BACKGROUND: Parkinson's disease is a condition of the brain affecting approximately six million people. It is most commonly characterized by slowness of movement, stiffness, shaking, and loss of balance. Parkinson's often develops after the age of 50. Although Parkinson's disease is one of the most common nervous system disorders for the elderly, it can affect young people too, usually because a form of the disease runs in their family. Nerve cells use a brain chemical called dopamine to control muscles. When the nerve cells in the brain that produce dopamine are destroyed as a result of Parkinson’s, the nerve cells in that particular part of the brain will not properly send messages. The result is the loss of muscle control. The damage gets worse over time. (

SYMPTOMS: Usually symptoms are mild at first. There might be a slight feeling that one foot may be stiff or there might be a small tremor when the disease first makes its appearance. As the disease progresses symptoms can include: slow blinking, difficulty swallowing, constipation, drooling, no expression in the face problems with balance, muscle pains, trouble moving, stiff muscles, shaking (tremors), stooped position, slowed speech or monotone voice, low blood pressure, confusion, anxiety, hallucinations, memory loss, fainting, depression, or dementia. (Source:

TREATMENT: A doctor may be able to diagnose the disease based on symptoms alone, but symptoms can be difficult to access in the elderly. Unfortunately, there is no known cure only a treatment plan to control symptoms. Medicines for Parkinson’s are designed to control symptoms usually by increasing levels of dopamine in the brain. Throughout the day the medications can wear off and symptoms can return. Parkinson’s requires the patient and doctor to work closely with each other to find the right treatment plan that works best. Common medications are Levodopa (L-dopa), Pramipexole (Mirapex), Selegiline (Eldepryl, Deprenyl), Amantadine or anticholinergic medications to reduce early or mild tremors, or Entacapone to help control movement. Other medications include: Memantine for cognitive difficulties, Antidepressants, Gabapentin for pain, Fludrocortisone for autonomic dysfunction, and Armodafinil for sleep disorders. (Source:

NEW TECHNOLOGY: Testing for Parkinson's can be expensive and time consuming. One of the newest breakthroughs for this disease is the Parkinson's Voice Initiative. Technology has been developed to test for symptoms using voice recordings. The voice tests are just as accurate as clinical tests with 99 percent accuracy and can be administered over the phone, resulting in reduced costs. The Parkinson's Voice Initiative believes that the impact of this test will reduce logistical difficulties (no need to do routine checkups), will become a cost-effective mass recruitment for treatment trials (perhaps obtaining a large database for new treatments to speed up the search for a cure), will have a high-frequency monitoring for individualized treatment options, and will result in population-scale screening programs. Calls can be placed based out of your county, including: USA, Brazil, Mexico, UK, France, Spain, Argentina, Canada, and New Zealand. (Source:

Max Little, Post Doctoral Research Fellow at MIT Media Lab talks about using the voice as a biomarker for Parkinson’s Disease.

How did the Parkinson's Voice Initiative start?

Dr. Little: We've been doing a lot of research on the extent to which voice could be used as a kind of 'dry biomarker' for Parkinson's Disease. We were interested in the question of whether or not this technology could be deployed over the telephone. We’ve been doing a lot of lab studies: lab recording is important to test the idea but the problem is, of course, that these lab recordings will not be accessible to a large number of people. In previous research we’ve been able to show that we can get a very high accuracy detection rate using lab-based voice recordings. It would seem natural that the telephone could be one of the ways of deploying this technology. So that was the purpose of the Parkinson’s Voice Initiative: to test out whether we can make this work over the telephone.

What kind of program did it take to implement this kind of study?

Dr. Little: What's required to implement this sort of research is an interactive voice recording service. We have a service in the UK that captures voice recordings using the standard telephony infrastructure that’s now very accessible. The service itself just captures the voice recordings but then we need to do the processing of these recordings afterwards; and this processing is fairly intensive. It requires a number of algorithms that are looking for specific features in the voice. It then requires machine learning algorithms that can make sense of those features.

So pretty complex stuff?

Dr. Little: It is quite complex. Certainly it’s using leading edge technologies -- for example computer science departments in universities around the world have been working on these kind of machine learning algorithms. We require those sorts of algorithms but we do have an advantage in the sense that the computing hardware is now becoming cheaper and faster so we can anticipate that in a few years time, the latest algorithms could run, for example on a smart phone in someone’s pocket.

So you could have it on your smart phone and just have doctors do diagnostic tests through their own smart phone?

Dr. Little: Yes, if that arrangement was valuable in a clinical practice of course.

You've done lab studies already, what were the results?

Dr. Little: In the lab studies we’ve done we’ve been able to show that we can get high detection accuracy – this is, accurately determining whether somebody has Parkinson’s or not. We are up to around 99% accuracy. This is now good enough to demonstrate screening capability. That’s the kind of technique that could be used in order to do triage, for example, to work out who might be at high risk of having the disease. The next stage is to pass that on to clinicians who could then do a more in-depth diagnosis, and as a result make appropriate treatment decisions.

What's wrong with the test we have right now for Parkinson’s?

Dr. Little: Well, one of the problems with test that we have right now is that it requires you to be in the clinic. It’s going to be very difficult to get a large number of people to visit in order to screen for the signs of the disease, for example. When you have to go to the clinic you have all these associated logistical difficulties. So part of the motivation for developing this technology is about trying to bring these tests to a wider audience, and to reduce the cost involved in trying to do mass screening.

It can even help without lining drug timing and dosage?

Dr. Little: This is one clinical application that we think we can address with this sort of technology. If you have something as simple as a voice test then it’s feasible for you to take that test frequently during the daytime. And in this case what we can do is get accurate measurements of symptoms, so that you can have something like a day by day symptom diary showing how your symptoms are changing very regularly. Currently, the problem with measuring Parkinson’s is that because you have to go to the clinic, it’s very rare that people will actually get an objective measurement of their symptoms. Most of the time you have a consultation with a neurologist and it’s really all just anecdotal – they will ask you how you feel, that is, whether you feel that your symptoms are improving on this current treatment regime. A lot of that actually comes down to questions of timing and dosage. Having an objective symptom diary would really optimize that process, because it would allow clinicians to have an objective record of how someone’s symptoms have been changing over the day.

If they had the right dosage would they lose some of the tremor that you hear in their voice?

Dr. Little: We would expect that because tremor is one of the ‘canonical symptoms’. It is not the only symptom – there are many others which is why we’re looking at a lot of different features – but, yes, certainly that is what our research shows. So, as the drug wears off during the day then the symptoms come back and cease to be suppressed. This should also be evident in the voice.

You say you look for a hundred and thirty different things in the voice, what are some of them?

Dr. Little: All told now we’re looking for about a hundred and thirty different features. We’ve managed to reduce that down to an informative set of about ten different features. This set is what we would actually be using for practical computations in decision making. We have identified three different ‘classes’ of symptoms that we’re currently focusing on. The first class of symptoms has to do with vocal tremor – this is a ‘canonical symptom’ of Parkinson’s. The next cluster of symptoms have largely to do with breathiness, and what is perceived as weakness in the voice. The third cluster of symptoms are relatively new – we have identified these in our latest research. We’ve discovered that vocal tremor caused by involuntary movements in the lips and jaw seems indicative, and these are turning out to be quite a useful cluster of symptoms.

And these things that you’re looking for are evident from your first study?

Dr. Little: I should explain that what we’re doing is replicating the clinical diagnosis. So, someone goes to their neurologist and they get what a neurologist would consider as being a definitive diagnosis of Parkinson’s. Now, of course that doesn’t mean that there aren’t some people who are inaccurately diagnosed by that process, but we think it should be very, very small. What we’re able to do is to replicate that clinical diagnosis. What that says about the prevalence of voice symptoms in Parkinson’s may well conflict somewhat with what is known in with reference to less exhaustive studies of voice in Parkinson’s. Unfortunately, there are very few circumstances in which you have a clinical study which looks at voice in Parkinson’s as a primary outcome. They may well look at another primary outcome measure, e.g. contained in a scoring system called the Unified Parkinson’s Disease Rating Scale, and voice only accounts for a very small part of that. Unfortunately, most neurologists are not explicitly trained in voice analysis. Therefore, part of what we’re doing is trying to elaborate what is currently known about voice in Parkinson’s.