Evidence map›Paper›PMID 27246897›Full record

ArticleHuman brain mapping2016

Brain activity and connectivity in response to negative affective stimuli: Impact of dysphoric mood and sex across diagnoses.

Klara Mareckova, Laura M Holsen, Roee Admon, Nikos Makris, Larry Seidman, Stephen Buka, Susan Whitfield-Gabrieli, Jill M Goldstein

Open access · greenAbstract readComparative Study
In one paragraph

Article in Human brain mapping, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.1field-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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
  2. Article
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  9. Impact of prenatal maternal cytokine exposure on sex differences in brain circuitry regulating stress in offspring 45 years later.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Article
  12. Impact of sex and depressed mood on the central regulation of cardiac autonomic function.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  13. Review
  14. Article
  15. Sex differences in major depression and comorbidity of cardiometabolic disorders: impact of prenatal stress and immune exposures.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Review
  16. Article
  17. Article
  18. Sex- and Estrus-Dependent Differences in Rat Basolateral Amygdala.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  19. Article
  20. 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

8 authors at 6 institutions in 2 countries.

Klara MareckovaConnors Center for Women's Health & Gender Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Laura M HolsenConnors Center for Women's Health & Gender Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Roee AdmonCenter for Depression, Anxiety and Stress Research, McLean Hospital, Harvard Medical School, Boston, Massachusetts.
Nikos MakrisDivision of Psychiatric Neuroscience, Department of Psychiatry, Athinoula a. Martinos Center, Massachusetts General Hospital, Boston, Massachusetts.
Larry SeidmanDivision of Public Psychiatry, Beth Israel Deaconess Medical Center, Massachusetts Mental Health Center and Harvard Medical School, Boston, Massachusetts.
Stephen BukaDepartment of Community Health, Brown University, Providence, Rhode Island.
Susan Whitfield-GabrieliMcGovern Institute for Brain Research, Massachusetts Institute of Technology, Boston, Massachusetts.
Jill M GoldsteinConnors Center for Women's Health & Gender Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts. jill_goldstein@hms.harvard.edu.
Brigham and Women's Hospital · USAthinoula A. Martinos Center for Biomedical Imaging · USBrown University · USMassachusetts Institute of Technology · USMassachusetts Mental Health Center · USMcLean Hospital · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
Sex-Specific Programming of the HPA Axis by GlucocorticoidsP50MH082679 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M · 2007 to 2011
$5.9M
SEX &STRUCTURAL BRAIN ABNORMALITIES IN SCHIZOPHRENIA IIR01MH056956 · NIMH · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GOLDSTEIN, JILL M · 1997 to 2010
$4.5M
Ghrelin Modulation of Mesolimbic Reward Signaling in Stress-induced HyperphagiaR01DK104772 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI HOLSEN, LAURA MCGRATH · 2016 to 2020
$2.7M
Prenatal & Adult Immune Biomarkers of the Negative Valence BiosignatureR03MH105585 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M · 2015 to 2016
$177k
NCRR NIH HHS UL1 RR025758NIDDK NIH HHS R01 DK104772NIMH NIH HHS P50 MH082679NIMH NIH HHS R01 MH056956NIMH NIH HHS R03 MH105585
6 · The paper itself

Abstract

Negative affective stimuli elicit behavioral and neural responses which vary on a continuum from adaptive to maladaptive, yet are typically investigated in a dichotomous manner (healthy controls vs. psychiatric diagnoses). This practice may limit our ability to fully capture variance from acute responses to negative affective stimuli to psychopathology at the extreme end. To address this, we conducted a functional magnetic resonance imaging study to examine the neural responses to negative valence/high arousal and neutral valence/low arousal images as a function of dysphoric mood and sex across individuals (n = 99) who represented traditional categories of healthy controls, major depressive disorder, bipolar psychosis, and schizophrenia. Observation of negative (vs. neutral) stimuli elicited blood oxygen-level dependent responses in the following circuitry: periaqueductal gray, hypothalamus (HYPO), amygdala (AMYG), hippocampus (HIPP), orbitofrontal cortex (OFC), medial prefrontal cortex (mPFC), and greater connectivity between AMYG and mPFC. Across all subjects, severity of dysphoric mood was associated with hyperactivity of HYPO, and, among females, right (R) AMYG. Females also demonstrated inverse relationships between severity of dysphoric mood and connectivity between HYPO - R OFC, R AMYG - R OFC, and R AMYG - R HIPP. Overall, our findings demonstrated sex-dependent deficits in response to negative affective stimuli increasing as a function of dysphoric mood state. Females demonstrated greater inability to regulate arousal as mood became more dysphoric. These findings contribute to elucidating biosignatures associated with response to negative stimuli across disorders and suggest the importance of a sex-dependent lens in determining these biosignatures. Hum Brain Mapp 37:3733-3744, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

Sex CharacteristicsAdultAffectAnxietyBipolar DisorderBrainBrain MappingCerebrovascular CirculationFactor Analysis, StatisticalFemaleHumansMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedNeural PathwaysOxygendysphoric mood statefunctional magnetic resonance imaginggeneralized psychophysiological interactionInternational Affective Picture Systemnegative affectResearch Domain Criteriasex

Identifiers

PMID27246897
PMCPMC5053909
OpenAlexW2418379501

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.