Evidence map›Paper›PMID 28867943›Full record

ReviewDialogues in clinical neuroscience2017

Oxytocin and social functioning.

Candace Jones, Ingrid Barrera, Shaun Brothers, Robert Ring, Claes Wahlestedt

Open access · diamondAbstract readReview
In one paragraph

Review in Dialogues in clinical neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 3 pooled it
8.9field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 3 syntheses or guidelines pooled it, 127 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Candace JonesUniversity of Miami Miller School of Medicine, Miami, Florida, USA.
Ingrid BarreraUniversity of Miami Department of Psychiatry and Behavioral Sciences, Miami, Florida, USA.
Shaun BrothersUniversity of Miami Department of Psychiatry and Behavioral Sciences, Miami, Florida, USA.
Robert RingDrexel University Department of Pharmacology and Physiology, Philadelphia, Pennsylvania, USA.
Claes WahlestedtUniversity of Miami Department of Psychiatry and Behavioral Sciences, Miami, Florida, USA.
University of Miami · USDrexel University · US

Funding

Development of Nociceptin Receptor Agonists for Post-Traumatic Stress DisorderR01MH110441 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BROTHERS, SHAUN P · 2016 to 2019
$3.0M
Epigenetic Signaling Pathways Contributing to Alcohol DependenceR01AA023781 · NIAAA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI HEILIG, MARKUS ALEXANDER, WAHLESTEDT, CLAES ROBERT · 2015 to 2019
$2.1M
Small Molecule Identification for the Nociceptin Receptor to Treat Cocaine AbuseR01DA035055 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WAHLESTEDT, CLAES ROBERT · 2012 to 2016
$1.7M
Upregulation of Iduronidase Enzyme in MPSI DiseaseR01NS092671 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BROTHERS, SHAUN P · 2016 to 2020
$1.7M
Long noncoding RNAs and chromatin regulation in cocaine addictionR21DA035592 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WAHLESTEDT, CLAES ROBERT · 2014 to 2015
$381k
NIAAA NIH HHS R01 AA023781NIDA NIH HHS R01 DA035055NIDA NIH HHS R21 DA035592NIMH NIH HHS R01 MH110441NINDS NIH HHS R01 NS092671
6 · The paper itself

Abstract

Social anxiety is a form of anxiety characterized by continuous fear of one or more social or performance situations. Although multiple treatment modalities (cognitive behavioral therapy, selective serotonin reuptake inhibitors/selective norepinephrine reuptake inhibitors, benzodiazepines) exist for social anxiety, they are effective for only 60% to 70% of patients. Thus, researchers have looked for other candidates for social anxiety treatment. Our review focuses on the peptide oxytocin as a potential therapeutic option for individuals with social anxiety. Animal research both in nonprimates and primates supports oxytocin's role in facilitation of prosocial behaviors and its anxiolytic effects. Human studies indicate significant associations between social anxiety and oxytocin receptor gene alleles, as well as social anxiety and oxytocin plasma levels. In addition, intranasal administration of oxytocin in humans has favorable effects on social anxiety symptomology. Other disorders, including autism, schizophrenia, and anorexia, have components of social anxiety in their pathophysiology. The therapeutic role of oxytocin for social dysfunction in these disorders is discussed.

Indexed as

Administration, IntranasalAnimalsAnti-Anxiety AgentsFearHumansOxytocinPhobia, SocialAnti-Anxiety AgentsOxytocinanxietyhumanoxytocinprimaterodentsocial

Identifiers

PMID28867943
PMCPMC5573563
OpenAlexW2772095365

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.