The Use of Vitamin K2 in Patients With Parkinson's Disease and Mitochondrial Dysfunction (PD-K2): A Theranostic Pilot Study in a Placebo-Controlled Parallel Group Design
Despite rapid advances in research on Parkinson's disease (PD), in particular in the elucidation of genetic contributions, no disease-modifying therapy has become available to date. In the proposed project, we aim to investigate the potential effects of vitamin K2 (long-chain menaquinone 7, MK-...
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Published in | Frontiers in neurology Vol. 11; p. 592104 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
11.01.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Despite rapid advances in research on Parkinson's disease (PD), in particular in the elucidation of genetic contributions, no disease-modifying therapy has become available to date.
In the proposed project, we aim to investigate the potential effects of vitamin K2 (long-chain menaquinone 7, MK-7) in genetically determined PD with mitochondrial dysfunction.
A total of 130 study participants (26 biallelic
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mutation carriers, 52 sporadic PD patients, and 52 healthy controls) will receive the trial medication (MK-7 or placebo for 1 week). 31P-Magnetic resonance spectroscopy imaging of the forebrain and basal ganglia (31P-MRSI, primary endpoint) as well as other advanced neuroimaging methods, clinical assessment, including quantitative movement analysis, and biomarker sampling will be applied pre- and post-intervention.
The proposed project is highly translational as it builds on compelling mechanistic data from animal studies as well as on a small preliminary data set in humans. Patients are selected based on their mutation-related mitochondrial dysfunction and compared to disease and a healthy control group in a personalized medicine approach. We will further investigate how neuroimaging and blood-derived biomarkers can predict individual treatment response in sporadic PD.
This study was registered at the German Clinical Trial Registry (DRKS, DRKS00019932) on the 19th of December 2019. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Giuseppe De Michele, University of Naples Federico II, Italy This article was submitted to Movement Disorders, a section of the journal Frontiers in Neurology Reviewed by: Jamie Near, McGill University, Canada; Derek Narendra, National Institutes of Health (NIH), United States |
ISSN: | 1664-2295 1664-2295 |
DOI: | 10.3389/fneur.2020.592104 |