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. 2017 Apr 4:8:45865.
doi: 10.1038/srep45865.

Comparison for Efficacy and Tolerability among Ten Drugs for Treatment of Parkinson's Disease: A Network Meta-Analysis

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Comparison for Efficacy and Tolerability among Ten Drugs for Treatment of Parkinson's Disease: A Network Meta-Analysis

Chuanjun Zhuo et al. Sci Rep. .

Abstract

Parkinson's disease (PD) is a long term disorder affects the central nervous system and we aim to determine the relative efficacy of the current available drugs used in PD. Firstly, we performed a systematic review in current literature and eligible studies were retrieved from online databases, relevant data were extracted. Efficacy of these medications was assessed by different Unified Parkinson's Disease Rating Scales (UPDRS). Mean difference (MD) and odds ratio (OR) were produced by pairwise or network meta-analysis (NMA). Finally, we performed a cluster analysis for the included medications with respect to their surface under the cumulative ranking curve (SUCRA). Pairwise meta-analysis suggests that selegiline had a higher ranking in UPDRS II, UPDRS III and UPDRS total than bromocriptine and levodopa. Selegiline was more tolerable than bromocriptine (OR = 0.62, CI: 0.39 to 0.98) and pramipexole was less tolerable than levodopa (OR = 1.43, CI = 1.00 to 2.04). Results of NMA indicate that patients with levodopa, pramipexole, ropinirole and selegiline exhibited a significantly improved UPDRS III than those with lazabemide. To sum up, levodopa, selegiline, ropinirole and rotigotine were recommended for PD patients as they appeared relatively high efficacy and tolerability.

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Conflict of interest statement

The authors declare no competing financial interests.

Figures

Figure 1
Figure 1. The network plot of included trials.
Each node represents a therapy of PD, the number beside the nodes represents the number of people involved and the number between two nodes represents the number of study involved in the head-to-head comparison.
Figure 2
Figure 2. Clustered ranking plot of the network.
The plot is based on cluster analysis of surface under the cumulative ranking curves (SUCRA) values. Each plot shows SUCRA values for two outcomes. Each color represents a group of treatments that belong to the same cluster. Treatments lying in the upper right corner are more effective and safe than the other treatments.
Figure 3
Figure 3. Net heat plot.
The size of the gray squares indicates the contribution of the direct evidence (shown in the column) to the network evidence (shown in the row). The colors are associated with the change in inconsistency between direct and indirect evidence (shown in the row). Blue colors indicate an increase of inconsistency and warm colors indicate a decrease.

References

    1. Barzilai A. & Melamed E. Molecular mechanisms of selective dopaminergic neuronal death in Parkinson’s disease. Trends Mol Med. 9, 126–132 (2003). - PubMed
    1. Hindle J. V. Ageing, neurodegeneration and Parkinson’s disease. Age Ageing. 39, 156–161 (2010). - PubMed
    1. Hennis M. R., Marvin M. A., Taylor C. M. 2nd & Goldberg M. S. Surprising behavioral and neurochemical enhancements in mice with combined mutations linked to Parkinson’s disease. Neurobiol Dis. 62, 113–123 (2014). - PMC - PubMed
    1. Twelves D., Perkins K. S. & Counsell C. Systematic review of incidence studies of Parkinson’s disease. Mov Disord. 18, 19–31 (2003). - PubMed
    1. Calabrese V. P. Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurology. 69, 223–224, author reply 224 (2007). - PubMed

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