Evidence map›Paper›PMID 28880494›Full record

ArticleEarly intervention in psychiatry2019

Clinical psychopathology in youth at familial high risk for psychosis.

Jai L Shah, Neeraj Tandon, Debra M Montrose, Diana Mermon, Shaun M Eack, Jean Miewald, Matcheri S Keshavan

Abstract read
In one paragraph

Article in Early intervention in psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.5field-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

4 citing papers in PubMed, 26 citations in OpenAlex.

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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

7 authors at 4 institutions in 2 countries.

Jai L ShahMassachusetts Mental Health Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Neeraj TandonMassachusetts Mental Health Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Debra M MontroseWestern Psychiatric Institute and Clinic, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Diana MermonWestern Psychiatric Institute and Clinic, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Shaun M EackUniversity of Pittsburgh School of Social Work, Pittsburgh, Pennsylvania.
Jean MiewaldWestern Psychiatric Institute and Clinic, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Matcheri S KeshavanMassachusetts Mental Health Center, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
University of Pittsburgh · USWestern Pennsylvania Hospital · USBaylor College of Medicine · USHarvard University · US

Funding

Stability of Biotypes: a Longitudinal EvaluationR01MH078113 · NIMH · WAYNE STATE UNIVERSITY · PI KESHAVAN, MATCHERI S. · 2007 to 2019
$6.2M
Brain Maturation and Vulnerability to SchizophreniaR01MH064023 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KESHAVAN, MATCHERI S. · 2003 to 2008
$3.0M
CORTICAL PRUNING AND SCHIZOPHRENIAK02MH001180 · NIMH · WAYNE STATE UNIVERSITY · PI KESHAVAN, MATCHERI S. · 1995 to 2005
$648k
NIMH NIH HHS K02 MH001180NIMH NIH HHS MH01180NIMH NIH HHS R01 MH064023NIMH NIH HHS R01 MH078113
6 · The paper itself

Abstract

aimWhile the course of psychopathology has been explored from an index mental health diagnosis onwards, there are few detailed, prospective studies of the occurrence of clinical psychopathology in youth with familial risk for severe mental illnesses such as psychosis. We sought to describe the appearance of Axis I psychopathology in a unique sample of adolescents with a family history of schizophrenia (FHR).

methodsOne hundred and sixty two first- and second-degree relatives (mean age 15.7 ± 3.6; range 8-25) of probands with schizophrenia or schizoaffective disorder were assessed at baseline and annual intervals for up to 3 years, focusing on Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) Axis I psychopathology.

resultsFourteen individuals (8.6%) developed a psychotic disorder. One hundred and five subjects (65%) met criteria for an Axis I disorder over the course of the study, the most common of which was a depressive episode (40 subjects; 25%). Of the 148 individuals who did not develop psychosis, 91 (61%) had one or more Axis I disorders compared with 10/14 converters who had a comorbid Axis I disorder (71%). Ordered by increasing age of onset, diagnoses included cognitive and externalizing disorders, anxiety disorders, affective disorders, substance use disorders and psychotic disorders.

conclusionsIn addition to an elevated risk of psychosis, young FHR relatives manifest a broad range of non-psychotic Axis I psychopathology in childhood and adolescence. This breadth of diagnoses has implications for the structure and function of mental health services for young people.

Indexed as

Schizophrenic PsychologyAdolescentAdultAge of OnsetAnxiety DisordersDepressive DisorderDisease SusceptibilityFemaleHumansMaleMental DisordersMood DisordersProspective StudiesPsychopathologyPsychotic DisordersRisk Factorscharacteristicsdiagnosisemergencefamilial high riskpsychopathologypsychosis

Identifiers

PMID28880494
PMCPMC5897185
OpenAlexW2751877738

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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.