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Abstract Details

Dysautonomia as a Prognostic Marker for Phenoconversion and Functional Dependence in Prodromal Parkinson's Disease
Movement Disorders
P4 - Poster Session 4 (8:00 AM-9:00 AM)
5-002

To determine whether particular dysautonomia measures predict later Parkinson's disease (PD) phenoconversion and functional dependence in populations without PD but with other PD risk markers, and whether specific risk markers modify associations between dysautonomia and risk of the outcomes.

Identifying populations that will develop PD is important for recruitment into studies of putative disease-modifying therapies. Dysautonomia is a prodromal feature of PD that may help risk-stratify individuals in the presence of other risk markers.

Data were obtained from Parkinson’s Progression Markers Initiative; cohorts without PD but with PD risk markers (hyposmia and/or RBD, LRRK2 gene mutation, GBA gene mutation) were included. Dysautonomia measures included Scales for Outcomes in Parkinson’s Disease Autonomic (SCOPA-AUT), 7 SCOPA-AUT subscales, +/- neurogenic orthostasis, +/- supine hypertension, +/- low pulse pressure. Outcome measures were phenoconversion and Schwab and England Activities of Daily Living Scale (SE-ADL) ≤70. Cox proportional-hazards regression was used to evaluate phenoconversion/SE-ADL≤70 hazard for each dysautonomia measure, adjusting for relevant demographic/clinical variables in multivariable models. If a significant association was identified, a likelihood-ratio test was employed to evaluate for an interaction between the measure and cohort. If an interaction was identified, regression analysis was repeated stratified by cohort.

Median follow-up was 30 months. On multivariable analysis, female sexual dysfunction SCOPA-AUT score was associated with phenoconversion hazard (HR=2.19, 95% CI 1.35-3.54), and total, gastrointestinal, cardiovascular SCOPA-AUT scores, neurogenic orthostasis were associated with increased hazard of SE-ADL≤70. The association for gastrointestinal SCOPA-AUT score was driven by the LRRK2 cohort (HR=2.71, 95% CI 1.25-5.84) and cardiovascular SCOPA-AUT score was driven by the hyposmia/RBD cohort (HR=1.85, 95% CI 1.07-3.20).
Female sexual dysfunction as measured by the SCOPA-AUT may be an important variable for inclusion in prodromal PD diagnostic criteria. Particular risk marker combinations may be associated with increased risk of functional dependence in prodromal PD.
Authors/Disclosures
Cameron C. Miller-Patterson, MD
PRESENTER
Dr. Miller-Patterson has nothing to disclose.
Jesse Hsu (University of Pennsylvania) No disclosure on file
Lana Chahine, MD, FAAN Dr. Chahine has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Gray Matters Technology. The institution of Dr. Chahine has received research support from UPMC. The institution of Dr. Chahine has received research support from MJFF. The institution of Dr. Chahine has received research support from Denali/Biogen. Dr. Chahine has received publishing royalties from a publication relating to health care.
James F. Morley, MD, PhD Dr. Morley has nothing to disclose.
Allison Wright Willis, MD (University of Pennsylvania) Dr. Wright Willis has received personal compensation in the range of $0-$499 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Pharmacoepidemiology and Drug Safety. Dr. Wright Willis has received personal compensation in the range of $0-$499 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for JAMA Neurology. The institution of Dr. Wright Willis has received research support from NIH. The institution of Dr. Wright Willis has received research support from NIA. The institution of Dr. Wright Willis has received research support from Biogen. The institution of Dr. Wright Willis has received research support from Parkinson Foundation. The institution of Dr. Wright Willis has received research support from Arcadia.