Evidence map›Paper›PMID 30529716›Full record

ArticlePsychoneuroendocrinology2019

Resting amygdala connectivity and basal sympathetic tone as markers of chronic hypervigilance.

Olena Kleshchova, Jenna K Rieder, Jack Grinband, Mariann R Weierich

Open access · greenAbstract read
In one paragraph

Article in Psychoneuroendocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 32% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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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

4 authors at 2 institutions in 1 country.

Olena KleshchovaHunter College, The City University of New York, 695 Park Avenue, New York, NY 10065, USA; The Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY 10016, USA.
Jenna K RiederHunter College, The City University of New York, 695 Park Avenue, New York, NY 10065, USA; The Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY 10016, USA.
Jack GrinbandDepartment of Radiology and Neurology, Columbia University, 622 W 168th St, New York, NY 10032, USA.
Mariann R WeierichHunter College, The City University of New York, 695 Park Avenue, New York, NY 10065, USA; The Graduate Center, The City University of New York, 365 Fifth Avenue, New York, NY 10016, USA. Electronic address: mariann.weierich@hunter.cuny.edu.
The Graduate Center, CUNY · USColumbia University · US

Funding

WILD TYPE &MUTANT P53 INTERACTIONS WITH HIV LTR DNAG12RR003037 · NCRR · HUNTER COLLEGE · PI DOTTIN, ROBERT P · 1985 to 2011
$27.6M
Basic and Translational Research Center for Reducing Health DisparitiesG12MD007599 · NIMHD · HUNTER COLLEGE · PI ANGULO, JESUS A · 2012 to 2017
$14.6M
BP-ENDURE at Hunter and NYUR25NS080686 · NINDS · HUNTER COLLEGE · PI Nesha Star Burghardt, GLENN E SCHAFE · 2012 to 2026
$9.2M
Neurobiology of Addiction &Impulsive BehaviorR24DA012136 · NIDA · HUNTER COLLEGE · PI QUINONES-JENAB, VANYA · 1999 to 2016
$5.2M
NCRR NIH HHS G12 RR003037NIDA NIH HHS R24 DA012136NIMHD NIH HHS G12 MD007599NINDS NIH HHS R25 NS080686
6 · The paper itself

Abstract

backgroundChronic hypervigilance, a state of sustained alertness and hyperarousal in the absence of threat, has been shown to predict poorer clinical outcomes post-trauma. An exaggerated and persistent amygdala alerting response to affective information has been proposed as a reactivity-based, and thus indirect, marker of hypervigilance. However, because chronic hypervigilance is a persistent rather than reactive state, it should be directly observable under resting-state conditions without the need for exposure to affectively charged stimuli.

objectiveWe tested resting amygdala connectivity and basal sympathetic and hypothalamic-pituitary-adrenal axis activity as direct neural and neuroendocrine markers of chronic hypervigilance.

participants24 trauma-exposed women (age M = 22.9, SD = 5.5) and 20 no-trauma controls (age M = 21.1, SD = 3.2). MEASURES: Amygdala connectivity was measured using functional magnetic resonance imaging at rest and during viewing of novel and familiar affective scenes. Elevated amygdala connectivity during the viewing of novel scenes (exaggerated alerting response) and familiar scenes (persistent alerting response) was used as a reactivity-based index of hypervigilance. Resting amygdala connectivity and basal salivary alpha-amylase (sAA) and cortisol were tested as neural and neuroendocrine markers of hypervigilance, respectively.

resultsCompared to no-trauma controls, trauma-exposed women showed greater connectivity between the left amygdala and the ventral anterior cingulate cortex (vACC) both during affective processing and at rest. Exaggerated neural novelty response was associated with greater resting left amygdala-vACC connectivity and higher basal sAA, but not cortisol.

conclusionsGreater synchronization of threat-detection circuitry in the absence of threat and basal sympathetic tone might serve as complementary resting-state markers of the cognitive and physiological components of chronic hypervigilance, respectively.

Indexed as

AdultAmygdalaAnxietyBiomarkersFemaleGyrus CinguliHumansHydrocortisoneHypothalamo-Hypophyseal SystemMagnetic Resonance ImagingNeural PathwaysPituitary-Adrenal SystemRestWounds and InjuriesYoung AdultBiomarkersHydrocortisoneAmygdala connectivityHypervigilanceResting-state fMRISalivary alpha-amylaseTraumaVentral anterior cingulate cortex

Identifiers

PMID30529716
PMCPMC6605037
OpenAlexW2902447379

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.