Evidence map›Paper›PMID 29168420›Full record

ArticleJournal of clinical and experimental neuropsychology2018

Vulnerabilities in sequencing and task switching in healthy youth offspring of parents with mood disorders.

Manpreet K Singh, Sara M Leslie, Kalpa Bhattacharjee, Melina Gross, Elizabeth F Weisman, Laila M Soudi, Owen R Phillips, Alexander Onopa

Abstract read
In one paragraph

Article in Journal of clinical and experimental neuropsychology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 45 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

8 authors at 1 institution in 1 country.

Manpreet K Singha Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Sara M Lesliea Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Kalpa Bhattacharjeea Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Melina Grossa Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Elizabeth F Weismana Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Laila M Soudia Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Owen R Phillipsa Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Alexander Onopaa Department of Psychiatry and Behavioral Sciences , Stanford University School of Medicine , Stanford , CA , USA.
Stanford University · US

Funding

Emotion Regulation in Children of Parents with Bipolar DisorderK23MH085919 · NIMH · STANFORD UNIVERSITY · PI SINGH, MANPREET K · 2009 to 2013
$866k
NIMH NIH HHS K23 MH085919
6 · The paper itself

Abstract

introductionVisuospatial processing and task switching are impaired in individuals with mood disorders. It is unknown whether early deficits are present before mood symptom on set or are related to risk for a specific type of mood disorder. To investigate, we compared visual attention and task switching during sequencing among never-disordered youth with parental family histories of bipolar (BD) and major depressive disorders (MDD) and healthy controls (HC) with no personal or family history of psychopathology.

method8-17-year-old youth of parents with BD (n = 31, "BD-risk"), youth of parents with MDD (n = 49, "MDD-risk"), and demographically similar HC (n = 31, "HC") were examined using the Delis-Kaplan Executive Functioning System Trail Making Test. Seed-based resting-state functional connectivity (RSFC) was collected from a subset of 88 participants (25 BD-risk, 37 MDD-risk, 26 HC) to investigate group differences in RSFC related to visuospatial processing.

resultsBD-risk and MDD-risk offspring had impaired sequencing and task switching, demonstrated by reduced scores on visual scanning, F(2, 108) = 4.12, p = .02, number sequencing, F(2, 88) = 4.75, p = .01, letter sequencing, F(2, 108) = 4.24, p = .02, and number-letter sequencing, F(2, 108) = 4.66, p = .01, compared to scores in HC. RSFC between the posterior cingulate (PCC) and clusters in the subcallosal cortex, amygdala, and hippocampus significantly differed among HC, BD-risk, and MDD-risk groups. PCC-subcallosal/limbic RSFC was positively coupled in the MDD-risk and BD-risk groups and negatively coupled in HCs.

conclusionsYouth at familial risk for mood disorders demonstrate visuospatial deficits early in the processing stream. Improved methods for identifying at-risk children with the earliest possible neurocognitive impairments may inform remediation strategies that could prevent mood disorders.

Indexed as

Psychomotor PerformanceAdolescentAttentionBipolar DisorderBrainChildExecutive FunctionFemaleHealth StatusHumansMagnetic Resonance ImagingMajor Depressive DisorderMaleMood DisordersNeural PathwaysNeuropsychological TestsBipolar disorderfamily riskmajor depressive disorderoffspringresting statetask switchingvisuospatial processing

Identifiers

PMID29168420
PMCPMC6167013
OpenAlexW2770465581

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.