The structural and functional organisation of the brain as shown on MRI can predict the progression of brain atrophy in patients with early-stage, mild Parkinson’s disease, according to a study.
Researchers wanted to see if mapping the structural and functional connections across the brain could be used to predict patterns of atrophy spread in patients with mild Parkinson’s disease.
They used MRI data from 86 patients with mild Parkinson’s disease and 60 healthy control participants to generate the connectome, a structural/functional map of the brain’s neural connections.
The researchers used the connectome to develop an index of disease exposure.
Disease exposure at one year and two years was correlated with atrophy at two years and three years post-baseline.
Models including disease exposure predicted grey matter atrophy accumulation over three years in several areas of the brain.
Federica Agosta, M.D., Ph.D. is associate professor of neurology at the Neuroimaging Research Unit of IRCCS San Raffaele Scientific Institute in Milan, Italy.
The researcher said: “In the present study, brain connectome, both structural and functional, showed the potential to predict progression of grey matter alteration in patients with mild Parkinson’s disease.”
Parkinson’s disease affects more than 8.5 million people worldwide, and prevalence has doubled in the past 25 years, according to the World Health Organization (WHO).
One of the distinctive features of Parkinson’s disease is the presence of altered versions of the protein alpha-synuclein in the brain.
Normally present in the brain, this protein accumulates as misfolded clumps inside nerve cells in Parkinson’s disease, forming structures known as Lewy bodies and Lewy neurites.
These clumps spread to other brain regions, damaging nerves.
The research findings support the theory that functional and structural connections between brain regions may significantly contribute to Parkinson’s disease progression.
Agosta said: “The loss of neurons and accumulation of abnormal proteins can disrupt neural connections, compromising the transmission of neural signals and the integration of information across different brain regions.”
The study results point to a role for MRI in intervention trials to prevent or delay the disease progression—especially when individual patient information is incorporated into the model.
Since Parkinson’s disease progression likely differs among individuals, future models should consider different starting conditions and incorporate individual-specific information for optimal effectiveness, according to Prof Agosta.
She said: “We believe that understanding the organisation and dynamics of the human brain network is a pivotal goal in neuroscience, achievable through the study of the human connectome.
“The idea that this approach could help identify different biomarkers capable of modulating Parkinson’s disease progression inspires our work.”
