4.7 Article

Uterine Blood Flow in a Psychiatric Population: Impact of Maternal Depression, Anxiety, and Psychotropic Medication

Journal

BIOLOGICAL PSYCHIATRY
Volume 72, Issue 6, Pages 483-490

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2012.05.006

Keywords

Bupropion; depression; neurobehavioral development; pregnancy; psychopathology; SSRIs; uterine blood flow

Funding

  1. Translational Research Center in Behavioral Sciences [P50 MH077928]
  2. National Alliance for Research on Schizophrenia and Depression (NARSAD) award
  3. March of Dimes
  4. Wharton Fund
  5. Sackler Foundation
  6. Eli Lilly
  7. GlaxoSmithKline (GSK)
  8. Janssen
  9. NIH
  10. NARSAD
  11. Wyeth
  12. Veteran Affairs
  13. Bristol-Myers Squibb
  14. Cyberonics
  15. Forest
  16. Novartis
  17. GSK
  18. Pfizer
  19. National Institutes of Health (NIH)

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Background: Accumulating evidence suggests that fetal exposure to maternal psychiatric symptoms is associated with future risk for psychopathology. One potential pathway is distress-linked constriction in uterine or umbilical blood flow (UBF). With approximately 6.6% of pregnant women taking an antidepressant, an ecologically valid investigation of this hypothesis must consider the potential concomitant influence of pharmacotherapy on UBF. Methods: Pregnant women (n = 101) with lifetime histories of mental illness were evaluated every 4 to 6 weeks during gestation for mood symptoms and medication use; women underwent an ultrasound examination for UBF at approximately 25 weeks gestation. Results: No associations were observed between UBF and three assessments of maternal prenatal depression and anxiety (acute: coincident with the UBF scan; proximal: within 2 weeks of the scan; chronic: serial symptom ratings). Chronic and acute use of bupropion was associated with reduced UBF, even after controlling for pregnancy complications. Chronic use of atypical antipsychotics also was associated with decreased UBF. There were no associations between serotonergic antidepressant use and UBF. Conclusions: Contrary to a popular hypothesis, depression and anxiety-associated reductions in UBF may not be a pathway by which risk is conferred during prenatal development. However, while requiring replication, our findings suggest that prenatal bupropion exposure may be associated with reductions in UBF.

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