Abstract
Parkinson’s disease (PD) is one of the most common neurodegenerative diseases, and its prevalence is expected to increase as the population ages. The earliest symptoms of PD are subtle and nonspecific, complicating diagnosis at early stages, when novel treatments would be most likely to alter the disease course. Therefore, biomarkers for PD, capable of improving clinical diagnostic practices, as well as monitoring disease progression and the effects of therapeutic treatments, are urgently needed. Different techniques have been applied for identifying PD biomarkers, with neuroimaging and biochemical biomarkers showing the most promise for the most common, idiopathic forms of the disease, while genetic markers that confer risk of PD are also under intense investigation. Due to the complexity and overlapping syndromes of neurodegenerative diseases, it is very challenging to validate PD biomarkers with high sensitivity and specificity for clinical practice. This chapter reviews the advantages and pitfalls of each type of biomarker, and further discovery of novel PD markers and integration of current biomarkers are proposed.
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Abbreviations
- 18F-AV-133:
-
18F-(+) fluoropropyldihydrotetrabenazine
- 2DGE:
-
Two-Dimensional Gel Electrophoresis
- AADC:
-
Aromatic l-amino Acid Decarboxylase
- AD:
-
Alzheimer’s Disease
- CBD:
-
Cortical Basal Degeneration
- CNS:
-
Central Nervous System
- CβE:
-
Conduritol-β-Epoxide
- DAergic:
-
Dopaminergic
- DLB:
-
Dementia with Lewy Bodies
- DTBZ:
-
11C-(±)-α-Dihydrotetrabenazine
- DTI:
-
Diffusion Tensor Image
- DWI:
-
Diffusion-Weighted Image
- EC-SOD:
-
Extracellular Superoxide Dismutase
- EGF:
-
Epidermal Growth Factor
- F-dopa:
-
6-[18F]-Fluoro-l-3,4-Dihydroxyphenylalanine
- F-FDG:
-
Fluorine-18-Labelled Fluorodeoxyglucose
- GWAS:
-
Genome-Wide Association Studies
- iPD:
-
Idiopathic PD
- iTRAQ:
-
Isobaric Tags for Relative and Absolute Quantification
- LRRK2:
-
Leucine-Rich Repeat Kinase 2
- MAPT:
-
Microtubule-Associated Protein
- MRI:
-
Magnetic Resonance Imaging
- MS:
-
Mass Spectrometry
- MSA:
-
Multiple System Atrophy
- PBMCs:
-
Peripheral Blood Mononuclear Cells
- PD:
-
Parkinson’s Disease
- PET:
-
Positron Emission Tomography
- PIGD:
-
Postural Instability Gait Difficulty
- PINK1:
-
PTEN-Induced Putative Kinase 1
- PSP:
-
Progressive Supranuclear Palsy
- PTMs:
-
Posttranslational Modifications
- RBCs:
-
Fragile Red Blood Cells
- SNCA:
-
α-Synuclein
- SNpc:
-
Substantia Nigra Pars Compacta
- SPECT:
-
Single Emission Computed Tomography
- TD:
-
Tremor Dominant
- UCHL1:
-
Ubiquitin Carboxyl-Terminal Hydrolase L1
- UCP:
-
Uncoupling Protein
- UPDRS:
-
Unified Parkinson’s Disease Rating Scale
- VMAT2:
-
Vesicular Monoamine Transporter Type 2
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Acknowledgements
This work was supported by grants from the Michael J. Fox Foundation, the Parkinson Study Group, and the National Institutes of Health [NIEHS T32ES015459 to T.S., AG033398, ES004696-5897, ES007033-6364, ES016873, ES019277, NS057567, NS060252, NS062684-6221, and NS082137 to J.Z.].
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Fang, F., Stewart, T., Zhang, J. (2015). Biomarkers of Parkinson’s Disease. In: Preedy, V., Patel, V. (eds) General Methods in Biomarker Research and their Applications. Biomarkers in Disease: Methods, Discoveries and Applications. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-7696-8_17
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