Brain and Systemic Inflammation in De Novo Parkinson's Disease

Author:

Yacoubian Talene A.1ORCID,Fang Yu‐Hua Dean2,Gerstenecker Adam1,Amara Amy1,Stover Natividad1,Ruffrage Lauren1,Collette Christopher1,Kennedy Richard3,Zhang Yue3,Hong Huixian4,Qin Hongwei4ORCID,McConathy Jonathan2,Benveniste Etty N.4,Standaert David G.1

Affiliation:

1. Department of Neurology University of Alabama at Birmingham Birmingham Alabama USA

2. Department of Radiology University of Alabama at Birmingham Birmingham Alabama USA

3. Department of Medicine University of Alabama at Birmingham Birmingham Alabama USA

4. Department of Cell, Developmental, and Integrative Biology University of Alabama at Birmingham Birmingham Alabama USA

Abstract

AbstractObjectiveTo assess the presence of brain and systemic inflammation in subjects newly diagnosed with Parkinson's disease (PD).BackgroundEvidence for a pathophysiologic role of inflammation in PD is growing. However, several key gaps remain as to the role of inflammation in PD, including the extent of immune activation at early stages, potential effects of PD treatments on inflammation and whether pro‐inflammatory signals are associated with clinical features and/or predict more rapid progression.MethodsWe enrolled subjects with de novo PD (n = 58) and age‐matched controls (n = 62). Subjects underwent clinical assessments, including the Movement Disorder Society‐United Parkinson's Disease rating scale (MDS‐UPDRS). Comprehensive cognitive assessment meeting MDS Level II criteria for mild cognitive impairment testing was performed. Blood was obtained for flow cytometry and cytokine/chemokine analyses. Subjects underwent imaging with 18F‐DPA‐714, a translocator protein 18kd ligand, and lumbar puncture if eligible and consented.ResultsBaseline demographics and medical history were comparable between groups. PD subjects showed significant differences in University of Pennsylvania Smell Identification Test, Schwab and England Activities of Daily Living, Scales for Outcomes in PD autonomic dysfunction, and MDS‐UPDRS scores. Cognitive testing demonstrated significant differences in cognitive composite, executive function, and visuospatial domain scores at baseline. Positron emission tomography imaging showed increased 18F‐DPA‐714 signal in PD subjects. 18F‐DPA‐714 signal correlated with several cognitive measures and some chemokines.Conclusions18F‐DPA‐714 imaging demonstrated increased central inflammation in de novo PD subjects compared to controls. Longitudinal follow‐up will be important to determine whether the presence of inflammation predicts cognitive decline. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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