Evidence map›Paper›PMID 41951830›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2026

Identification of an intrusive-hypervigilant phenotype of posttraumatic stress symptoms with unique stress peptide and amygdala functional connectivity profiles.

Kevin J Clancy, Caitlin Ravichandran, Sydney A Jobson, Victor May, Sayamwong E Hammack, William A Carlezon, Kerry J Ressler, Scott L Rauch, Isabelle M Rosso

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Fine mapping of PTSD GWAS reveals a role for amygdalabioRxiv : the preprint server for biology · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Kevin J ClancyDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA. kclancy@mclean.harvard.edu.ORCID http://orcid.org/0000-0001-6581-357X
Caitlin RavichandranDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA.
Sydney A JobsonDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA.
Victor MayLarner College of Medicine, University of Vermont, Burlington, VT, USA.
Sayamwong E HammackDepartment of Psychology, University of Vermont, Burlington, VT, USA.
William A CarlezonDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA.ORCID http://orcid.org/0000-0002-4162-3947
Kerry J ResslerDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA.ORCID http://orcid.org/0000-0002-5158-1103
Scott L RauchDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA.
Isabelle M RossoDivision of Depression and Anxiety Disorders, McLean Hospital, Belmont, MA, USA. irosso@mgb.org.ORCID http://orcid.org/0000-0001-6988-3858

Funding

SPARED CenterP50MH115874 · NIMH · MCLEAN HOSPITAL · PI BERRETTA, SABINA · 2019 to 2023
$13.7M
PACAP and the Response to Stressors: Neural MechanismsR01MH097988 · NIMH · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HAMMACK, SAYAMWONG E., MAY, VICTOR · 2012 to 2023
$3.7M
Multimodal imaging of hippocampal-cortical networks and mechanisms of trauma-related intrusionsR01MH120400 · NIMH · MCLEAN HOSPITAL · PI ROSSO, ISABELLE M · 2019 to 2023
$3.3M
Progressive social withdrawal in trauma-exposed older adolescents and young adults: neurocircuitry predictorsR01MH125852 · NIMH · MCLEAN HOSPITAL · PI ROSSO, ISABELLE M · 2021 to 2025
$2.4M
A Multilevel Characterization of Sensory Cortical Disinhibition in Post-Traumatic IntrusionsK23MH137459 · NIMH · MCLEAN HOSPITAL · PI Kevin Clancy · 2024 to 2026
$537k
NIMH NIH HHS K23 MH137459NIMH NIH HHS P50 MH115874NIMH NIH HHS R01 MH097988NIMH NIH HHS R01 MH120400NIMH NIH HHS R01 MH125852U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) K23-MH137459U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) P50-MH115874U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01-MH120400U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01-MH125852U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01-MH97988
6 · The paper itself

Abstract

Posttraumatic stress disorder (PTSD) is a highly heterogeneous psychiatric disorder, complicating efforts to identify consistent biological markers and develop targeted treatments for individuals exposed to trauma. Recent research has identified a distinct intrusive-hypervigilant (IH) phenotype, which is characterized by heightened intrusive reexperiencing and hypervigilance symptoms along with elevated levels of pituitary adenylate cyclase-activating polypeptide (PACAP), a neuropeptide involved in stress response via amygdala signaling. In an independent sample of 172 symptomatic trauma-exposed adults, we replicated this IH phenotype using latent profile analysis of Clinician-Administered PTSD Scale for DSM-5 symptom severity ratings and expanded its biological characterization using resting-state functional magnetic resonance imaging (rs-fMRI). Consistent with prior work, the identified IH group demonstrated more severe intrusive reexperiencing (Cohen's d's = 0.61-6.93) and hypervigilance symptoms (d's = 0.57-0.88) and higher PACAP levels compared to groups with generally High (d = 0.35) or Low (d = 0.44) symptom severity. Additionally, the IH phenotype exhibited stronger functional connectivity of the centromedial, but not basolateral, amygdala with regions in the occipital cortex (d's = 0.78-0.95), precuneus (d's = 1.20-1.21), and medial prefrontal cortex (d's = 0.81-1.18)-areas primarily within the Default Mode and Visual Networks. Meta-analytic decoding linked these regions to mental imagery, memory processing, fear, and threat perception. These findings support the existence of an IH phenotype of posttraumatic stress that may exhibit a distinct biological profile, characterized by exaggerated interactions between memory, threat, and arousal systems that may be mediated by PACAP and its effects on amygdala connectivity. This phenotype may serve as a promising target for precision psychiatry approaches, including pharmacological and neurotherapeutic interventions that modulate PACAP signaling and amygdala connectivity.

Indexed as

AmygdalaPituitary Adenylate Cyclase-Activating PolypeptideStress Disorders, Post-TraumaticAdultFemaleHumansMagnetic Resonance ImagingMaleNeural PathwaysPhenotypeYoung AdultPituitary Adenylate Cyclase-Activating Polypeptide

Identifiers

PMID41951830
PMCPMC13598154

What Socratic holds

Textmetadata
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 Socratic graph.