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. Author manuscript; available in PMC: 2022 Apr 18.
Published in final edited form as: Prog Neurobiol. 2011 Sep 14;95(4):629–635. doi: 10.1016/j.pneurobio.2011.09.005

Table 2.

Scheme for incorporating imagine and biospecimen biomarkers.

Modality Target Ligand
A. Imaging markers
TIER 1 – in use in PPMI in all or sub set of sites
 SPECT Dopamine transporter DaTSCAN
 MRI DTI/resting state
TIER II – supportive data and clear rationale for biomarker for PD, but limited data in disease progression
 PET VMAT2 DTZB, AV133
 PET Glucose metabolism FDG
 Ultrasound Substantia nigra
 PET Amyloid AV45, BAY94, PIB
 SPECT Cardiac sympathetic function MIBG
TIER III – limited data in PD but rationale for biomarker for PD
 PET/SPECT PBR – inflammation PK11195, PBR06, PBR111
 PET/SPECT Striatal function – MGluR5, CB1, A2a, GlyT1 FPEB, MK9640, FCPyPB
 PET/SPECT DASB, MZIENT, INER, MPPF SERT, NET, 5HT1a, 5HT2a
 Optical coherence tomography (OCT) Retinal morphology
TIER IV – strong rationale for biomarker for PD, no data for PD
 PET/SPECT Alpha-synuclein
 PET/SPECT Tau
B. Biospedmen biomarkers
TIER I – plans for use in PPMI. Markers for which there is some evidence for a disease association, preliminary data around the detection of the marker in a biochemical assay exist CSF alpha synuclein, DJ1, amyloid, tau, blood urate
TIER II – putative markers with weak data correlating to PD, standardized assays exist and are straightforward to study in PD subjects EGF, cytokines, inflammatory markers, glutamine/glutamate
TIER III – minimal data available, relationship to PD hypotheses and mechanisms of disease exist Proteomics, glutathione, 8-OHdG