Abnormal brain activation during working memory in children with prenatal exposure to drugs of abuse: The effects of methamphetamine, alcohol, and polydrug exposure

NeuroImage

Volumn 54, Issue 4, 2011, Pages 3067-3075

  Roussotte, Florence F ^a,b   Bramen, Jennifer E ^a   Nunez, S Christopher ^a   Quandt, Lorna C ^a   Smith, Lynne ^c   O'Connor, Mary J ^a   Bookheimer, Susan Y ^a   Sowell, Elizabeth R ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c HARBOR UCLA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; METHAMPHETAMINE;

ADOLESCENT; ALCOHOLISM; ARTICLE; BRAIN DAMAGE; BRAIN FUNCTION; BRAIN REGION; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CORPUS STRIATUM; DEPTH PERCEPTION; DRUG DEPENDENCE; FEMALE; FRONTAL LOBE; HUMAN; LEFT HEMISPHERE; MALE; NERVE CELL NETWORK; PRENATAL EXPOSURE; PRIORITY JOURNAL; PUTAMEN; QUANTITATIVE ANALYSIS; SCHOOL CHILD; TASK PERFORMANCE; WORKING MEMORY;

ADOLESCENT; ALCOHOL DRINKING; BRAIN; CENTRAL NERVOUS SYSTEM DEPRESSANTS; CENTRAL NERVOUS SYSTEM STIMULANTS; CHILD; FEMALE; HUMANS; IMAGE INTERPRETATION, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MEMORY; METHAMPHETAMINE; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; SUBSTANCE-RELATED DISORDERS;

EID: 78650939781     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2010.10.072     Document Type: Article

References (57)

1. Alexander G.E., DeLong M.R., Strick P.L. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Ann. Rev. Neurosci. 1986, 9:357-381.
2. Archibald S.L., Fennema-Notestine C., Gamst A., Riley E.P., Mattson S.N., Jernigan T.L. Brain dysmorphology in individuals with severe prenatal alcohol exposure. Dev. Med. Child Neurol. 2001, 43:148-154.
3. Astley S.J. Diagnostic guide for fetal alcohol spectrum disorders: the 4-digit diagnostic code 2004, University of Washington, Seattle, WA.
4. Astley S.J., Clarren S.K. Measuring the facial phenotype of individuals with prenatal alcohol exposure: correlations with brain dysfunction. Alcohol Alcohol. 2001, 36(2):147-159.
5. Belger A., Puce A., Krystal J.H., Gore J.C., Goldman-Rakic P., MvVarthy G. Dissociation of mnemonic and perceptual processes during spatial and nonspatial working memory using fMRI. Hum. Brain Mapp. 1998, 6:14-32.
6. Braver T.S., Cohen J.D., Nystrom L.E., Jonides J., Smith E.E. A parametric study of prefrontal cortex involvement in human working memory. Neuroimage 1997, 5:49-62.
7. Braver T.S., Barch D.M., Kelley W.M., Buckner R.L., Cohen N.J., Miezin F.M., Snyder A.Z., Ollinger J.M., Akbudak E., Conturo T.E., Petersen S.E. Direct comparison of prefrontal cortex regions engaged by working and long-term memory tasks. Neuroimage 2001, 14:48-59.
8. Callicott J.H., Mattay V.S., Bertolino A., Finn K., Coppola R., Frank J.A., Goldberg T.E., Weinberger D.R. Physiological characteristics of capacity constraints in working memory as revealed by functional MRI. Cereb. Cortex 1999, 9:20-26.
9. Carlson S., Martinkauppi S., Rama P., Salli E., Korvenoja A., Aronen H.J. Distribution of cortical activation during visuospatial n-back tasks as revealed by functional magnetic resonance imaging. Cereb. Cortex 1998, 8:743-752.
10. Casey B.J., Cohen J.D., O'Craven K., Davidson R.J., Irwin W., Nelson C.A., Noll D.C., Hu X., Lowe M.J., Rosen B.R., Truwitt C.L., Turski P.A. Reproducibility of fMRI results across four institutions using a spatial working memory task. Neuroimage 1998, 8:249-261.
11. Chang L., Smith L.M., LoPresti C., Yonekura M.L., Kuo J., Walot I., Ernst T. Smaller subcortical volumes and cognitive deficits in children with prenatal methamphetamine exposure. Psychiatry Res. Neuroimaging 2004, 132:95-106.
12. Chang L., Cloak C., Jiang C.S., Farnham S., Tokeshi B., Buchthal S., Hedemark B., Smith L.M., Ernst T. Altered neurometabolites and motor integration in children exposed to methamphetamine in utero. Neuroimage 2009, 48:391-397.
13. Clark A.M., Li D., Conry J., Conry R., Loock C. Structural and functional brain integrity of fetal alcohol syndrome in nonretarded cases. Pediatrics 2000, 105(5):1096-1099.
14. Cloak C.C., Ernst T., Fujii L., Hedemark B., Chang L. Lower diffusion in white matter of children with prenatal methamphetamine exposure. Neurology 2009, 72:2068-2075.
15. Colby JB, Smith L, O'Connor MJ, Bookheimer SY, Van Horn JD, Sowell ER (submitted) The effects of prenatal methamphetamine/polydrug exposure on white matter microstructure: A tract-based diffusion imaging study.
16. Colliver J.D., Kroutil L.A., Dai L., Gfroerer J.C. Misuse of prescription drugs: Data from the 2002, 2003, and 2004 National Surveys on Drug Use and Health In. Substance Abuse and Mental Health Services Administration 2006, Office of Applied Studies, Rockville, MD.
17. Cortese B.M., Moore G.J., Bailey B.A., Jacobson S.W., Delaney-Balck V., Hannigan J.H. Magnetic resonance and spectroscopic imaging in prenatal alcohol-exposed children: preliminary findings in the caudate nucleus. Neurotoxicol. Teratol. 2006, 28:597-606.
18. Courtney S.M., Ungerleider L.G., Keil K., Haxby J.F. Object and spatial visual working memory activate separate neural systems in the human cortex. Cereb. Cortex 1996, 6:39-49.
19. Cummings J.L. Frontal-subcortical circuits and human behavior. Arch. Neurol. 1993, 50:873-880.
20. Desmond J.E., Gabrieli J.D., Wagner A.D., Ginier B.L., Glover G.H. Lobular patterns of cerebellar activation in verbal working memory and finger-tapping tasks as revealed by functional MRI. J. Neurosci. 1997, 17:9675-9685.
21. Friston K.J., Worsley K.J., Frackowiak R.S.J., Mazziotta J.C., Evans A.C. Assessing the significance of focal activations using their spatial extent. Hum. Brain Mapp. 1994, 1:214-220.
22. Fryer S.L., Tapert S.F., Mattson S.N., Paulus M.P., Spadoni A.D., Riley E.P. Prenatal alcohol exposure affects frontal-striatal BOLD response during inhibitory control. Alcohol. Clin. Exp. Res. 2007, 31(8):1415-1424.
23. Frost D.O., Cadet J.L. Effects of methamphetamine-induced neurotoxicity on the development of neural circuitry: a hypothesis. Brain Res. Rev. 2000, 34:103-118.
24. Goldman-Rakic P.S. Topography of cognition: parallel distributed networks in primate association cortex. Annu. Rev. Neurosci. 1988, 11:1137-1156.
25. Goldman-Rakic P.S. Cellular basis of working memory. Neuron 1995, 14:477-485.
26. Graham V.W., Goldman-Rakic P.S. Modulation of memory fields by dopamine D1 receptors in prefrontal cortex. Nature 1995, 376:572-575.
27. Gruber A.J., Dayan P., Gutkin B.S., Solla S.A. Dopamine modulation in the basal ganglia locks the gate to working memory. J. Comput. Neurosci. 2006, 20:153-166.
28. Helmich R.C., Derikx L.C., Bakker M., Scheeringa R., Bloem B.R., Toni I. Spatial remapping of cortico-striatal connectivity in Parkinson's disease. Cereb. Cortex 2010, 20(5):1175-1186.
29. Jenkinson M., Smith S. A global optimization method for robust affine registration of brain images. Med. Image Anal. 2001, 5:143-156.
30. Jenkinson M., Bannister P., Brady M., Smith S. Improved optimization for the robust and accurate linear registration and motion correction of brain images. Neuroimage 2002, 17:825-841.
31. Jonides J., Schumacher E.H., Smith E.E., Koeppe R.A., Awh E., Reuter-Lorenz P.A., Marshuetz C., Willis C.R. The role of parietal cortex in verbal working memory. J. Neurosci. 1998, 18:5026-5034.
32. Kirschen M.P., Chen S.H., Schraedley-Desmond P., Desmond J.E. Load- and practice-dependent increases in cerebro-cerebellar activation in verbal working memory: an fMRI study. Neuroimage 2005, 24:462-472.
33. Klingberg T., O'Sullivan B.T., Roland P.E. Bilateral activation of fronto-parietal networks by incrementing demand in a working memory task. Cereb. Cortex 1997, 7:465-471.
34. Lewis S.J.G., Dove A., Robbins T.W., Barker R.A., Owen A.M. Striatal contributions to working memory: a functional magnetic resonance imaging study in humans. Eur. J. Neurosci. 2004, 19:755-760.
35. Lu L.H., Johnson A., O'Hare E.D., Bookheimer S.Y., Smith L.M., O'Connor M.J., Sowell E.R. Effects of prenatal methamphetamine exposure on verbal memory revealed with functional magnetic resonance imaging. J. Dev. Behav. Pediatr. 2009, 30:185-192.
36. Mattson S.N., Riley E.P., Sowell E.R., Jernigan T.L., Sobel D.F., Jones K.L. A decrease in the size of the basal ganglia in children with fetal alcohol syndrome. Alcohol. Clin. Exp. Res. 1996, 20(6):1088-1093.
37. McNab F., Klingberg T. Prefrontal cortex and basal ganglia control access to working memory. Nat. Neurosci. 2008, 11:103-107.
38. O'Connor M.J., Frankel F., Paley B., Schonfeld A.M., Carpenter E., Laugeson E.A., Marquardt R. A controlled social skills training for children with fetal alcohol spectrum disorders. J. Consult. Clin. Psychol. 2006, 74:639-648.
39. Riley E.P., McGee C.L. Fetal alcohol spectrum disorders: an overview with emphasis on changes in brain and behavior. Exp. Biol. Med. (Maywood) 2005, 230:357-365.
40. Roussotte, F.F., Soderberg, L., Sowell, E.R., 2010. Structural, metabolic, and functional brain abnormalities as a result of prenatal exposure to drugs of abuse: evidence from neuroimaging. Neuropsychol. Rev. PMID: 20978945. doi:10.1007/s11065-010-9150-x.
41. Rypma B., Prabhakaran V., Desmond J.E., Glover G.H., Gabrieli J.D. Load-dependant roles of frontal brain regions in the maintenance of working memory. Neuroimage 1999, 9:216-226.
42. Scherf K.S., Sweeney J.A., Luna B. Brain basis of deveopmental change in visuospatial working memory. J. Cogn. Neurosci. 2006, 18(7):1045-1058.
43. Schneider M.L., Moore C.F., Barnhart T.E., Larson J.A., DeJesus O.T., Mukherjee J., Nickles R.J., Converse A.K., Roberts A.D., Kraemer G.W. Moderate-level prenatal alcohol exposure alters striatal dopamine system function in rhesus monkeys. Alcohol. Clin. Exp. Res. 2005, 29(9):1685-1697.
44. Schneider M.L., Moore C.F., Gajewski L.L., Larson J.A., Roberts A.D., Converse A.K., DeJesus O.T. Sensory processing disorder in a primate model: evidence from a longitudinal study of prenatal alcohol and prenatal stress effects. Child Dev. 2008, 79(1):100-113.
45. Slotkin T.A. Fetal nicotine or cocaine exposure: which one is worse?. J. Pharmacol. Exp. Ther. 1998, 285:931-945.
46. Smith E.E., Jonides J. Dissociating verbal and spatial working memory using PET. Cereb. Cortex 1996, 6:11-20.
47. Smith L.M., Chang L., Yonekura M.L., Grob C., Osborn D., Ernst T. Brain proton magnetic resonance spectroscopy in children exposed to methamphetamine in utero. Neurology 2001, 57:255-260.
48. Smith L.M., LaGasse L.L., Derauf C., Grant P., Shah R., Arria A., Huestis M., Haning W., Strauss A., Grotta S.D., Liu J., Lester B.M. The infant development environment, and lifestyle study: effects of prenatal methamphetamine exposure, polydrug exposure, and poverty on intrauterine growth. Pediatrics 2006, 118:1149-1156.
49. Smith L.M., LaGasse L.L., Derauf C., Grant P., Shah R., Arria A., Huestis M., Haning W., Strauss A., Grotta S.D., Fallone M., Liu J., Lester B.M. Prenatal methamphetamine use and neonatal neurobehavioral outcome. Neurotoxicol. Teratol. 2008, 30:20-28.
50. Smith S.M. Fast robust automated brain extraction. Hum. Brain Mapp. 2002, 17(3):143-155.
51. Smith S.M., Jenkinson M., Woolrich M.W., et al. Advances in functional and structural MR image analysis and implementation as FSL. Neuroimage 2004, 23(S1):208-219.
52. Sowell E.R., Leow A.D., Bookheimer S.Y., Smith L.M., O'Connor M.J., Kan E., Rosso C., Houston S., Dinov I.D., Thompson P.M. Differentiating prenatal methamphetamine from alcohol exposure using tensor based brain morphometry and discriminant analysis. J. Neurosci. 2010, 30(11):3876-3885.
53. Thompson B.L., Levitt P., Stanwood G.D. Prenatal exposure to drugs: effects on brain development and implications for policy and education. Nat. Rev. Neurosci. 2009, 10:303-312.
54. Wechsler D. The Wechsler Intelligence Scale for Children-Fourth Edition 2003, The Psychological Corporation, San Antonio, TX.
55. Woolrich M.W., Ripley B.D., Brady M., Smith S.M. Temporal autocorrelation in univariate linear modeling of FMRI data. Neuroimage 2001, 14:1370-1386.
56. Worsley K.J. Statistical analysis of activation images. Ch 14 in Functional MRI: An Introduction to Methods 2001, P. Jezzard, P.M. Matthews, S.M. Smith (Eds.).
57. Worsley K.J., Marrett S., Neelin P., Vandal A.C., Friston K.J., Evans A.C. A unified statistical approach for determining significant signals in images of cerebral activation. Hum. Brain Mapp. 1996, 4:58-73.