Joseph Friedman, M.D. |
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.
I AM NOT RESPONSIBLE FOR IT'S CONTENTS. I AM JUST A COPIER OF INFORMATION SEARCHED ON THE COMPUTER. PLEASE UNDERSTAND THE COPIES ARE JUST THAT, COPIES AND AT TIMES, I AM UNABLE TO ENLARGE THE WORDING OR KEEP IT UNIFORMED AS I WISH. IT IS IMPORTANT TO UNDERSTAND I AM A PERSON WITH PARKINSON'S DISEASE. I HAVE NO MEDICAL EDUCATION,
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.
PLEASE DISCUSS THIS WITH YOUR DOCTOR, SHOULD YOU HAVE ANY QUESTIONS, OR CONCERNS. NEVER DO ANYTHING WITHOUT TALKING TO YOUR DOCTOR FIRST..
I DO NOT MAKE ANY MONEY FROM THIS WEBSITE. I VOLUNTEER MY TIME TO HELP ALL OF US TO BE INFORMED.
I WILL NOT ACCEPT ANY ADVERTISEMENT OR HEALING POWERS, HEALING FROM HERBS AND ETC. UNLESS IT HAS GONE THROUGH TRIALS AND APPROVED BY FDA. IT WILL GO INTO SPAM.
THIS IS A FREE SITE FOR ALL WITH NO ADVERTISEMENTS
THANK YOU FOR VISITING! TOGETHER WE CAN MAKE A DIFFERENCE!
TRANSLATE
Saturday, December 6, 2014
Psychosis in Parkinson's disease: An LTC perspective
Say No to Parkinson's with Regular Exercise
By Express News Service
Friday, December 5, 2014
Off switch' for pain discovered: Activating the adenosine A3 receptor subtype is key to powerful pain relief
sciences at SLU, demonstrated that turning on a receptor in the brain and spinal cord counteracts
chronic nerve pain in male and female rodents. Activating the A3 receptor -- either by its native
chemical stimulator, the small molecule adenosine, or by powerful synthetic small molecule drugs
invented at the NIH -- prevents or reverses pain that develops slowly from nerve damage without
causing analgesic tolerance or intrinsic reward (unlike opioids).
multi-billion dollar societal cost. Current treatments are problematic because they cause intolerable
side effects, diminish quality of life and do not sufficiently quell pain.
"pathways": circuits involving opioid, adrenergic, and calcium channels.
interactions between molecular-level components that lead to pain. While adenosine had shown
potential for pain-killing in humans, researchers had not yet successfully leveraged this particular
pain pathway because the targeted receptors engaged many side effects.
receptor subtype is key in mediating the pain relieving effects of adenosine.
provide a breakthrough step towards an effective treatment for chronic pain," Salvemini said. "Our
findings suggest that this goal may be achieved by focusing future work on the A3AR pathway, in
particular, as its activation provides robust pain reduction across several types of pain."
inflammatory and anticancer agents and show good safety profiles. "These studies suggest that A3AR
activation by highly selective small molecular weight A3AR agonists such as MRS5698 activates a
pain-reducing pathway supporting the idea that we could develop A3AR agonists as possible new
therapeutics to treat chronic pain," Salvemini said.
- J. W. Little, A. Ford, A. M. Symons-Liguori, Z. Chen, K. Janes, T. Doyle, J. Xie, L. Luongo, D. K. Tosh, S. Maione, K. Bannister, A. H. Dickenson, T. W. Vanderah, F. Porreca, K. A. Jacobson, D. Salvemini. Endogenous adenosine A3 receptor activation selectively alleviates persistent pain states. Brain, 2014; DOI: 10.1093/brain/awu330
Preliminary study suggests Parkinson's drugs safe for the heart Last updated: 4 December 2014
Stem Cells from Adult Nose Tissue Used to Cure Parkinson’s Disease in Rats
ITSCs are stem cells taken from tissue that would generally be discarded after an adult patient undergoes sinus surgery.
The team then tested how the ITSCs would behave when transplanted into a group of rats with Parkinson’s disease. Prior to transplantation, the animals showed severe motor and behavioral deficiencies. However, 12 weeks after receiving the ITSCs, the cells had migrated into the animals’ brains and functional ability was not only fully restored, but significant behavioral recovery was witnessed, too. In another positive sign, no tumors were found in any of the animals after the transplantations, something that also has been a concern in stem cell therapy.
“Due to their easy accessibility and the resulting possibility of an autologous transplantation approach, ITSCs represent a promising cell source for regenerative medicine,” said UB’s Barbara Kaltschmidt, Ph.D., who led the study along with Alexander Storch, M.D., and Christiana Ossig, M.D., both of Dresden University. “The lack of ethical concerns associated with human embryonic stem cells is a plus, too.”
“In contrast to fighting the symptoms of Parkinson’s disease with medications and devices, this research is focused on restoring the dopamine-producing brain cells that are lost during the disease,” said Anthony Atala, M.D., Editor-in-Chief of STEM CELLS Translational Medicine and director of the Wake Forest Institute for Regenerative Medicine. "These cells are easy to access and isolate from nasal tissue, even in older patients, which adds to their attraction as a potential therapeutic tool.”
###
The full article, “Intrastriatal transplantation of adult human neural crest-derived stem cells improves functional outcome in Parkinsonian rats” can be accessed at http://www.StemCellsTM.com.
http://bio-medicine.org/medicine-news-1/Stem-Cells-from-Adult-Nose-Tissue-Used-to-Cure-Parkinson-u2019s-Disease-in-Rats-138259-2/
Wednesday, December 3, 2014
SONOGRAPHY FOR DIAGNOSIS OF PARKINSON'S DISEASE
Transcranial sonography is a non-invasive diagnostic technique that makes use of sound waves to create a digital image to aid the diagnosis of Parkinson's Disease. The sound waves are typically produced by a transducer. Strong, short electrical pulses from the ultrasound machine make the transducer ring at the desired frequency. Materials on the face of the transducer enable the sound to be transmitted efficiently into the body. The sound wave is partially reflected from layers between different tissues. Sound is reflected anywhere there are density changes in the body. Some of the reflections return to the transducer. The return sound wave vibrates the transducer, which turns the vibrations into electrical pulses that travel to the ultrasonic scanner where they are processed and transformed into a digital image
For more information go to : http://www.biomedcentral.com/1471-2377/10/9
The primary area of the brain concerning Parkinson's Disease is the substantia nigra. The substantia nigra echogenic area was found to be larger in those people with Parkinson's Disease. Substantia nigra echogenicity was also larger in
males than in females. Age did not correlate with substantial nigra echogenicity in any group. After multivariate analysis, only the substantia nigra hyperechogenicity was associated with the diagnosis of Parkinson's Disease.
Transcranial sonography consequently showed good diagnostic validity for the diagnosis of Parkinson's Disease.
However, in a previous study the diagnostic accuracy in the early stages of Parkinson's Disease was not sufficient for routine clinical use.
Reference : Journal of Ultrasound in Medicine [2014] 33 (12) : 2069-2074 (A.AlonsoCánovas,
J.L.López-Sendón, J.Buisán, A.deFelipe-Mimbrera, M.Guillán, N.GarcÃa-Barragán,
I.Corral, M.C.Matute-Lozano, J.Masjuan, J.C.MartÃnez-Castrillo, U.Walter)
Complete abstract : http://www.ncbi.nlm.nih.gov/pubmed/25425362
http://www.viartis.net/parkinsons.disease/news/141202.pdf
mail@viartis.net
©2014 Viartis
Proper copper levels essential to spontaneous neural activity
Two New Therapies for Parkinson’s Disease Patients to get Excited About: Vaccines and Monoclonal Antibodies
In September 2012, the What’s Hot in Parkinson’s Disease? blog featured a new therapy that at that time had entered into human testing. The Austrian company AFFiRiS A.G. launched a two-year long clinical trial of a vaccine designed to stop Parkinson’s disease progression. In this month’s What’s Hot Column we will bring you an update on the vaccine and an update on another therapy (monoclonal antibodies) for the treatment of Parkinson’s disease.
Parkinson’s disease is a neurodegenerative condition associated with deposition of a brain protein known as alpha-synuclein. This protein clumps and spreads throughout the brain, and the spread of the protein parallels the progression of Parkinson’s disease. Many experts believe that much of the damage in Parkinson’s disease traces to the brain’s failure to process, and to clear these bad proteins.
The idea underpinning the Parkinson’s disease vaccine is simple. Patients receive injections with the hope that these injections will stimulate an immune system response against alpha-synuclein, and that antibodies will attack these brain proteins; and ultimately clear them. Thirty-two human Parkinson’s disease patients were part of a two year safety and tolerability study called the PD01A project. The study ultimately would be the first step in modifying disease progression in human Parkinson’s disease patients.
The preliminary results of the study revealed the vaccine was safe and well-tolerated, though relatively few people were tested. Half of those in the study developed antibodies against alpha-synuclein, and for those patients the investigators believe that the appearance of antibodies was a positive sign. Why some patients did not develop antibodies remains unknown, and a follow-up study will address the use of booster vaccine shots.
Using a different approach, Prothena and Roche are developing monoclonal antibodies (i.e. antibodies that are specific and only bind to a single substance) that will directly target alpha-synuclein. What is the difference between monoclonal antibodies and a vaccine? The monoclonal antibodies are injected into the patient as a direct therapy, whereas the vaccine shot stimulates the immune system to produce antibodies against alpha-synuclein. Both are considered under the umbrella of “immunotherapies.” Two dose-finding and human safety trials of the first Parkinson’s monoclonal antibody PRX002 are underway.
It is important to keep in mind that not all experts believe that removal of these brain proteins will result in clinically meaningful changes and/or disease modification. Additionally, we must keep in mind that one highly publicized attempt to target amyloid in Alzheimer’s patients led to serious safety concerns, and termination of a vaccine study known as AN1792 because several patients developed a meningoencephalitis.
What patients need to know about the vaccine and about monoclonal antibodies is that both are still in the very early stages of testing, but that the idea of boosting immunity and using immunotherapy is novel and promising. Safety, tolerability, and clinical efficacy will need to be demonstrated before the vaccine and the monoclonal antibodies can move into the next phase of clinical testing. Our hope is that clearance of the Parkinson’s associated brain proteins will translate into disease modification. A similar approach is also being tested in other diseases such as Alzheimer’s disease, diabetes, and atherosclerosis. These are definitely potential Parkinson’s disease therapies to get excited about.
Selected References:
- Lindström V, Ihse E, Fagerqvist T, Bergström J, Nordström E, Möller C, Lannfelt L, Ingelsson M. Immunotherapy targeting α-synuclein, with relevance for future treatment of Parkinson's disease and other Lewy body disorders. Immunotherapy. 2014 Feb;6(2):141-53. doi: 10.2217/imt.13.162. Review. PubMed PMID: 24491088.
- Ghochikyan A, Petrushina I, Davtyan H, Hovakimyan A, Saing T, Davtyan A, Cribbs DH, Agadjanyan MG. Immunogenicity of epitope vaccines targeting different B cell antigenic determinants of human α-synuclein: feasibility study. Neurosci Lett. 2014 Feb 7;560:86-91. doi: 10.1016/j.neulet.2013.12.028. Epub 2013 Dec 19. PubMed PMID: 24361548; PubMed Central PMCID: PMC3928627.
- Sanchez-Guajardo V, Annibali A, Jensen PH, Romero-Ramos M. α-Synuclein vaccination prevents the accumulation of parkinson disease-like pathologic inclusions in striatum in association with regulatory T cell recruitment in a rat model. J Neuropathol Exp Neurol. 2013 Jul;72(7):624-45. doi:10.1097/NEN.0b013e31829768d2. PubMed PMID: 23771222.
- Rohn TT. Targeting alpha-synuclein for the treatment of Parkinson's disease. CNS Neurol Disord Drug Targets. 2012 Mar;11(2):174-9. Review. PubMed PMID:22483285.
- Ha D, Stone DK, Mosley RL, Gendelman HE. Immunization strategies for Parkinson's disease. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S218-21. doi:10.1016/S1353-8020(11)70067-0. Review. PubMed PMID: 22166440.
- Schneeberger A, Mandler M, Mattner F, Schmidt W. Vaccination for Parkinson's disease. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S11-3. doi:10.1016/S1353-8020(11)70006-2. Review. PubMed PMID: 22166404.
- Hutter-Saunders JA, Mosley RL, Gendelman HE. Pathways towards an effective immunotherapy for Parkinson's disease. Expert Rev Neurother. 2011 Dec;11(12):1703-15. doi: 10.1586/ern.11.163. Review. PubMed PMID: 22091596; PubMed Central PMCID: PMC3263336.
Help with dignity ! Medications possibly free for those in need!
I will run this several times during the year. This could happen to anyone of us. Don't go without your medicine. This may help you.
Help with dignity
The mission of NeedyMeds has been to make information about assistance programs available to low-income patients and their advocates at no cost. Databases such as Patient Assistance Programs and Disease-Based Assistance, government programs and other types of assistance programs are the crux of the free information we offer online.
RxAssist
RxAssist offers a comprehensive database of pharmaceutical companies’patient assistance programs which provide free medications to people who cannot afford to buy their medicine. RxAssist also provides practical tools, news and articles so that health care professionals and patients can find the information that they need. All in one place.
Rx Outreach is managed by Express Scripts Specialty Distribution Services, Inc. (ESSDS), a fully-licensed mail order pharmacy that is committed to making the use of prescription drugs safer and more affordable. Rx Outreach is not a prescription insurance program nor an Internet pharmacy.
1-888-4PPA-NOW (1-888-477-2669) Their mission is to increase awareness of patient assistance programs and boost enrollment of those who are eligible. The Partnership for Prescription Assistance offers a single point of access to more than 475 public and private patient assistance programs, including more than 180 programs offered by pharmaceutical companies.
There is an app for smartphones called Good RX .
HELPFUL ITEMS TO GIVE TO THOSE WITH PARKINSON'S DISEASE COPIED FROM PARKINSON'S JOURNEY
Posted: 28 Nov 2014 09:54 AM PST
It’s that time of year again and so, here’s the 3rd annual list of great ideas for gifts for people with Parkinson’s disease and is suitable for those who live with other chronic illnesses. If you have ideas/suggestions not on the list, feel free to add to the list by leaving a comment.
Readers Choices:
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Tuesday, December 2, 2014
Google's Latest: A Spoon That Steadies Tremors
New Online Tool Trains Doctors to Diagnose and Treat Parkinson's
Tue Dec 2, 2014 6:00am ESTis not responsible for the content in this press release.
Kelly Mills
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