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The Pharmaceutical Journal
Vol 271 No 7262 p200
16 August 2003

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Warn patients treated for Parkinson's disease about gambling behaviour risk

Patients with Parkinson’s disease should be warned that treatment could be associated with an increased risk of gambling, suggest American researchers (Neurology 2003;61:422).

After a review of 1,884 patients with Parkinson’s disease who were seen at the Muhammad Ali Parkinson Research Centre, Barrow Neurological Institute, Phoenix, Arizona, over a 12-month period, Dr Mark Stacy and colleagues found that seven men and two women showed signs of pathological gambling.

Of these nine patients, eight were being treated with pramipexole (Mirapexin, mean dose 4.3mg/day, range 2 to 8mg/day) and one was being treated with pergolide (Celance, 4.5mg/day) when they started gambling.

The researchers report that the overall incidence of gambling among the patients was 0.05 per cent. The incidence of this behaviour among pramipexole-treated patients was 1.5 per cent and 0.3 per cent for pergolide-treated patients. The researchers point out that the rate of pathological gambling found in subjects taking pramipexole is only slightly higher than the reported rate in the general population (0.3 to 1.3 per cent) and other factors could have contributed to the development of this behaviour.

“However, this clinical observation suggests that higher dosages of dopamine agonists may be a catalyst to bringing out this destructive behaviour,” said Dr Stacy.

He added that it might be appropriate to inform patients of this potential risk, “particularly patients taking relatively high dosages of a dopamine agonist, and with a documented history of depression or anxiety disorder”.

The patients identified as pathological gamblers had been taking pramipexole or pergolide for between six and 64 months. Seven patients started gambling within one month of an increase in their dopamine agonist dose.

For six of the patients the gambling was controlled by switching treatment to ropinirole (Requip). Another patient, who did not tolerate a change in dopamine agonist therapy, improved after the pramipexole dose was reduced from 8mg/day to 3mg/day with a concurrent increase in the levodopa dose.

Pfizer, manufacturer of Mirapexin, said that long-term, controlled clinical trials of pramipexole involving nearly 1,000 patients with Parkinson’s disease did not suggest an association between the product and excessive gambling or other impulsive behaviours.

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