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PARKINSON'S DISEASE |
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PARKINSON'S DISEASE NEWS
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SEPTEMBER 2011
19th September 2011 - New researchSAFINAMIDE CLINICAL TRIAL RESULTS Movement Disorders [2011] Sep 12 [Epub ahead of print] (F.Stocchi, R.Borgohain, M.Onofrj, A.H.Schapira, M.Bhatt, V.Lucini, R.Giuliani, R.Anand) Complete abstract Safinamide is a new type of drug being developed for Parkinson's Disease. Safinamide is believed to have both dopaminergic and non-dopaminergic actions, including the inhibition of monoamine oxidase B (MAO-B) and inhibition of glutamate release. It is intended to be added on to the existing use of L-dopa or dopamine agonists. In people with early Parkinson's Disease taking a dopamine
agonist, the effect of 200mg safinamide was found to be little different from
that of a placebo. The effect of 100mg safinamide was found to be significantly
better than a placebo. In previous clinical trials, after six months, once daily
dosages of 50mg to 100mg Safinamide improved
18th September 2011 - New bookPARKINSON'S DISEASE : NON-MOTOR AND NON-DOPAMINERGIC FEATURES C.Warren Olanow (Editor), Fabrizio Stocchi (Editor), Anthony Lang (Editor)
15th September 2011 - News release IRON CHELATOR FOR PARKINSON'S DISEASE
A clinical trial is to be carried out with the iron chelator Deferiprone (Ferriprox)
in Parkinson’s Disease. The clinical trial is being sponsored by Parkinson's UK.
It has been claimed in medical studies that iron accumulates in the brains of
people with Parkinson's Disease, and that iron can therefore cause further
deterioration. Deferipone is
There are a number of weaknesses in the theory behind the method used : (1) The claims made in studies that there is an accumulation of iron in Parkinson's Disease are not matched by the details of the results of those studies. When the results are age controlled, most people with Parkinson's Disease have only a mild accumulation of iron or no iron accumulation at all. (2) Iron is absolutely essential for the formation of dopamine, due to it being a cofactor for the formation of L-dopa. A restriction or lowering of iron intake can therefore be seriously counterproductive. (3) When L-dopa formation is low as occurs in Parkinson's Disease, iron, as an essential cofactor for L-dopa formation, can accumulate in order to overcome that deficiency. It is a compensatory mechanism rather than a cause of Parkinson's Disease. (4) If iron accumulation caused Parkinson's Disease, those people with Hereditary Haemochromatosis, which causes an accumulation of iron, would all have Parkinson's Disease. Yet in a study of people with Hereditary Haemochromatosis, none of them had Parkinson's Disease. (5) When iron was used therapeutically in Parkinson's Disease, all of the people tested reduced rather than increased their Parkinson's Disease symptoms. In order to refer to this article on its own click here.
4th September 2011 - New research MALNUTRITION IS PREVALENT IN PARKINSON'S DISEASE Nutrition Reviews [2011] 69 (9) : 520-532 (J.M.Sheard, S.Ash, P.A.Silburn, G.K.Kerr) Complete abstract Malnutrition has been found to occur in up to 24% of people with Parkinson's Disease. Up to 60% of people with Parkinson's Disease have been found to be at risk of malnutrition. However, the studies assessed vary greatly in their figures. People with Parkinson's Disease may be at higher risk of malnutrition because of the symptoms associated with Parkinson's Disease and the side effects of the medication used to manage it. A decline in nutritional status is associated with many adverse outcomes related to health and quality of life. The researchers consequently suggest that it is important to screen for malnutrition at the time of Parkinson's Disease diagnosis.
3rd September 2011 - New book THE COGNITIVE NEUROPSYCHIATRY OF PARKINSON'S DISEASE Patrick McNamara
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