IQ and a higher prevalence of psychiatric disorders, brain abnormalities in BDo appear less pronounced (but are not absent) than in SZo. Lower ICV in SZo implies that familial risk for schizophrenia has a stronger association with stunted early brain development than familial risk for bipolar disorder.

Indexed as

Bipolar DisorderIntelligence TestsPsychopathologySchizophreniaAdolescentAdultBrainChildDisease SusceptibilityFemaleHumansMagnetic Resonance ImagingMaleNeuroimagingBipolar disorderneurodevelopmentoffspringschizophreniastructural magnetic resonance imaging

Identifiers

PMID32093799
PMCPMC8057400
OpenAlexW3004279176

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.