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Abstract Details

CSF biomarkers in Parkinson patients with and without freezing of gait
Movement Disorders
P4 - Poster Session 4 (5:30 PM-6:30 PM)
3-001

To validate the ability of candidate CSF biomarkers to distinguish between patients with and without freezing of gait (FOG) in Parkinson’s disease (PD).

Freezing of gait (FOG) is a common, poorly understood symptom complex that has potentially grave consequences to Parkinson’s disease (PD) patients. However, the pathophysiology underlying this symptom remains unknown. Here, we compared levels of potential CSF biomarkers previously implicated in PD progression in patients with FOG versus those without FOG.

CSF samples were collected from PD patients with FOG (N=12), PD patients without FOG (N=20) and healthy control individuals (N=11) for analysis. Levels of 14 putative CSF biomarkers were measured using independent assays and compared across groups with ANOVAs. P values for factors representing presence of PD and presence of FOG were calculated and adjusted to control Type I error with the Holm procedure.
The anti-inflammatory marker Fractalkine was significantly decreased in PD compared to non-PD (P=0.0238, adjusted), and further decreased in PD with FOG compared to PD without FOG or non-PD (P=0.0350, adjusted). The Alzheimer’s disease-related protein amyloid-beta(42) (Aβ42) was significantly increased in FOG compared to PD without FOG or non-PD (P=0.0025, adjusted). Phosphorylated tau (ptau181) was also significantly decreased in PD compared to non-PD (P=0.0129, adjusted).

These results suggest that FOG may be associated with characteristic changes in specific CSF biomarkers including Fractalkine, Aβ42, and ptau181. These results suggest that the potential exists to identify reproducible, validated CSF biomarkers for FOG. The use of CSF biomarkers for FOG may increase the power of clinical trials to select the appropriate patients for target-specific therapies. The presence of differential biomarkers for PD and FOG provides additional evidence that FOG may not represent continued progression of PD symptoms, but may result from a separate underlying pathophysiology.

Authors/Disclosures
Johnathan L. McKay, PhD (Emory University)
PRESENTER
The institution of Dr. McKay has received research support from NIH. The institution of Dr. McKay has received research support from the McCamish Foundation.
Jaime Hatcher-Martin, MD, PhD, FÂé¶¹´«Ã½Ó³»­ (Synapticure) Dr. Hatcher-Martin has received personal compensation for serving as an employee of Synapticure. Dr. Hatcher-Martin has received personal compensation for serving as an employee of HD Genetics. Dr. Hatcher-Martin has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Science37. Dr. Hatcher-Martin has received personal compensation in the range of $10,000-$49,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Neurocrine. Dr. Hatcher-Martin has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Takeda. Dr. Hatcher-Martin has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Neurocrine. Dr. Hatcher-Martin has received personal compensation in the range of $0-$499 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for npc Parkinson's Disease Journal.
No disclosure on file
William T. Hu, MD, PhD, FÂé¶¹´«Ã½Ó³»­ (Rutgers Biomedical and Health Sciences) Dr. Hu has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Fujirebio. Dr. Hu has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Beckman Coulter. Dr. Hu has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Apellis Pharmaceuticals. The institution of Dr. Hu has received research support from NIA. The institution of Dr. Hu has received research support from TMCity Foundation. The institution of Dr. Hu has received research support from Atlanta Family Foundation. The institution of Dr. Hu has received research support from Fujirebio Diagnostics.
Stewart A. Factor, DO, FÂé¶¹´«Ã½Ó³»­ (Emory University School of Medicine) Dr. Factor has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Neurocrine. Dr. Factor has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Dr. Factor has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Takeda. The institution of Dr. Factor has received research support from Biohaven. The institution of Dr. Factor has received research support from Neurocrine. The institution of Dr. Factor has received research support from Supernus. The institution of Dr. Factor has received research support from Sun Pharmaceuticals Advanced Research Company. The institution of Dr. Factor has received research support from Aspen. The institution of Dr. Factor has received research support from RHO. Dr. Factor has received publishing royalties from a publication relating to health care. Dr. Factor has received publishing royalties from a publication relating to health care. Dr. Factor has received publishing royalties from a publication relating to health care. Dr. Factor has received publishing royalties from a publication relating to health care.