2018
DOI: 10.3389/fneur.2018.00170
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Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients

Abstract: BackgroundNon-motor symptoms (NMSs) are a real burden in Parkinson’s disease (PD). They may appear in early pre-symptomatic stage as well as throughout the disease course. However, their relationship with the deterioration of the patient’s quality of life (QoL) is still under debate. This study aimed to investigate the prevalence of NMSs and their impact on the QoL in a cohort of Moroccan patients.MethodsWe carried out a cross-transactional study, where a total of 117 patients were submitted to a structured cl… Show more

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Cited by 101 publications
(76 citation statements)
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“…Autonomic dysfunction is a core clinical feature underlying all of the α‐synucleinopathies and includes bladder dysfunction, constipation, cardiovascular abnormalities, sexual dysfunction, sialorrhea, dry eyes, excessive sweating, and altered thermoregulation. These symptoms are a greater contributor to loss of quality of life than are the motor symptoms in PD (Estrada‐Bellmann et al, ; Martinez‐Martin, Rodriguez‐Blazquez, Kurtis, Chaudhuri,, & NMSS Validation Group, ; Müller et al, ; Prakash et al, ; Tibar et al, ), yet have been challenging to investigate in model organisms. Although common to all of the α‐synucleinopathies, autonomic dysfunction is particularly important in MSA (Fanciulli & Wenning, ), where it is required to make the diagnosis (Gilman et al, ).…”
Section: Discussionmentioning
confidence: 99%
“…Autonomic dysfunction is a core clinical feature underlying all of the α‐synucleinopathies and includes bladder dysfunction, constipation, cardiovascular abnormalities, sexual dysfunction, sialorrhea, dry eyes, excessive sweating, and altered thermoregulation. These symptoms are a greater contributor to loss of quality of life than are the motor symptoms in PD (Estrada‐Bellmann et al, ; Martinez‐Martin, Rodriguez‐Blazquez, Kurtis, Chaudhuri,, & NMSS Validation Group, ; Müller et al, ; Prakash et al, ; Tibar et al, ), yet have been challenging to investigate in model organisms. Although common to all of the α‐synucleinopathies, autonomic dysfunction is particularly important in MSA (Fanciulli & Wenning, ), where it is required to make the diagnosis (Gilman et al, ).…”
Section: Discussionmentioning
confidence: 99%
“…For example, PD patients carrying PARKIN , PINK1, or LRRK2 mutation does not always present Lewy bodies [ 216 , 217 ]. Moreover, patients differ in the age of onset, ailment severity, neurodegeneration progression, and symptoms (including motor and non-motor) [ 218 , 219 ].…”
Section: Neurotoxin-induced Experimental In Vivo Models Of Pdmentioning
confidence: 99%
“…Understanding the inner working mechanisms of PD is one of the most intriguing scientific questions. Studies in neuroscience strongly suggest intervention during early therapeutic windows (Vu et al, 2012;Tibar et al, 2018). Although positron emitted topography/computed tomography is accurate (Meles et al, 2017) the diagnosis of PD at present is mainly dependent on clinical features and scores.…”
Section: Introductionmentioning
confidence: 99%