Evidence map›Paper›PMID 29018407›Full record

ArticleFrontiers in endocrinology2017

Dose-Dependent and Lasting Influences of Intranasal Vasopressin on Face Processing in Men.

Daniel Price, Debra Burris, Anna Cloutier, Carol B Thompson, James K Rilling, Richmond R Thompson

Erratum issued Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT01327027 (Phase 2 Study of Vasopressin Effects on Human Social Communication), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 10% 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.

NCT01327027 phase1completednot on this map

Phase 2 Study of Vasopressin Effects on Human Social Communication

TypeinterventionalSponsorBowdoin CollegeRan2011 to 2017Enrolled225ConditionsHealthyArmsVasopressin, Arginine, ADH, Placebo, Sterile Saline
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 17 citations in OpenAlex.

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  10. Is Oxytocin "Nature's Medicine"?Pharmacological reviews · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Daniel PriceMaine Medical Center, Department of Psychiatry, Portland, ME, United States.
Debra BurrisMaine Medical Center, Department of Psychiatry, Portland, ME, United States.
Anna CloutierMaine Medical Center, Department of Psychiatry, Portland, ME, United States.
Carol B ThompsonBiostatistics Center, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, United States.
James K RillingDepartment of Anthropology, Emory University, Atlanta, GA, United States.
Richmond R ThompsonPsychology Department and Neuroscience Program, Bowdoin College, Brunswick, ME, United States.
Maine Medical Center · USBowdoin College · USCenter for Neurosciences · USJohns Hopkins University · US

Funding

Vasopressin Effects on Emotional Social CommunicationR01MH087721 · NIMH · BOWDOIN COLLEGE · PI RILLING, JAMES K, THOMPSON, RICHMOND R · 2010 to 2014
$1.6M
NIMH NIH HHS R01 MH087721
6 · The paper itself

Abstract

Arginine vasopressin (AVP) and related peptides have diverse effects on social behaviors in vertebrates, sometimes promoting affiliative interactions and sometimes aggressive or antisocial responses. The type of influence, in at least some species, depends on social contexts, including the sex of the individuals in the interaction and/or on the levels of peptide within brain circuits that control the behaviors. To determine if AVP promotes different responses to same- and other-sex faces in men, and if those effects are dose dependent, we measured the effects of two doses of AVP on subjective ratings of male and female faces. We also tested if any influences persist beyond the time of drug delivery. When AVP was administered intranasally on an initial test day, 20 IU was associated with decreased social assessments relative to placebo and 40 IU, and some of the effects persisted beyond the initial drug delivery and appeared to generalize to novel faces on subsequent test days. In single men, those influences were most pronounced, but not exclusive, for male faces, whereas in coupled men they were primarily associated with responses to female faces. Similar influences were not observed if AVP was delivered after placebo on a second test day. In a preliminary analysis, the differences in social assessments observed between men who received 20 and 40 IU, which we suggest primarily reflect lowered social assessments induced by the lower dose, appeared most pronounced in subjects who carry what has been identified as a risk allele for the V1a receptor gene. Together, these results suggest that AVP's effects on face processing, and possibly other social responses, differ according to dose, depend on relationship status, and may be more prolonged than previously recognized.

Indexed as

face processingintranasalsocial behaviorsocial contextV1a receptor

Identifiers

PMID29018407
PMCPMC5614924
OpenAlexW2758786296

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.