parkinson's disease

New trial: Fetal Transplantation Usage for Treatment of PD: By Dr. De Leon

Nearly 30 years ago, the novel treatment which propel me into medicine but not just medicine but neurology and Parkinson’s disease was fetal brain transplantation into PD person’s brain in an attempt to halt disease. After several decades the procedure was banned here in the States and an unofficial moratorium was placed elsewhere on this type of trial. For those 300 plus patients which did receive this “novel” treatment, the results were a mixed bag. While the procedure showed some improvement in younger and less severely affected Parkinson’s patients, “many patients experienced off-drug ‘runaway‘ dyskenesias which resembled a lot like chorea at times. These patients then had to be treated with Tetrabenazine, Reserpine as well as pallidotomies and DBS to attempt to control symptoms.

Now, using a different technique by researchers with a new PD population a trial is underway to test the cell based therapy, which according to Dr. Roger Baker (lead investigator) professor of clinical neuroscience at Cambridge University in the United Knigdom is by any means designed to be a cure but rather another method by which dopamine is better (hopefully) delivered into the brain.

some of the previous trials problems were believed to be due to site implantation since the fetal nigral cells containing dopamine could not be directly placed into the hosts nigra, they were placed in the near by striatum. Uneven re-enervation of these cells is believed to be one of the causes of ‘runaway’ dyskenesias as well as the presence of serotonergic neurons from the donor raphe nucleus which can also produce dopamine in unregulated fashion. Further problem seen with initial procedure back in the 1980’s and 90’s  is the yet unaccounted reason for  the development of Lewy bodies in the grafted (donor) cells.

Because the European community ( where trials began) have always insisted on the merit of this procedure as a possible treatment a TRANSEURO consortium was gather to further discuss results. they have found there is a specific type of patient that responds best- so now they are recruiting patients between ages of 30-68 who have mild to moderate illness with minimal to no dyskenesias. now these patients will receive 3 fetal nigras on each side vs. the 2 used on each side in the past. these patients will receive a year worth of immunosuppression and be observed for 3 years ( believed to be time frame for maximal effect). they hope to control some of the emergence of dyskenesias by their new harvesting protocol which will decrease or minimize the number of serotonin containing neurons. hope is to improve dopamine related symptoms however, the non-dopaminergic effects will still remain unaffected.

Once again, I see hope ( but a smaller ray of sunshine than when I first began this trajectory) for a future generation of PD patients for a better life as I had once envision as a young neuroscientist. If this proves to be successful it will undoubtedly unleash a whole new era in the science of stem cell therapy research for the treatment of neurological diseases.  However, I along with other more prominent neurologists like Dr. Anthony  Lang  caution those considering participating in such trial for it will be not a cure PD and if it works it will only provide limited  results affecting only the symptoms related to dopamine.  Keep in mind that a big part of the spectrum of PD is non-dopamine related and these are in fact the things which I believe as a doctor and patient which cause most PD persons problems such as gait instability, mood and sleep problem’s, along with declining cognition. so in the end, aside from boosting science in a new direction I don’t foresee this to replace DBS which has a long trajectory of excellent outcome and compared to fetal transplantation a much les invasive and aggressive surgery without the need for whole body immunosuppression which is known to carry many risks of its own accord. perhaps may have a niche for usage if works in those with young onset PD with Parkin gene mutation

Others of course like Dr. Baker are much more optimistic and believe that this may actually some day be first line therapy. highly doubt based on my years of experience with this disease and its complexities but one never knows….

Food for thought….

Sources:

Robinson, R. (October 20, 2016); “Fifteen years later, a new trial set to test fetal transplants again is for Parkinson’s Disease.” Neurology Today. 16(20)13,23.

 

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Thinking Outside the Brain for a Parkinson’s Cure : By Dr. De Leon

Thinking Outside the Brain for a Parkinson's Cure : By Dr. De Leon

I don’t think inside the box, I don’t think OUTSIDE the box, I don’t EVEN KNOW where the box is!”- unknown

The other day while I was giving a talk about how to diagnose PD, I was giving my usual spill about ” in the hands of a specialist like myself- accuracy is 95%,” when someone in the audience asked me a very thought provoking question. So, how early can you diagnose with such certainty? Therein lies the BIG Problem in why we need biomarkers and be able to think outside of our current diagnostic criteria!

In reality, I told her it is still very accurate above 90% for someone that has a lot of experience -that’s where art meets medicine …you get your “intuition” about things based on past knowledge and experience and are able to predict with fair accuracy and since at this point there is NO difference in treatment really between one type of Parkinson syndrome or another it does not much matter at the beginning…However, where it becomes a problem is being able to predict outcome and assign patients to studies because you have to follow strict criteria and even if you just KNOW that someone has Parkinson’s or an atypical variant you have to back it up…and as you all know EVERYONE is different so it may take some one ten years to develop all 4 cardinal symptoms of Parkinson’s while someone else only 2. So, it is hard to at present time to make a lot of head way in the discovery of new medications that might be beneficial to slow or stop the progression of early stage of Parkinson’s because unfortunately there is still a lot of variability in early diagnostic accuracy depending on the field. Even among neurologist not Parkinson’s specialist, a published study indicated that for PD patients who had symptoms less than 5 years, they were wrong 50% of the time. These patients turned up to have another reason for their Parkinsonism which translates to automatic failure of any drug being studied since 50% of the patients in any given trial of early PD may not even respond because they don’t have the right diagnosis!

So, I realized that in order for us to start thinking OUTSIDE the BOX we need to FIRST get a CLUE of where the BOX is – what Parkinson’s looks like- acts like, presents like so THAT EVERYONE IS on the same page and able to diagnose with same degree of accuracy!!! This needs of course to go back to medical school, residency and communities and we all as PD advocates can play a role in educating health staff and other health professionals about Parkinson’s. The better we are at recognizing early symptoms the better chance we have for participating in neuro-protective trials as well as be able to determine biomarkers early on.

A lot of money and research is being channeled to the finding of these biomarkers in the recent years. According to research initiated by the MJFOX foundation, we may have insight into possible new biomarkers coming from the retina, colon, or skin which could lead to not early detection but a cure for PD.

For a number of years, neuroscientist have known that alpha-synuclein the abnormal protein seen in Parkinson’s is also found outside of the central nervous system. This protein is a major constituent of Lewy body disease another Parkinson’s like disease. However, alpha-synuclein which is located largely at the ends of neurons plays a part in both familial and sporadic Parkinson’s disease as well.

Through the usage of very powerful machines and equipment known as optical coherence tomography (OCT) which takes high resolution pictures of the retina, scientists and doctors have found that PD patients have thinner retinas compared to healthy individuals.
At this point, they are not sure if there is enough evidence to use as a biomarker because they are not certain how specific it is to Parkinson’s since it also has been seen in Alzheimer’s patients who had Parkinson’s as a co-morbidity.
Alpha-synuclein is normally present in several types of retinal cells…so the possibility of serving as a biomarker exists either by accumulation or (absence) at this time no cells have been found in PD patients.

Another place that accumulates alpha-synuclein outside the brain is the colon. Published studies have revealed that immunostaining for Alpha-synuclein in living Parkinson’s individuals results in a positive outcome in 69-100% of the time but not seen in MSA ( multi -system atrophy) patients. Another study showed that these findings preceded the clinical motor symptoms. So far, results which are small have been mixed. They are easy to attain because of flexible sigmoidoscopy can access distal colon easily plus screening is required of all over 50 years of age. However, not all pd people showed pathology. Some explanations have been given which include variation of tissue involvement, change in pathology over time and perhaps unsuitability of this being used as a biomarker.

The third place where scientists are looking for a possible biomarker outside the central nervous system which is also full of alpha -synuclein is the skin. One reason, people are interested in this area is because of the new wave of knowledge and thinking about the etiology of Parkinson’s. Since, we now know that there is a prodrome period of non- motor & autonomic symptoms that precede the development of the motor symptoms, researchers believe that perhaps alpha-synuclein pathology starts outside the brain and migraines to the brainstem.
Also, studies have suggested that peripheral nervous system is equally involved in Parkinson’s. Evidence of this was suggested in an issue of Brain in 2008 where Parkinson’s patients were found to have cutaneous denervation resulting in higher threshold for heat and touch but decrease for pain.

Because the skin is not only easily accessible but also has a plethora of autonomic involvement, and many autonomic nerves making it a great candidate for study.
A study in the Journal of Neuropathology & Experimental Neurology proposed that the skin may be a beneficial site for diagnostic predictability since 70% of PD cases and 40% of PD with dementia revealed positive alpha-synuclein immunoreactivity while absent in other Parkinson plus syndromes like MSA ( multisystem atrophy) , PSP( Progressive supranuclear palsy), & CBGD (Cortico-basal-ganglia-degeneration). The results are very promising but still need to be validated and compared longitudinally and with autopsy confirmed cases of PD.

Out of all these the most promising is the skin biopsies as a possible biomarker..easy and readily accessible and this far able to differentiate between Parkinson’s and other Parkinson’s plus syndromes.
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For more information on the topic: MJFOX research on biomarkers
Haugh, Zac., Movement Disorder Focus: Alpha-synuclein :Thinking Outside the Brain. Practical Neurology. Vol. 13, No.2, March 2014

Dr. M. De Leon is a movement disorder specialist on sabbatical, PPAC member and research advocate for PDF (Parkinson’s Disease Foundation); Texas State Assistant Director for PAN (Parkinson’s Action Network). You can learn more about her work at http://www.facebook.com/defeatparkinsons101 you can also learn more about Parkinson’s disease at www.pdf.org or at www.wemove.org; http://www.aan.org, http://www.defeatparkinsons.blogspot.com

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