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      Alexithymia Is Associated with Reduced Quality of Life and Increased Caregiver Burden in Parkinson’s Disease

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          Abstract

          Parkinson’s disease (PD) is the second most frequent neurodegenerative disease of people who are beyond 50 years of age. People with PD (PwP) suffer from a large variety of motor and non-motor symptoms resulting in reduced health-related quality of life (HR-QoL). In the last two decades, alexithymia was identified as an additional non-motor symptom in PD. Alexithymia is defined as a cognitive affective disturbance resulting in difficulty to identify and distinguish feelings from bodily sensations of emotional arousal. In PD, the frequency of patients suffering of alexithymia is increased compared to healthy controls. The aim of the present study was to determine the relationship of alexithymia to HR-QoL of the PwP and caregiver burden of the corresponding caregiver. This cross-sectional questionnaire-based study used disease specific questionnaires for HR-QoL and caregiver burden. In total 119 PwP and their corresponding caregivers were included in the study. HR-QoL of the PwP correlated significantly with alexithymia ( p < 0.001), especially the sub-components “identifying feelings” ( p < 0.001) and “difficulties describing feelings” ( p = 0.001). Caregiver burden also correlated significantly with PwP alexithymia ( p < 0.001). However, caregiver burden was associated with sub-components “identifying feelings” ( p < 0.008) and “external oriented thinking” ( p < 0.004). These data support the importance of alexithymia as a non-motor symptom in PD.

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          Most cited references48

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          PDQ-39: a review of the development, validation and application of a Parkinson's disease quality of life questionnaire and its associated measures.

          Parkinson's disease is a common degenerative neurological condition. A number of general instruments exist to measure quality of life, but these were not designed to address areas salient to a specific disease. This contribution reviews the development and validation of the PDQ-39, a short 39-item quality of life questionnaire for Parkinson's disease. PDQ-39 data can be presented either in profile form or as a single index. This report also reviews the development and validation of a briefer measure (PDQ-8) derived from the PDQ-39, and of two summary indices (PDQ-39SI and PDQ-8SI.
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            Determinants of health-related quality of life in Parkinson's disease: a systematic review.

            This systematic review critically evaluates the literature to identify the demographic and clinical factors that predict the health-related quality of life (HRQOL) of people with Parkinson's disease (PD). Understanding how these factors relate to HRQOL in people with PD may assist clinicians minimise the functional and social impact of the disease by optimising their assessment and clinical decision making processes. A tailored search strategy in six databases identified 29 full-text reports that fulfilled the pre-defined inclusion and exclusion criteria. The quality of included studies was assessed by two independent reviewers using a customized assessment form. A best-evidence synthesis was used to summarise the demographic and clinical factors that were examined in relation to HRQOL. Depression was the most frequently identified determinant of HRQOL in people with idiopathic PD. Disease severity and disease disability were also found to be predictive of poor HRQOL outcomes in many studies. The motor symptoms that contributed most often to overall life quality were gait impairments and complications arising from medication therapy. To minimise the impact of PD on HRQOL, it may be necessary to consider the extent to which demographic factors and motor and non-motor symptoms contribute to life quality. © 2010. Published by Elsevier Ltd. All rights reserved.
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              Cognitive performance and neuropsychiatric symptoms in early, untreated Parkinson's disease.

              This study was undertaken to determine the prevalence and correlates of cognitive impairment (CI) and neuropsychiatric symptoms (NPS) in early, untreated patients with Parkinson's disease (PD).
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                Author and article information

                Journal
                Brain Sci
                Brain Sci
                brainsci
                Brain Sciences
                MDPI
                2076-3425
                24 June 2020
                June 2020
                : 10
                : 6
                : 401
                Affiliations
                [1 ]Department of Neurology, Hannover Medical School, Carl-Neuberg-Straße 1, 30625 Hannover, Germany; Theresa.Schnur@ 123456stud.mh-hannover.de (T.S.); Simon.C.Drexel@ 123456stud.mh-hannover.de (S.C.D.); Paracka.Lejla@ 123456mh-hannover.de (L.P.); Huber.Meret@ 123456mh-hannover.de (M.K.H.); Dressler.Dirk@ 123456mh-hannover.de (D.D.); Hoeglinger.Guenter@ 123456mh-hannover.de (G.U.H.); Wegner.Florian@ 123456mh-hannover.de (F.W.)
                [2 ]Behavioral Engineering Research Group, KU Leuven, Naamsestraat 69, 3000 Leuven, Belgium; florian.lange@ 123456kuleuven.be
                Author notes
                [* ]Correspondence: Klietz.Martin@ 123456mh-hannover.de ; Tel.: +49-511-5323122
                Author information
                https://orcid.org/0000-0002-3054-9905
                https://orcid.org/0000-0002-8336-5608
                Article
                brainsci-10-00401
                10.3390/brainsci10060401
                7348697
                32599704
                4136fe1e-7904-4747-af3c-3d40bb11b2d9
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 04 May 2020
                : 22 June 2020
                Categories
                Article

                parkinson’s disease,caregiver burden,alexithymia,health-related quality of life

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