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1.
J Neurol ; 262(11): 2433-9, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26210749

ABSTRACT

The pathophysiology of the postural instability gait difficulty (PIGD) subtype of Parkinson's disease (PD) is unclear. Information on the spectrum of non-motor symptoms (NMS) in PIGD phenotype is limited. Our objective is to compare the spectrum of NMS in PIGD subtype compared to non-PIGD subgroup in PD patients and to determine predictive factors that are associated with PIGD phenotype. A total of 432 PD patients comprising 158 PIGD and 274 non-PIGD patients were recruited. NMS burden (frequency and severity) was assessed using non-motor symptom scale (NMSS). In the univariable analysis, NMSS total score (P = 0.0132), NMSS domain 3 (mood/apathy) score (P = 0.0108), NMSS domain 5 (attention/memory) score (P = 0.0048) and NMSS domain 8 (sexual function) score (P = 0.0052) were significantly higher in the PIGD group than in the non-PIGD group. Using multivariable logistic regression, UPDRS tremor score, UPDRS PIGD score, H&Y staging score and NMSS domain 8 (sexual function) score were found to be significantly different in the PIGD group compared to the non-PIGD group. We disclosed for the first time that PIGD patients demonstrated a greater overall NMS burden and sexual dysfunction and was an independent predictor of PIGD phenotype. Early intervention of sexual dysfunction symptoms in PIGD patients may improve their clinical management.


Subject(s)
Gait Disorders, Neurologic/physiopathology , Parkinson Disease/physiopathology , Postural Balance/physiology , Sexual Dysfunction, Physiological/physiopathology , Adult , Aged , Aged, 80 and over , Comorbidity , Female , Gait Disorders, Neurologic/epidemiology , Gait Disorders, Neurologic/etiology , Humans , Male , Middle Aged , Parkinson Disease/complications , Parkinson Disease/epidemiology , Sexual Dysfunction, Physiological/epidemiology , Sexual Dysfunction, Physiological/etiology
2.
Parkinsonism Relat Disord ; 21(8): 843-7, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25997863

ABSTRACT

BACKGROUND: Non-motor symptoms (NMS) are common among patients with Parkinson's disease (PD) however little is known about their progression in terms of severity or burden after referral to expert care. OBJECTIVE: This study was aimed to establish the progression of NMS burden in PD patients after referral to tertiary healthcare centre and factors affecting it. METHODS: Newly referred PD patients were prospectively enrolled and follow-up for up to 18 months. Non-motor symptoms scale (NMSS) was used to evaluate the burden of non-motor symptoms. RESULTS: There was a significant median reduction of total NMS burden over the follow-up period. Similarly all NMS domains except domains 2 (sleep/fatigue), 3 (mood/cognition), 6 (gastrointestinal) and 7 (urinary) showed significant median reduction of scores. In the univariate regression analysis, Hoehn & Yahr staging, disease duration, visit, Schwab & England Activities of Daily Living score and UPDRS motor scores were individually predictive of change in total NMS burden. However, in the multivariable regression analysis only the latter three were significantly predictive of change in the total NMS burden. CONCLUSION: There was a significant reduction of total NMS burden over the study period. The severity of motor and activity of daily living impairments as well as subsequent visit were the best predictors of NMS change.


Subject(s)
Disease Progression , Parkinson Disease/physiopathology , Severity of Illness Index , Aged , Female , Humans , Longitudinal Studies , Male , Middle Aged , Parkinson Disease/complications , Parkinson Disease/therapy , Referral and Consultation , Tertiary Healthcare
3.
Neurodegener Dis Manag ; 5(2): 147-53, 2015.
Article in English | MEDLINE | ID: mdl-25894878

ABSTRACT

Besides the classical motor symptoms, Parkinson's disease (PD) patients experience a wide range of nonmotor symptoms (NMS) throughout the disease course. However, due to the lack of recognition and understanding of the pathogenesis, NMS symptoms may be overlooked. Familial PD is a well-defined group that can provide a good model to investigate the mechanisms for both motor and NMS in PD. Some studies suggest that the frequency of NMS is not different between genetic and sporadic form of PD while others suggest that specific domains (such as neuropsychiatric symptoms) are more common in the genetic form. Early recognition of NMS may facilitate early diagnosis and monitoring of both sporadic and genetic PD.


Subject(s)
Parkinson Disease/genetics , Parkinson Disease/physiopathology , Animals , Humans , Parkinson Disease/psychology , Parkinson Disease/therapy
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