Dopamine genes and ADHD.

@article{citeulike:2915270, abstract = {Family, twin, and adoption studies have documented a strong genetic basis for ADHD/HKD, but these studies do not identify specific genes linked to the disorder. Molecular genetic studies can identify allelic variations of specific genes that are functionally associated with ADHD/HKD, and dopamine genes have been the initial candidates based on the site of action of the stimulants drugs, which for a half century have provided the primary pharmacological treatment for ADHD/HKD. Two candidate dopamine genes have been investigated and reported to be associated with ADHD/HKD: the dopamine transporter (DAT1) gene [Cook et al., American Journal of Human Genetics 1995;56:993-998, Gill et al., Molecular Psychiatry 1997;2:311-313] and the dopamine receptor D4 (DRD4) gene [LaHoste et al., Molecular Psychiatry 1996;1:121-124: Smalley et al., 1998;3:427-430; Swanson et al., Molecular Psychiatry 1998;3:38-41]. Speculative hypotheses [Swanson and Castellanos, NIH Consensus Development Conference: Diagnosis and Treatment of Attention Deficit Hyperactivity Disorder, November 1998. p. 37-42] have suggested that specific alleles of these dopamine genes may alter dopamine transmission in the neural networks implicated in ADHD/HKD (e.g. that the 10-repeat allele of the DAT1 gene may be associated with hyperactive re-uptake of dopamine or that the 7-repeat allele of the DRD4 gene may be associated with a subsensitive postsynaptic receptor). These and other variants of the dopamine hypothesis of ADHD will be discussed.}, address = {Child Development Center, University of California at Irvine, 92715, USA. jmswanso@uci.edu}, author = {Swanson, J. M. and Flodman, P. and Kennedy, J. and Spence, M. A. and Moyzis, R. and Schuck, S. and Murias, M. and Moriarity, J. and Barr, C. and Smith, M. and Posner, M. }, citeulike-article-id = {2915270}, issn = {0149-7634}, journal = {Neuroscience and biobehavioral reviews}, keywords = {adhd, dopamine, gene, theory}, month = {January}, number = {1}, pages = {21--25}, posted-at = {2008-06-22 16:26:28}, priority = {2}, title = {Dopamine genes and ADHD.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/10654656}, volume = {24}, year = {2000} }

TY - JOUR ID - citeulike:2915270 L3 - citeulike-article-id:2915270 TI - Dopamine genes and ADHD. JF - Neuroscience and biobehavioral reviews VL - 24 IS - 1 SP - 21 EP - 25 AD - Child Development Center, University of California at Irvine, 92715, USA. jmswanso@uci.edu SN - 0149-7634 N2 - Family, twin, and adoption studies have documented a strong genetic basis for ADHD/HKD, but these studies do not identify specific genes linked to the disorder. Molecular genetic studies can identify allelic variations of specific genes that are functionally associated with ADHD/HKD, and dopamine genes have been the initial candidates based on the site of action of the stimulants drugs, which for a half century have provided the primary pharmacological treatment for ADHD/HKD. Two candidate dopamine genes have been investigated and reported to be associated with ADHD/HKD: the dopamine transporter (DAT1) gene [Cook et al., American Journal of Human Genetics 1995;56:993-998, Gill et al., Molecular Psychiatry 1997;2:311-313] and the dopamine receptor D4 (DRD4) gene [LaHoste et al., Molecular Psychiatry 1996;1:121-124: Smalley et al., 1998;3:427-430; Swanson et al., Molecular Psychiatry 1998;3:38-41]. Speculative hypotheses [Swanson and Castellanos, NIH Consensus Development Conference: Diagnosis and Treatment of Attention Deficit Hyperactivity Disorder, November 1998. p. 37-42] have suggested that specific alleles of these dopamine genes may alter dopamine transmission in the neural networks implicated in ADHD/HKD (e.g. that the 10-repeat allele of the DAT1 gene may be associated with hyperactive re-uptake of dopamine or that the 7-repeat allele of the DRD4 gene may be associated with a subsensitive postsynaptic receptor). These and other variants of the dopamine hypothesis of ADHD will be discussed. KW - adhd KW - dopamine KW - gene KW - theory AU - Swanson, JM AU - Flodman, P AU - Kennedy, J AU - Spence, MA AU - Moyzis, R AU - Schuck, S AU - Murias, M AU - Moriarity, J AU - Barr, C AU - Smith, M AU - Posner, M PY - 2000/01// UR - http://view.ncbi.nlm.nih.gov/pubmed/10654656 ER -