Evidence map›Paper›PMID 28674759›Full record

ArticleBrain imaging and behavior2018

Impaired sensory processing measured by functional MRI in Bipolar disorder manic and depressed mood states.

Joseph J Shaffer, Casey P Johnson, Jess G Fiedorowicz, Gary E Christensen, John A Wemmie, Vincent A Magnotta

Abstract read
In one paragraph

Article in Brain imaging and behavior, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  13. Association between the epigenetic lifespan predictor GrimAge and history of suicide attempt in bipolar disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
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  20. Cerebellum and Emotion in Social Behavior.Advances in experimental medicine and biology · 2022
    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

6 authors at 1 institution in 1 country.

Joseph J ShafferDepartment of Radiology, University of Iowa, Iowa City, IA, USA. joseph-shaffer@uiowa.edu.ORCID http://orcid.org/0000-0003-0459-1568
Casey P JohnsonDepartment of Radiology, University of Iowa, Iowa City, IA, USA.
Jess G FiedorowiczDepartment of Psychiatry, University of Iowa, Iowa City, IA, USA.
Gary E ChristensenDepartment of Electrical and Computer Engineering, University of Iowa, Iowa City, IA, USA.
John A WemmieDepartment of Psychiatry, University of Iowa, Iowa City, IA, USA.
Vincent A MagnottaDepartment of Radiology, University of Iowa, Iowa City, IA, USA.
University of Iowa · US

Funding

VASOPRESSIN IN CARDIOVASCULAR REGULATIONP01HL014388 · NHLBI · UNIVERSITY OF IOWA · PI CHAPLEAU, MARK W · 1985 to 2018
$40.3M
Cerebellar metabolism, neural circuits, and symptoms in bipolar disorderR01MH111578 · NIMH · UNIVERSITY OF IOWA · PI VINCENT A MAGNOTTA, John A Wemmie · 2017 to 2026
$5.7M
University of Iowa Institute for Clinical and Translational ScienceU54TR001013 · NCATS · UNIVERSITY OF IOWA · PI ROSENTHAL, GARY E · 2014 to 2014
$4.2M
Interdisciplinary Training Program in Pain ResearchT32NS045549 · NINDS · UNIVERSITY OF IOWA · PI KATHLEEN A SLUKA, Yuriy M Usachev · 2004 to 2026
$3.7M
Regulation of Cerebral Blood Flow by Acid-Sensing Ion Channels (ASICs)R01HL113863 · NHLBI · UNIVERSITY OF IOWA · PI FARACI, FRANK M, WEMMIE, JOHN A · 2012 to 2016
$1.9M
Modeling CO2-evoked fear in mice: role of acid-sensing ion channelsR01MH085724 · NIMH · UNIVERSITY OF IOWA · PI WEMMIE, JOHN A · 2009 to 2013
$1.8M
Antipsychotics and Vascular Function in Bipolar DisordersK23MH083695 · NIMH · UNIVERSITY OF IOWA · PI FIEDOROWICZ, JESS G · 2010 to 2014
$869k
Brain pH and Acid Sensing in Depression-Related BehaviorI01BX000741 · VA · IOWA CITY VA MEDICAL CENTER · PI WEMMIE, JOHN A · 2011 to 2018
–
BLRD VA I01 BX000741National Alliance for Research on Schizophrenia and Depression Independent InvestigatorNational Alliance for Research on Schizophrenia and Depression Independent Investigator AwardNational Alliance for Research on Schizophrenia and Depression Young InvestigatorNCATS NIH HHS U54 TR001013NHLBI NIH HHS P01 HL014388NHLBI NIH HHS P01HL014388NHLBI NIH HHS R01 HL113863NHLBI NIH HHS R01HL113863NIMH NIH HHS 5R01MH085724NIMH NIH HHS K23 MH083695NIMH NIH HHS K23MH083695NIMH NIH HHS R01 MH085724NIMH NIH HHS R01 MH111578NINDS NIH HHS T32 NS045549Roger Koch Private DonationUniversity of Iowa Institute for Clinical and Translational Science U54TR001013U.S. Department of Veterans Affairs Merit Award
6 · The paper itself

Abstract

Bipolar disorder is characterized by recurring episodes of depression and mania. Defining differences in brain function during these states is an important goal of bipolar disorder research. However, few imaging studies have directly compared brain activity between bipolar mood states. Herein, we compare functional magnetic resonance imaging (fMRI) responses during a flashing checkerboard stimulus between bipolar participants across mood states (euthymia, depression, and mania) in order to identify functional differences between these states. 40 participants with bipolar I disorder and 33 healthy controls underwent fMRI during the presentation of the stimulus. A total of 23 euthymic-state, 16 manic-state, 15 depressed-state, and 32 healthy control imaging sessions were analyzed in order to compare functional activation during the stimulus between mood states and with healthy controls. A reduced response was identified in the visual cortex in both the depressed and manic groups compared to euthymic and healthy participants. Functional differences between bipolar mood states were also observed in the cerebellum, thalamus, striatum, and hippocampus. Functional differences between mood states occurred in several brain regions involved in visual and other sensory processing. These differences suggest that altered visual processing may be a feature of mood states in bipolar disorder. The key limitations of this study are modest mood-state group size and the limited temporal resolution of fMRI which prevents the segregation of primary visual activity from regulatory feedback mechanisms.

Indexed as

Magnetic Resonance ImagingAdultAffectBipolar DisorderBrainBrain MappingFemaleHumansMaleMiddle AgedPhotic StimulationVisual PerceptionBipolar disorderDepressionfMRIManiaMood stateVisual cortex

Identifiers

PMID28674759
PMCPMC5752628
OpenAlexW2727261861

What OpenQuestion holds

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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.