WELCOME TO OUR PARKINSON'S PLACE!

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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I JUST WANT TO SHARE WITH YOU WHAT I READ ON THE INTERNET. IT IS UP TO YOU TO DECIDE WHETHER TO READ IT AND TALK IT OVER WITH YOUR DOCTOR. I AM JUST THE COPIER OF DOCUMENTS FROM THE COMPUTER. I DO NOT HAVE PROOF OF FACT OR FICTION OF THE ARTICLE. I ALSO TRY TO PLACE A LINK AT THE BOTTOM OF EACH ARTICLE TO SHOW WHERE I RECEIVED THE INFORMATION SO THAT YOU MAY WANT TO VISIT THEIR SITE.

THIS IS FOR YOU TO READ AND TO ALWAYS KEEP AN OPEN MIND.

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Saturday, May 31, 2014

What are the Symptoms of Anxiety Disorders and Treatments ?

There are many different ways in which a person with Parkinson’s can experience anxiety. The following is a list of common anxiety disorders and a description of symptoms associated with each form. As many as two out of five people with Parkinson’s will experience one of these forms during the course of their illness.

1. Generalized Anxiety Disorder

Generalized anxiety disorder (GAD) is characterized by feelings of nervousness and recurring thoughts of worry and fear. This worrying is in excess of what would normally be expected given the situation and often leaves the person feeling out of control. Physical symptoms that may accompany these feelings include butterflies in the stomach, trouble breathing or swallowing, racing of the heart, sweating and increased tremors.

2. Anxiety Attacks

Anxiety, or panic, attacks usually start suddenly with a sense of severe physical and emotional distress. Individuals may feel as if they cannot breathe or are having a heart attack. They may feel they are experiencing a medical emergency. These episodes usually last less than an hour, particularly when associated with “off” periods, though they can last for longer periods of time.

3. Social Avoidance

Social avoidance, or social anxiety disorder, involves avoiding everyday social situations because of a fear of embarrassment at having Parkinson's symptoms, such as tremor, dyskinesias, or trouble walking noticed in public. Exposure to social situations can lead to severe anxiety in these individuals, which goes away when the person is removed from the situation.

4. Obsessive-Compulsive Disorder

People with obsessive-compulsive disorder (OCD ) may be plagued by persistent, unwelcome thoughts or images (obsessions), and by the urgent need to engage in certain rituals (compulsions) to try to control or rid themselves of these thoughts. As an example, they may be obsessed with germs or dirt, and wash their hands over and over. Performing these so-called rituals, however, only provides temporary relief, and not performing them markedly increases anxiety.


What are the Treatment Options for Anxiety?

There are two main types of treatment options for anxiety:  medications and psychological counseling (psychotherapy).  Depending on the severity of symptoms, psychotherapy can be used alone or combination with medication. NPF recommends a holistic, comprehensive strategy for the treatment of mental health problems, meaning that care should be tailored to each person’s individual health needs and preferences.
The following are treatment options for anxiety disorders:

Medication Therapy

SSRIs (antidepressants)

A newer class of antidepressant drugs called selective serotonin reuptake inhibitors (SSRIs) are typically the first-line treatment for depression and anxiety disorders. All of these medications have been shown to be helpful for one or more anxiety disorder. They include:
  • fluoxetine (Prozac®)
  • sertraline (Zoloft®)
  • paroxetine (Paxil®)
  • citalopram (Celexa®)
  • escitalopram (Lexapro®)
For patients with anxiety attacks, very low dosages should be used at first, as there is evidence that these medications can actually increase attacks when first started at higher dosages. An added benefit of using SSRIs is that they also work for depression, which often occurs simultaneously. 

Benzodiazepines (anti-anxiety medications)

An older class of medications called benzodiazepines is used to treat anxiety disorders and target the brain chemical GABA. Most of these medications have been around for many years.  They include:
  • diazepam (Valium®)
  • lorazepam (Ativan®)
  • clonazepam (Klonopin®)
  • alprazolam (Xanax®)
These medications can be very effective for anxiety, sometimes working better than antidepressants. They take effect very quickly, often providing some relief after a single dose, though they have to be taken regularly for a lasting effect. Also, they can help with other symptoms of Parkinson’s, including certain types of tremor, muscle cramping and sleep changes. Major drawbacks of using benzodiazepines include memory difficulties, confusion, increase in balance problems and tiredness. These medications should not be stopped suddenly, as patients can have serious withdrawal symptoms.
NOTE: Benzodiazepines should be used with caution in older patients with Parkinson’s or in those with dementia. If used regularly, they should never be stopped suddenly to avoid serious withdrawal symptoms.

Psychotherapy

Psychotherapy or “talk therapy” is a term used to refer to the many varieties of counseling available today. This type of treatment can help people diagnosed with an anxiety disorder understand their illness and better manage their symptoms. Mental health professionals who provide therapy include psychologists, social workers, psychiatrists, licensed professional counselors, and specially-trained nurses. Importantly, the first step is to find a compatible therapist. Here are ways that quality therapy can be beneficial.
  • Cognitive behavioral therapy (CBT) is a popular technique that has been shown to be very effective at helping people change negative thinking patterns and behaviors in order to solve their problems and engage in life.
  • Counseling sessions can provide vital support, understanding and education. Patients may be seen alone, as a couple or family, or in a group.
  • For those who do not want to take medication, psychotherapy offers two advantages: no drug side effects and coping skills that can be used over the long term.

Friday, May 30, 2014

New treatment targeting versatile protein may protect brain cells in Parkinson's disease


May 16, 2014
Source:
Lund University

 In Parkinson’s disease (PD), dopamine-producing nerve         cells that control our movements waste away. Current treatments for PD therefore aim at restoring dopamine contents in the brain. In a new study, researchers are attacking the problem from a different angle, through early activation of a protein that improves the brain's capacity to cope with a host of harmful processes.

In Parkinson's disease (PD), dopamine-prodcing nerve cells that control our movements waste away.


Current treatments for PD therefore aim at restoring dopamine contents in the brain. In a new study from Lund University, researchers are attacking the problem from a different angle, through early activation of a protein that improves the brain's capacity to cope with a host of harmful processes. Stimulatingthe protein, called Sigma-1 receptor, sets off a battery of defence mechanisms and restores lost motor function. The results were obtained in mice, but clinical trials in patients may not be far away.
By activating the Sigma-1 receptor, a versatile protein involved in many cellular functions, levels of several molecules that help nerve cells build new connections increased, inflammation decreased, while dopamine levels also rose. The results, published in the journalBrain, show a marked improvement of motor symptoms in mice with a Parkinson-like condition that had been treated with a Sigma-1-stimulating drug for 5 weeks.
This treatment has never before been studied in connection with Parkinson's disease. However, various publications linked to stroke and motor neurone disease have reported positive results with drugs that stimulate the Sigma-1 receptor, and a biotech company in the US will soon begin clinical trials on Alzheimer's patients. The fact that substances stimulating this protein are already available for clinical use is a major advantage, according to Professor M. Angela Cenci Nilsson, head of the research team at Lund University.
"It is a huge advantage that these substances have already been tested in people and approved for clinical application. It means that we already know that the body tolerates this treatment. Clinical trials for Parkinson's disease could theoretically start any time."
Boosting the brain's in-built defence mechanisms with approaches like this is a rather new idea in Parkinson's research. Professor Cenci Nilsson, however, believes that the number of targets for future treatments is increasing as we learn more and more about the complex effects of PD on many different types of cells in the brain.
"The motor improvements we have seen in mice are disproportionately large compared to the recovery of dopamine levels. We believe this is because the treatment has protected the brain against a series of indirect consequences triggered by the Parkinson-like lesion. For example, we know today that a loss of dopamine causes the target neurons to lose synapses, and also alters both neural pathways and non-neuronal cells in the brain. Since the Sigma-1 receptor is widely expressed in many cell types, the treatment could intervene in many of these damaging processes ."
The treatment was shown to be significantly more effective when started at the beginning of the most aggressive phase of dopamine cell death. As a future potential therapy for Parkinson's disease, this treatment would therefore need to be started as soon as possible after diagnosis in order to deliver maximum impact.
"In order to accelerate a possible clinical translation of our findings, we will now seek further evidence in support of this type of treatment. We are now discussing various opportunities with different collaborating partners, and we will try to procure funding for clinical studies in Parkinson´s disease as soon as possible," concludes M. Angela Cenci Nilsson.
Story Source:
The above story is based on materials provided by Lund UniversityNote: Materials may be edited for content and length.

Journal Reference:
  1. V. Francardo, F. Bez, T. Wieloch, H. Nissbrandt, K. Ruscher, M. A. Cenci.Pharmacological stimulation of sigma-1 receptors has neurorestorative effects in experimental parkinsonismBrain, 2014; DOI: 10.1093/brain/awu107

Tuesday, May 27, 2014

Partners in Parkinson's,

Partners in Parkinson's, a new initiative from the Michael J. Fox Foundation, offers on online tool to help patients locate a movement-disorder specialist, in collaboration with the International Parkinson and Movement Disorder Society, whose members include medical specialists. With funding from pharmaceutical company AbbVie Inc., which has a Parkinson's drug in development, the Fox foundation is holding patient and family events where specialists from local clinics demonstrate a comprehensive evaluation.
                                                                       
Dennis Ploszaj, 65, exercises and volunteers to help patients 
at the University of Toledo's Gardner-McMaster Parkinson Center.
 Dennis Ploszjad

Patients visiting the University of Florida Center for Movement Disorders and Neurorestoration, in Gainesville, are screened for depression, which can be caused by changes in the brain as well as by sadness about the disease's effects, said Michael Okun, the center's co-director and author of the book "Parkinson's Treatment: 10 Secrets to a Happier Life." Patients receive a neurologist's evaluation of motor function, including their gait and balance, as well as their lung function.
Dr. Okun says the aim is to prevent falls, fractures and a respiratory ailment called aspiration pneumonia, which are the leading causes of injury and death in Parkinson's patients. They can see several specialists in a single day, including mental-health and speech and communication therapists, who can help with issues like swallowing.
A study led by Peter Schmidt, vice president of research at the National Parkinson Foundation, estimates that neurologist care prevents more than 4,500 deaths a year in Parkinson's patients. The foundation trains medical teams and is conducting a large study at 20 clinics in its Centers of Excellence network to identify factors that result in longer and more active lives for Parkinson's patients.
Dennis Ploszaj, 65, of Findlay, Ohio, was diagnosed with Parkinson's in 2005 at age 56, after experiencing shakiness and balance issues while volunteering as a high-school sports referee. He says his doctor told him he might have a decade or so to live and provided little information about lifestyle changes that could help.
"Movement disorder specialist wasn't in my vocabulary," Mr. Ploszaj says. A year later, he attended a seminar held by Lawrence Elmer, director of the University of Toledo's Gardner-McMaster Parkinson Center, and signed on as a new patient.
"There is so much more to offer patients now than just, 'Here, take a pill,' " says Dr. Elmer. He told Mr. Ploszaj that it would be possible for him to delay the disease's progression and lead a good life. Dr. Elmer advised regular exercise.
Mr. Ploszaj signed up for clinical drug trials and hearing and speech therapy. With his disease under control, Mr. Ploszaj now volunteers to help other patients. "A lot of people come in very down and don't yet understand the disease, so I try to pick up their spirits." he says.

Specialized Care Urged for Treating Parkinson's Disease






Advocacy Groups Urge Patients to See Specialists for Movement Diseases

Updated May 26, 2014 8:00 p.m. ET

Beth Hochstein (center) gave up a career as a podiatrist several years after a diagnosis of young-onset Parkinson's disease.. She now is a Zumba instructor and leads classes for people with Parkinson's near her home in Great Neck, N.Y. Zumba Fitness
A new push is on to provide more specialized care for millions of people with Parkinson's disease and related conditions that impair control of body movement.
Advocacy groups say many doctors aren't extensively trained in treating these conditions, yet studies have shown that only some 40% to 60% of patients ever seek care from a specialist.
Patients benefit most under the care of a neurologist with extra training in movement disorders, backed up by a team including mental health professionals and physical and occupational therapists who can help with the diseases' physical and emotional toll, advocates say.
World-wide, the number of Parkinson's patients alone is projected to double by 2030. The aging population accounts for much of the rise in movement disorders, but they are also being diagnosed in younger patients and can be inherited. Parkinson's affects an estimated 1 million to 1.5 million people in the U.S.
For unknown reasons, Parkinson's leads to degeneration in brain structures called basal ganglia, as well as a loss of chemicals, especially dopamine. The loss causes nerve cells to go haywire and can result in tremors, stiffness and loss of motor control, as well as depression and thinking problems. Dystonia, or involuntary, prolonged and often painful muscle contractions, is caused by dysfunction in similar brain regions and affects about 500,000 people, including some Parkinson's patients. Another condition known as essential tremor, which affected the actress Katharine Hepburn, occurs in as many as 10 million people, and some will develop Parkinson's or dystonia.
Movement disorders often progress slowly and can be controlled with drugs including the central nervous system agent levodopa. There are side effects, such as fluctuations in the ability to control movements, low blood pressure and confusion.
Some patients are candidates for surgical procedures such as deep brain stimulation, in which abnormal movements are regulated with electrical impulses from electrodes implanted in the brain. Side effects can include seizure and mood changes and there can be problems with hardware or poor placement of electrodes, among other issues.
New drugs are in the pipeline, and genetic research is yielding promising clues for future treatment. But the least expensive and most accessible treatment often isn't stressed by doctors unaware of its benefits: Exercise, including dance, has been shown to lead to sharp improvements in some symptoms and may even delay progression of Parkinson's.
Beth Hochstein, who was diagnosed with young-onset Parkinson's in 2007 at age 36, was on medication to control tremors. In 2010, she had to give up her career as a podiatrist in Great Neck, N.Y., because of side effects from medication to control her hands during surgery.
A movement-disorder specialist she consulted early on had advised her that exercise "was the best nonmedical help I could get."
Dr. Hochstein had grown up dancing and took it up again, starting with hip-hop and then popular Zumba classes. She trained with a program called Dance for PD led by the Brooklyn, N.Y.-based Mark Morris Dance Company and now teaches a class affiliated with a hospital near her home.
She starts by telling participants how dance helped her control her symptoms.
Treatment centers specializing in movement disorders have expanded around the country in recent years, with funding from the federal government and nonprofits including the National Parkinson Foundation and the Bachmann-Strauss Dystonia & Parkinson Foundation.
A survey by Harris Poll that included more than 500 patients for the Michael J. Fox Foundation, named for its founder, the actor who has the disease, found that fewer than half were aware of movement-disorder specialists.
Only about 28% of Parkinson's patients surveyed were currently seeing one, and only about half felt "informed" or "very informed" about how to control their symptoms, the survey found.
Conventional treatment may not give proper weight to the link between movement disorders and mental health. Patients may experience anxiety and embarrassment caused by uncontrollable movements and tics, as well as a social stigma.
According to the National Parkinson Foundation, most physicians, especially those who lack training in movement disorders, don't know how to deliver a diagnosis of Parkinson's and often leave the patient feeling lost and alone.
In Wallstreet Journal

Saturday, May 24, 2014

PRAMIPEXOLE CLINICAL TRIAL RESULTS IN PARKINSON'S DISEASE

20th May 2014 - New research

Barone, Y.Mizuno, O.Rascol, M.Busse, C.Debieuvre, M.Fraessdorf, W.Poewe
European Journal of Neurology [2014] 21 (5) : 736-743 (R.A.Hauser, A.H.Schapira, P.
Barone,Complete abstract : http://www.ncbi.nlm.nih.gov/pubmed/24834511
The long term safety and efficacy of pramipexole was assessed as an extended-release oral
formulation and immediate release formulation in early or advanced Parkinson's Disease.
Pramipexole, which is marketed as Mirapex, Mirapexin, and Sifrol, is a dopamine agonist.
For more information go to Pramipexole : http://www.rxlist.com/mirapex-drug.htm
In those people with early Parkinson's Disease the reported side
effects were somnolence (15%), peripheral edema (11%) and back
pain (10%). The scores on the Parkinson's Disease symptom score
(UPDRS) after over 2 years were down by 6.6 when using extended
release pramipexole and 6.3 when using immediate release
pramipexole. In those people with advanced Parkinson's Disease the
reported side effects were dyskinesia (27%), somnolence (13%),
and impulse control disorders (1%). The scores on the Parkinson's
Disease symptom score (UPDRS) after over 2 years were down by
11.5 when using extended release pramipexole and 9.1 when using
immediate release pramipexole.
In both early and advanced Parkinson's Disease better efficacy was achieved when using the
extended release version of pramipexole. The adverse events were typical for dopaminergic
drugs.
©2014 Viartis

Upcoming Challenges for Neurologists in the United States



With the rapidly changing economy, new healthcare laws, and a plethora of cuts from the government, neurologists and their practices should expect a severe decrease in revenue. According to JAMA Neurology Volume 70, Number 9, the sweeping changes due to Obamacare are effecting many medical institutions and practices, but for a number of reasons, neurology is in a crisis of its own. To give you an idea of impact of current neurological practices, here are some of the big cuts that’ve already been implemented:

"...as of January 1, 2013, the Centers for Medicare and Medicaid Services, by regulation, reduced the payment for nerve conduction testing services by more than 50%. Jonathan Blum, a Centers for Medicare and Medicaid Services administrator, indicated that these cuts reduce total neurologic revenue by 7% on average. Implemented March 1, 2013, sequestration cuts further reduced Medicare payments to physicians by 2%. Because the typical neurologic practice has an overhead percentage of greater than 50%, the 9% cut to revenue translates to a greater than 18% reduction in neurologist income.”
…"every deficit reduction proposal targets GME payments. The most prominent, the 2010 Simpson/Bowles bipartisan commission (updated in 2012), proposed a 60% reduction in GME payments. President Barack Obama’s recently released 2014 budget recommends a $780 million cut to GME payments, approximately a 7% cut."

Not only are current small neurology practices being short-changed, but those looking to train to become neurologists are also in trouble:

"As neurologic practices struggle to stay afloat, the viability of training programs is also imperiled. In addition to the loss of clinical revenues, 2 other sources of revenue that support the educational mission are at risk: hospital facility fees and federal graduate educational payments. The facility fee—an additional charge for outpatient services charged by hospitals that materially adds to the reimbursement for these services—is on the hit list for deficit reduction."

As if these cuts weren’t enough, research grants will also be greatly reduced:

”...new grants are projected to be sharply reduced to 17% to 18% of the proposals. Successful awardees now comprise only half of the percentage of those who succeeded in attaining them in the 1980s.”
“…Academic and research programs can find replacement for some of the lost federal revenues through well-coordinated efforts to attract charitable support.”
“...GME funding of neurology training must be protected. Finally, the president’s announced initiative provides a key opportunity to educate the public and Congress as to the need for research and access to care for this patient population.”

Unfortunately in rough economic times, science and medicine tend to get defunded. Neurological disorders are prevalent throughout the world, and as a society we understand that they need serious research and treatments. In your next email, letter, or call to your representatives, consider pressuring them to support laws that strengthen neurological science, treatments, and practices.

Visit JAMA Neurology’s site to susbcribe to their journal for further reading and sources. JAMA Neurology September 2013 Volume 70, Number 9 page 1097, 1098 written by Orly Avitzur, MD, MBA and Bruce Sigsbee, MD, MS.


A Finger Sensor & App could make Parkinson’s disease Symptom Monitoring more Scalable

April 16, 2014 





Thanks in part to a $1.5 million grant from NIH, Great Lakes Neurotechnologies thinks it can make its Parkinson’s disease symptom monitoring technology more scalable and flexible by taking it mobile.
GLN makes the FDA-cleared Kinesia technology platform, which uses a patient-worn sensor and PC tablet-based software to quantify and monitor motor-related symptoms of Parkinson’s. While it’s found traction in the clinical trials market with companies developing new treatments for Parkinson’s, the company says the price point has kept it from widespread use in traditional patient care.
The current system comprises a sensor device that a patient with Parkinson’s disease wears on his finger as he performs tasks. Along with the sensor, the patient kit includes a tablet with broadband connectivity that instructs the patient through assessments, collects data from the sensors and pushes data to the cloud. Via a web portal, clinicians can access reports on patients’ progress.
The app should be available by the end of 2014 in the U.S. and Europe, Cleveland-based GLN said.side from use in monitoring disease progression and evaluating how new therapies affect clinical trial participants’ Parkinson’s systems, the Kinesia system can also help neurologists fine-tune the settings of deep brain stimulation devices after they’ve been implanted. The sensor captures linear acceleration and angular velocities, and clinically validated algorithms in GLN’s software turn them into scores that can help clinicians gauge the severity of a tremor at a given time more: http://medcitynews.com/2014/04/remote-monitoring-parkinsons-disease-symptoms/#ixzz32da3dhPF


By Deanna Pogorelc MedCity News

Wednesday, May 21, 2014

"LIFT” SPOON NOT JUST FOR CONVENIENCE

 
Lift Labs, a San Francisco based business, developed the “Lift” spoon basically to enable people with movement disorders and tremors to eat comfortably without spilling their “soup” before getting it from the bowl to their mouth.  The device senses a tremor when it is first picked up and uses stabilizers to counter the tremor, keeping the contents of the spoon steady.  It has a rechargeable battery so it will always be ready to use.  Lift Labs is promising more attachments beside the spoon, such as a fork and a key holder will be available soon.
Now a young researcher from the University of Michigan, Dr. Kelvin L. Chou, has found that the “spoon” is not just convenient, but actually helps reduce tremors.   This clever fellow tested 15 PARKINSON’S DISEASE patients on three different tasks: holding something in the spoon; eating with the spoon and transferring objects from the spoon to a cup about a foot away.  (He actually used small foam blocks instead of actual food.)  Subjects were tested with the “spoon” turned off and then again with it turned on.  While both subjects and the investigator were supposedly blinded, because of the effect of the device, true blinding might not be possible.
With the exception of two subjects hose tremors were so severe that use of the device was not helpful, the rest saw a reduction of their tremors of between 71% and 76% as measured with an accelerometer.  Using the Fahn-Tolosa-Marin Tremor Rating Scale (TRS), all subjects showed a significant improvement on all three tasks when the device was turned on.  Improvement in this case meant going from “spilling to minimal spilling”.  Tremor was still present, but most of the subjects were impressed with the device and wanted to buy one when it becomes commercially available.
The device, called the Lift Ware Stabilizer, is now available and can be ordered from liftlabsdesign.com.  It costs $295.00, but comes with a 30-day money back guarantee.  Lift Labs says the cost works out to about 27 cents a meal for a year.
Handheld Device Reduced Tremors. Medscape. Mar. 11, 2014 
Review by Marcia McCallPicture Credit

GENETICS OF PARKINSON’S DISEASE IS TOPIC OF NEW RESEARCH

genetics
 
The Parkinson’s Progression Markers Initiative  (PPMI) is an ongoing study looking for biomarkers in biological samples and imaging data from an international base of people with Parkinson’s disease who are part of a large national study.  Presently, over 800 individuals are involved with PPMI clinical trials at 32 sites.  In looking for biomarkers, such as a particular blood substances, or other physical processes that might predict the risk of PARKINSON’S DISEASE, researchers are hoping to find ways and means to both predict and treat the disease as early as possible and to target areas where drugs can be developed faster and more effectively.  Symptoms that have a demonstrated risk factor are loss of sense of smell and sleep behavior disorders are the subjects of other areas of research the PPMI. This study has already identified some blood markers such as the LRRK2 gene and the presence of alpha synuclein (SNCA gene) that are clearly connected to the disease, but the mechanism of operation is not yet clear.
Now they are further refining the search and are enrolling 250 subjects who are known to carry these genes and have symptoms of PARKINSON’S DISEASE and another 250 subjects who carry the genes but have no symptoms.  These subjects will be followed for at least 5 years.  At present, only about five or ten percent of all people with PARKINSON’S carry the genetic mutation.  However, knowledge learned from the genetics of these people will ultimately inform better understanding of the disease process. Of special interest are people of Eastern European descent who have relatives affected by PARKINSON’S DISEASE.
“Studying individuals with genetic mutations associated with PARKINSON’S can accelerate our research toward a PD biomarker and more effective treatments: said Stuart Factor, D.O., who is director of the Emory University Comprehensive Parkinson’s Disease Center and the director of the Emory Movement Disorders Center.  The large-scale extent of the PPMI research is already bringing scientific insights that will strengthen the efforts to find therapies that will modify or change the course of this disease.  This is an observational study that is seeking information and samples from participants.  Participants will not be involved in taking any experimental medication or undergoing any experimental procedures. Individuals who would like to be a part of this large undertaking should visit the Michael J. Fox Parkinson’s Progression Markers Initiative web page for further information.
 
http://medical express.com/news/2014-03-genetics-parkinson-disease.html
 
written by Marcia McCall
 
Picture Credits

EARLY ASSESSMENT OF DEMENTIA RISK IN PARKINSON’S DISEASE

dementia magnet
 
PARKINSON’S DISEASE is usually considered a “movement disorder”, with symptoms of tremor, rigidity and slowness that affect a person’s ability to move.  But a small percentage of people diagnosed with PARKINSON’S DISEASE go on to develop cognitive impairments, dementia or even Lewy body dementias.
“This study opens the door to further research, for example, on medication or on non-pharmacological approaches such as transcranial magnetic stimulation.  It’s important for these patients to be identified very quickly before they develop dementia so that a therapeutic approach can be adapted to their specific needs”, says Dr. Oury Monchi, the principal investigator of this study.
Dr. Monchi and Dr. Hanganu and their team of researchers affiliated with the Universitè de Montrèal, used magnetic resonance imaging to find there was a thinning and atrophy in some brain regions of people with mild cognitive impairment who were diagnosed in early stages of PARKINSON’S DISEASE.  They discovered that as the disease progressed, the thinning and atrophy of these areas progressed along with an increase in cognitive decline.  The study followed a cohort of 32 subjects in the early stages of PARKINSON’S DISEASE and a control group of 18 healthy subjects for a period of 20 months.
Cortical thinning has been proven to occur corresponding to the progression of the disease but has not been studied in relation to the development of cognitive impairment.  This study found a more rapid progression of thinning in the temporal, occipital, parietal and supplementary motor areas of patients with mild cognitive decline as compared to patients who had no cognitive impairments and healthy controls. They also found that the amygdala and nucleus accumbens also lost significant volume in patients with cognitive impairments. As a specific pattern of deterioration in these brain regions correlates to the presence of mild cognitive impairment in the early stages of PARKINSON’S DISEASE, these findings could lead to a biomarker predicting the subsequent development of dementia.
A. Hanganu, C. Bedetti, C. Degroot, B. Mejia-Constain, A.-L. Lafontaine, V. Soland, S. Chouinard, M.-A. Bruneau, S. Mellah, S. Belleville, O. Monchi. Mild cognitive impairment is linked with faster rate of cortical thinning in patients with Parkinson’s disease longitudinallyBrain, 2014; DOI:10.1093/brain/awu036
 
Review by Marcia McCall
 
Picture Credits