Evidence map›Paper›PMID 22221140›Full record

Trial reportAlimentary pharmacology & therapeutics2012

Neurokinin-1-receptor antagonism decreases anxiety and emotional arousal circuit response to noxious visceral distension in women with irritable bowel syndrome: a pilot study.

K Tillisch, J Labus, B Nam, J Bueller, S Smith, B Suyenobu, J Siffert, J McKelvy, B Naliboff, E Mayer

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Alimentary pharmacology & therapeutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Endocannabinoid signaling in stress, nausea, and vomiting.Neurogastroenterology and motility · 2025
    Review
  5. Article
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  20. New treatments for IBS.Nature reviews. Gastroenterology & hepatology · 2013
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

K TillischCenter for Neurobiology of Stress, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. ktillisch@mednet.ucla.edu
J Labus
B Nam
J Bueller
S Smith
B Suyenobu
J Siffert
J McKelvy
B Naliboff
E Mayer
University of California, Los Angeles · US

Funding

Central and Peripheral Autonomic Responses in Irritable Bowel SyndromeK23DK073451 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TILLISCH, KIRSTEN · 2006 to 2010
$625k
Effective connectivity of central response to Irritable Bowel Syndrome (IBS)K08DK071626 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LABUS, JENNIFER S · 2006 to 2010
$607k
NIDDK NIH HHS K08 DK071626NIDDK NIH HHS K23 DK073451NIDDK NIH HHS K23DK073451
6 · The paper itself

Abstract

backgroundIrritable bowel syndrome is characterised by chronic abdominal pain and frequent comorbid anxiety. The substance P ⁄ neurokinin-1 receptor system is implicated in the regulation of both pain and anxiety, suggesting a potential therapeutic target in IBS.

aimTo determine whether inhibition of the neurokinin-1 receptor (NK1R) will change pain ratings and brain responses to experimental visceral pain and anxiety symptoms in women with IBS or not.

methodsRome II positive IBS women were recruited for a double-blind, placebo-controlled, cross-over study of NK1R antagonist AV608. Treatment periods were 3 weeks with a 2-week washout period. Functional MRI during a visceral distension paradigm was performed before first treatment and after treatment blocks. SPM8 was used to compare brain activity during painful and nonpainful visceral stimuli in regions associated with emotional arousal and interoception. Negative affect, anxiety symptoms and pain ratings were assessed.

resultsEleven subjects completed the study and eight subjects provided fMRI data. AV608, compared with placebo, was associated with reduced anxiety, negative affect, and pain ratings. During AV608 treatment, the amygdala, hippocampus and anterior cingulate gyrus showed decreased activity during visceral distension. AV608 was also associated with decreases in activity in brain regions associated with interoception (posterior insula, anterior mid-cingulate gyrus).

conclusionsChronic treatment with AV608 in IBS is associated with improved mood and pain ratings and activity of emotional arousal related brain regions. This suggests that further exploration of NK1R antagonists is warranted in visceral pain disorders, particularly in patients with comorbid anxiety symptoms.

Indexed as

Neurokinin-1 Receptor AntagonistsAbdominal PainAdolescentAdultAgedAnxietyArousalCross-Over StudiesDilatation, PathologicDouble-Blind MethodEmotionsFemaleHumansIrritable Bowel SyndromeMiddle AgedPain4-aminopiperidineNeurokinin-1 Receptor AntagonistsPiperidinesReceptors, Neurokinin-1

Identifiers

PMID22221140
PMCPMC4073664
OpenAlexW1943020141

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.