Resumen
Effects of prenatal exposure to cocaine on the reactivity and regulation of the motor system of 825 four-month-old infants enrolled in the Maternal Lifestyle Study were examined. Videotaped assessments of 338 cocaine-exposed (CE) infants and 487 non-exposed comparison infants were coded by examiners masked to exposure status. Exposure status was determined by meconium assay and maternal self-report of prenatal cocaine use. Infants were presented with a series of 17 visual, auditory and tactile stimuli for 30-s each. Intensity and latency of limb movement responses on a subset of items were analyzed to test the following hypotheses: CE infants are more active in general; CE infants exhibit increased movement levels for a larger proportion of time in response to stimulation; the motor systems of CE infants are more reactive to stimulation (e.g., shorter latencies to respond); and CE infants are poorer regulators of the motor system. Results: CE infants were not more active in general and data do not indicate a more highly reactive motor system. However, CE infants exhibited increased movement levels for a larger proportion of time in response to stimulation. Additional analysis of movement exhibited during three tactile items found increased movement lability in CE infants and different patterns of responding, suggesting that the effects of prenatal cocaine exposure on the motor system may vary by context. Covariate effects for tobacco, alcohol, and marijuana are also reported.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 25-32 |
| Número de páginas | 8 |
| Publicación | Neurotoxicology and Teratology |
| Volumen | 43 |
| DOI | |
| Estado | Published - may 2014 |
Nota bibliográfica
Funding Information:This research was supported by the National Institute on Child Health and Human Development through cooperative agreements ( U10 HD 27904 ; U10 HD 21397 ; U10 HD 21385 ; U10 HD 27856 ; U10 HD 19897 ), NICHD contract HD23159, intra-agency agreements with the National Institute on Drug Abuse (NIDA) , Administration for Youth and Families (ACYF) and the Center for Substance Abuse Treatment (CSAT) , and a New Faculty Research Fellowship from the College of Health and Human Services at Missouri State University .
Financiación
This research was supported by the National Institute on Child Health and Human Development through cooperative agreements ( U10 HD 27904 ; U10 HD 21397 ; U10 HD 21385 ; U10 HD 27856 ; U10 HD 19897 ), NICHD contract HD23159, intra-agency agreements with the National Institute on Drug Abuse (NIDA) , Administration for Youth and Families (ACYF) and the Center for Substance Abuse Treatment (CSAT) , and a New Faculty Research Fellowship from the College of Health and Human Services at Missouri State University .
| Financiadores | Número del financiador |
|---|---|
| Youth and Families (ACYF) | |
| Administration for Youth and Families | |
| College of Health and Human Services at Missouri State University | |
| National Institute on Drug Abuse | |
| NIH National Institute of Child Health and Human Development National Center for Medical Rehabilitation Research | N01HD023159, U10 HD 27904, U10 HD 27856, U10 HD 21385, U10 HD 21397, U10 HD 19897 |
| NIH National Institute of Child Health and Human Development National Center for Medical Rehabilitation Research | |
| Center for Substance Abuse Treatment | |
| Eunice Kennedy Shriver National Institute of Child Health and Human Development |
ASJC Scopus subject areas
- Toxicology
- Developmental Neuroscience
- Cellular and Molecular Neuroscience
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