2022
DOI: 10.1016/j.neuropharm.2022.108959
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New approaches to treatments for sleep, pain and autonomic failure in Parkinson's disease - Pharmacological therapies

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Cited by 7 publications
(8 citation statements)
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“…A high proportion (87.05%) of PD patients developed more than one NMS in the past month and the autonomic disorders were the most common NMSs. Besides, in accordance with others, pain and depression were relatively common in this study [34] . PD patients often complain pain symptoms, especially musculoskeletal and dystonia pain [35] .…”
Section: Overview Of Nmsssupporting
confidence: 92%
“…A high proportion (87.05%) of PD patients developed more than one NMS in the past month and the autonomic disorders were the most common NMSs. Besides, in accordance with others, pain and depression were relatively common in this study [34] . PD patients often complain pain symptoms, especially musculoskeletal and dystonia pain [35] .…”
Section: Overview Of Nmsssupporting
confidence: 92%
“…Treatments for pain in PwP have been very recently reviewed by Rukavina et al , who summarised that, to date, only three drugs (rotigotine, oxycodone/naloxone, and duloxetine) had been investigated specifically for their analgesic effects in PwP in double-blind RCT setting [ 125 ]. None of the studies met their primary endpoint [ 122 , 126 , 127 ].…”
Section: Painmentioning
confidence: 99%
“…To date, the exploitation of the central pharmacology of the A 2A receptor has centered on the use of antagonist molecules for the treatment of PD, and for that reason, it will form the backbone of this review. However, since PD is characterized by both motor and non-motor symptoms, including a range of neuropsychiatric symptoms (depression, cognitive decline, sleep disturbance), this may hint at the potential of adenosinergic modulation as a target for central nervous system disorders in general [ 28 , 29 , 30 ]. A limitation with the current symptomatic therapies for PD is that they are almost entirely based on dopamine-replacement therapy (levodopa, dopamine agonists, enzymatic inhibitors) that shows a loss of efficacy (response fluctuations such as ‘wearing off’) with disease duration and severity, and where significant side effects occur (dyskinesia, hallucinations, impulse control disorders, sleep disturbance) [ 31 ].…”
Section: Adenosine a 2a Receptors And Parkinson’s ...mentioning
confidence: 99%
“…In addition, most non-motor symptoms are only partially responsive to dopaminergic drugs, leaving a high degree of unmet need [ 8 ]. However, the widespread adaptive changes that occur within the basal ganglia as a result of the loss of dopaminergic neurons affect multiple neuronal systems that are non-dopaminergic in nature, offering potential new targets for treating both motor and non-motor symptoms [ 30 , 32 ].…”
Section: Adenosine a 2a Receptors And Parkinson’s ...mentioning
confidence: 99%