Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease

Introduction: Mutations in the Parkin gene are the most common cause of autosomal recessive early-onset Parkinson's disease (PD). However, little is known about the quality of life (QoL) in Parkin-related PD. Here, we investigated the patterns of QoL in newly diagnosed Parkin-related PD patient...

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Main Authors: Xin-Yue Zhou, Feng-Tao Liu, Chen Chen, Su-Shan Luo, Jue Zhao, Yi-Lin Tang, Bo Shen, Wen-Bo Yu, Chuan-Tao Zuo, Jian-Jun Wu, Zheng-Tong Ding, Jian Wang, Yi-Min Sun
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-12-01
Series:Frontiers in Neurology
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Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2020.580910/full
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spelling doaj-f0f8893f645a4fd9ba70aad52cd11abe2020-12-18T06:20:36ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-12-011110.3389/fneur.2020.580910580910Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's DiseaseXin-Yue Zhou0Feng-Tao Liu1Chen Chen2Su-Shan Luo3Jue Zhao4Yi-Lin Tang5Bo Shen6Wen-Bo Yu7Chuan-Tao Zuo8Jian-Jun Wu9Zheng-Tong Ding10Jian Wang11Yi-Min Sun12Department of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaPositron Emission Tomography (PET) Center, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of Neurology, National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, ChinaIntroduction: Mutations in the Parkin gene are the most common cause of autosomal recessive early-onset Parkinson's disease (PD). However, little is known about the quality of life (QoL) in Parkin-related PD. Here, we investigated the patterns of QoL in newly diagnosed Parkin-related PD patients.Methods: Newly diagnosed PD patients (diagnosis made within 12 months) who had an age of onset (AOO) below 40 and underwent a PD-related genetic testing, were recruited (n = 148). Among them, 24 patients carried bi-allelic variants in Parkin (PD-Parkin) and 24 patients did not have any known causative PD mutations, or risk variants (GU-EOPD). The clinical materials, relevant factors and determinants of QoL were analyzed.Results: PD-Parkin patients had a younger AOO (p = 0.003) and longer disease duration (p = 0.005). After adjustment for AOO and disease duration, more dystonia (p = 0.034), and worse scores of non-motor symptoms including Beck depression inventory (BDI, p = 0.035), Epworth sleepiness scale (ESS, p = 0.044), and subdomains of depression/anxiety (p = 0.015) and sleep disorders (p = 0.005) in Non-motor symptoms questionnaire, were found in PD-Parkin comparing with GU-EOPD. PD-Parkin patients had poorer QoL (adjusted p = 0.045), especially in the mobility (adjusted p = 0.025), emotional well-being (adjusted p = 0.015) and bodily discomfort dimensions (adjusted p = 0.016). BDI scores (p = 0.005) and ESS scores (p = 0.047) were significant determinants of QoL in PD-Parkin.Conclusion: Newly diagnosed PD-Parkin patients showed worse QoL. More depression and excessive daytime sleepiness predicted worse QoL. For clinicians, management of depression and excessive daytime sleepiness is suggested to better improve QoL in patients with Parkin mutations.https://www.frontiersin.org/articles/10.3389/fneur.2020.580910/fullParkinson's diasesequality of lifeParkin (PARK2) gene mutationnewly diagnosedearly-onsetgenetics
collection DOAJ
language English
format Article
sources DOAJ
author Xin-Yue Zhou
Feng-Tao Liu
Chen Chen
Su-Shan Luo
Jue Zhao
Yi-Lin Tang
Bo Shen
Wen-Bo Yu
Chuan-Tao Zuo
Jian-Jun Wu
Zheng-Tong Ding
Jian Wang
Yi-Min Sun
spellingShingle Xin-Yue Zhou
Feng-Tao Liu
Chen Chen
Su-Shan Luo
Jue Zhao
Yi-Lin Tang
Bo Shen
Wen-Bo Yu
Chuan-Tao Zuo
Jian-Jun Wu
Zheng-Tong Ding
Jian Wang
Yi-Min Sun
Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease
Frontiers in Neurology
Parkinson's diasese
quality of life
Parkin (PARK2) gene mutation
newly diagnosed
early-onset
genetics
author_facet Xin-Yue Zhou
Feng-Tao Liu
Chen Chen
Su-Shan Luo
Jue Zhao
Yi-Lin Tang
Bo Shen
Wen-Bo Yu
Chuan-Tao Zuo
Jian-Jun Wu
Zheng-Tong Ding
Jian Wang
Yi-Min Sun
author_sort Xin-Yue Zhou
title Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease
title_short Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease
title_full Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease
title_fullStr Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease
title_full_unstemmed Quality of Life in Newly Diagnosed Patients With Parkin-Related Parkinson's Disease
title_sort quality of life in newly diagnosed patients with parkin-related parkinson's disease
publisher Frontiers Media S.A.
series Frontiers in Neurology
issn 1664-2295
publishDate 2020-12-01
description Introduction: Mutations in the Parkin gene are the most common cause of autosomal recessive early-onset Parkinson's disease (PD). However, little is known about the quality of life (QoL) in Parkin-related PD. Here, we investigated the patterns of QoL in newly diagnosed Parkin-related PD patients.Methods: Newly diagnosed PD patients (diagnosis made within 12 months) who had an age of onset (AOO) below 40 and underwent a PD-related genetic testing, were recruited (n = 148). Among them, 24 patients carried bi-allelic variants in Parkin (PD-Parkin) and 24 patients did not have any known causative PD mutations, or risk variants (GU-EOPD). The clinical materials, relevant factors and determinants of QoL were analyzed.Results: PD-Parkin patients had a younger AOO (p = 0.003) and longer disease duration (p = 0.005). After adjustment for AOO and disease duration, more dystonia (p = 0.034), and worse scores of non-motor symptoms including Beck depression inventory (BDI, p = 0.035), Epworth sleepiness scale (ESS, p = 0.044), and subdomains of depression/anxiety (p = 0.015) and sleep disorders (p = 0.005) in Non-motor symptoms questionnaire, were found in PD-Parkin comparing with GU-EOPD. PD-Parkin patients had poorer QoL (adjusted p = 0.045), especially in the mobility (adjusted p = 0.025), emotional well-being (adjusted p = 0.015) and bodily discomfort dimensions (adjusted p = 0.016). BDI scores (p = 0.005) and ESS scores (p = 0.047) were significant determinants of QoL in PD-Parkin.Conclusion: Newly diagnosed PD-Parkin patients showed worse QoL. More depression and excessive daytime sleepiness predicted worse QoL. For clinicians, management of depression and excessive daytime sleepiness is suggested to better improve QoL in patients with Parkin mutations.
topic Parkinson's diasese
quality of life
Parkin (PARK2) gene mutation
newly diagnosed
early-onset
genetics
url https://www.frontiersin.org/articles/10.3389/fneur.2020.580910/full
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