Groundbreaking research to identify early signs of multiple sclerosis

Notice: News releases are not subject to review by MedLink Neurology’s Editorial Board.

In a major step towards early detection, University of South Australia researchers are investigating the biology behind multiple sclerosis (MS) to help predict people’s genetic risk of developing the disease, long before any symptoms appear.

Funded by an MS Australia Incubator Grant announced today, the Australian-first study will use a powerful new research method known as ‘recall by genotype’ to explore genetic causes of multiple sclerosis.

Specifically, the study will explore links between multiple sclerosis and the Epstein-Barr virus – a common virus best known for causing glandular fever, but increasingly believed to be a trigger for multiple sclerosis.

Multiple sclerosis is a chronic autoimmune disease that disrupts communication between the brain, spinal cord and body. Affecting more than 33,000 Australians, the exact cause of multiple sclerosis remains unknown, though genetics and environmental factors are thought to play a key role.

Lead researcher, UniSA’s Dr David Stacey, says the research aims to untangle how the Epstein-Barr virus might lead to multiple sclerosis in some people but not others.

“For many years we’ve known that the Epstein-Barr virus is a likely precursor for multiple sclerosis,” Dr Stacey says.

“But because the virus affects up to 90% of the population, it’s difficult to pin down why some people go on to develop multiple sclerosis while others don’t.

“We believe the way a person’s immune system responds to the Epstein-Barr virus may be a key factor, and genetics can help us uncover that.”

The study will calculate multiple sclerosis genetic risk scores for more than 1000 South Australian participants without an multiple sclerosis diagnosis, then compare biological traits in a subset of participants with either high or low genetic risk.

“By grouping people based on their genetic profile, we expect to find those with a high genetic risk for multiple sclerosis will also show biological differences – even if they don’t have the disease,” Dr Stacey says. “That could reveal how the Epstein-Barr virus and multiple sclerosis are connected and identify early warning signs or biomarkers for multiple sclerosis.”

To enable this study, the researchers will use an innovative research design called ‘recall by genotype’ – or RbG for short. RbG studies use naturally occurring genetic variants that are strongly associated with a disease to group people for research. Participants are then ‘recalled’ for further testing based on their DNA, allowing researchers to study differences in a more targeted and reliable way.

The researchers have been working to establish resources to enable RbG studies in Australia, which until now have not been possible. This study will therefore help to establish standard operating procedures for participant recall and tackle important ethical questions about sharing genetic risk with research participants.

“If we identify people who are at risk of developing multiple sclerosis, we need to consider how – and whether – to share that information, particularly as this information may not yet be clinically actionable,” Dr Stacey says.

“This study will explore those ethical, legal, and social questions to guide how future studies approach personal genetic risk.”

Ultimately, the research team – which includes collaborators from the Perron Institute and the University of Adelaide – hopes the study will pave the way for larger investigations and help support the development of early diagnostic tools and future preventative strategies for multiple sclerosis.

Source: News Release
University of South Australia
July 29, 2025