Evidence map›Paper›PMID 35811000›Full record

ArticleBehavioural brain research2022

Resting-state neural signal variability in women with depressive disorders.

Sally Pessin, Erin C Walsh, Roxanne M Hoks, Rasmus M Birn, Heather C Abercrombie, Carissa L Philippi

Open access · greenAbstract read
In one paragraph

Article in Behavioural brain research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Trial
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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 3 institutions in 1 country.

Sally PessinDepartment of Psychological Sciences, University of Missouri-St. Louis, 1 University Blvd., St. Louis, MO 63121, USA.
Erin C WalshDepartment of Psychiatry, University of North Carolina at Chapel Hill School of Medicine, CB# 7167, Chapel Hill, NC 27599, USA.
Roxanne M HoksCenter for Healthy Minds, University of Wisconsin-Madison, 625W. Washington Ave., Madison, WI 53703, USA.
Rasmus M BirnDepartment of Psychiatry, University of Wisconsin-Madison, 6001 Research Park Blvd., Madison, WI 53719, USA.
Heather C AbercrombieCenter for Healthy Minds, University of Wisconsin-Madison, 625W. Washington Ave., Madison, WI 53703, USA.
Carissa L PhilippiDepartment of Psychological Sciences, University of Missouri-St. Louis, 1 University Blvd., St. Louis, MO 63121, USA. Electronic address: philippic@umsl.edu.
University of Wisconsin–Madison · USUniversity of Missouri–St. Louis · USUniversity of North Carolina at Chapel Hill · US

Funding

North Carolina Translational and Clinical Science Institute (NC TraCS) KL2KL2TR002490 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEINBERGER, MORRIS · 2018 to 2022
$11.0M
North Carolina Translational & Clinical Sciences Institute (NC TraCS)KL2TR001109 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, CAREY, TIMOTHY S · 2013 to 2017
$5.7M
Learning, neural signaling of cortisol, and early adversity in depressionR01MH094478 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI ABERCROMBIE, HEATHER C · 2012 to 2016
$2.2M
NCATS NIH HHS KL2 TR001109NCATS NIH HHS KL2 TR002490NIMH NIH HHS R01 MH094478
6 · The paper itself

Abstract

Aberrant activity and connectivity in default mode (DMN), frontoparietal (FPN), and salience (SN) network regions is well-documented in depression. Recent neuroimaging research suggests that altered variability in the blood oxygen level-dependent (BOLD) signal may disrupt normal network integration and be an important novel predictor of psychopathology. However, no studies have yet determined the relationship between resting-state BOLD signal variability and depressive disorders nor applied BOLD signal variability features to the classification of depression history using machine learning (ML). We collected resting-state fMRI data for 79 women with different depression histories: no history, past history, and current depressive disorder. We tested voxelwise differences in BOLD signal variability related to depression group and severity. We also investigated whether BOLD signal variability of DMN, FPN, and SN regions could predict depression history group using a supervised random forest ML model. Results indicated that individuals with any history of depression had significantly decreased BOLD signal variability in the left and right cerebellum and right parietal cortex (p

Indexed as

Depressive DisorderMagnetic Resonance ImagingBrainBrain MappingFemaleGyrus CinguliHumansNeural PathwaysParietal LobeBOLD variabilityDefault mode networkDepressionFrontoparietal networkMachine learningNeural signal variabilitySalience network

Identifiers

PMID35811000
PMCPMC9559753
OpenAlexW4284883680

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.