(PSYCHIATRIC TIMES) - In the United States, approximately 2% to 6% of school-age children are diagnosed with attention-deficit/hyperactivity disorder. Data show that stimulant medication is the most consistently successful form of treatment in ADHD, with psychostimulants such as dextroamphetamine (Adderall, Dexedrine) and methylphenidate (Ritalin) exerting therapeutic effects via modulation of the noradrenergic and dopaminergic systems. In the United States, methylphenidate is used to treat over 2 million children with ADHD annually. Methylphenidate acts primarily by blocking the dopamine transporter and increasing extracellular dopamine in the striatum. Despite more than 50 years of clinical and neuroscientific research, appropriate diagnostic and therapeutic interventions for ADHD are still an issue for many people, and although reports summarize the current knowledge (American Academy of Pediatrics Subcommittee on Attention-Deficit/Hyperactivity Disorder and Committee on Quality Improvement, 2001), they use parameters that are still based on the same descriptive determinations that have plagued the field for years. Stimulants are thus widely prescribed for the treatment of ADHD even though the mechanisms subserving their calming effects are not easily understood.
The past two decades have ushered in a new era of methodological advances in tools for noninvasive imaging of the living brain. Brain imaging has forged an impressive link between psychology, psychiatry and neuroscience. The information gleaned from such advances has been used to study both the anatomical and functional aspects of neural processing. Functional neuroimaging methods allow measurement of changes in brain activity associated with simultaneous changes in behavior or in response to a wide variety of stimuli. Event-related potentials, functional magnetic resonance imaging (fMRI), magnetoencephalography, near infrared spectroscopy, positron emission tomography (PET), and single photon emission computed tomography (SPECT) can all measure changes in brain activity. Neuroimaging allows scientists to study the ways in which medications affect neurophysiology and is beginning to provide more precise insights into ADHD--its etiology, diagnosis and treatment.
Neuropsychological studies have implicated the frontal cortical regions of the brain and the circuits linking them to the basal ganglia as critical to executive function, attention and the ability to exercise inhibition. Anatomical assays using quantitative MRI of the brain have provided insights into the neuroanatomical substrate. Early studies suggested that individuals with ADHD had smaller total cerebral volume and showed loss of the normal asymmetry in the size of the caudate nucleus (Castellanos et al., 1996). These data also showed decreased volumes of the right globus pallidus, right anterior frontal region and cerebellum. While PET studies in adult volunteers have provided new knowledge about the pharmacokinetic properties of methylphenidate at its primary site of action in the brain, morphometric and functional neuroimaging have illuminated the neural correlates of abnormalities in both children and adults diagnosed with ADHD (Castellanos and Tannock, 2002; Giedd et al., 2001). Replicable findings using larger samples have implicated brain regions long suspected to play a role in ADHD, but have also identified neural circuitry not previously considered in the context of pathophysiological models.
Neuroimaging assays have most consistently implicated abnormalities of the dorsal prefrontal cortex and basal ganglia in the pathophysiology of ADHD. Reduced metabolic rates have been reported in the left sensorimotor area in children with ADHD (Lou et al., 1989) and in the premotor and superior prefrontal cortices of adults with ADHD (Zametkin et al., 1990). Positron emission tomography data from 10 adolescents with ADHD found reduced metabolic rates versus healthy controls in, among other regions, the left anterior frontal area, showing negative correlation with numerous symptom severity measures (Zametkin et al., 1993). Smaller volumes of the right prefrontal cortex have been reported in children with ADHD compared with healthy controls (Castellanos et al., 1996). This result has generally been replicated but not always with regard to laterality (Aylward et al., 1996; Filipek et al., 1997). Magnetic resonance imaging data demonstrated smaller right globus pallidus nuclei in boys with ADHD relative to a control group (Castellanos et al., 1996).
More recent data compared regional brain volumes at initial scan and their change over time in medicated and previously unmedicated male and female study participants with ADHD versus healthy controls (Castellanos et al., 2002). Individuals with ADHD had significantly smaller brain volumes in all regions, even after adjustment for significant covariates. This global difference was reflected in smaller total cerebral volumes and in significantly smaller cerebellar volumes. Compared with controls, previously unmedicated children with ADHD demonstrated significantly smaller total cerebral volumes and cerebellar volumes. Unmedicated children with ADHD also exhibited smaller total white matter volumes compared with controls and with medicated children with ADHD. Volumetric abnormalities in total and regional cerebral measures and in the cerebellum persisted with age. Caudate nucleus volumes were initially abnormal for patients with ADHD, but differences disappeared as caudate volumes decreased throughout adolescence. Developmental trajectories for all structures except the caudate remained roughly parallel for patients and controls during childhood and adolescence, suggesting that genetic and/or early environmental influences on brain development in ADHD were unrelated to stimulant treatment.
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