How Effective is Deep Brain Stimulation in Reducing the Symptoms of Parkinson’s Disease?
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This article discusses the effectiveness of deep brain stimulation (DBS) in reducing the symptoms of Parkinson’s disease (PD). It explores the history and prevalence of PD, the procedure of DBS, and its impact on motor symptoms. The article also highlights recent research advancements and potential future applications of DBS.
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Running head: MEDS2001 SID: Title: how effective is deep brain stimulation in reducing the symptoms of Parkinson’s disease and how far has the research progressed? Name of the University Author Note
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2MEDS2001 Parkinson’s disease (PD) refers to a degenerative disorder that affects the central nervous system and creates an impact on motor functioning (Postumaet al.2015). The widespread prevalence of the disease can be associated with the fact that an estimated 340 Australians suffer from the degenerative disorder and 32 people get diagnosed with PD, every day (Parkinson’s Queensland 2018). The mean age of onset of PD is roughly 60-65 years, however, in rare cases it occurs among people aged between 20-50 years (Pringsheimet al. 2014). Recent reports also provide evidence for the fact that PD is the second most prevalent neurological disorder in Australia and was associated with an estimated$10 billion cost in 2014 (Deloitte Access Economics 2015). Although there are several treatment modalities for management of PD, deep brain stimulation is one procedure that has gained prominence in recent years and involves the implantation of electrodes within specific areas of the brain, thereby generating electrical impulses, and affecting the release of neurotransmitters. This assessment will determine the impacts of deep brain stimulation on reducing the symptoms of PD. According toBerget al.(2014)history of PD can be traced back to 1817, when the bookAn Essay on the Shaking Palsywas published by James Parkinson. Great enhancement in knowledge about the symptoms and treatment of the condition was made during the 20th century, prior to which the condition was referred to asparalysis agitans(Sagnaet al.2014). Some of the common signs and symptoms of the condition comprise of tremors, muscle rigidity, and alterations in patterns of gait and speech (Sveinbjornsdottir 2016). Movement difficulties that are found associated with PD are commonly referred to as Parkinsonism, which in turn is characterized by progressive decrease in speed and several repetitive actions like voluntary finger-tapping. Non-motor signs and symptoms of the condition comprise of neuropsychiatricproblemsthatencompassmood,behaviour,thoughalterations,and cognition (Pfeiffer 2016). Some other symptoms encompass autonomic dysfunction and
3MEDS2001 altered sensory perceptions. Taking into consideration the fact that the most commonly reported complaint involves slow and coarse tremor of the hands during rest, which typically disappears while showing voluntary movement of the arms that are affected, the major objective of all treatment modalities focus on reducing the severity of such tremor. Although there is no particular cure for PD management, physical treatment, surgery and medications prove effective in providing relief and lowering the severity of the symptoms. DBS is the most commonly implemented surgical procedure and is administered to patients who have been diagnosed with the condition for more than four years, in addition to the presence of dyskinesia, and a noteworthy “off time” (Shake It Up Australia 2018). The efficacy of DBS in PD were explained byAnderson, Beecher and Ba (2017) who suggested that some of the major targets of DBS were the globus pallidus pars interna (GPi), subthalamic nucleus (STN), and the ventral intermediate nucleus (VIM) located in the thalamus. They also elaborated on the fact that VIM-DBS helps in effectively suppressing tremors, while bringing aboutCMPf stimulation. Results from another study suggested that implementation of acute therapeutic DBS helps in bringing about a reversible reduction in phase-amplitude interactions, over a period of that is comparable to reduction in motor signs and symptoms of Parkinsonism (De Hemptinneet al.2015).Herrington, Cheng and Eskandar (2015) opined that most common form of DBS encompasses the usage of a four-contact electrode that is stereotactically implanted and connected to an implantable pulse generator (IPG), with the help of a subcutaneous wire. The efficacy of VIM thalamus DBS helps in providing relieffrom essentialtremorover seconds. Furthermore,lessprofound axial symptomsoften get delayed for days or hours, upon subjecting the patient to STN DBS. In addition, it has been found that DBS plays an important role in inhibiting the target neuronal networks, while activating efferent axons.
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4MEDS2001 Besidessuppressionof pathologicalrhythmsorimposingnewrhythmsitalso upregulates several neurotransmitter systems such as, GABA and dopamine, thus reducing PDsymptoms(Udupa and Chen 2015). Recentdevelopmentsin thisdomaininclude researchingfortechnologicaladvancesthathelpinincreasingthebatterylifeof the electrodes, in addition to facilitating specific targeting with multiple contacts. Research has also progressed towards determining the role of DBS in management of opioid addiction by accumbal stimulation (Kuhnet al.2014). Investigators have also tried to determine the effects of this treatment modality in management of depression and found a significant improvement in the signs of depression among patients, upon using the Hamilton Depression Rating Scale (Morishitaet al.2014). To conclude, DBS refers to a neurosurgical procedure that comprises of the placement of a neurostimulator for sending electrical impulses to particular targets in the brain, through electrodes. An analysis of the aforementioned articles suggest that DBS works effective in the treatment of PD by reducing specific motor symptoms such as,slowness, stiffness,and tremor. Further research should be done to determine whether the procedure of DBS has any impact on other PD signs such as, non-motor symptoms, cognitive difficulties, or freezing during walking.
5MEDS2001 References Anderson, D., Beecher, G. and Ba, F., 2017. Deep Brain Stimulation in Parkinson’s Disease: New and Emerging Targets for Refractory Motor and Nonmotor Symptoms.Parkinson’s Disease,2017. Berg, D., Postuma, R.B., Bloem, B., Chan, P., Dubois, B., Gasser, T., Goetz, C.G., Halliday, G.M., Hardy, J., Lang, A.E. and Litvan, I., 2014. Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease.Movement Disorders,29(4), pp.454-462. De Hemptinne, C., Swann, N.C., Ostrem, J.L., Ryapolova-Webb, E.S., San Luciano, M., Galifianakis, N.B. and Starr, P.A., 2015. Therapeutic deep brain stimulation reduces cortical phase-amplitude coupling in Parkinson's disease.Nature neuroscience,18(5), p.779. Deloitte Access Economics., 2015.Living with Parkinson's Disease – update.[online] Availableat:https://shakeitup.org.au/wp-content/uploads/2012/01/AER-2011-Living-with- PD-FINAL.pdf[Accessed 26 Feb. 2019]. Herrington,T.M.,Cheng,J.J.andEskandar,E.N.,2015.Mechanismsofdeepbrain stimulation.Journal of neurophysiology,115(1), pp.19-38. Kuhn, J., Möller, M., Treppmann, J.F., Bartsch, C., Lenartz, D., Gründler, T.O., Maarouf, M., Brosig, A., Barnikol, U.B., Klosterkötter, J. and Sturm, V., 2014. Deep brain stimulation of thenucleusaccumbensanditsusefulnessinsevereopioidaddiction.Molecular psychiatry,19(2), p.145. Morishita, T., Fayad, S.M., Higuchi, M.A., Nestor, K.A. and Foote, K.D., 2014. Deep brain stimulationfortreatment-resistantdepression:systematicreviewofclinical outcomes.Neurotherapeutics,11(3), pp.475-484.
6MEDS2001 Parkinson’s Queensland., 2018.STATISTICS.[online] Available at:http://www.parkinsons- qld.org.au/pqi-research/statistics/[Accessed 26 Feb. 2019] Pfeiffer, R.F., 2016. Non-motor symptoms in Parkinson's disease.Parkinsonism & related disorders,22, pp.S119-S122. Postuma, R.B., Berg, D., Stern, M., Poewe, W., Olanow, C.W., Oertel, W., Obeso, J., Marek, K., Litvan, I., Lang, A.E. and Halliday, G., 2015. MDS clinical diagnostic criteria for Parkinson's disease.Movement Disorders,30(12), pp.1591-1601. Pringsheim, T., Jette, N., Frolkis, A. and Steeves, T.D., 2014. The prevalence of Parkinson's disease: A systematic review and meta‐analysis.Movement disorders,29(13), pp.1583-1590. Sagna, A., Gallo, J.J. and Pontone, G.M., 2014. Systematic review of factors associated with depression and anxiety disorders among older adults with Parkinson's disease.Parkinsonism & related disorders,20(7), pp.708-715. Shake It Up Australia., 2018.DEEP BRAIN STIMULATION – DBS.[online] Available at: https://shakeitup.org.au/understanding-parkinsons/dbs-deep-brain-stimulation/[Accessed 26 Feb. 2019] Sveinbjornsdottir,S.,2016.TheclinicalsymptomsofParkinson'sdisease.Journalof neurochemistry,139, pp.318-324. Udupa, K. and Chen, R., 2015. The mechanisms of action of deep brain stimulation and ideas for the future development.Progress in neurobiology,133, pp.27-49.