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I HAVE PARKINSON'S DISEASES AND THOUGHT IT WOULD BE NICE TO HAVE A PLACE WHERE THE CONTENTS OF UPDATED NEWS IS FOUND IN ONE PLACE. THAT IS WHY I BEGAN THIS BLOG.

I COPY NEWS ARTICLES PERTAINING TO RESEARCH, NEWS AND INFORMATION FOR PARKINSON'S DISEASE, DEMENTIA, THE BRAIN, DEPRESSION AND PARKINSON'S WITH DYSTONIA. I ALSO POST ABOUT FUNDRAISING FOR PARKINSON'S DISEASE AND EVENTS. I TRY TO BE UP-TO-DATE AS POSSIBLE.

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Saturday, July 30, 2011

Increased risk of Parkinson’s disease in methamphetamine users, CAMH study finds

For Immediate Release - July 26, 2011- (Toronto) - People who abused methamphetamine or other amphetamine-like stimulants were more likely to develop Parkinson’s disease than those who did not, in a new study from the Centre for Addiction and Mental Health (CAMH).

The researchers examined almost 300,000 hospital records from California covering 16 years. Patients admitted to hospital for methamphetamine or amphetamine-use disorders had a 76 per cent higher risk of developing Parkinson’s disease compared to those with no diagnosis.

Globally, methamphetamine and similar stimulants are the second most commonly used class of illicit drugs.

“This study provides evidence of this association for the first time, even though it has been suspected for 30 years,” said lead researcher Dr. Russell Callaghan, a scientist with CAMH. Parkinson’s disease is caused by a deficiency in the brain’s ability to produce a chemical called dopamine. Because animal studies have shown that methamphetamine damages dopamine-producing areas in the brain, scientists have worried that the same might happen in humans.

It has been a challenge to establish this link, because Parkinson’s disease develops in middle and old age, and it is necessary to track a large number of people with methamphetamine addiction over a long time span.

The CAMH team took an innovative approach by examining hospital records from California – a state in which methamphetamine use is prevalent – from 1990 up to 2005. In total, 40,472 people, at least 30 years of age, had been hospitalized due to a methamphetamine- or amphetamine-use disorder during this period.

These patients were compared to two groups: 207,831 people admitted for appendicitis with no diagnosis of any type of addiction, and 35,335 diagnosed with cocaine use disorders. A diagnosis of Parkinson’s disease was identified from hospital records or death certificates. Only the methamphetamine group had an increased risk of developing Parkinson’s disease.

While the appendicitis group served as a comparison to the general population, the cocaine group was selected for two reasons. Because cocaine is another type of stimulant that affects dopamine, this group could be used to determine whether the risk was specific to methamphetamine stimulants. Cocaine users also served as a control group to account for the health effects or lifestyle factors associated with dependence on an illicit drug.

“It is important for the public to know that our findings do not apply to patients who take amphetamines for medical purposes, such as attention deficit hyperactivity disorder (ADHD), since these patients use much lower doses of amphetamines than those taken by patients in our study,” said Dr. Stephen Kish, a CAMH scientist and co-author.

To put the study findings into numbers, if 10,000 people with methamphetamine dependence were followed over 10 years, 21 would develop Parkinson’s, compared with 12 people out of 10,000 from the general population. “It is also possible that our findings may underestimate the risk because in California, methamphetamine users may have had less access to health-care insurance and consequently to medical care,” said Dr. Callaghan.

The current project is significant because it is one of the few studies examining the long-term association between methamphetamine use and the development of a major brain disorder. “Given that methamphetamine and other amphetamine stimulants are the second most widely used illicit drugs in the world, the current study will help us anticipate the full long-term medical consequences of such problematic drug use,” said Dr. Callaghan.

Media Contact: Michael Torres, Media Relations, CAMH; 416-595-6015


The Centre for Addiction and Mental Health (CAMH) is Canada's largest mental health and addiction teaching hospital, as well as one of the world's leading research centres in the area of addiction and mental health. CAMH combines clinical care, research, education, policy development and health promotion to help transform the lives of people affected by mental health and addiction issues. CAMH is fully affiliated with the University of Toronto, and is a Pan American Health Organization/World Health Organization Collaborating Centre.

RHINORRHEA IN PARKINSON'S DISEASE


26th July 2011 - New research

Movement Disorders [2011] 26 (2) : 320-323 (Chou KL, Koeppe RA, Bohnen NI.)

Rhinorrhea is nasal discharge, commonly referred to as a runny nose. For more information go to Rhinorrhea. Although, nasal discharge is usually assumed to occur for a variety of reasons such as colds, flu or allergies, it is a common symptom in Parkinson's Disease. Researchers have found that people with Parkinson's Disease multiplied the likelihood of nasal discharge 5 times the average. This is after other possible causes had been accounted for.
Over two thirds (68%) of people who had Parkinson's Disease reported nasal discharge. There was no relationship with age or severity of symptoms. The nasal discharge of over half (52%) of people with Parkinson's Disease was accompanied with light headedness. The symptom of lightheadedness is uncommon in people who do not have Parkinson's Disease, occurring in less than 1 in 10. Another recent study found similar results.  The frequency of nasal discharge can lead to a reduction in the sense of smell, which is common in Parkinson's Disease.
It is not clearly known what causes this relationship. Nasal discharge occurring so frequently in Parkinson's Disease is not directly due to low dopamine, and a previous study found no relationship between rhinorrhea and dopamine agonists.

Single and dual task gait training in people with Parkinson's Disease: A protocol for a randomised controlled trial

From Northwest  Parkinsons Foundation:      

 

Difficulty performing more than one task at a time (dual tasking) is a common and disabling problem experienced by people with Parkinson disease (PD). If asked to perform another task when walking, people with PD often take shorter steps or walk more slowly.

Currently there is uncertainty about whether clinicians should teach people with PD to avoid dual tasking or whether they should encourage them to practice dual tasking with the hope that practice will lead to enhanced performance. This study will address this issue by comparing single to dual task gait training.Methods and design: A prospective randomised clinical trial is being conducted.

Sixty participants with idiopathic PD will be recruited, provided they score I-IV on the modified Hoehn and Yahr (1967) scale, and fulfil other inclusion criteria. Participants will be randomly allocated to either a single or dual task gait training group.Both groups will receive 12 hours of walking training over 4 weeks. The single task group will undertake gait training with cueing strategies to increase step length.The dual task group will train to improve step length when walking and performing a variety of added tasks.

Both groups will receive a tailored home program for 6 months.Blinded assessors will conduct four assessments: two baseline assessments, one post intervention and one at 6 months follow-up.

The primary outcome measure will be step length when dual tasking over 8m.Secondary outcome measures include: spatiotemporal gait parameters when walking under single and dual task conditions, measures of executive function, the timed up and go test, measures of community mobility, and quality of life.

All analyses will be based on intention to treat principle. Discussion. This trial will examine the immediate and longer term effect of dual task walking training as compared to single task training in people with idiopathic PD, at the impairment, activity, and participation levels.

It has the potential to identify a new intervention that may improve and maintain walking beyond the laboratory. The results of this trial will provide guidance forclinicians in the development of walking training programs for people with PD.Trial Registration: ACTRN12609000791235

Tuesday, July 19, 2011

PARKINSON'S DISEASE FOUNDATION FUNDS ELEVEN NEW PROJECTS

11th July 2011 - News release



The Parkinson’s Disease Foundation has announced awards totalling more than $1 million for 11 novel research projects, which they claim are "designed to understand the cause(s) of and find a cure for Parkinson’s disease." The research ranges from basic science investigations to studies of potential new therapies and symptomatic relief.

The primary cause of Parkinson's Disease is the insufficient formation of dopamine in the dopaminergic neurons, which are the brain cells specialised in producing dopamine. Yet most of the projects are quite remote from this basic biochemistry of Parkinson's Disease. One of them aims at studying "the role of norepinephrine" and "the potential of norepinephrine-targeted therapies to treat" Parkinson's Disease. However, norepinephrine is not produced by the cells affected in Parkinson's Disease, and the formation or lack of formation of norepinephrine has never been shown to cause Parkinson's Disease. Another project is to assess "the role of the mitochondria in Parkinson’s" Disease using "Transparent Zebrafish". The mitochondria is the energy producing part of all brain cells. It is not directly involved in dopamine formation, and its deficiency has never been shown to cause Parkinson's Disease. Another project concerns the "Identification of Genes for Parkinson's Disease in an Isolated Greek Community". However, genetic mutations have only ever been proven to make Parkinson's Disease more likely in a small number of people. Other studies include looking at the use of "Electrical Stimulation", "Identification of Neuroprotective Factors in Tobacco", generating "interest in Parkinson’s research and patient care among basic scientists and clinicians", and "Small Aromatic Molecules as Novel Inhibitors of Alpha-Synuclein Aggregation".

A THIRD OF PEOPLE WITH PARKINSON'S DISEASE HAVE DYSPHAGIA

14th July 2011 - New research

Dysphagia [2011] 26 (1) : 92-96 (Walker RW, Dunn JR, Gray WK.)

A third of people with Parkinson's Disease have been found to experience dysphagia. Dysphagia is difficulty with swallowing. This can cause eating and drinking problems, and more seriously causes choking, which can be fatal.  The reason why dysphagia is so common in Parkinson's Disease is that the insufficient dopamine in Parkinson's Disease can affect all muscles, including those needed for swallowing, of which there are many. In Parkinson's Disease dysphagia has been found to be unrelated to age, gender or duration of Parkinson's Disease. However, dysphagia is very common in those people with sever motor skills. Although Parkinson's Disease underlies the problem in many cases, there are practical means of dealing with dysphagia. The recently published "Swallow Safely", which is "A caregiver's guide to recognition, treatment, and prevention" deals with the problem, particularly as it relates to Parkinson's Disease.  For information about DYSPHAGIA:
http://www.nidcd.nih.gov/health/voice/dysph.html

DUAL LAYER L-DOPA CLINICAL TRIAL RESULTS

16th July 2011 - New research

Movement Disorders [2011] Jul 13 [Epub ahead of print] (R.A.Hauser, A.L.Ellenbogen, L.V.Metman, A.Hsu, M.J. O'Connell, N.B.Modi, H.M.Yao, S.H.Kell, S.K.Gupta)
L-dopa combined with carbidopa usually comes in two different forms : either the immediate release version (such as Regular Sinemet), which satisfies the immediate need for L-dopa, or the controlled release version (such as Sinemet CR), which avoids the excessive effects of L-dopa by spreading out the effects of the L-dopa over time.

Dual layer L-dopa combines the two types of L-dopa and carbidopa - an immediate release form and a controlled release form, all in the same tablet. Dual layer L-dopa is consequently being developed as a possible replacement for Sinemet and Sinemet CR. Dual layer L-dopa (IPX054) was shown to be slightly more effective than conventional forms of L-dopa, despite having to be taken only twice a day instead of throughout the day. Dual layer L-dopa (IPX066) increased L-dopa levels at the same rate as immediate release L-dopa and carbidopa, and also provided more sustained L-dopa concentrations. It also substantially reduced the variability in plasma concentrations of L-dopa, despite being taken less often.

NEWLY DISCOVERED FORM OF GENETIC PARKINSON'S DISEASE

19th July 2011 - New research

American Journal of Human Genetics [2011] 89 (1) : 162-167 (Vilariño-Güell C, et al) 
American Journal of Human Genetics [2011] 89 (1) : 168-175 (Zimprich A, et al)

A new form of genetic Parkinson's Disease called VPS35 has been discovered by two different lots of researchers. One of the studies concerned a Swiss family and other families who have late-onset Parkinson's Disease. The Swiss family has tremor-predominant L-dopa responsive Parkinsonism with an average of onset at 50 years old. The other study concerned an Austrian family with 16 affected individuals and others with an average of onset at 53 years old.
The VPS35 gene produces a protein called VPS35 (Vacuolar protein sorting-associated protein 35). The function of VPS35 is known, but it is not explained how this function not taking place causes Parkinson's Disease symptoms. Unlike other genetic causes of Parkinson's Disease, VPS35 appears to eventually cause Parkinson's Disease symptoms rather than make them more likely.
Although Parkinson's Disease uncommonly has a genetic cause or increased likelihood, the prevalence of genetic Parkinson's Disease is not known, and may be more than is assumed. This is because there are a variety of genetic causes of Parkinson's Disease, and most people are never tested for them. Therefore, there are many people with Parkinson's Disease who have unknowingly been inclined, but not inevitably, to develop Parkinson's Disease all their life.

Wednesday, July 13, 2011

WHY DO PEOPLE WITH PARKINSON'S DISEASE TAKE PART IN CLINICAL TRIALS ?

3rd July 2011 - New research

Parkinsonism Related Disorders [2011] Jun 27 [Epub ahead of print] (Valadas A, Coelho M, Mestre T, Guedes LC, Finisterra M, Noronha A, Rosa MM, Sampaio C, Ferreira JJ.)

Limited data is available regarding the motivations and concerns of people with Parkinson's Disease when participating in clinical trials. Knowledge of these factors may improve the recruitment and quality of future trials.

When asked for their reasons the main reasons for participating in clinical trials were : to help the advance of science (63%), to gain access to a better treatment (56%), and to benefit others (51%). The major concerns were : the risk of adverse events (49%) and the negative effects of treatment (35%). 90% reported they had understood the informed consent. Only 64% understood what the placebo effect meant. 66% of patients would participate in another clinical trial, but only 41% of patients would participate in a placebo-controlled trial.

Parkinson's Disease Foundation Announces $1 Million for Novel Studies Into Parkinson’s

PDF Press Releases and Statements

 - Jul 07 2011
(New York, NY) The Parkinson’s Disease Foundation (PDF) is pleased to announce awards totaling more than $1 million for 11 novel investigator-initiated research projects designed to understand the cause(s) of and find a cure for Parkinson’s disease.
Investigator-driven projects are a core piece of PDF’s philosophy to empower the community – of scientists, clinicians, people with Parkinson’s and health care professionals – to find creative solutions benefitting the seven to 10 million people worldwide living with Parkinson’s. The projects are funded through two key programs: the International Research Grants program and the Research Fellowships program, which both seek to encourage novel ideas by respectively funding “high-risk/high-reward” projects and supporting scientists in the early stages of their careers.

A review committee that was chaired by Robert Burke, M.D., and included PDF’s Scientific Director, Stanley Fahn, M.D., chose the 11 projects, which range from basic science investigations of the cellular mechanisms that underlie the disease, to studies of potential new therapies. They also include ideas that may lead to symptomatic relief for the people who are living with Parkinson’s today.

For example, Parkinson’s research has typically focused on dopamine and its role in an area of the brain called the substantia nigra. Elena Vazey, Ph.D., of the Medical University of South Carolina in Charleston, SC, will use her research fellowship to cast a wider net, studying the role of norepinephrine released from brain stem neurons and its impact on the brain as a whole. Initial research suggests that changes in norepinephrine in the brain may contribute to changes in cognition, sleep and mood in Parkinson’s. Dr. Vazey’s investigations may help us to better understand the impact of brain norepinephrine upon Parkinson’s and the potential of norepinephrine-targeted therapies to treat the disease.

Her fellow awardees, Sarah B. Berman, M.D., Ph.D., and Edward Burton, M.D., D.Phil., of the University of Pittsburgh in Pittsburgh, PA, are using their International Research Grant to investigate a more popular topic, the role of the mitochondria (the power plant of the cell) in Parkinson’s. But their approach is unique. They will look for clues about the mitochondria by observing their movements in transparent zebrafish. By recording the motion of mitochondria as they migrate within the dopamine neurons and axons of a living animal, Dr. Berman and Dr. Burton hope to yield new insights into the role of the mitochondria in Parkinson’s.

PDF Executive Director, Robin Anthony Elliott commented on the nature of this year’s projects, “Time is of the essence for people with Parkinson’s. Part of our responsibility to the community is to provide promising scientists with opportunities to pursue creative strategies to understanding the disease. Each of this year’s research projects, in its own way, represents an innovative approach to solving Parkinson’s. We look forward to seeing how they progress. ”

Thomas Shiftan, M.D., a PDF research advocate who was part of the review committee noted, “After seeing first-hand the scientific debate among some of the world’s leading Parkinson’s experts, I am hopeful that we are pursuing Parkinson’s from every angle possible. I am glad to play a role in PDF’s team – of researchers, advocates, clinicians and supporters – in making a difference for people living with Parkinson’s.”


International Research Grants | $825,000


Designed to promote innovative research projects that have high potential to significantly advance the knowledge of Parkinson’s.

Evaluating the Role of Mitochondrial Dynamics in Parkinson's Disease in an In Vivo Vertebrate Model: Real-Time Live Imaging of Mitochondrial Dynamics in Dopamine Neurons in Whole Zebrafish
Sarah Berman, M.D., Ph.D., and Edward Burton M.D., D.Phil., F.R.C.P.
University of Pittsburgh

Impact of Low- and High-Frequency Electrical Stimulation on the Inputs, Integrative Properties and Output of the Subthalamic Nucleus
Mark Bevan, Ph.D.
Northwestern University

Telomere Biology in Patients with Incident Parkinson’s Disease*
Tobias Kurth, M.D., Sc.D., and Robert Y.L. Zee, Ph.D., M.P.H.
Brigham and Women’s Hospital

Identification of Neuroprotective Factors in Tobacco*
Leo J. Pallanck, Ph.D.
University of Washington

Small Aromatic Molecules as Novel Inhibitors of Alpha-Synuclein Aggregation
Daniel Segal, Ph.D.
Tel Aviv University, Israel

Identification of Genes for Parkinson's Disease in an Isolated Greek Community and a Greek Population Cohort

Georgia Xiromerisiou M.D., Ph.D., and Henry Houlden M.D., Ph.D., M.R.C.P.
University of Thessaly, Greece and University College London, England

Research Fellowships | $250,000


Aim to generate interest in Parkinson’s research and patient care among basic scientists and clinicians.

Functional Dissection of a Novel Dopaminergic Inhibitory Circuit in Parkinson's Disease
Jun Ding, Ph.D.
Harvard Medical School

The Regulation of Somatodendritic Dopamine Release*
James Maas, M.D., Ph.D.
University of California, San Francisco

Evaluating Pedunculopontine Nucleus Stimulation as a Treatment for L-DOPA- Resistant Gait Disorders in Advanced Parkinson's Disease
Abirami Muralidharan, Ph.D.
University of Minnesota

The Role of Parkin in Regulating Mitochondrial Dynamics and Homeostasis in Cortical and Dopaminergic Neurons
Victor Van Laar, Ph.D.
University of Pittsburgh

The Locus Coeruleus as a Substrate for Parkinsonian Cognitive Inflexibility
Elena Vazey, Ph.D.
Medical University of South Carolina

*Denotes second year of funding


About Parkinson’s Disease
Parkinson’s disease is a progressive neurological disorder that affects nearly one million people in the US and seven to 10 million people worldwide. Although promising research is being conducted, there is currently no cure for Parkinson’s.

About PDF Research
Central to the mission of the Parkinson’s Disease Foundation (PDF) is funding research of the highest caliber. In fiscal year 2011, PDF will contribute a total of $5.5 million towards Parkinson’s research programs, funding 40 scientific projects around the world. These include projects and mentored fellowships initiated by individual investigators from the global scientific grassroots community and collaborative projects being conducted by research teams at major institutions. Grants are reviewed by PDF’s Scientific Advisory Committee, which includes leading researchers, clinicians and people living with Parkinson’s who work as trained research advocates with PDF’s Parkinson’s Advocates in Research (PAIR) program. A full list of 2012 research projects appears below and is available on the PDF website at www.pdf.org/en/results_funded.

About the Parkinson’s Disease Foundation (PDF)
The Parkinson’s Disease Foundation® (PDF®) is a leading national presence in Parkinson’s disease research, education and public advocacy. We are working for the nearly one million people in the US who live with Parkinson’s by funding promising scientific research while supporting people living with Parkinson’s through educational programs and services. Since its founding in 1957, PDF has dedicated over $90 million to fund the work of leading scientists throughout the world and over $37 million to support national education and advocacy programs.
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Source Date: Jul 07 2011

Friday, July 1, 2011

Promising new Parkinson's Disease drug


TriCities.com - Parkinson's patients are hoping a promising new drug will help them get the most out of their current medications. Those medications often bring complications to Parkinson's patients but a non-dopamine drug may be able to help smooth things out.

Terry Bogard's clarinet has been a hobby for years. He's determined that his parkinson's Disease won't rob him of his music.

Terry Bogard said, "gradually, as it's gotten worse, my left hand is less able to, particularly my little finger, operate the keys that they're supposed to."

That's pretty common for patients taking the standard treatment for Parkinson's, Levodopa.

Dr. Robert Hauser said, "the problem is with levodopa it's a medication that gets absorbed, peaks, and is cleared. So we're trying to take a target that we'd like to have nice and smooth and we're usually a bullet that goes up and down to shoot at that target."

When the fluctuations are mild, doctors can move the Levodopa closer together, or add other dopamine medication. but Doctor Hauser is studying a non-dopamine drug to help

Preladenant is in the category called A2A or adenosine 2A inhibitors. And what these medications do is they interact with the dopamine system in the brain but they're unique and different because they're not dopamine.

Terry, who spent his career in clinical research, was happy to travel to take part in Doctor Hauser's study.

Dr. Hauser said, "this drug interacts with that dopamine system past where dopamine does its thing and it tends to move the system back toward normal. So it does have a more prolonged effect uh but it works right now we think in concert with levodopa. So you still have the fluctuations from levodopa but overall it helps smooth out that clinical response."

The Phase 3 study of Preladenant is underway now at multiple sites (find them at http://clinicaltrials.gov/ct2/show/nct01155479).


Doctor Hauser says if all goes well with FDA approval, perhaps as soon as two to three years from now, it will be the first non-dopamine treatment for Parkinson’s Disease.