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Published Online: 1 March 2012

Striatal Dopamine Transporter Alterations in ADHD: Pathophysiology or Adaptation to Psychostimulants? A Meta-Analysis

Abstract

Background:

Striatal dopamine transporter abnormalities are thought to underlie the pathophysiology and psychostimulant treatment of attention deficit hyperactivity disorder (ADHD). However, individual studies using single photon emission tomography (SPECT) or positron emission tomography (PET) have yielded inconsistent results, i.e., both high and low striatal dopamine transporter levels.

Method:

Nine SPECT and PET studies investigating striatal dopamine transporter density in ADHD patients (N=169) and age-, gender-, and IQ-matched healthy comparison subjects (N=173) were included in a quantitative meta-analysis. Binding potentials in the striatum and demographic, clinical, and methodological variables were extracted from each publication or obtained directly from authors. Hedges' g was used as a measure of effect size in an analysis using Comprehensive Meta-Analysis software. Publication bias was assessed with funnel plots and Egger's intercept. Heterogeneity was addressed with the Q statistic and I2 index.

Results:

Striatal dopamine transporter density was 14% higher on average in the ADHD group than in the healthy comparison group. However, heterogeneity across studies was large and statistically significant. Meta-regression analyses showed that the percentage of subjects without exposure to psychostimulants was negatively correlated with dopamine transporter density; density was higher in patients with previous medication exposure and lower in medication-naive patients. There was no moderating effect for age, comorbidity, gender, year of publication, or imaging technique. There was no publication bias, and sensitivity analysis confirmed robustness of the results.

Conclusions:

Striatal dopamine transporter density in ADHD appears to depend on previous psychostimulant exposure, with lower density in drug-naive subjects and higher density in previously medicated patients.

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Information & Authors

Information

Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 264 - 272
PubMed: 22294258

History

Received: 20 June 2011
Revision received: 25 September 2011
Revision received: 22 October 2011
Accepted: 27 October 2011
Published online: 1 March 2012
Published in print: March 2012

Authors

Details

Paolo Fusar-Poli, Ph.D.
From the Department of Psychosis Studies and the Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King's College London; the Child Neuropsychiatry Unit, IRCCS C. Mondino National Institute of Neurology Foundation, University of Pavia, Pavia, Italy; and the Department of Psychology, University of Padua, Padua, Italy.
Katya Rubia, Ph.D.
From the Department of Psychosis Studies and the Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King's College London; the Child Neuropsychiatry Unit, IRCCS C. Mondino National Institute of Neurology Foundation, University of Pavia, Pavia, Italy; and the Department of Psychology, University of Padua, Padua, Italy.
Giorgio Rossi, M.D.
From the Department of Psychosis Studies and the Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King's College London; the Child Neuropsychiatry Unit, IRCCS C. Mondino National Institute of Neurology Foundation, University of Pavia, Pavia, Italy; and the Department of Psychology, University of Padua, Padua, Italy.
Giuseppe Sartori, Ph.D.
From the Department of Psychosis Studies and the Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King's College London; the Child Neuropsychiatry Unit, IRCCS C. Mondino National Institute of Neurology Foundation, University of Pavia, Pavia, Italy; and the Department of Psychology, University of Padua, Padua, Italy.
Umberto Balottin, M.D., Ph.D.
From the Department of Psychosis Studies and the Department of Child and Adolescent Psychiatry, Institute of Psychiatry, King's College London; the Child Neuropsychiatry Unit, IRCCS C. Mondino National Institute of Neurology Foundation, University of Pavia, Pavia, Italy; and the Department of Psychology, University of Padua, Padua, Italy.

Notes

Address correspondence to Dr. Fusar-Poli ([email protected]).

Funding Information

Dr. Rubia has received speakers' honoraria from Eli Lilly, Medice, Novartis, and Shire. Dr. Rossi served as principal investigator in Shire study SPD503-316 in 2011 and as an investigator in Eli Lilly study B4Z-IT- LICY in 2006. The other authors report no financial relationships with commercial interests.

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