STAT-PD: Preventing Levodopa Induced Dyskinesia in Parkinson's Disease With HMG-CoA Reductase Inhibitors

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Recruiting
CT.gov ID
NCT04064294
Collaborator
Oregon Health and Science University (Other)
120
3
94
40
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Study Details

Study Description

Brief Summary

In this study, the investigators will examine the association of statin use and dyskinesia in a convenience sample Parkinson's disease patients in the Veterans Administration Health Care System.

Condition or Disease Intervention/Treatment Phase
  • Drug: Intravenous Infusion

Detailed Description

Long term treatment with levodopa, the gold standard treatment of Parkinson's disease (PD), can lead to the development of abnormal involuntary movements called levodopa induced dyskinesia (LID). The severity of LID can range from mild to severely debilitating. A majority of PD patients will develop LID in their treatment life-time. In a recent study of the MPTP monkey model of PD, statin use was found to reduce LID (45%) without a worsening of Parkinsonism symptoms1. Another study showed rats treated with lovastatin prior to and with initiation of levodopa after substantia nigra lesioning showed dramatically less LID evolution compared to animals without lovastatin exposure2. In this study, the investigators will examine the association of statin use and dyskinesia in a convenience sample Parkinson's disease patients in the Veterans Administration Health Care System. This study is a retrospective three cohort design and will compare statin exposure BEFORE beginning LD, versus statin exposure AFTER LD is begun, versus NO statin exposure in PD subjects controlling for disease characteristics (severity), gender, and total LD exposure The primary endpoint is the severity of LID between the groups after years of opportunity to develop LID. Levodopa-Induced dyskinesia is a major cause of reduced quality of life for Veterans with PD and, in some cases, leads to costly surgical interventions. This project examines the impact of statin use on the presence of LID, and could lead to a future intervention trial. The reduction, delayed onset, or elimination of LID could improve the quality of life of many Veterans nationwide.

Study Design

Study Type:
Observational
Anticipated Enrollment :
120 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Preventing Levodopa Induced Dyskinesia in Parkinson?s Disease With Statins
Actual Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
Dec 31, 2026
Anticipated Study Completion Date :
Mar 31, 2027

Arms and Interventions

Arm Intervention/Treatment
Statin Before Levodopa

Historical use of a statin (simvastatin or lovastatin) BEFORE beginning levodopa

Drug: Intravenous Infusion
Intravenous levodopa given 1.0 to 1.5 mg/kg/hr from 0930 - 1130 on a single visit day.
Other Names:
  • levodopa
  • Statin After Levodopa

    Historical use of a statin (simvastatin or lovastatin) AFTER beginning levodopa

    Drug: Intravenous Infusion
    Intravenous levodopa given 1.0 to 1.5 mg/kg/hr from 0930 - 1130 on a single visit day.
    Other Names:
  • levodopa
  • No Statin

    No historical use of a statin (simvastatin or lovastatin)

    Drug: Intravenous Infusion
    Intravenous levodopa given 1.0 to 1.5 mg/kg/hr from 0930 - 1130 on a single visit day.
    Other Names:
  • levodopa
  • Outcome Measures

    Primary Outcome Measures

    1. Peak Unified Dyskinesia Rating Score (UDysRS) [11:00 am]

      The Unified Dyskinesia Rating Scale (UDysRS) combines patient, caregiver, and treating physician perspectives on both historical (Parts 1 & 2) and objective (Part 3 & 4) assessments of dyskinesia and dystonia. The historical portion and the objective ratings are added together to form total score ranging from 0 to 104 with higher scores indicating more severe dyskinesia.

    Secondary Outcome Measures

    1. phosphorylated ERK1/2 Levels in CD3/CD20 lymphocytes [11:15 am]

      Immunodetection of pERK with antibody against the phosphorylated forms of Tyrosine202 and 204 of ERK1/2 (AlexaFluor488 BD Biosciences) will occur in lymphocytes isolated from whole blood using flow cytometry.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Parkinson's Disease

    • Age diagnosed with Parkinson's Disease greater than or equal to 50 years

    • Treatment with levodopa greater than or equal to 5 years

    Exclusion Criteria:
    • Deep Brain stimulation

    • Unable to stand for 1 minute intervals, or sensory deficits in the feet

    • Significant cognitive impairment as measured by the Montreal Cognitive Assessment score of < 18

    • Subjects with unstable medical or psychiatric conditions (including hallucinations).

    • History of unstable medical conditions (i.e. active cardiac disease, recent unwellness, surgery etc.)

    • Current use of drugs that may affect parkinsonism or dyskinesia:

    • dopamine receptor blocking medications

    • depakote

    • lithium

    • amiodarone

    • tetrabenazine

    • metoclopramide

    • dronabinol

    • and illicit drugs such as marijuana (THC)

    • cocaine

    • methamphetamine

    • Statins other than simvastatin or lovastatin ie atorvastatin, fluvastatin

    • rationale is that while all other statins are thought to not cross the blood brain barrier well, the central nervous system penetrating nature of others is not perfectly clear and could confound results

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Oregon Health & Science University Portland Oregon United States 97239not
    2 VA Portland Health Care System, Portland, OR Portland Oregon United States 97239
    3 VA Puget Sound Health Care System Seattle Division, Seattle, WA Seattle Washington United States 98108

    Sponsors and Collaborators

    • VA Office of Research and Development
    • Oregon Health and Science University

    Investigators

    • Principal Investigator: Kathryn Anne Chung, MD, VA Portland Health Care System, Portland, OR

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    VA Office of Research and Development
    ClinicalTrials.gov Identifier:
    NCT04064294
    Other Study ID Numbers:
    • NURE-004-18S
    • 17302
    • 3869
    • 5273
    • 1635227
    First Posted:
    Aug 21, 2019
    Last Update Posted:
    May 5, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 5, 2022