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Prenatal methamphetamine exposure and neonatal neurobehavioral outcome in the USA and New Zealand
Authors:Linda L. LaGasse  Trecia WouldesElana Newman  Lynne M. SmithRizwan Z. Shah  Chris DeraufMarilyn A. Huestis  Amelia M. ArriaSheri Della Grotta  Tara WilcoxBarry M. Lester
Affiliation:
  • a Center for the Study of Children at Risk, Warren Alpert Medical School of Brown University, Women & Infants Hospital, Providence, RI, USA
  • b Department of Psychological Medicine, University of Auckland, Auckland, New Zealand
  • c Department of Psychology, The University of Tulsa, Tulsa, OK, USA
  • d Los Angeles Biomedical Institute at Harbor-UCLA Medical Center and David Geffen School of Medicine at UCLA, Los Angeles, CA, USA
  • e Blank Hospital Regional Child Protection Center-Iowa Health, Des Moines, IA, USA
  • f John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA
  • g Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD, USA
  • h Center for Substance Abuse Research (CESAR), University of Maryland, College Park, MD, USA
  • Abstract:

    Background

    Methamphetamine (MA) use among pregnant women is a world-wide problem, but little is known of its impact on exposed infants.

    Design

    The prospective, controlled longitudinal Infant Development, Environment and Lifestyle (IDEAL) study of prenatal MA exposure from birth to 36 months was conducted in the US and NZ. The US cohort has 183 exposed and 196 comparison infants; the NZ cohort has 85 exposed and 95 comparison infants. Exposure was determined by self-report and meconium assay with alcohol, marijuana, and tobacco exposures present in both groups. The NICU Neurobehavior Scale (NNNS) was administered within 5 days of life. NNNS summary scores were analyzed for exposure including heavy exposure and frequency of use by trimester and dose-response relationship with the amphetamine analyte.

    Results

    MA exposure was associated with poorer quality of movement, more total stress/abstinence, physiological stress, and CNS stress with more nonoptimal reflexes in NZ but not in the USA. Heavy MA exposure was associated with lower arousal and excitability. First trimester MA use predicted more stress and third trimester use more lethargy and hypotonicity. Dose-response effects were observed between amphetamine concentration in meconium and CNS stress.

    Conclusion

    Across cultures, prenatal MA exposure was associated with a similar neurobehavioral pattern of under arousal, low tone, poorer quality of movement and increased stress.
    Keywords:Prenatal exposure   Methamphetamine   Neurodevelopment   Meconium
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