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In reply
We appreciated the interest in our article1 by Dr Morgan and colleagues. We agree that any drug that increases cerebral dopaminergic neurotransmission may facilitate development of impulse control disorders. We specifically focused on pathological gambling, however, and were struck by the association with dopamine agonist therapy and most notably pramipexole. As we commented in our article, levodopa may have been a contributory factor, and that seems likely in those cases where agonists were adjunctively administered.
Levodopa has been the foundation of PD treatment for decades, often as monotherapy. However, none of our patients in the study with pathological gambling or those in prior published series were treated with levodopa monotherapy; all were taking therapeutic doses of agonists. As we indicated in our article, Molina et al2 failed to specify drugs other than levodopa: adjunctive drugs were employed but not listed; hence, we could not include their series in our compilation.
We thank Dr Morgan and colleagues for bringing to our attention the abstract by Tyne et al,3 who did report pathologic gambling in a single patient on levodopa monotherapy, although their other 6 pathologic gamblers were taking dopamine agonists. They also commented, “In those discontinuing dopamine agonist therapy the urge to gamble ceased quickly.”3
For the reasons discussed in our article, disproportionate dopamine D3 agonism as a substrate for pathologic gambling seems too obvious to ignore. Effective risperidone treatment of pergolide-associated pathologic gambling4 cited by Dr Morgan and colleagues is consistent, given that risperidone is also a potent dopamine D3 antagonist.5
Correspondence: Dr Dodd, Department of Psychiatry and Psychology, Mayo Clinic, 200 First St SW, Rochester, MN 55905 (dodd.maryellen@mayo.edu).
Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature
Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal
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