Guest guest Posted October 23, 2002 Report Share Posted October 23, 2002 Subject: Coenzyme Q10 for Early Parkinson's Disease Date: 10/14/2002 Effects of coenzyme Q10 in early Parkinson disease: Evidence of slowing of the functional decline CW Shults, D Oakes, K Kieburtz, et al., and the Parkinson's Study Group Arch Neurol 2002;59:1541-1550 High-dose Coenzyme Q10 slows the development of disability in early PD patients, according to this study. Eighty PD patients not yet on levodopa therapy were randomized to receive placebo or one of three doses of coenzyme Q10: 300, 600, or 1200 mg/day. All study medications included 300 IU vitamin E as a lipophilic carrier. The primary outcome variable was the change in UPDRS total score from the initial visit to the final visit. The final visit was either 16 months after entry or the point at which levodopa was needed, whichever came first. Four patients dropped out or were lost to follow-up. Adverse events were mild, and were similar among all groups. No clinically significant changes in laboratory values were seen in any group. Mean changes in UPDRS by group from baseline to last visit were: Placebo: +11.99 300 mg: +8.81 600 mg: +10.82 1200 mg: +6.69 (p=0.04 vs. placebo) The effect was significant in all three domains of the UPDRS, but the greatest effect was in part II, ADLs. No significant effect was seen on Hoehn & Yahr score or timed tapping. Treatment did not delay the time until levodopa was needed, but the authors state that evidence from the DATATOP study indicated this would be a less informative measure and hence was not included as a primary variable in the present study. The authors conclude, " The mechanism(s) through which coenzyme Q10 exerted its beneficial effect cannot be determined from our clinical trial, but our data are consistent with an effect on mitochondrial function…To our knowledge, our study is the first trial to systematically explore the safety and efficacy of high dosages of coenzyme Q10. Our data suggest that in treatment of neurological disorders in which evidence of complex I or II dysfunction are found, such as PD and Huntington disease, dosages much higher than those previously used may be required. The benefit was greatest in the group receiving the highest dosage, 1200 mg/d. It is conceivable that a greater effect could be seen at even higher dosages of coenzyme Q10. Future studies of coenzyme Q10 in PD and other disorders will need to explore the effect of dosages of 1200 mg/d and higher. " In our study, coenzyme Q10 treatment at high dosages was safe and well tolerated and reduced the worsening of PD, as reflected in the total UPDRS score. It would be premature to recommend the use of coenzyme Q10 for the treatment of PD. Our results need to be confirmed in a larger, phase 3 study, and the appropriate dosage and the magnitude of effect need to be better defined. " An editorial by Roger Rosenberg accompanies the study. *** See: Mitochondrial Therapy for Parkinson Disease Roger N. Rosenberg, MD http://archneur.ama-assn.org/issues/v59n10/ffull/ned20014.html The abstract of this study is available online *** See: Effects of Coenzyme Q10 in Early Parkinson Disease Evidence of Slowing of the Functional Decline http://archneur.ama-assn.org/issues/v59n10/abs/noc20145.html ---------------------------------------------------------------------------- ---- Copyright 2002 WE MOVE Editor: (rrobinson@...) PRIVATE DONATIONS ARE NEEDED TO SUPPORT WE MOVE's VALUABLE, FREE SERVICES LIKE THIS ELECTRONIC NEWS SERVICE. Please donate online, or send your tax-deductible contribution to WE MOVE, 204 West 84th Street New York, NY 10024. TEL 800-437-MOV2 or . Thank you so much! This document may be freely redistributed by email only in its unedited form. We encourage you to share it with your colleagues. Visit http://www.wemove.org/emove for E-MOVE archives and free subscriptions. Patient subscribers: Information presented in the above article(s) should not be interpreted as medical advice. Contact your physician if you have questions about the information presented by the E-MOVE news service or archives. It is not possible, nor appropriate for WE MOVE to respond directly to questions regarding medical management, including diagnosis and treatment. WE MOVE Worldwide Education and Awareness for Movement Disorders 204 West 84th Street New York, NY 10024 TEL 800-437-MOV2 TEL FAX Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 23, 2002 Report Share Posted October 23, 2002 Subject: Coenzyme Q10 for Early Parkinson's Disease Date: 10/14/2002 Effects of coenzyme Q10 in early Parkinson disease: Evidence of slowing of the functional decline CW Shults, D Oakes, K Kieburtz, et al., and the Parkinson's Study Group Arch Neurol 2002;59:1541-1550 High-dose Coenzyme Q10 slows the development of disability in early PD patients, according to this study. Eighty PD patients not yet on levodopa therapy were randomized to receive placebo or one of three doses of coenzyme Q10: 300, 600, or 1200 mg/day. All study medications included 300 IU vitamin E as a lipophilic carrier. The primary outcome variable was the change in UPDRS total score from the initial visit to the final visit. The final visit was either 16 months after entry or the point at which levodopa was needed, whichever came first. Four patients dropped out or were lost to follow-up. Adverse events were mild, and were similar among all groups. No clinically significant changes in laboratory values were seen in any group. Mean changes in UPDRS by group from baseline to last visit were: Placebo: +11.99 300 mg: +8.81 600 mg: +10.82 1200 mg: +6.69 (p=0.04 vs. placebo) The effect was significant in all three domains of the UPDRS, but the greatest effect was in part II, ADLs. No significant effect was seen on Hoehn & Yahr score or timed tapping. Treatment did not delay the time until levodopa was needed, but the authors state that evidence from the DATATOP study indicated this would be a less informative measure and hence was not included as a primary variable in the present study. The authors conclude, " The mechanism(s) through which coenzyme Q10 exerted its beneficial effect cannot be determined from our clinical trial, but our data are consistent with an effect on mitochondrial function…To our knowledge, our study is the first trial to systematically explore the safety and efficacy of high dosages of coenzyme Q10. Our data suggest that in treatment of neurological disorders in which evidence of complex I or II dysfunction are found, such as PD and Huntington disease, dosages much higher than those previously used may be required. The benefit was greatest in the group receiving the highest dosage, 1200 mg/d. It is conceivable that a greater effect could be seen at even higher dosages of coenzyme Q10. Future studies of coenzyme Q10 in PD and other disorders will need to explore the effect of dosages of 1200 mg/d and higher. " In our study, coenzyme Q10 treatment at high dosages was safe and well tolerated and reduced the worsening of PD, as reflected in the total UPDRS score. It would be premature to recommend the use of coenzyme Q10 for the treatment of PD. Our results need to be confirmed in a larger, phase 3 study, and the appropriate dosage and the magnitude of effect need to be better defined. " An editorial by Roger Rosenberg accompanies the study. *** See: Mitochondrial Therapy for Parkinson Disease Roger N. Rosenberg, MD http://archneur.ama-assn.org/issues/v59n10/ffull/ned20014.html The abstract of this study is available online *** See: Effects of Coenzyme Q10 in Early Parkinson Disease Evidence of Slowing of the Functional Decline http://archneur.ama-assn.org/issues/v59n10/abs/noc20145.html ---------------------------------------------------------------------------- ---- Copyright 2002 WE MOVE Editor: (rrobinson@...) PRIVATE DONATIONS ARE NEEDED TO SUPPORT WE MOVE's VALUABLE, FREE SERVICES LIKE THIS ELECTRONIC NEWS SERVICE. Please donate online, or send your tax-deductible contribution to WE MOVE, 204 West 84th Street New York, NY 10024. TEL 800-437-MOV2 or . Thank you so much! This document may be freely redistributed by email only in its unedited form. We encourage you to share it with your colleagues. Visit http://www.wemove.org/emove for E-MOVE archives and free subscriptions. Patient subscribers: Information presented in the above article(s) should not be interpreted as medical advice. Contact your physician if you have questions about the information presented by the E-MOVE news service or archives. It is not possible, nor appropriate for WE MOVE to respond directly to questions regarding medical management, including diagnosis and treatment. WE MOVE Worldwide Education and Awareness for Movement Disorders 204 West 84th Street New York, NY 10024 TEL 800-437-MOV2 TEL FAX Quote Link to comment Share on other sites More sharing options...
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