Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 May 21;3(5):e258.
doi: 10.1038/tp.2013.34.

Sniffing around oxytocin: review and meta-analyses of trials in healthy and clinical groups with implications for pharmacotherapy

Affiliations
Review

Sniffing around oxytocin: review and meta-analyses of trials in healthy and clinical groups with implications for pharmacotherapy

M J Bakermans-Kranenburg et al. Transl Psychiatry. .

Abstract

The popularity of oxytocin (OT) has grown exponentially during the past decade, and so has the number of OT trials in healthy and clinical groups. We take stock of the evidence from these studies to explore potentials and limitations of pharmacotherapeutic applications. In healthy participants, intranasally administered OT leads to better emotion recognition and more trust in conspecifics, but the effects appear to be moderated by context (perceived threat of the 'out-group'), personality and childhood experiences. In individuals with untoward childhood experiences, positive behavioral or neurobiological effects seem lowered or absent. In 19 clinical trials, covering autism, social anxiety, postnatal depression, obsessive-compulsive problems, schizophrenia, borderline personality disorder and post-traumatic stress, the effects of OT administration were tested, with doses ranging from 15 IU to more than 7000 IU. The combined effect size was d=0.32 (N=304; 95% confidence interval (CI): 0.18-0.47; P<0.01). However, of all disorders, only studies on autism spectrum disorder showed a significant combined effect size (d=0.57; N=68; 95% CI: 0.15-0.99; P<0.01). We hypothesize that for some of the other disorders, etiological factors rooted in negative childhood experiences may also have a role in the diminished effectiveness of treatment with OT.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Effects of oxytocin administration on face recognition, trust to in-group and trust to out-group in healthy participants: combined effect sizes (d) and 95% confidence intervals. The combined effect size for distrust to out-group is not significant.
Figure 2
Figure 2
Randomized controlled trials with oxytocin administration in clinical groups: effect sizes (Cohen's d, 95% confidence interval) and significance.
Figure 3
Figure 3
A contextual psychoneurobiological model of oxytocin (OT) treatment: moderation by childhood experiences.

References

    1. Guastella AJ, Howard AL, Dadds MR, Mtchell P, Carson DS. A randomized controlled trial of intranasal oxytocin as an adjunct to exposure therapy for social anxiety disorder. Psychoneuroendocrinology. 2009b;34:917–923. - PubMed
    1. Striepens N, Kendrick KM, Maier W, Hurlemann R. Prosocial effects of oxytocin and clinical evidence for its therapeutic potential. Front Neuroendocrinol. 2011;32:426–450. - PubMed
    1. Yamasue H, Yee JR, Hurlemann R, Rilling JK, Chen FS, Meyer-Lindenberg A, et al. Integrative approaches utilizing oxytocin to enhance prosocial behavior: from animal and human social behavior to autistic social dysfunction. J Neurosci. 2012;32:14109–14117. - PMC - PubMed
    1. Feldman R. Oxytocin and social affiliation in humans. Horm Behav. 2012;61:380–391. - PubMed
    1. Churchland PS, Winkielman P. Modulating social behavior with oxytocin: How does it work? What does it mean. Horm Behav. 2012;61:392–399. - PMC - PubMed

MeSH terms