We hypothesize that because of cocaine's effect on the developing catecholamine system, prenatal cocaine exposure (CE) should interfere with the infant's ability to regulate and control arousal. This effect produces a style of responding to the environment that is characterized by seeking stimulation more than usual and is hypothesized to affect normal development of attention and subsequent behavior. Thus, CE infants will differ in how they integrate arousal and attention as compared to (a) non- CE infants, and (b) infants with other CNS risk conditions. Furthermore, we hypothesize that these differences should persist through the first 19 months of age and be detected primarily using tasks that require control of stimulation. Strong evidence now indicates that CE infants tend to look at more stimulating events regardless of manipulations of arousal that would normally shift attention to less stimulating events. Current aims are designed to manipulate a vanity of situations for which hypothesized responses with respect to stimulation can be evaluated. First, we predict that CE infants during the newborn period, in contrast to both normal infants and infants with documented CNS pathology, will display this stimulus-seeking behavior in a number of different converging tasks in which arousal is manipulated by feeding or amount of stimulation. Second, we propose to extend the study of the interaction of early CE with developmental changes in attention and perception to determine whether development of short-term memory and of response to stimulus change, complex patterns, and auditory-visual synchrony are altered. We predict that CE, acting through the substrate of early arousal/attention organization, will interfere with the normal development of these processes when evaluated at specific intervals during the first year. Third, we propose to determine if there is a relationship of early cocaine exposure with (a) perceptual and motivational development between 10 and 19 months, as measured by focused attention, distractibility, and exploratory behavior and (b) general cognitive growth particularly as altered by CNS status. Finally we wish to determine if the different developmental trajectory of mental function observed in CE infants reflects CNS injury, differential environmental experience, or intrauterine CE by studying infants of cocaine using mothers seeking rehabilitation program. A 5-year project initially studying 384 infants, with 192 completing all aspects of the study is proposed.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA006644-09
Application #
6174631
Study Section
Special Emphasis Panel (SRCD (31))
Program Officer
Frascella, Joseph
Project Start
1990-08-01
Project End
2003-07-31
Budget Start
2000-08-01
Budget End
2003-07-31
Support Year
9
Fiscal Year
2000
Total Cost
$527,038
Indirect Cost
Name
Institute for Basic Research in Dev Disabil
Department
Type
DUNS #
167205090
City
Staten Island
State
NY
Country
United States
Zip Code
10314
Geva, R; Gardner, J M; Karmel, B Z (1999) Feeding-based arousal effects on visual recognition memory in early infancy. Dev Psychol 35:640-50
Freedland, R L; Karmel, B Z; Gardner, J M et al. (1998) Prenatal cocaine exposure and stimulus-seeking behaviors during the first year of life. Ann N Y Acad Sci 846:386-90
Karmel, B Z; Gardner, J M; Freedland, R L (1998) Neonatal neurobehavioral assessment Bayley I and II scores of CNS-injured and cocaine-exposed infants. Ann N Y Acad Sci 846:391-5
Lewkowicz, D J; Karmel, B Z; Gardner, J M (1998) Effects of prenatal cocaine exposure on responsiveness to multimodal information in infants between 4 and 10 months of age. Ann N Y Acad Sci 846:408-11
Karmel, B Z; Gardner, J M (1996) Prenatal cocaine exposure effects on arousal-modulated attention during the neonatal period. Dev Psychobiol 29:463-80
Karmel, B Z; Gardner, J M; Freedland, R L (1996) Arousal-modulated attention at four months as a function of intrauterine cocaine exposure and central nervous system injury. J Pediatr Psychol 21:821-32