Document Type
Article
Publication Date
10-1-2015
Abstract
OBJECTIVE: Increased caffeine intake is associated with a lower risk of Parkinson disease (PD) and is neuroprotective in mouse models of PD. However, in a previous study, an exploratory analysis suggested that, in patients taking creatine, caffeine intake was associated with a faster rate of progression. In the current study, we investigated the association of caffeine with the rate of progression of PD and the interaction of this association with creatine intake.
METHODS: Data were analyzed from a large phase 3 placebo-controlled clinical study of creatine as a potentially disease-modifying agent in PD. Subjects were recruited for this study from 45 movement disorders centers across the United States and Canada. A total of 1741 subjects with PD participated in the primary clinical study, and caffeine intake data were available for 1549 of these subjects. The association of caffeine intake with rate of progression of PD as measured by the change in the total Unified Parkinson Disease Rating Scale score and the interaction of this association with creatine intake were assessed.
RESULTS: Caffeine intake was not associated with the rate of progression of PD in the main analysis, but higher caffeine intake was associated with significantly faster progression among subjects taking creatine.
CONCLUSIONS: This is the largest and longest study conducted to date that addresses the association of caffeine with the rate of progression of PD. These data indicate a potentially deleterious interaction between caffeine and creatine with respect to the rate of progression of PD.
Recommended Citation
Simon, David K.; Wu, Cai; Tilley, Barbara C.; Wills, Anne-Marie; Aminoff, Michael J.; Bainbridge, Jacquelyn; Hauser, Robert A.; Schneider, Jay S.; Sharma, Saloni; Singer, Carlos; Tanner, Caroline M.; Truong, Daniel; and Wong, Pei Shieen, "Caffeine and Progression of Parkinson Disease: A Deleterious Interaction With Creatine." (2015). Department of Pathology, Anatomy, and Cell Biology Faculty Papers. Paper 205.
https://jdc.jefferson.edu/pacbfp/205
PubMed ID
26366971
Comments
This article has been peer reviewed. It is the authors' final version prior to publication in Clinical Neuropharmacology
Volume 38, Issue 5, October 2015, Pages163-169.
The published version is available at DOI: 10.1016/j.jamcollsurg.2008.06.341.Copyright © Wolters Kluwer Health, Inc.