Evidence map›Paper›PMID 32878667›Full record

ArticlePsychological medicine2022

Heritable anisotropy associated with cognitive impairments among patients with schizophrenia and their non-psychotic relatives in multiplex families.

K M Prasad, J Gertler, S Tollefson, J A Wood, D Roalf, R C Gur, R E Gur, L Almasy, M F Pogue-Geile, V L Nimgaonkar

Open access · greenAbstract read
In one paragraph

Article in Psychological medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 6 citations in OpenAlex.

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  5. Distinct neurocognitive profiles and clinical phenotypes associated with copy number variation at the 22q11.2 locus.Autism research : official journal of the International Society for Autism Research · 2023
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

K M PrasadDepartments of Psychiatry and Bioengineering, University of Pittsburgh, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.ORCID 0000-0003-0245-1393
J GertlerDepartments of Psychiatry and Bioengineering, University of Pittsburgh, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.
S TollefsonDepartments of Psychiatry and Bioengineering, University of Pittsburgh, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.
J A WoodDepartments of Psychiatry and Bioengineering, University of Pittsburgh, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.
D RoalfDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
R C GurDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
R E GurDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
L AlmasyDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
M F Pogue-GeileDepartment of Psychology, University of Pittsburgh, Pittsburgh, PA, USA.
V L NimgaonkarDepartments of Psychiatry and Bioengineering, University of Pittsburgh, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA.
University of Pittsburgh · USUniversity of Pennsylvania · US

Funding

NEUROBEHAVIORAL STUDY OF SCHIZOPHRENIAR01MH042191 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 1987 to 2018
$7.1M
A Neurobehavioral Family Study of SchizophreniaR01MH063480 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIMGAONKAR, VISHWAJIT LAXMIKANT · 2001 to 2018
$6.1M
A Neurobehavioral Family Study of SchizophreniaR01MH061622 · NIMH · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 2001 to 2018
$4.9M
Ultra-high field GluCEST MRI and MRS in youth at risk for psychosisR01MH120174 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI ROALF, DAVID R · 2020 to 2024
$3.8M
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
Olfactory and facial markers of developmental risk for psychosis in 22q11 deletion syndromeR01MH119185 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI ROALF, DAVID R · 2019 to 2024
$3.5M
Synaptic Pruning and Complement Gene in Schizophrenia: Imaging & Cellular StudiesR01MH115026 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PRASAD, KONASALE M · 2018 to 2022
$3.1M
Dimensional outcomes and neural circuitry associated with psychosis riskR01MH112584 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PRASAD, KONASALE M · 2018 to 2021
$2.1M
3/3: Pedigree-Based Whole Genome Sequencing of Affective and Psychotic DisordersU01MH105634 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 2015 to 2018
$714k
NIMH NIH HHS R01 MH042191NIMH NIH HHS R01 MH061622NIMH NIH HHS R01 MH063480NIMH NIH HHS R01 MH112584NIMH NIH HHS R01 MH115026NIMH NIH HHS R01 MH119185NIMH NIH HHS R01 MH119219NIMH NIH HHS R01 MH120174NIMH NIH HHS U01 MH105634
6 · The paper itself

Abstract

backgroundTo test the functional implications of impaired white matter (WM) connectivity among patients with schizophrenia and their relatives, we examined the heritability of fractional anisotropy (FA) measured on diffusion tensor imaging data acquired in Pittsburgh and Philadelphia, and its association with cognitive performance in a unique sample of 175 multigenerational non-psychotic relatives of 23 multiplex schizophrenia families and 240 unrelated controls (total = 438).

methodsWe examined polygenic inheritance (h2r) of FA in 24 WM tracts bilaterally, and also pleiotropy to test whether heritability of FA in multiple WM tracts is secondary to genetic correlation among tracts using the Sequential Oligogenic Linkage Analysis Routines. Partial correlation tests examined the correlation of FA with performance on eight cognitive domains on the Penn Computerized Neurocognitive Battery, controlling for age, sex, site and mother's education, followed by multiple comparison corrections.

resultsSignificant total additive genetic heritability of FA was observed in all three-categories of WM tracts (association, commissural and projection fibers), in total 33/48 tracts. There were significant genetic correlations in 40% of tracts. Diagnostic group main effects were observed only in tracts with significantly heritable FA. Correlation of FA with neurocognitive impairments was observed mainly in heritable tracts.

conclusionsOur data show significant heritability of all three-types of tracts among relatives of schizophrenia. Significant heritability of FA of multiple tracts was not entirely due to genetic correlations among the tracts. Diagnostic group main effect and correlation with neurocognitive performance were mainly restricted to tracts with heritable FA suggesting shared genetic effects on these traits.

Indexed as

Cognitive DysfunctionSchizophreniaWhite MatterAnisotropyBrainDiffusion Tensor ImagingHumansBrain connectivitydiffusion tensor imagingfamilial riskheritabilityneuroimagingschizophreniawhite matter fibers

Identifiers

PMID32878667
PMCPMC8218223
OpenAlexW3083142180

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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.