Early detection of Parkinson’s disease before classic symptoms are present may get a boost from a new technique that identifies the build-up of abnormal protein deposits linked to the illness, researchers reported on Wednesday in The Lancet Neurology.
An editorial published with the study calls the findings “a game-changer in Parkinson’s disease diagnostics, research, and treatment trials.”
Researchers looked for the protein alpha-synuclein using a “seed amplification assay” on samples of cerebrospinal fluid obtained from 1,123 volunteers with either a Parkinson’s disease diagnosis, “prodromal” or early signs and symptoms that may predict development of the disease, or gene variants linked to the condition.
Nearly 90% of individuals with Parkinson’s disease had a positive result.
Most prodromal participants also had positive results, despite not yet being diagnosed with Parkinson’s disease. Scans of these patients’ brains did not show a decline in brain cells that is usually present before diagnosis, suggesting that build-up of alpha-synuclein aggregates may be a very early indicator of disease onset.
In participants with genetic risk variants but without Parkinson’s disease or prodromal symptoms, fewer than 10% had positive results for alpha-synuclein.
Eventually, researchers say, blood tests for the protein will be developed.
“Validation of this biomarker launches a new, biological era in Parkinson’s research,” Dr. Kenneth Marek of the Institute for Neurodegenerative Disorders in New Haven, Connecticut, one of the study’s principal investigators, said in a statement.
“We are already unlocking new understanding of Parkinson’s, which will transform every aspect of drug development and ultimately clinical care,” he said.
The study was funded by The Michael J. Fox Foundation for Parkinson’s Research and a consortium of more than 40 private and philanthropic partners.
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