Aimee R Kroll-Desrosiers1, Benjamin C Nephew2, Jessica A Babb3, Yurima Guilarte-Walker4, Tiffany A Moore Simas5, Kristina M Deligiannidis6,7. 1. Department of Quantitative Health Sciences, University of Massachusetts Medical School, Worcester, MA, USA. 2. Department of Biomedical Sciences, Tufts University Cummings School of Veterinary Medicine, North Grafton, MA, USA. 3. Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children's Hospital, Boston, MA, USA. 4. Department of Information Technology - Research Computing, University of Massachusetts Medical School, Worcester, MA, USA. 5. Departments of Obstetrics & Gynecology, Pediatrics, and Psychiatry, University of Massachusetts Medical School and UMass Memorial Medical Center, Worcester, MA, USA. 6. Women's Mental Health Program, Departments of Psychiatry and Obstetrics and Gynecology, University of Massachusetts Medical School, Worcester, MA, USA. 7. Departments of Psychiatry and Obstetrics & Gynecology, Hofstra Northwell School of Medicine and Zucker Hillside Hospital, Northwell Health, NY, USA.
Abstract
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.
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.
Authors: Andrea Jobst; Daniela Krause; Carina Maiwald; Kristin Härtl; Aye-Mu Myint; Ralph Kästner; Michael Obermeier; Frank Padberg; Benedikt Brücklmeier; Elif Weidinger; Susann Kieper; Markus Schwarz; Peter Zill; Norbert Müller Journal: Arch Womens Ment Health Date: 2016-06-20 Impact factor: 3.633
Authors: Taylor A Thul; Elizabeth J Corwin; Nicole S Carlson; Patricia A Brennan; Larry J Young Journal: Psychoneuroendocrinology Date: 2020-07-06 Impact factor: 4.905
Authors: Benjamin C Nephew; Marcelo Febo; Wei Huang; Luis M Colon-Perez; Laurellee Payne; Guillaume L Poirier; Owen Greene; Jean A King Journal: J Affect Disord Date: 2018-01-02 Impact factor: 4.839
Authors: A B Witteveen; C A I Stramrood; J Henrichs; J C Flanagan; M G van Pampus; M Olff Journal: Arch Womens Ment Health Date: 2019-08-06 Impact factor: 3.633