Evidence map›Paper›PMID 31883930›Full record

ArticleSchizophrenia research2020

Characteristics of youth with reported family history of psychosis spectrum symptoms in the Philadelphia Neurodevelopmental Cohort.

Jerome H Taylor, Nana Asabere, Monica E Calkins, Tyler M Moore, Sunny X Tang, Rose Mary Xavier, Alison K Merikangas, Daniel H Wolf, Laura Almasy, Ruben C Gur and 1 more

Open access · greenAbstract read
In one paragraph

Article in Schizophrenia research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.5field-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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Issues in Estimating Interpretable Lower Order Factors in Second-Order Hierarchical Models: Commentary on Clark et al. (2021).Clinical psychological science : a journal of the Association for Psychological Science · 2022
    Article
  9. Article
  10. Psychotic-like Experiences and Polygenic Liability in the Adolescent Brain Cognitive Development Study.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2022
    Article
  11. Article
  12. Familial and socioeconomic contributions to premorbid functioning in psychosis: Impact on age at onset and treatment response.European psychiatry : the journal of the Association of European Psychiatrists · 2020
    Article
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

11 authors at 2 institutions in 1 country.

Jerome H TaylorLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: taylorje@pennmedicine.upenn.edu.
Nana AsabereLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Monica E CalkinsLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Tyler M MooreLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Sunny X TangLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Rose Mary XavierThe University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Alison K MerikangasLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Daniel H WolfLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Laura AlmasyLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Ruben C GurLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Raquel E GurLifespan Brain Institute, Children's Hospital of Philadelphia Department of Child and Adolescent Psychiatry and Behavioral Sciences, Perelman School of Medicine Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
Children's Hospital of Philadelphia · USUniversity of North Carolina at Chapel Hill · US

Funding

Neurodevelopmental Genomics: Trajectories of Complex PhenotypesRC2MH089983 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 2009 to 2011
$14.3M
Institutional Clinical and Translational Science AwardKL2TR001879 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$13.7M
NMDA Receptor Hypofunction in the Amygdala of Schizophrenia PatientsP50MH096891 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BILKER, WARREN B. · 2012 to 2016
$10.6M
SCHIZOPHRENIA: A NEUROPSYCHIATRIC PERSPECTIVET32MH019112 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 1990 to 2024
$6.2M
Evolution of Psychosis in Youth: Multimodal Risk and Resilience MarkersR01MH119219 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E, GUR, RUBEN C. · 2019 to 2023
$3.8M
Adolescent Neurodevelopment and Impaired Intrinsic Motivation in Psychosis RiskR01MH113565 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI WOLF, DANIEL H · 2018 to 2022
$2.9M
Multimodal brain maturation indices modulating psychopathology and neurocognitionR01MH107235 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RUBEN C. · 2015 to 2017
$1.5M
A Prospective Study of Endophenotypes in At-Risk Youths and Their SiblingsK08MH079364 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI CALKINS, MONICA E · 2007 to 2011
$750k
NCATS NIH HHS KL2 TR001879NIMH NIH HHS K08 MH079364NIMH NIH HHS P50 MH096891NIMH NIH HHS R01 MH107235NIMH NIH HHS R01 MH113565NIMH NIH HHS R01 MH119219NIMH NIH HHS RC2 MH089983NIMH NIH HHS T32 MH019112
6 · The paper itself

Abstract

Little is known about the impact of family history of psychosis on youth from community samples. To fill this gap, we compared youth with a first-degree relative with psychosis spectrum symptoms (i.e. family history of psychosis spectrum symptoms, FHPS) to youth without FHPS in a cross-sectional analysis of the Philadelphia Neurodevelopmental Cohort (PNC). The PNC is a racially diverse community sample of 9498 youth ages 8-21 years old, of whom 8928 completed the Family Interview for Genetic Studies to determine FHPS status. Polygenic risk score for schizophrenia (PRSS) was available for a subsample of 4433 European Americans. FHPS youth (n = 489) constituted 5.5% of the analytic sample. After adjusting for environmental risk factors (sociodemographic variables and traumatic stressful events), FHPS youth had lower functioning on the Children's Global Assessment Scale and elevated psychosis spectrum, mood, externalizing, and fear symptoms compared to non-FHPS youth (all p < .001). In the European-American subsample, FHPS status was associated with poorer functioning and greater symptom burden in all four psychopathology domains (all p < .001), even after covarying for PRSS. Thus, ascertaining FHPS is important because it is uniquely associated with symptoms and functional impairment in community youth beyond PRS-S and the environmental risk factors we investigated. Future research identifying environmental causes of FHPS-associated impairment could inform the development of interventions for the broad array of symptoms observed in FHPS youth.

Indexed as

Psychotic DisordersSchizophreniaAdolescentAdultChildCohort StudiesCross-Sectional StudiesHumansYoung AdultAdolescentsChildrenCognitionFamilial high riskPolygenic risk scoreSchizophrenia

Identifiers

PMID31883930
PMCPMC7239716
OpenAlexW2997344373

What OpenQuestion holds

Textmetadata
LicenceTDM
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.