Podcasts

Episode 113: Cell-Based Therapies for Parkinson’s Disease

Researchers have been investigating cell-based therapies for treating Parkinson’s disease (PD) for some time now, using a variety of materials and methods. Two approaches have been to implant dopamine-producing cells or to induce cells already in the brain to become dopamine-producers. We asked Dr. Roger Barker, Professor of Clinical Neuroscience at the University of Cambridge in the United Kingdom, to summarize what has been learned so far and based on that, to give his perspective on where the field may be headed. The field is still in the experimental stages, and he cautions about what people with PD should ask when considering entering a clinical trial of cell-based therapy and what they may expect in terms of symptom management and disease progression.

Released: September 21, 2021

Podcasts

Episode 17: Stem Cells and Parkinson’s

Stem cells – those cells that can give rise to so many cell types in the body – have been touted as the cure-all for a variety of diseases, including Parkinson’s. But to date, attempts at stem cell transplantation into the brain have fallen short. Parkinson’s is one of the most complex diseases, with a variety of motor and non-motor symptoms and an impact on many systems of the body. Just inducing a cell to make dopamine is not the whole answer. But stem cells are still useful for drug screening and disease modeling. Dr. Michael Okun, National Medical Advisor of the Parkinson’s Foundation, Chairman of the University of Florida Department of Neurology and Co-Director of the University of Florida Center for Movement Disorders and Neurorestoration, a Parkinson’s Foundation Center of Excellence, puts the field into perspective and where it’s going.

Released: December 5, 2017

Podcasts

Episode 108: The Golden Year for Testing Disease Modifying Drugs

Most people with Parkinson’s disease (PD) first seek medical care when they recognize or are troubled by symptoms – often stiffness, slowness of movement, or tremor. They may go on drug therapy at the time of diagnosis or, typically, within six to twelve months to relieve those symptoms.

In order for researchers and drug developers to test and ultimately find drugs that can slow the progression of the disease, they need to test those drugs in people who are not already on medications to alleviate symptoms and compare them to similar people taking a placebo. Currently there is no blood test or other biomarker to measure progression, so the most common and straightforward way for drug trials to judge progression is to observe signs and symptoms in people not receiving symptomatic medications such as levodopa, dopamine agonists, or other drugs that make symptoms less apparent.

Dr. Robert Hauser, Director of the Parkinson’s Disease and Movement Disorders Center at the University of South Florida in Tampa, urges people early in the course of their disease to enter a clinical trial as soon as they receive a PD diagnosis and before they go on medication. The longer that they can be observed before taking a potential disease-modifying medication, the greater the ability of researchers to detect changes, or in the case of a drug in development, if successful, not to see changes. However, patients who can go up to a year without medication are in short supply, in part because patients often wait to seek medical help until they want medication. As Dr. Hauser wrote in a medical publication a few years ago, “… why see a doctor when you don’t need treatment?”

But the answer is because people very early in the course of their disease are vital to finding drugs that can slow progression. Dr. Hauser terms the critical period of about one year between the time of first motor symptoms appearing to initiating symptomatic therapy the “Golden Year” for participation in disease modifying clinical trials. So, he wrote, “It is critical that care providers and patients don’t unknowingly waste this golden year.” In this episode he lays out the problem, has messages for patients and providers, and tells how such a system of referral to entry into clinical trials can work.

Released: July 13, 2021

Podcasts

Episode 16: Can an Asthma Drug Prevent Parkinson’s?

Alpha-synuclein is a protein in the human brain that is linked with the development of Parkinson’s disease. An important scientific paper came out in September 2017 describing how some common drugs, already approved by the Food and Drug Administration for other purposes, may lower the production of alpha-synuclein – and potentially protect against Parkinson’s. Dr. David K. Simon, Director of the Parkinson's Disease and Movement Disorders Center at Beth Israel Deaconess Medical Center in Boston, a Parkinson’s Foundation Center of Excellence, describes what the researchers did and what they found.

Released: November 21, 2017

Podcasts

Episode 79: How Clinical Studies Help People with PD

Clinical studies fall into two main categories – observational and interventional. An observational study is non-experimental. Researchers observe the effects of a risk factor, such as an inherited gene, or air quality, or a treatment that has already been applied. Researchers have no control over the variables. Such a study can show a correlation between the variable and the observed outcome but cannot prove that one caused the other. In an interventional study, such as a clinical trial, researchers introduce an intervention, such as a drug treatment, exercise, or meditation and then observe the results. A rigorous form of an interventional trial divides people into two or more groups, one receiving the intervention and, for example, the other receiving a placebo or standard treatment. Both types of study are valuable, and sometimes the findings from an observational study can suggest a hypothesis and lead investigators to design a clinical trial.

The Parkinson’s Foundation PDGENEration: Mapping the Future of Parkinson’s Disease study is a flagship initiative providing free genetic testing and genetic counseling to look at specific Parkinson’s-related genes and connect their presence with disease course, medication usage, and other outcomes. Besides potentially helping people with Parkinson’s manage their disease better, the results may empower clinical trial design, such as seeing how a medication may affect the disease depending on what type of gene is present. Dr. Tanya Simuni, Chief of Movement Disorders at the Northwestern University Feinberg School of Medicine in Chicago and Dr. Michael Schwarzschild, director of the Molecular Neurobiology Laboratory at Massachusetts General Hospital in Boston, discuss some aspects of clinical studies in PD and why it is important for people with PD to participate in them. Both institutions are Parkinson’s Foundation Centers of Excellence.

Released: April 21, 2020

Videos & Webinars

Neuro Talk: Top 3 Parkinson’s Disease Research Areas We Fund

Why is research important for understanding Parkinson’s disease (PD)? In our latest Neuro Talk, Parkinson's Foundation Chief Scientific Officer James Beck, PhD, outlines the Foundation’s research strategy and some exciting Parkinson’s research being conducted right now. Dr. Beck highlights three key areas of PD research funded by Parkinson’s Foundation grants: biology, neural circuitry and symptoms.

Videos & Webinars

Neuro Talk: How Does Basic Parkinson’s Research Get Us Closer to a Cure?

How can understanding the basic biology of Parkinson’s disease (PD) help us prevent Parkinson’s altogether? In our latest Neuro Talk, Parkinson's Foundation Chief Scientific Officer James Beck, PhD, discusses what basic research is and how funding researchers early in their careers can lead to scientific breakthroughs. He also highlights the role that Parkinson’s Foundation initiatives like PD GENEration: Mapping the Future of Parkinson’s Disease and Reach Further play in furthering PD research.

Videos & Webinars

Neuro Talk: What To Know About Parkinson’s Disease Statistics

Did you know that Parkinson’s disease (PD) cases in the U.S. are expected to surpass 1.2 million by the year 2030? In our latest Neuro Talk, Parkinson's Foundation Chief Scientific Officer James Beck, PhD, outlines key statistics related to PD. He also shares insights from the Parkinson’s Prevalence Project, a research study conducted by the Parkinson’s Foundation to calculate the prevalence of Parkinson’s throughout North America.

Podcasts

Episode 73: Genetics and PD: What do we know so far?

New tools in genetics are providing researchers with insights into diseases never before obtainable. For Parkinson’s disease (PD), research promises to reveal specific genes and mutations that contribute to the risk of developing PD as well as mechanisms by which these genes act. Along these lines, the Parkinson’s Foundation has launched PD GENEration, a flagship initiative that offers free genetic testing and genetic counseling for people with PD. Participating and contributing one’s genetic data, DNA, and blood can help scientists advance their understanding of the disease, improve research and care, accelerate enrollment in clinical trials, and aid in the development of better treatments.

The PD GENEration initiative is another step in the development of personalized medicine. Participants receive results of their genetic testing as it pertains to PD, which may allow them to better manage their disease in the future.

In this podcast Dr. Martha Nance, medical director of the Struthers Parkinson’s Center in Minneapolis, Minnesota, a Parkinson’s Foundation Center of Excellence, talks about some of the genes related to PD that are under investigation, how they work, and what their effects are, both biologically and in terms of how they may influence the course of the disease.

Released: January 28, 2020

Videos & Webinars

Neuro Talk: Top Findings from the Parkinson’s Outcomes Project

What challenges are people with Parkinson’s disease (PD) facing and how can research help improve their lives? In our latest Neuro Talk, Parkinson's Foundation Chief Scientific Officer James Beck, PhD, outlines top findings from the largest-ever clinical study of Parkinson’s disease, the Parkinson’s Outcomes Project. This study captures the experiences of people with Parkinson’s and their care partners over time, to identify new and better ways to provide care and manage Parkinson’s disease.

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