A simple blood test for Parkinson’s disease could soon become a reality.

A research team led by Chalmers University of Technology in Sweden has identified biomarkers for the disease in its earliest stages, before extensive brain damage occurs.

The biological processes leave measurable traces in the blood, but only for a limited period. The discovery thus reveals a window of opportunity that could be crucial for future treatment, but also for early diagnosis through blood tests. Those tests could begin trials within five years.

Parkinson’s is an endemic disease with over 10 million people affected globally but that number is projected to more than double by 2050 as the world’s population grows older. There currently is neither an effective cure nor an established screening method for detecting this chronic neurological disorder at an early stage before it has caused significant damage to the brain.

In a new study published in npj Parkinson’s Disease, a research team from Chalmers University of Technology and Oslo University Hospital, Norway, reports on decisive steps towards an early Parkinson’s diagnosis.

“By the time the motor symptoms of Parkinson’s disease appear, 50% to 80% of the relevant brain cells are often already damaged or gone. The study is an important step towards facilitating early identification of the disease and counteracting its progression before it has gone this far,” said first study author Danish Anwer, a doctoral student at the Department of Life Sciences at Chalmers.

Important Window of Opportunity Discovered

In the study, the researchers focused on two processes believed to be involved in the disease’s very early phase, which can last up to 20 years before motor symptoms are fully developed. One of the processes is the body’s DNA damage repair, which is the cells’ built-in system for detecting and correcting damage. The second is the cells’ stress response, a survival reaction activated by threats, in which cells prioritize repair and protection by pausing normal functions.

The researchers used machine learning and other techniques to discover a pattern of distinct gene activities linked to DNA damage repair and stress response in patients in the early phase of Parkinson’s disease. This pattern was not found in either healthy individuals or diagnosed patients who already displayed symptoms.

“This means that we have found an important window of opportunity in which the disease can be detected before motor symptoms caused by nerve damage in the brain appear. The fact these patterns only show at an early stage and are no longer activated when the disease has progressed further also makes it interesting to focus on the mechanisms to find future treatments,” stated Annikka Polster, assistant professor at the Department of Life Sciences at Chalmers, who led the study.

In the global research into Parkinson’s disease, several other biological indicators associated with the disease’s early stage have been examined, including those linked to brain imaging or brain fluid analyses. However, validated tests suitable for widespread screening to detect the disease before symptoms appear are not yet available.

“In our study, we highlighted biomarkers that likely reflect some of the early biology of the disease and showed they can be measured in blood. This paves the way for broad screening tests via blood samples: a cost-effective, easily accessible method,” Polster noted.

Blood Tests in Five Years?

In the next stage, the researchers will try to understand exactly the ways in which the mechanisms activated in the disease’s early stage work, and develop tools to make it even easier to detect them.

Within five years, the research team believes that blood tests for early diagnosis of Parkinson’s disease could begin to be tested in healthcare. In the longer term, it is hoped the research will also contribute to the development of drugs to prevent or treat the disease.

“If we can study the mechanisms as they happen, it could provide important keys to understanding how they can be stopped and which drugs might be effective. This may involve new drugs, but also drug repurposing, where we can use drugs developed for diseases other than Parkinson’s because the same gene activities or mechanisms are active,” Polster said.

The study, “Longitudinal assessment of DNA repair signature trajectory in prodromal versus established Parkinson’s disease” has been published in npj Parkinson’s Disease. The authors are Danish Anwer, Nicola Pietro Montaldo, Elva Maria Novoa-del-Toro, Diana Domanska, Hilde Loge Nilsen, and Annikka Polster. The researchers work at Chalmers University of Technology, Sweden, and Oslo University Hospital, Norway.

The research has been funded by Chalmers Health Engineering Area of Advance, Sweden, the Michael J. Fox Foundation, the Research Council of Norway, NAISS (National Academic Infrastructure for Supercomputing in Sweden), and the Swedish Research Council.

Parkinson’s disease is a neurological disorder that makes it difficult for the brain to control the nerve signals that control movement. The disease develops slowly and usually starts after the age of 55 to 60. Parkinson’s disease is the second most common neurodegenerative disease worldwide, after Alzheimer’s.

Sources: The Swedish Parkinson’s Association, The BMJ, global projection study, 2024.