Abstract

Parkinson's disease is the second most common neurodegenerative disease and its prevalence has been projected to double over the next 30 years. An accurate diagnosis of Parkinson's disease remains challenging and the characterisation of the earliest stages of the disease is ongoing. Recent developments over the past 5 years include the validation of clinical diagnostic criteria, the introduction and testing of research criteria for prodromal Parkinson's disease, and the identification of genetic subtypes and a growing number of genetic variants associated with risk of Parkinson's disease. Substantial progress has been made in the development of diagnostic biomarkers, and genetic and imaging tests are already part of routine protocols in clinical practice, while novel tissue and fluid markers are under investigation. Parkinson's disease is evolving from a clinical to a biomarker-supported diagnostic entity, for which earlier identification is possible, different subtypes with diverse prognosis are recognised, and novel disease-modifying treatments are in development.

Keywords

DiseaseParkinson's diseaseGenetic testingMedicineBiomarkerIdentification (biology)Diagnostic testClinical PracticeIntensive care medicinePathologyBioinformaticsBiologyInternal medicinePediatricsPhysical therapyGenetics

MeSH Terms

DiagnosisDifferentialDisease ProgressionHumansMagnetic Resonance ImagingParkinson DiseaseSymptom Assessment

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Publication Info

Year
2021
Type
review
Volume
20
Issue
5
Pages
385-397
Citations
1458
Access
Closed

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1458
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Cite This

Eduardo Tolosa, Alícia Garrido, Sonja W. Scholz et al. (2021). Challenges in the diagnosis of Parkinson's disease. The Lancet Neurology , 20 (5) , 385-397. https://doi.org/10.1016/s1474-4422(21)00030-2

Identifiers

DOI
10.1016/s1474-4422(21)00030-2
PMID
33894193
PMCID
PMC8185633

Data Quality

Data completeness: 86%