Increased reflection impulsivity in patients with ephedrone-induced Parkinsonism.

Increased reflection impulsivity in patients with ephedrone-induced Parkinsonism.
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DOI:
10.1111/add.12080
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发表时间:
2013-04
期刊:
Addiction (Abingdon, England)
影响因子:
--
通讯作者:
Averbeck BB
Averbeck BB
中科院分区:
其他
文献类型:
--
作者:
Djamshidian A;Sanotsky Y;Matviyenko Y;O'Sullivan SS;Sharman S;Selikhova M;Fedoryshyn L;Filts Y;Bearn J;Lees AJ;Averbeck BB

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To examine a syndrome of chronic manganism that occurs in drug addicts in Eastern Europe who use intravenous methcathinone (ephedrone) contaminated with potassium permanganate. The basal ganglia, especially the globus pallidus and the putamen, are damaged irreversibly in many cases. Routine neuropsychological assessment has revealed no cognitive deficits despite widespread abnormalities on brain imaging studies and severe extrapyramidal motor handicap on clinical examination. Case control study. Ephedrone patients and patients with opioid dependence were recruited from Lviv, Ukraine. We tested 15 patients with ephedrone induced toxicity, 13 opiate dependent patients, who were receiving opioid replacement therapy and 18 matched healthy volunteers. The ‘beads task’, an information gathering task to assess reflection impulsivity was used and feedback learning, working memory and risk taking were also assessed. Opiate dependent patients differed from controls on three out of four tasks, whereas ephedrone patients differed from controls on only one task. More specifically both patient groups were more impulsive and made more irrational choices on the beads task than controls (p<0.001). However, ephedrone patients had no deficits in working memory (p>0.1) or risk taking (p>0.1) compared with controls. Opioid dependent patients had significantly worse working memory (p<0.001) and were significantly more risk prone than controls (p=0.002). Ephedrone patients may have similar deficits in information gathering and decision making to opiate dependent patients, with preservation of working memory and risk taking. This may reflect specific damage to anterior cingulate- basal ganglia loops.
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