Category: Parkinson's Disease: Non-Motor Symptoms
Objective: The aims of the present study were to investigate the levels of inflammatory cytokines in the cerebrospinal fluid (CSF) of drug-naïve Parkinson’s Disease (PD) patients and to investigate correlations between non-motor symptoms (NMS) and cytokines in PD patients.
Background: NMS in PD are associated with a variety of poor outcomes. Research and clinical data suggest that the etiology of PD and of NMS is multifactorial [1,2]. Even if the pathophysiological mechanisms behind NMS, mood disorders in particular, are poorly understood, recent advance in neuroinflammation have provide a better knowledge of these symptoms [3,4] .
Method: CSF was collected in new diagnosed, drug-naïve PD patients. Exclusion criteria were autoimmune or inflammatory diseases, anti-inflammatory or antidepressant medication, evidence of an inflammatory process at the time of CSF withdrawal or blood-tinged CSF. Cytokines were assessed using a Bio-Plex multiplex assay. Motor disability was evaluated using UPDRS part-III. Cognitive status and quality of life were assessed by MoCA and PDQ-8. Depression and anxiety were investigated with the Beck Depression Inventory (BDI)-II and the State-Trait Anxiety Inventory (STAI-Y). The sleep quality and the daytime sleepiness were assessed using the PD Sleep Scale (PDSS-2) and the Epworth Sleepiness Scale (ESS) respectively.
Results: The study population comprised 28 patients with a median of disease duration of 12 months. Disease duration, UPDRS-III, MoCA, PDSS-2 and ESS scores did not correlate significantly with CSF cytokines levels. BDI-II score correlated significantly and positively with IL-6 (r=0.52, p=0.005) and IL-10 (r=0.44, p=0.01). STAI-st score correlated significantly and positively with IL-6 (r=0.58, p=0.001) and IL-10 (r=0.43, p=0.02). STAI-tr score correlated significantly and positively with IL-6 (r=0.54, p=0.003) and IL-10 (r=0.44, p=0.02). These correlations remain significant also after controlling for disease duration, motor impairment and age.
Conclusion: In our study, we found that CSF levels of IL-6 and IL-10 were significantly related to severity of depression and anxiety in PD patients. Although further investigations are needed, the assessment of CSF cytokines could be proposed as a biomarker of specific non-motor phenotypes in early PD patients and may lead to the development of novel therapies.
Abstract presented at 5th LIMPE-DISMOV Congress, 23/05/2019
References: [1] Kaur R, Mehan S, Singh S. Understanding multifactorial architecture of Parkinson’s disease: pathophysiology to management. Neurol Sci. 2019 Jan;40(1):13-23. [2] Pfeiffer RF. Non-motor symptoms in Parkinson’s disease. Parkinsonism Relat Disord. 2016 Jan; 22 Suppl 1():S119-22. [3] Halliday GM, Stevens CH. Glia: initiators and progressors of pathology in Parkinson’s disease. Mov Disord 2011;26(1):6-17. [4] McGeer PL, McGeer EG. Inflammation and neurodegeneration in Parkinson’s disease. Parkinsonism Relat Disord 2004;10 Suppl 1:S3-7.
To cite this abstract in AMA style:
E. Olivola, M. Stampanoni Bassi, L. Gilio, C. Femiano, G. Ricciardo Rizzo, F. Sica, L. Belli, R. Furlan, A. Finardi, D. Centonze, N. Modugno. CSF inflammatory cytokines and correlation with clinical features in early, untreated PD patients [abstract]. Mov Disord. 2020; 35 (suppl 1). https://www.mdsabstracts.org/abstract/csf-inflammatory-cytokines-and-correlation-with-clinical-features-in-early-untreated-pd-patients/. Accessed November 22, 2024.« Back to MDS Virtual Congress 2020
MDS Abstracts - https://www.mdsabstracts.org/abstract/csf-inflammatory-cytokines-and-correlation-with-clinical-features-in-early-untreated-pd-patients/