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The Journal of Parkinson’s Disease is dedicated to providing an open forum for original research in basic science, translational research and clinical medicine that will expedite our fundamental understanding and improve treatment of Parkinson’s disease. The journal is international and multidisciplinary and aims to promote progress in the epidemiology, etiology, genetics, molecular correlates, pathogenesis, pharmacology, psychology, diagnosis and treatment of Parkinson’s disease.
It will publish research reports, reviews, short communications, and letters-to-the-editor and offers very rapid publication and an affordable open access option.
Authors: Barnish, Maxwell S. | Whibley, Daniel | Horton, Simon M.C. | Butterfint, Zoe R. | Deane, Katherine H.O.
Article Type: Research Article
Abstract: Background: Communication is fundamental to human interaction and the development and maintenance of human relationships and is frequently affected in Parkinson’s disease (PD). However, research and clinical practice have both tended to focus on impairment rather than participation aspects of communicative deficit in PD. In contrast, people with PD have reported that it is these participation aspects of communication that are of greatest concern to them rather than physical speech impairment. Objective: To systematically review the existing body of evidence regarding the association between cognitive status and/or intelligibility and everyday communication in PD. Methods: Five …online databases were systematically searched in May 2015 (Medline Ovid, EMBASE, AMED, PsycINFO and CINAHL) and supplementary searches were also conducted. Two reviewers independently evaluated retrieved records for inclusion and then performed data extraction and quality assessment using standardised forms. Articles were eligible for inclusion if they were English-language original peer-reviewed research articles, book chapters or doctoral theses investigating the associations between at least one of cognitive status and level of intelligibility impairment and an everyday communication outcome in human participants with PD. Results: 4816 unique records were identified through database searches with 16 additional records identified through supplementary searches. 41 articles were suitable for full-text screening and 15 articles (12 studies) met the eligibility criteria. 10 studies assessed the role of cognitive status and 9 found that participants with greater cognitive impairment had greater everyday communication difficulties. 4 studies assessed the role of intelligibility and all found that participants with greater intelligibility impairment had greater everyday communication difficulties, although effects were often weak and not consistent. Conclusions: Both cognitive status and intelligibility may be associated with everyday communicative outcomes in PD. The contribution of intelligibility to everyday communication appears to be of small magnitude, suggesting that other factors beyond predominantly motor-driven impairment-level changes in intelligibility may play an important role in everyday communication difficulties in PD. Show more
Keywords: Parkinson disease, cognition disorders, speech disorders, communication, social participation, international classification of functioning, disability and health, review, systematic
DOI: 10.3233/JPD-150757
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 453-462, 2016
Authors: Baille, Guillaume | De Jesus, Anna Maria | Perez, Thierry | Devos, David | Dujardin, Kathy | Charley, Christelle Monaca | Defebvre, Luc | Moreau, Caroline
Article Type: Review Article
Abstract: In contrast to some other neurodegenerative diseases, little is known about ventilatory dysfunction in Parkinson’s disease (PD). To assess the spectrum of ventilation disorders in PD, we searched for and reviewed studies of dyspnea, lung volumes, respiratory muscle function, sleep breathing disorders and the response to hypoxemia in PD. Among the studies, we identified some limitations: (i) small study populations (mainly composed of patients with advanced PD), (ii) the absence of long-term follow-up and (iii) the absence of functional evaluations under “off-drug” conditions. Although there are many reports of abnormal spirometry data in PD (mainly related to impairment of the …inspiratory muscles), little is known about hypoventilation in PD. We conclude that ventilatory dysfunction in PD has been poorly studied and little is known about its frequency and clinical relevance. Hence, there is a need to characterize the different phenotypes of ventilation disorders in PD, study their relationships with disease progression and assess their prognostic value. Show more
Keywords: Parkinson’s disease, pathophysiology, ventilatory function, review
DOI: 10.3233/JPD-160804
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 463-471, 2016
Authors: Barnish, Jean | Atkinson, Rachel A. | Barran, Susannah M. | Barnish, Maxwell S.
Article Type: Research Article
Abstract: Background: There is evidence that participation in performing arts brings psychosocial benefits in the general population and in recent years there has been substantial interest in the potential therapeutic benefit of performing arts, including singing, for people with chronic medical conditions including those of neurological aetiology. Objective: To systematically review the existing body of evidence regarding the potential benefit of singing on clinical outcomes of people with PD. Methods: Seven online bibliographic databases were systematically searched in January 2016 and supplementary searches were conducted. Full-text original peer-reviewed scientific papers that investigated the potential benefit of …singing on at least one of speech, functional communication, cognitive status, motor function and quality of life in human participants with PD were eligible for inclusion. Results: 449 unique records were identified, 25 full-text articles were screened and seven studies included in the review. All seven studies assessed the impact of singing on speech, five found partial evidence of benefit and two found no evidence of benefit. One study assessed each of functional communication and quality of life and no significant benefit was found. No included study assessed the impact of singing on motor function or cognitive status. Conclusions: Singing may benefit the speech of people with PD, although evidence is not unequivocal. Further research is required to assess wider benefits including on functional communication, cognitive status, motor function and quality of life. Substantial methodological limitations were identified in the existing literature. Recommendations are made for advancing the state of the literature. Show more
Keywords: Parkinson disease, rehabilitation, singing, speech therapy, music therapy, review, systematic
DOI: 10.3233/JPD-160837
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 473-484, 2016
Authors: Margraf, N.G. | Wrede, A. | Deuschl, G. | Schulz-Schaeffer, W.J.
Article Type: Review Article
Abstract: Camptocormia is a disabling pathological, non-fixed, forward bending of the trunk. The clinical definition using only the bending angle is insufficient; it should include the subjectively perceived inability to stand upright, occurrence of back pain, typical individual complaints, and need for walking aids and compensatory signs (e.g. back-swept wing sign). Due to the heterogeneous etiologies of camptocormia a broad diagnostic approach is necessary. Camptocormia is most frequently encountered in movement disorders (PD and dystonia) and muscles diseases (myositis and myopathy, mainly facio-scapulo-humeral muscular dystrophy (FSHD)). The main diagnostic aim is to discover the etiology by looking for signs of the …underlying disease in the neurological examination, EMG, muscle MRI and possibly biopsy. PD and probably myositic camptocormia can be divided into an acute and a chronic stage according to the duration of camptocormia and the findings in the short time inversion recovery (STIR) and T1 sequences of paravertebral muscle MRI. There is no established treatment of camptocormia resulting from any etiology. Case series suggest that deep brain stimulation (DBS) of the subthalamic nucleus (STN-DBS) is effective in the acute but not the chronic stage of PD camptocormia. In chronic stages with degenerated muscles, treatment options are limited to orthoses, walking aids, physiotherapy and pain therapy. In acute myositic camptocormia an escalation strategy with different immunosuppressive drugs is recommended. In dystonic camptocormia, as in dystonia in general, case reports have shown botulinum toxin and DBS of the globus pallidus internus (GPi-DBS) to be effective. Camptocormia in connection with primary myopathies should be treated according to the underlying illness. Show more
Keywords: Camptocormia, bent spine syndrome, stooped posture, postural abnormality, back pain
DOI: 10.3233/JPD-160836
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 485-501, 2016
Authors: Pagan, Fernando | Hebron, Michaeline | Valadez, Ellen H. | Torres-Yaghi, Yasar | Huang, Xu | Mills, Reversa R. | Wilmarth, Barbara M. | Howard, Hellen | Dunn, Connell | Carlson, Alexis | Lawler, Abigail | Rogers, Sean L. | Falconer, Ramsey A. | Ahn, Jaeil | Li, Zhaoxia | Moussa, Charbel
Article Type: Research Article
Abstract: Background : We evaluated the effects of low doses of the tyrosine kinase Abelson (Abl) inhibitor Nilotinib, on safety and pharmacokinetics in Parkinson’s disease dementia or dementia with Lewy bodies. Objectives : The primary outcomes of this study were safety and tolerability; pharmacokinetics and target engagement were secondary, while clinical outcomes were exploratory. Methods : Twelve subjects were randomized into 150 mg (n = 5) or 300 mg (n = 7) groups and received Nilotinib orally every day for 24 weeks. Results : This study shows that 150 mg and 300 mg doses of Nilotinib appear to be safe and tolerated in subjects …with advanced Parkinson’s disease. Nilotinib is detectable in the cerebrospinal fluid (CSF) and seems to engage the target Abl. Motor and cognitive outcomes suggest a possible beneficial effect on clinical outcomes. The CSF levels of homovanillic acid are significantly increased between baseline and 24 weeks of treatment. Exploratory CSF biomarkers were measured. Conclusions : This small proof-of-concept study lacks a placebo group and participants were not homogenous, resulting in baseline differences between and within groups. This limits the interpretations of the biomarker and clinical data, and any conclusions should be drawn cautiously. Nonetheless, the collective observations suggest that it is warranted to evaluate the safety and efficacy of Nilotinib in larger randomized, double-blind, placebo-controlled trials. Show more
Keywords: Parkinson, Lewy bodies, Nilotinib, synuclein, dopamine, homovanillic acid, tau
DOI: 10.3233/JPD-160867
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 503-517, 2016
Authors: Wyse, Richard K. | Brundin, Patrik | Sherer, Todd B.
Article Type: Article Commentary
Abstract: We discuss a report in the current issue on clinical and biochemical findings from a safety trial using the cAbl tyrosine kinase inhibitor Nilotinib (150 mg or 300 mg given daily for 24 weeks) in a small group of patients with either advanced Parkinson’s disease or Dementia with Lewy Bodies. Despite some side effects (one serious), the authors claim that Nilotinib, which is normally used at much higher doses for treating leukemia, is safe and tolerated. Furthermore, they report a possible benefit on motor and cognitive outcomes. We debate the safety of Nilotinib and the reported efficacy signals. We emphasize that due …to the small sample size, and lack of a control group, it is impossible to rule out a placebo effect. We briefly discuss a range of aspects surrounding the current and possible future use of this cAbl inhibitor in patients with alpha-synucleinopathy, and what must now be done to obtain definitive information about its safety and efficacy in this population of patients. Show more
Keywords: Drug repositioning, neuroprotection, Nilotinib
DOI: 10.3233/JPD-160904
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 519-522, 2016
Authors: He, Lu | Lee, Eun-Young | Sterling, Nicholas W. | Kong, Lan | Lewis, Mechelle M. | Du, Guangwei | Eslinger, Paul J. | Huang, Xuemei
Article Type: Research Article
Abstract: Background: The impact of motor- and non-motor symptoms on health-related quality of life (HRQOL) in Parkinson’s disease (PD) has received increasing attention. Objectives: To address this, the study explored a large cohort of patients enrolled in the PD Biomarker Program. Methods: The PD Questionnaire-39 (PDQ-39) measured HRQOL, whereas the Unified PD Rating Scale (UPDRS) assessed motor and non-motor symptoms. Determinants of HRQOL in PD patients were identified by stepwise linear regression analysis. The relationship between the PDQ-39 and UPDRS subscale scores then was explored through structural equation modeling. Results: The mean disease duration …was 6.8 years and the mean PDQ-39 summary index (PDQ-39SI) was 18.4. UPDRS-I (non-motor function) and UPDRS-II (motor questionnaire) scores demonstrated the strongest correlations with PDQ-39SI (r Ϡ 0.4, P < 0.05), whereas UPDRS-III (motor exam) and UPDRS-IV (motor complications) scores were correlated moderately with PDQ-39SI (0.3 < r < 0.4, P < 0.05). Multiple linear stepwise regression analyses showed that age (β= –0.13, P < 0.001), education (β= –0.07, P = 0.008), UPDRS-I (β= 0.32, P = 0.000), and UPDRS-II (β= 0.44, P < 0.001) significantly contributed to HRQOL, and cumulatively accounted for 69.1% of the PDQ-39SI variance. UPDRS-II score was the primary predictor of PDQ-39SI, accounting for 57.3% of the variance, whereas UPDRS-I score accounted for 7.5%. UPDRS-III and -IV and other factors measured did not survive stepwise regression. Structural equation modeling confirmed the association of UPDRS-II (β= 0.67, P < 0.001) and UPDRS-I (β= 0.35, P < 0.001) with the PDQ-39SI. Conclusion: Both motor and non-motor function scores impacted significantly HRQOL in PD. UPDRS-III, however, has limited contributions to HRQOL although it is used as a main outcome in many clinical trials. Show more
Keywords: Parkinson’s disease, quality of life, motor symptoms, non-motor symptoms, structural equation modeling, Unified Parkinson’s disease rating scales, structure, review
DOI: 10.3233/JPD-160851
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 523-532, 2016
Authors: Nijhuis, Frouke A.P. | van Heek, Jolien | Bloem, Bastiaan R. | Post, Bart | Faber, Marjan J.
Article Type: Research Article
Abstract: Background: In advanced Parkinson’s disease (PD), neurologists and patients face a complex decision for an advanced therapy. When choosing a treatment, the best available evidence should be combined with the professional’s expertise and the patient’s preferences. Objective: The objective of this study was to explore current decision-making in advanced PD. Methods: We conducted focus group discussions and individual interviews with patients (N = 20) who had received deep brain stimulation, Levodopa-Carbidopa intestinal gel, or subcutaneous apomorphine infusion, and with their caregivers (N = 16). Furthermore, we conducted semi-structured interviews with neurologists (N = 7) and PD nurse specialists …(N = 3) to include the perspectives of all key players in this decision-making process. Data were analyzed by two researchers using a qualitative thematic analysis approach. Results: Four themes representing current experiences with the decision-making process were identified: 1) information and information needs, 2) factors influencing treatment choice and individual decision strategies, 3) decision-making roles, and 4) barriers and facilitators to shared decision-making (SDM). Patient preferences were taken into account, however patients were not always provided with adequate information. The professional’s expertise influenced the decision-making process in both positive and negative ways. Although professionals and patients considered SDM essential for the decision of an advanced treatment, they mentioned several barriers for the implementation in current practice. Conclusions: In this study we found several factors explaining why in current practice, evidence-based decision-making in advanced PD is not optimal. An important first step would be to develop objective information on all treatment options. Show more
Keywords: Parkinson’s disease, evidence-based medicine, shared decision-making, qualitative research
DOI: 10.3233/JPD-160816
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 533-543, 2016
Authors: Gu, Quanquan | Zhang, Huan | Xuan, Min | Luo, Wei | Huang, Peiyu | Xia, Shunren | Zhang, Minming
Article Type: Research Article
Abstract: Background: Patients with the postural instability and gait difficulty subtype (PIGD) of Parkinson’s disease (PD) are a refractory challenge in clinical practice. Despite previous attempts that have been made at studying subtype-specific brain alterations across PD population, conclusive neuroimaging biomarkers on patients with the PIGD subtype are still lacking. Machine learning-based classifications are a promising tool for differential diagnosis that effectively integrate complex and multivariate data. Objective: Our present study aimed to introduce the machine learning-based automatic classification for the first time to distinguish patients with the PIGD subtype from those with the non-PIGD subtype of PD …at the individual level. Methods: Fifty-two PD patients and forty-five normal controls (NCs) were recruited and underwent multi-modal MRI scans including a set of resting-state functional, 3D T1-weighted and diffusion tensor imaging sequences. By comparing the PD patients with the NCs, features that were not conducive to the subtype-specific classification were ruled out from massive brain features. We applied a support vector machine classifier with the recursive feature elimination method to multi-modal MRI data for selecting features with the best discriminating power, and evaluated the proposed classifier with the leave-one-out cross-validation. Results: Using this classifier, we obtained satisfactory diagnostic rates (accuracy = 92.31%, specificity = 96.97%, sensitivity = 84.21% and AUCmax = 0.9585). The diagnostic agreement evaluated by the Kappa test showed an almost perfect agreement with the existing clinical categorization (Kappa value = 0.83). Conclusions: With these favorable results, our findings suggested the machine learning-based classification as an alternative technique to classifying clinical subtypes in PD. Show more
Keywords: Parkinson’s disease, functional neuroimaging, diagnosis, machine learning, support vector machines
DOI: 10.3233/JPD-150729
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 545-556, 2016
Authors: Sterling, N.W. | Lewis, M.M. | Du, G. | Huang, X.
Article Type: Review Article
Abstract: Parkinson’s disease (PD) is a progressive age-related neurodegenerative disorder. Although the pathological hallmark of PD is dopaminergic cell death in the substantia nigra pars compacta, widespread neurodegenerative changes occur throughout the brain as disease progresses. Postmortem studies, for example, have demonstrated the presence of Lewy pathology, apoptosis, and loss of neurotransmitters and interneurons in both cortical and subcortical regions of PD patients. Many in vivo structural imaging studies have attempted to gauge PD-related pathology, particularly in gray matter, with the hope of identifying an imaging biomarker. Reports of brain atrophy in PD, however, have been inconsistent, most likely due …to differences in the studied populations (i.e. different disease stages and/or clinical subtypes), experimental designs (i.e. cross-sectional vs. longitudinal), and image analysis methodologies (i.e. automatic vs. manual segmentation). This review attempts to summarize the current state of gray matter structural imaging research in PD in relationship to disease progression, reconciling some of the differences in reported results, and to identify challenges and future avenues. Show more
Keywords: Parkinson’s disease, MRI, structure, review
DOI: 10.3233/JPD-160824
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 557-567, 2016
Authors: Izumi, Yasuhiko | Kondo, Naoto | Takahashi, Ryosuke | Akaike, Akinori | Kume, Toshiaki
Article Type: Research Article
Abstract: Background: The formation of intracellular aggregates containing α-synuclein (α-syn) is a main pathological feature of Parkinson disease. The propagation of α-syn aggregation via cell-to-cell transmission has been implicated in the progression of Parkinson disease. Objective: Our aim is to clarify the molecular mechanisms underlying the formation of intracellular aggregation by extracellular α-syn. Methods: We investigated the effects of exogenous α-syn aggregates on intracellular α-syn immunoreactivity in α-syn-overexpressing SH-SY5Y cells using two antibodies to distinct epitopes of α-syn. To obtain α-syn aggregates, α-syn solution was aged with continuous agitation. Results: Immunoreactivity against the acidic …C-terminal domain of the intracellular α-syn was reduced by exposure to agedα-syn, whereas that against the hydrophobic non-amyloid component region was not changed. The reduction in immunoreactivity was not suppressed by protease inhibitors but was mimicked by neutralization of the negative charges on the C-terminal of the intracellular α-syn induced by spermine or extracellular acidification. Conclusions: These results suggest that the reduction in immunoreactivity is attributed not to proteolytic cleavage but to a conformational change at the C-terminus of the intracellular α-syn. The conformational change at the C-terminus of the intracellular α-syn might be involved in an initial step of fibril formation by exogenous α-syn aggregates. Show more
Keywords: α-synuclein, conformational change, fibril, Parkinson disease, proteolysis
DOI: 10.3233/JPD-160835
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 569-579, 2016
Authors: Olsson, Yvonne | Clarén, Lena | Alvariza, Anette | Årestedt, Kristofer | Hagell, Peter
Article Type: Research Article
Abstract: Background: Being a family caregiver for a person with Parkinson’s disease (PD) can negatively impact health and wellbeing, but it appears less clear to what extent caregivers’ health/social service needs are met. Objective: We explored the extent to which PD family caregivers experience sufficient access to health/social services, as compared to age-matched controls; and the associations between this and demographic and health-related variables. Methods: A cross-sectional survey of 66 PD family caregivers and 79 age-matched control subjects including the SF-36 health survey, the Nottingham Health Profile Sleep section (NHP-Sleep), and questions regarding contacts with various …health/social related services and whether these were perceived as sufficient. Results: People reporting insufficient access (n = 29) were more often PD family caregivers than controls (83% vs. 37%), did more often have a disease of their own (79% vs. 46%), and reported poorer health according to the SF-36 and the NHP-Sleep. Being a PD family caregiver (OR, 8.90), reporting more pain (OR, 1.02) and having an own disease (OR, 3.46) were independently associated with insufficient health/social service access. Conclusions: Our results imply that those in greatest need for health/social services (i.e., those with poorer health, an own disease, and who are PD family caregivers) are those whose health/social service needs are least met. Larger studies are needed for firmer conclusions and regarding how unmet health/social service needs impacts caregiver health and wellbeing. Health/social service providers should not only focus on patients but also consider their family members’ needs. Show more
Keywords: Caregivers, health, health services needs and demand, Parkinson disease
DOI: 10.3233/JPD-160811
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 581-587, 2016
Authors: Szeto, Jennifer Y.Y. | Mowszowski, Loren | Gilat, Moran | Walton, Courtney C. | Naismith, Sharon L. | Lewis, Simon J.G.
Article Type: Research Article
Abstract: Background: Recent attempts to standardise the definition of Mild Cognitive Impairment (MCI) in Parkinson’s disease (PD) by the Movement Disorder Society Task Force has led to a greater understanding of this entity but to date, there has been a paucity of research regarding the impact of PD-MCI on caregiver outcomes. Objective: The aim of this study was to utilise the newly established PD-MCI diagnostic criteria to investigate caregiver outcomes in relation to four specific aspects: (1) caregiver burden, (2) quality of life (QoL), (3) caregiving experience, and (4) psychological distress. Methods: This study included a …total of 166 patient-caregiver dyads. Caregiver outcomes including quality of life, caregiver burden, mood disturbances, and caregiver experience were compared between caregivers of PD patients classified as having normal cognition (PD-NC) and PD-MCI. Results: Despite the two groups being matched on demographic and clinical features, caregivers of PD-MCI patients reported a lower level of QoL with regard to physical health and more interruptions with usual activities. On the other hand, a higher impact on finances was reported in caregivers of PD-NC patients, relative to caregivers of PD-MCI patients. Conclusions: This study has shown that even at earlier stages of cognitive impairment, PD-MCI caregivers already experience elevated levels of distress in the role of providing care to their care-recipients. These findings highlight the need to include management of caregiver distress and associated sequelae alongside the management of PD-MCI patients, early on in the disease course. Show more
Keywords: Mild cognitive impairment, Parkinson’s disease, caregiver burden, quality of life, caregiver outcomes
DOI: 10.3233/JPD-160823
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 589-596, 2016
Authors: Ossig, Christiana | Sippel, Daniel | Fauser, Mareike | Gandor, Florin | Jost, Wolfgang H. | Ebersbach, Georg | Storch, Alexander
Article Type: Research Article
Abstract: Background: Since previous studies aimed to study nonmotor symptom (NMS) fluctuations in direct conjunction with motor oscillations, there are no data available on the temporal context of NMS fluctuations and motor oscillations in advanced Parkinson’s disease (PD). Objective: To evaluate circadian patterns and temporal connections of NMS and motor fluctuations in PD. Methods: 15 controls, 17 non-fluctuating and 15 fluctuating PD patients completed two diaries by rating 4 key psychiatric (anxiety, depressive mood, inner restlessness, concentration/attention deficits), fatigue and 4 autonomic NMS (excessive sweating, sialorrhea, bladder urgency, dizziness) absent or present and motor function (Off, …On with/without dyskinesia, and asleep) for every hour for 5 consecutive days. Results: NMS Off state hours (hours with NMS rated as present) were less frequent compared to motor Off state hours and NMS On-Off-switches were less prevalent compared to those of the motor state. Off time and number of On-Off-switches of psychiatric NMS were moderately correlated with motor Off time and number of motor On-Off switches on the individual patient level. Changes in NMS state occurred largely independent of changes in motor states with concordance rates of only 26–43% of all NMS changes for psychiatric and 7–17% for autonomic NMS. In controls and non-fluctuating PD patients, there were no NMS state switches in concordance to motor state switches. Conclusion: We provide first data on the temporal context of NMS fluctuations showing similar frequencies of psychiatric NMS Off, fatigue Off and motor Off times as well as their On-Off-fluctuations, but low concordance rates of NMS with motor On-Off-state switches. We found no evidence for NMS fluctuations in non-fluctuating PD patients. Our data implicate similar fluctuation patterns of mood NMS and motor function without close timing and/or different kinetics. Show more
Keywords: Nonmotor symptoms, nonmotor fluctuations, motor complications, psychiatric symptoms, autonomic dysfunction, Parkinson’s disease
DOI: 10.3233/JPD-150764
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 597-607, 2016
Authors: Johnson, Andrew R. | Lawrence, Blake J. | Corti, Emily J. | Booth, Leon | Gasson, N. | Thomas, Meghan G. | Loftus, A.M. | Bucks, Romola S.
Article Type: Research Article
Abstract: Background: The Depression, Anxiety, and Stress Scale –21 (DASS-21) is a frequently used measure of emotional disturbance symptoms in Parkinson’s disease (PD). However, the factor structure of the DASS-21 in PD has yet to be explored. Objective: To assess whether the scale is measuring these symptoms in PD in the same way as the general population. Methods: The present study fit a series of established DASS-21 factor structures with both confirmatory factor analysis (CFA) and exploratory structural equation modelling (ESEM) using data from 251 participants with PD. Results: The 3-factor ESEM provided the …best fit. The depression and stress scales fit well, however, few items on the anxiety subscale loaded clearly, with several items significantly loading onto the depression or stress factors. Conclusions: Whilst the depression and stress subscales appear suitable in PD, poor loadings and internal consistency indicate the anxiety subscale may not accurately assess anxiety symptomology in PD. This may be due to the scale’s reliance on physiological symptoms as indicators of anxiety, when many of these are present in PD. Thus, the anxiety subscale of the DASS-21 may not be a suitable measure of anxiety in PD. Show more
Keywords: Parkinson’s disease, DASS-21, ESEM, structure
DOI: 10.3233/JPD-160842
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 609-616, 2016
Authors: Chekani, Farid | Bali, Vishal | Aparasu, Rajender R.
Article Type: Research Article
Abstract: Background: Parkinson’s disease (PD) is a debilitating neurological disorder that has a significant impact on activities of daily living (ADL). Limited data exists regarding the functional status of nursing home residents with PD. Objective: The study examined the nature, extent, and predictors of limitation of ADL in patients with PD residing in nursing homes. Methods: This study used cross-sectional design involving data from the National Nursing Home Survey (NNHS). The dependent variable was the total number of ADL for which the patient needed assistance. Assistance for ADL comprised of five items of transferring, dressing, eating, …toileting and bathing. Multivariable linear regression was used to examine the individual, biological and environmental factors associated with assistance needed for ADL. Results: The nationally representative study sample was of 98,093 nursing home residents with PD for an overall prevalence of 6.57%. The mean age of the study sample was 81.03±0.34 years. Mood symptoms (45%), behavioral symptoms (24%)and dementia (8%) were common among PD patients. Assistance needed for each ADL ranged from 68.24% for eating to 99.25% for bathing. Older age, being married, living in metropolitan statistical area (MSA), living in other place prior to admission, and presence of mood symptoms were positively related to assistance for ADL. Presence of behavioral symptoms and use of levodopa combination therapy were negatively related to assistance for ADL. Conclusions: Majority of the nursing home residents with PD had disability in all the five items of ADL. Various individual, environmental and biological factors were associated with ADL in nursing home residents with PD. Show more
Keywords: Parkinson’s disease, activities of daily living, ADL, nursing home patients, nursing home residents, elderly
DOI: 10.3233/JPD-160822
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 617-624, 2016
Authors: Gunnery, Sarah D. | Habermann, Barbara | Saint-Hilaire, Marie | Thomas, Cathi A. | Tickle-Degnen, Linda
Article Type: Research Article
Abstract: Background: Though hypomimia, also called facial masking , is experienced by many people with Parkinson’s disease (PD), little is known about how the experience of this motor impairment relates to their own and their care partners’ (CP) social life and relationship quality. Objective: To test if the experience of facial masking relates to social wellbeing in people with PD and their CPs. Method: Forty individuals with PD and their CPs rated PD’s difficulty showing facial expression (facial masking), and completed questionnaires about their own social wellbeing and depression. Results: PD-reported and CP-reported facial …masking of PD were positively correlated with experience of social rejection in both partners, though this relationship was diminished when controlling for depression. CPs’ rating of their partner’s facial masking was negatively associated with enjoyment interacting with their partner. This relationship remained when controlling for CP and PD depression. Conclusions: The findings suggest that the experience of facial masking is negatively associated with social wellbeing particularly for the CPs, and especially so for the quality of CPs interpersonal relationship with their partner with PD. Show more
Keywords: Parkinson’s disease, caregivers, facial expression, quality of life
DOI: 10.3233/JPD-160782
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 625-630, 2016
Authors: Heldman, Dustin A. | Giuffrida, Joseph P. | Cubo, Esther
Article Type: Research Article
Abstract: Background: Advanced therapies, such as deep brain stimulation and levodopa-carbidopa intestinal gel, can significantly improve quality of life in advanced Parkinson’s disease (PD). However, determining who should be referred for advanced therapy is a challenging problem. Objective: The objective was to determine the impact of remote monitoring using objective, wearable sensors on the advanced therapy referral rate in patients with advanced PD and if sensor data differed in patients who were referred and those who were not. Methods: A retrospective, exploratory, secondary analysis was performed on data collected in a study that followed forty individuals …with advanced PD for one year with half receiving standard care and half using motion sensor-based remote monitoring once per month in conjunction with standard care. Advanced therapy referral rates were compared between groups. For the group who underwent remote monitoring, objective motor features representing symptoms, dyskinesias, and fluctuations were examined to determine if objective kinematic features differed between patients who were and were not recommended for advanced therapy. Results: The advanced therapy referral rate was significantly higher for patients when a clinician had access to remote monitoring reports compared to standard care alone (63.6% versus 11.8%, p < 0.01). Bradykinesia severity, bradykinesia fluctuations, and dyskinesia severity differed significantly (p < 10e-8, p < 10e-5, and p < 0.01, respectively) between patients recommended and not recommended for advanced therapy. Conclusions: Remote monitoring technologies can capture motor features that may be clinically useful in identifying patients who may be candidates for advanced therapy. This could lead to development of automated screening algorithms, improve referral efficiency, and expand access to advanced therapies for patients with advanced PD. Show more
Keywords: Parkinson’s disease, telemedicine, deep brain stimulation, levodopa-carbidopa intestinal gel
DOI: 10.3233/JPD-160830
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 631-638, 2016
Authors: Mak, Margaret K.Y. | Cheung, Vinci | Ma, Shuangye | Lu, Zhong L. | Wang, Defeng | Lou, Wutao | Shi, Lin | Mok, Vincent C.T. | Chu, Winnie C.W. | Hallett, Mark
Article Type: Research Article
Abstract: Background: Previous studies employed demanding and complex hand tasks to study the brain activation in people with Parkinson’s Disease (PD). There is inconsistent finding about the cerebellar activity during movement execution of this patient population. Objectives: This study aimed to examine the brain activation patterns of PD individuals in the on-state and healthy control subjects in a simple finger tapping task. Methods: Twenty-seven patients with PD and 22 age-matched healthy subjects were recruited for the study. Subjects were instructed to perform simple finger tapping tasks under self- and cue-initiated conditions in separate runs while their …brain activations were captured using fMRI. Results: Healthy subjects had higher brain activity in contralateral precentral gyrus during the self-initiated task, and higher brain activity in the ipsilateral middle occipital gyrus during the cue-initiated task. PD patients had higher brain activity in the cerebellum Crus I (bilateral) and lobules VI (ipsilateral) during the self-initiated task and higher brain activity in the contralateral middle frontal gyrus during the cue-initiated task. When compared with healthy controls, PD patients had lower brain activity in the contralateral inferior parietal lobule during the self-initiated task, and lower brain activity in the ipsilateral cerebellum lobule VIII, lobule VIIB and vermis VIII, and thalamus during the cue-initiated task. Conjunction analysis indicated that both groups had activation in bilateral cerebellum and SMA and ipsilateral precentral gyrus and postcentral gyrus during both self- and cue-initiated movement. Individuals with PD exhibited higher brain activity in the executive zone (cerebellum Crus I and II) during self-initiated movement, and lower brain activity in the sensorimotor zone (i.e. lobule VIIb and VIII of the cerebellum) during cue-initiated movement. Discussions: The findings suggest that individuals with PD may use more executive control when performing simple movements. Show more
Keywords: Cerebellum, cognition, fMRI, movement disorders, Parkinson’s disease
DOI: 10.3233/JPD-160849
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 639-650, 2016
Authors: Carriere, Nicolas | Bourriez, Jean-Louis | Delval, Arnaud | Derambure, Philippe | Defebvre, Luc | Dujardin, Kathy
Article Type: Research Article
Abstract: Background: Impulse control disorders (ICDs) in Parkinson’s disease (PD) are related to treatment with dopamine agonists, which is thought to deregulate the dopaminergic mesolimbic pathway and impair reward evaluation. EEG studies in healthy controls (HCs) have suggested that the increase in theta power observed after negative outcome is a marker of reward processing. Objective: To compare outcome-locked, event-related spectral perturbation in a gambling task in PD patients with and without ICDs and in HCs. Methods: Twelve PD patients with ICDs, 12 PD patients without ICDs and 14 HCs underwent EEG while performing a gambling task. …The groups were compared in terms of (i) the peak EEG power in the theta (4–7 Hz), alpha (8–14 Hz) and beta (15–30 Hz) frequency bands between 200 and 500 ms after the outcome, and (ii) time-frequency plots at Fz, FCz and Cz. Results: Positive outcomes were associated with greater theta power than negative outcomes in patients without ICDs and in HCs, but not in patients with ICDs. Patients with ICDs and HCs displayed greater theta power following unexpectedly high outcomes. HCs displayed greater beta power following high amplitude than low amplitude outcomes, whereas patients with ICD showed the opposite pattern. Conclusions: In PD, ICDs are associated with (i) weaker modulation of frontocentral theta power by reward valence, (ii) greater frontocentral theta power following unexpected, high outcomes, and (iii) a reversal of the effect of risk on beta oscillations. These observations are consistent with an impairment in prediction error computation in the medial prefrontal cortex. Show more
Keywords: Parkinson disease, disruptive, impulse control, and conduct disorders, electroencephalography, brain waves, gambling, reward
DOI: 10.3233/JPD-160828
Citation: Journal of Parkinson's Disease, vol. 6, no. 3, pp. 651-666, 2016
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