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Smell test cuts need for invasive Parkinson’s screening

Old woman smelling on a sample. Photo.
A new study shows that a simple smell test can reduce the need for invasive spinal fluid tests in early Parkinson’s diagnosis.Photo: ChatGTP

Early diagnosis is key to receiving proper care and advancing research on future therapies for neurodegenerative diseases such as Parkinson’s and dementia with Lewy bodies. New research from Skåne University Hospital and Lund University shows that combining a simple smell test with advanced spinal fluid analysis can predict these diseases with high accuracy, while sparing nearly half of patients from invasive testing.

Losing your sense of smell may be more than just a nuisance, it could be an early sign of serious brain disease. In Parkinson’s disease and dementia with Lewy bodies, abnormal protein deposits known as Lewy bodies often begin in the brain’s olfactory regions, making smell loss one of the earliest and easiest symptoms to test.

Fortunately, not all problems with reduced sense of smell are caused by Lewy body diseases. A more specific way of detecting these conditions is to measure traces of the protein α-synuclein in the spinal fluid. However, this method is both costly and more invasive for patients.

Now, researchers at MultiPark have found a way to reduce the number of invasive spinal fluid tests by 43% while still achieving 94% accuracy in predicting Lewy body pathology. Their new approach consists of a two-step diagnostic workflow: first, patients take a simple smell test. Only those who show reduced smell then undergo a lumbar puncture to measure levels of α-synuclein and thereby confirm or rule out the presence of Lewy body disease.

“This is a cost-effective way to increase diagnostic accuracy of diseases like Parkinson’s while reducing patient burden,” explains Sophie Mastenbroek.

“This is a cost-effective way to increase diagnostic accuracy of diseases like Parkinson’s while reducing patient burden,” explains Sophie Mastenbroek, PhD student at the Clinical Memory Research Unit and the first author of the study.

While the spinal fluid assay is still mainly used in research, smell tests are already available in clinics. Before the combined approach can be widely implemented in healthcare, the protocol needs to be validated in diverse patient groups and approved by regulatory authorities.

“We hope to see our combined strategy, with smell-function testing as a pre-screening method, become routine in patient care as soon as possible.

“We hope to see our combined strategy, with smell-function testing as a pre-screening method, become routine in patient care as soon as possible. More accessible diagnostics would make it possible to identify patients at earlier stages and provide better care,” concludes Rik Ossenkoppele and Oskar Hansson, senior authors of the study published in Nature Communications.

Sophie Mastenbroek. Photo.

Sophie Mastenbroek

Ph.D. student at Clinical Memory Research Unit

sophie [dot] mastenbroek [at] med [dot] lu [dot] se (sophie[dot]mastenbroek[at]med[dot]lu[dot]se)

Link to Sophie Mastenbroek's profile in the LU Research Portal

Profile photo of Rik Ossenkoppele.

Rik Ossenkoppele

Associate Senior Lecturer

rik [dot] ossenkoppele [at] med [dot] lu [dot] se (rik[dot]ossenkoppele[at]med[dot]lu[dot]se)

Link to Rik Ossenkoppele's profile in the LU Research Portal

Twitter: @RikOssenkoppele

Profile photo of Oskar Hansson in black and white
Photo: Kenneth Rouna

Oskar Hansson

Professor and senior consultant in neurology

oskar [dot] hansson [at] med [dot] lu [dot] se (oskar[dot]hansson[at]med[dot]lu[dot]se)

0722-26 77 45

Oskar Hanssons profile in Lund University research portal

Twitter: @oskarhansson9

Homepage: https://biofinder.se