4.2 Article

Placental aromatase expression decreased in severe neonatal opioid withdrawal syndrome

Journal

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE
Volume 34, Issue 5, Pages 670-676

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14767058.2019.1612870

Keywords

Buprenorphine; methadone; neonatal opioid withdrawal syndrome; opioids; placental aromatase; pregnancy

Funding

  1. John Dempsey Hospital
  2. Hartford Hospital
  3. Hospital of Central Connecticut

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The study found that the severity of severe neonatal opioid withdrawal syndrome (NOWS) may be associated with placental aromatase mRNA expression levels and umbilical cord drug and metabolite levels. Further investigation on placental aromatase in methadone- and buprenorphine-exposed pregnancies is warranted.
Background: Severe neonatal opioid withdrawal syndrome (NOWS) cannot be predicted. Placental aromatase metabolizes both methadone and buprenorphine and may contribute to the severity of NOWS.Objectives: To determine whether placental aromatase mRNA expression differs in methadone- or buprenorphine-exposed placentas and is associated with NOWS severity.Study design: Prospective multicenter observational cohort study from July 2016 to December 2017. Inclusion: pregnant, 18years old, singleton fetus, nonanomalous, 34weeks at delivery, documented methadone or buprenorphine use. Exclusion: declined sample collection. Severe NOWS is defined as three consecutive Finnegan scores 8 or sum of three consecutive scores 24 within 72hours of birth. Finnegan scoring was correlated with placental mRNA expression and compared to umbilical cord drug and metabolite levels. Data were analyzed using descriptive, parametric, and nonparametric statistics and regression analysis. p-Value <.05 was considered significant.Results: Thirty-eight out of 45 (84%) patients were included. Methadone and buprenorphine were used by 29/38 (76%) and 9/38 (24%) of patients, respectively. 19/38 (50%) infants had severe NOWS. Placental aromatase/actin mRNA expression was significantly lower in the placentas of infants with severe NOWS (p = .04). Mean umbilical cord 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP)/methadone ratios were significantly higher in infants with severe NOWS (p = .03). Placental aromatase mRNA expression was weakly to moderately correlated with umbilical cord methadone, buprenorphine, and their metabolite concentrations (r=0.4-0.8).Conclusion: Placental aromatase mRNA expression was lower and umbilical cord EDDP/methadone ratios were higher in infants with severe NOWS. Additional investigation of placental aromatase in methadone- and buprenorphine-exposed pregnancies is needed.

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