Evidence map›Paper›PMID 33620549›Full record

ArticlePsychopharmacology2021

Plasma gamma-aminobutyric acid (GABA) levels and posttraumatic stress disorder symptoms in trauma-exposed women: a preliminary report.

Kimberly A Arditte Hall, Sumaiya E DeLane, George M Anderson, Tiffany R Lago, Rachel Shor, Weiwei Wang, Ann M Rasmusson, Suzanne L Pineles

Abstract read
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In one paragraph

Article in Psychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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  5. Emphasizing the Crosstalk Between Inflammatory and Neural Signaling in Post-traumatic Stress Disorder (PTSD).Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2023
    Review
  6. Review
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  8. Dogs as a Natural Animal Model of Epilepsy.Frontiers in veterinary science · 2022
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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 5 institutions in 1 country.

Kimberly A Arditte HallDepartment of Psychology & Philosophy, Framingham State University, 100 State Street, Framingham, MA, 01701, USA. kardittehall@framingham.edu.
Sumaiya E DeLaneNational Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
George M AndersonChild Study Center, Yale University School of Medicine, New Haven, CT, 06519, USA.
Tiffany R LagoVA Boston Healthcare System, Boston, MA, 02130, USA.
Rachel ShorNational Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
Weiwei WangMEDKEC Keck Biotechnology Services, Yale University School of Medicine, New Haven, CT, 06519, USA.
Ann M RasmussonNational Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
Suzanne L PinelesNational Center for PTSD Women's Health Sciences Division at VA Boston Healthcare System, Boston, MA, 02130, USA.
VA Boston Healthcare System · USFramingham State University · USNational Center for PTSD · USW. M. Keck Foundation · USYale University · US

Funding

Facilitation of Extinction Retention and Reconsolidation Blockade by IV Allopregnanolone in PTSDR01MH122867 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI ANN M. RASMUSSON · 2020 to 2026
$3.6M
NIMH NIH HHS R01 MH122867
6 · The paper itself

Abstract

rationaleAberrations in the stress response are associated with posttraumatic stress disorder (PTSD) symptom development, maintenance, and severity. Gamma-aminobutyric acid (GABA), the brain's primary inhibitory neurotransmitter, may play a key role in stress recovery.

objectivesIn this preliminary study, we examined whether plasma GABA levels differed between women with PTSD and trauma-exposed healthy controls.

methodsThirty participants provided plasma samples during two phases of the menstrual cycle: the early follicular phase and the mid-luteal phase. During each phase, blood was drawn after 45 min of rest, and after mild and moderately stressful psychophysiological tasks. Plasma GABA levels were measured using HPLC-mass spectrometry (LC-MS/MS).

resultsIn analyses using PTSD diagnosis as a categorical group variable, women with and without a diagnosis of PTSD did not differ in plasma GABA levels (ps > .18). However, in analyses examining PTSD symptom severity as a continuous variable, there was a trend-level positive association between more severe PTSD symptoms and higher plasma GABA levels across the four blood draws (p = .06). In analyses examining DSM-IV PTSD symptom clusters separately, dysphoria symptoms were positively and significantly associated with plasma GABA levels (p = .03). Similarly, there was a trend-level positive association between avoidance cluster symptoms and plasma GABA levels (p = .06). Plasma GABA levels were not modulated by experimentally induced stress or menstrual cycle phase.

conclusionsDysregulation in GABA may be a neurobiological marker and/or potential treatment target for women with PTSD symptom profiles characterized by prominent dysphoria and avoidance cluster symptoms.

Indexed as

AdultChromatography, LiquidFemaleFollicular Phasegamma-Aminobutyric AcidHumansLuteal PhaseMenstrual CycleMiddle AgedStress Disorders, Post-TraumaticTandem Mass SpectrometryYoung Adultgamma-Aminobutyric AcidAvoidanceDysphoriaFear conditioningFemaleLoud tonesMenstrual cycleNeurotransmitterPrepulse inhibition taskPsychophysiologyTraumatic stress

Identifiers

PMID33620549
OpenAlexW3131049168

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Registered trials

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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.