As research has expanded in the area of Parkinson’s genetics, researchers have been able to uncover a number of genes which have been linked to an increased risk of developing Parkinson’s.

PD Frontline is a remote study offering online genetic testing for people with Parkinson’s, so they can be referred, if they wish, to appropriate clinical trials and other studies. The registration process is designed to be quick and easy to navigate.


About 20% of Parkinson’s diagnoses are associated with genetic variations. Researchers believe that by understanding how certain genes contribute to the development of Parkinson’s, such as the GBA and the LRRK2 genes, they will be able to develop new drugs which target specific biochemical pathways. To test whether these drugs work, the study teams need to identify people with abnormalities in these genes who can then be enrolled in appropriate clinical trials. 

PD Frontline is informing this targeted approach and the study team are encouraging participants to enroll now. The process is simple:

  • Visit the PD Frontline website, register your details, sign the consent form and login
  • Answer some straightforward questions
  • The team will send you a saliva kit with instructions to collect your DNA
  • Return this in the pre-paid envelope
  • The team will get in touch with you once your results are known

If your results show you are a carrier of a specific gene, you will receive an invitation for genetic counselling (over the phone). Both negative and positive results will be uploaded onto your study profile for you to view, and a letter will be sent to your GP and clinician, in accordance with your provided consent.

In the video, Dr Stephen Mullin talks about the importance of PD Frontline and how the team are helping people with Parkinson’s to #GetTrialReady   

You can also follow PD Frontline on social media to keep up to date with their news.

How helpful was this content?

/ 5. Vote count:

We are sorry that this content was not useful for you

Let us improve this content

Can you tell us how we can improve this content?