Cannabis use by women during pregnancy does not influence infant DNA methylation of the dopamine receptor DRD4

Am J Drug Alcohol Abuse. 2017 Nov;43(6):671-677. doi: 10.1080/00952990.2017.1314488. Epub 2017 Apr 27.

Abstract

Background: Maternal cannabis use in pregnancy is linked with long-term adverse behavioral outcomes in offspring. Epigenetic processes established in utero that affect dopaminergic (reward) signaling may mediate risks. Associations between cannabis use and offspring DNA methylation have not been investigated; however, maternal tobacco smoking in pregnancy is associated with distinct patterns of DNA methylation at birth and beyond.

Objectives: To determine whether maternal cannabis use is associated with methylation of the dopamine receptor gene DRD4 promoter in infants.

Methods: Mothers in the Triple B study provided detailed information on drug use in each trimester of pregnancy. Buccal swabs were collected from neonates at 8 weeks (n = 804, 51.7% male, and 48.3% female). DRD4 promoter DNA methylation was measured using SEQUENOM MassARRAY.

Results: Fifty-seven of the women in the study reported drug use during pregnancy, of whom 44 used cannabis. Of 19 cytosine-phosphate-guanine dinucleotides (CpG) units tested in DRD4, gestational cannabis use was associated with offspring methylation at 1 CpG unit in multivariate models (β + 1.48, CI: 0.02 to 2.93, and p = 0.047). At another site there was weak evidence that both cannabis and other drug use were independently associated with increased methylation, while the association with tobacco was in the reverse direction (cannabis use β + 0.67, CI: -0.12 to 1.46, and p = 0.09; other drug use β + 1.11, CI: 0.17 to 2.05, and p = 0.02; tobacco use β -0.41, CI: -0.85 to 0.03, and p = 0.07). None of the associations would remain significant after correction for multiple testing.

Conclusion: There is no strong evidence that maternal cannabis use in pregnancy is associated with offspring DRD4 methylation.

Keywords: Cannabis; DNA methylation; dopamine receptor (DRD4); epigenetics; fetal programming; perinatal; pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • DNA Methylation / drug effects*
  • Female
  • Humans
  • Infant
  • Male
  • Marijuana Smoking / metabolism*
  • Pregnancy
  • Prenatal Exposure Delayed Effects / metabolism*
  • Promoter Regions, Genetic
  • Receptors, Dopamine / metabolism*
  • Tobacco Smoking / adverse effects
  • Young Adult

Substances

  • Receptors, Dopamine

Grants and funding

This current study is funded by a grant from the Financial Markets Foundation for Children (Australia) (2015-252). The Triple B study was funded by an Australian National Health and Medical Research Council (NHMRC) Project Grant #GNT630517 for $2,196,179 and was financially supported by the National Drug and Alcohol Research Centre (NDARC), University of New South Wales. NDARC and the National Drug Research Institute (NDRI), Curtin University, are funded by the Australian Government under the Substance Misuse Prevention and Service Improvements Grants Fund. We also acknowledge financial support from Australian Rotary Health and the Foundation for Alcohol Research and Education (FARE).