Tuesday, 21st April 2026

Over 200,000 Australians are currently living with Parkinson’s disease, with a further 38 diagnosed every day. It’s the fastest growing neurological disorder in the world, and there is still no cure. In our ‘Solving the Parkinson’s Puzzle’ series, we speak to leading Australian researchers to find out how their work is helping to slow, stop and ultimately cure Parkinson’s disease.
Part of this work is to study conditions that share some aspects of Parkinson’s disease but have additional symptoms that may progress faster. We spoke with Associate Professor Kishore Kumar, from the ANZAC Research Institute, Sydney Local Health District and University of Sydney, about the AusPD Plus study. This research project aims to recruit 500 new participants with Parkinson’s Plus syndromes, to create a large genetic dataset in Australia that will provide in-depth and diverse insights.
“Parkinson’s Plus syndromes” (also called atypical parkinsonism) are a group of rare, progressive neurological conditions that share some movement symptoms with Parkinson’s disease—such as tremor, stiffness, and slowness—but have additional features and typically progress more rapidly. These conditions include:
People with Parkinson’s Plus often experience early balance problems, falls, speech or swallowing difficulties, and thinking or memory changes. They also tend to respond less well to standard Parkinson’s medications.
These disorders are challenging to diagnose and manage, which is why dedicated research programs like AusPD Plus are so important.
The AusPD Plus Study is a major national extension of the existing Monogenic Parkinson’s Disease Australia (MonoPDAus) program and the results will be integrated into the Australian Parkinson’s Genetics Study (APGS). It will recruit 500 people living with Parkinson’s Plus syndromes from across Australia.
The study will include:
AusPD Plus will be one of the largest national Parkinson’s Plus studies ever conducted in Australia. We are recruiting from major metropolitan movement disorder centres to ensure that the genetic and clinical data reflect the true diversity of Australians affected by Parkinson’s Plus syndromes.
AusPD Plus will provide the most comprehensive view to date of the genetic architecture of Parkinson’s Plus syndromes in Australia.
By combining detailed clinical assessments with advanced genomic analysis through GP2, the study aims to:
This work directly builds on the success of MonoPDAus, which has already identified clinically relevant genetic variants in participants.
For participants, the study will provide:
For the broader community, AusPD Plus will create an enduring dataset that supports discovery, improves diagnosis, and accelerates the development of new therapies. This is exactly the kind of catalytic, high‑impact research that the Shake It Up Foundation has championed across Australia.
Your support this Parkinson’s Awareness Month can help us fund research studies just like this one, which are making groundbreaking discoveries to slow, stop and cure Parkinson’s disease. By making a donation during April, you become part of a global community joining forces to change the future for people with Parkinson’s.