4.6 Article

Effects of Prenatal Exposure to Alcohol and Smoking on Fetal Heart Rate and Movement Regulation

期刊

FRONTIERS IN PHYSIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2021.594605

关键词

fetal heart rate; fetal movement; autonomic nervous system; prenatal; alcohol; smoking

资金

  1. Bill and Melinda Gates Foundation [OPP1184816]
  2. Office of the Director, National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism [U01HD055154, UH3OD023279, U01HD045935, U01HD055155, U01AA016501]
  3. National Institute on Deafness and Other Communication Disorders
  4. NIMH [T32MH016434]
  5. Eunice Kennedy Shriver National Institute of Child Health and Human Development
  6. Bill and Melinda Gates Foundation [OPP1184816] Funding Source: Bill and Melinda Gates Foundation

向作者/读者索取更多资源

This study investigated the effects of prenatal tobacco and alcohol exposure on fetal autonomic regulation, particularly on heart rate, movement, and heart rate variability. Differences were observed in the impact of exposure levels on fetal outcomes between the study sites in South Africa and the Northern Plains region of the United States.
Negative associations of prenatal tobacco and alcohol exposure (PTE and PAE) on birth outcomes and childhood development have been well documented, but less is known about underlying mechanisms. A possible pathway for the adverse fetal outcomes associated with PTE and PAE is the alteration of fetal autonomic nervous system development. This study assessed PTE and PAE effects on measures of fetal autonomic regulation, as quantified by heart rate (HR), heart rate variability (SD-HR), movement, and HR-movement coupling in a population of fetuses at >= 34 weeks gestational age. Participants are a subset of the Safe Passage Study, a prospective cohort study that enrolled pregnant women from clinical sites in Cape Town, South Africa, and the Northern Plains region, United States. PAE was defined by six levels: no alcohol, low quit early, high quit early, low continuous, moderate continuous, and high continuous; while PTE by 4 levels: no smoking, quit early, low continuous, and moderate/high continuous. Linear regression analyses of autonomic measures were employed controlling for fetal sex, gestational age at assessment, site, maternal education, household crowding, and depression. Analyses were also stratified by sleep state (1F and 2F) and site (South Africa, N = 4025, Northern Plains, N = 2466). The final sample included 6491 maternal-fetal-dyad assessed in the third trimester [35.21 +/- 1.26 (mean +/- SD) weeks gestation]. PTE was associated with a decrease in mean HR in state 2F, in a dose dependent fashion, only for fetuses of mothers who continued smoking after the first trimester. In state 1F, there was a significant increase in mean HR in fetuses whose mother quit during the first trimester. This effect was driven by the Norther Plains cohort. PTE was also associated with a significant reduction in fetal movement in the most highly exposed group. In South Africa a significant increase in mean HR both for the high quit early and the high continuous group was observed. In conclusion, this investigation addresses a critical knowledge gap regarding the relationship between PTE and PAE and fetal autonomic regulation. We believe these results can contribute to elucidating mechanisms underlying risk for adverse outcomes.

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