Association of peripartum synthetic oxytocin administration and depressive and anxiety disorders within the first postpartum year
Background Due to its potent effects on social behavior, including maternal behavior, oxytocin has been identified as a potential mediator of postpartum depression and anxiety. The objective of this study was to examine the relationship between peripartum synthetic oxytocin administration and the de...
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Published in | Depression and anxiety Vol. 34; no. 2; pp. 137 - 146 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.02.2017
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Subjects | |
Online Access | Get full text |
ISSN | 1091-4269 1520-6394 1520-6394 |
DOI | 10.1002/da.22599 |
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Summary: | Background
Due to its potent effects on social behavior, including maternal behavior, oxytocin has been identified as a potential mediator of postpartum depression and anxiety. The objective of this study was to examine the relationship between peripartum synthetic oxytocin administration and the development of depressive and anxiety disorders within the first year postpartum. We hypothesized that women exposed to peripartum synthetic oxytocin would have a reduced risk of postpartum depressive and anxiety disorders compared with those without any exposure.
Methods
Population‐based data available through the Massachusetts Integrated Clinical Academic Research Database (MiCARD) were used to retrospectively (2005–2014) examine this relationship and calculate the relative risk of peripartum synthetic oxytocin for the development of postpartum depressive and anxiety disorders in exposed (n = 9,684) compared to unexposed (n = 37,048) deliveries.
Results
Among deliveries to women with a history of prepregnancy depressive or anxiety disorder, exposure to peripartum oxytocin increased the risk of postpartum depressive or anxiety disorder by 36% (relative risk (RR): 1.36; 95% confidence interval (95% CI): 1.20–1.55). In deliveries to women with no history of prepregnancy depressive or anxiety disorder, exposure to peripartum oxytocin increased the risk of postpartum depressive or anxiety disorder by 32% compared to those not exposed (RR: 1.32; 95% CI: 1.23‐1.42).
Conclusions
Contrary to our hypothesis, results indicate that women with peripartum exposure to synthetic oxytocin had a higher relative risk of receiving a documented depressive or anxiety disorder diagnosis or antidepressant/anxiolytic prescription within the first year postpartum than women without synthetic oxytocin exposure. |
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Bibliography: | These authors contributed equally to this work. Grant sponsor: National Center for Advancing Translational Sciences; Grant sponsor: National Institutes of Health; Grant numbers: UL1TR000161 and 5K23MH097794; Grant sponsor: SAGE Therapeutics. Grant sponsor: National Institute of Mental Health Individual Postdoctoral Fellowship; Grant numbers: F32MH108247, NICHD R00 HD059943; Grant sponsor: Brain and Behavior Research Foundation NARSAD Young Investigator Award. Grant sponsor: Centers for Disease Control and Prevention Award; Grant number: 1U01DP006093‐01. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 equal contribution |
ISSN: | 1091-4269 1520-6394 1520-6394 |
DOI: | 10.1002/da.22599 |