Table · dataset · 2026
Data Sheet 2_A neuroimmune-enriched multibiofluid proteomic index associated with cognitive-motor progression in early Parkinson’s disease: a longitudinal PPMI cohort study.xlsx
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<p>Progression in early Parkinson's disease (PD) is heterogeneous, motivating transparent biological markers of group-level progression context.
Description
We analyzed longitudinal Parkinson’s Progression Markers Initiative (PPMI) data downloaded on 31 May 2026. The neuroimmune-enriched multibiofluid proteomic index (NEMPI) used 718 quality-control-eligible cerebrospinal fluid and plasma markers, organized into four source-context modules with equal marker and module weights.
Direct normalized protein quantification (NPQ) z-standardization was used for the primary reporting implementation, with the log1p implementation examined as a preprocessing sensitivity analysis. Among the 521 participants in the same-sample Cox comparison (173 first observed cognitive-status abnormalities), adding NEMPI to demographic, clinical, alpha-synuclein seed amplification assay, dopamine-transporter imaging, and apolipoprotein E (APOE) epsilon4 covariates yielded an NEMPI hazard ratio (HR) of 1.287 per 1-SD higher value (95% confidence interval (CI): 1.102–1.502; P = 0.001) and improved likelihood-based fit, but the C-index increment was small (0.0032; bootstrap 95% CI: -0.0093 to 0.0239).
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The consecutive-abnormality association was stronger but had fewer events, with fewer than 10 events per parameter; the persistent/irreversible estimate was weaker, and its confidence interval crossed 1. Higher NEMPI was also associated with a modest group-average Montreal Cognitive Assessment (MoCA) and motor trajectory differences, with 5-year translations below published minimal clinically important difference (MCID) ranges.
Results were similar under 5-year censoring, discrete-time analysis, stabilized inverse-probability weighting, age analyses, and measured confounder or preanalytic adjustments. NEMPI is therefore interpreted as an abundance-based, neuroimmune-enriched, multibiofluid proteomic composite associated with broad cognitive-motor progression, not as a patient-level prediction tool, clinical threshold, cognition-specific biomarker, or causal mechanism.</p>
Links
Where it is published
- DOI doi.org/10.3389/fimmu.2026.1928940.s001 ↗
DOI / persistent id · from figshare com
Catalogue records · 1
- OAI-PMH record api.figshare.com/v2/oai?verb=GetRecord&metadataPrefix=oai_dc&identifier=oai%3Af… ↗
metadata API · from figshare com
Topics
- From keywords
- Astronomy & Astrophysics · Chemistry · Computer Science & AI · Earth & Environmental Science · Economics & Finance · Engineering · Humanities · Life Sciences · Mass spectrometry · Medicine & Health · Ocean & Atmospheric Science · Psychology & Behavioral Science · Social Science
- Inferred from text
- Biochemistry and cell biology 72% · Disease 75% · Imaging 75% · Longitudinal study 65%
Provenance · 1 source records, 22 field assertions
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|---|---|---|---|
| figshare | oai:figshare.com:article/33717847 | 9 d ago | JSON v1 |
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| concepts[field].local:field:earth-environmental | mapping · figshare com | connector:figshare_com@1.0.0 | |
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| concepts[method].local:method:longitudinal-study | enrichment · figshare com | keyword-concept-rules@1.0.0 | title+description (65%) |
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| concepts[modality].local:modality:mass-spectrometry | mapping · figshare com | vocabulary-mapper@1.0.0 | keywords['proteomics'] |
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| license | source · figshare com | connector:figshare_com@1.0.0 | /metadata/dc/rights |
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| title | source · figshare com | connector:figshare_com@1.0.0 | /metadata/dc/title |