The association between plasma GPNMB and Parkinson's disease and multiple system atrophy

Parkinsonism Relat Disord. 2024 Mar:120:106001. doi: 10.1016/j.parkreldis.2024.106001. Epub 2024 Jan 9.

Abstract

Aims: Parkinson's disease (PD), as the second most common neurodegenerative disorder, often presents diagnostic challenges in differentiation from other forms of Parkinsonism. Recent studies have reported an association between plasma glycoprotein nonmetastatic melanoma protein B (pGPNMB) and PD.

Methods: A retrospective study was conducted, comprising 401 PD patients, 111 multiple system atrophy (MSA) patients, 13 progressive supranuclear palsy (PSP) patients and 461 healthy controls from the Chinese Han population, with an assessment of pGPNMB levels.

Results: The study revealed that pGPNMB concentrations were significantly lower in PD and MSA patients compared to controls (area under the receiver operating characteristics curve (AUC) 0.62 and 0.74, respectively, P < 0.0001 for both), but no difference was found in PSP patients compared to controls (P > 0.05). Interestingly, the level of pGPNMB was significantly higher in PD patients than in MSA patients (AUC = 0.63, P < 0.0001). Furthermore, the study explored the association between pGPNMB levels and disease severity in PD and MSA patients, revealing a positive correlation in PD patients but not in MSA patients with both disease severity and cognitive impairment.

Conclusion: This study successfully replicated prior findings, demonstrating an association between pGPNMB levels and disease severity, and also identified a correlation with cognitive impairment in PD patients of the Chinese Han population. Additionally, this study is the first to identify a significant difference in pGPNMB levels between MSA, PD, and normal controls. The data provide new evidence supporting the potential role of pGPNMB in the diagnosis and differential diagnosis of Parkinsonism.

Keywords: GPNMB; Multiple system atrophy; Parkinson's disease; Parkinsonism.

MeSH terms

  • Cognitive Dysfunction* / diagnosis
  • Diagnosis, Differential
  • Humans
  • Membrane Glycoproteins
  • Multiple System Atrophy* / diagnosis
  • Parkinson Disease* / diagnosis
  • Retrospective Studies
  • Supranuclear Palsy, Progressive* / diagnosis

Substances

  • GPNMB protein, human
  • Membrane Glycoproteins