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Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia

This study aimed to examine clinical features, sleep, abnormal sleep-wake transition and non-sleep disturbances as well as lab tests in Chinese fatal familial insomnia (FFI) subjects. Patients with confirmed clinical and laboratory diagnosis of FFI have been retrospectively reviewed. The clinical fe...

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Autores principales: Wu, Liyong, Lu, Hui, Wang, Xianling, Liu, Jia, Huang, Chaoyang, Ye, Jing, Li, Cuijiang, Lu, Jun, Wang, Yuping, Jia, Jianping, Zhan, Shuqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472586/
https://www.ncbi.nlm.nih.gov/pubmed/28620158
http://dx.doi.org/10.1038/s41598-017-03817-3
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author Wu, Liyong
Lu, Hui
Wang, Xianling
Liu, Jia
Huang, Chaoyang
Ye, Jing
Li, Cuijiang
Lu, Jun
Wang, Yuping
Jia, Jianping
Zhan, Shuqin
author_facet Wu, Liyong
Lu, Hui
Wang, Xianling
Liu, Jia
Huang, Chaoyang
Ye, Jing
Li, Cuijiang
Lu, Jun
Wang, Yuping
Jia, Jianping
Zhan, Shuqin
author_sort Wu, Liyong
collection PubMed
description This study aimed to examine clinical features, sleep, abnormal sleep-wake transition and non-sleep disturbances as well as lab tests in Chinese fatal familial insomnia (FFI) subjects. Patients with confirmed clinical and laboratory diagnosis of FFI have been retrospectively reviewed. The clinical features and the results of the complementary tests, including polysomnography (PSG), brain imaging and genetic analysis, were used. Two male and three female patients were recruited in this study. Three of the five patients had more comprehensive family medical records. The most typical clinical manifestations in all 5 patients were sleep disturbances, including insomnia, laryngeal stridor, sleep breath disturbance, and sleep-related involuntary movements. PSG of all these five cases showed reduction in total sleep time, sleep fragmentation, abnormal short non-rapid eye movement - rapid eye movement (REM) cycling, REM sleep reduction or loss, and REM sleep instruction in wakefulness. Patient 2's emission tomography scan demonstrated a reduction in glucose uptake in the left thalamus and bilateral inferior parietal lobe. In summary, Chinese FFI patients are typically characterized by organic sleep related symptoms, rapidly progressive dementia and sympathetic symptoms. We propose that structural damages in the thalamus and cortex are mostly responsible for clinical manifestations of FFI.
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spelling pubmed-54725862017-06-21 Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia Wu, Liyong Lu, Hui Wang, Xianling Liu, Jia Huang, Chaoyang Ye, Jing Li, Cuijiang Lu, Jun Wang, Yuping Jia, Jianping Zhan, Shuqin Sci Rep Article This study aimed to examine clinical features, sleep, abnormal sleep-wake transition and non-sleep disturbances as well as lab tests in Chinese fatal familial insomnia (FFI) subjects. Patients with confirmed clinical and laboratory diagnosis of FFI have been retrospectively reviewed. The clinical features and the results of the complementary tests, including polysomnography (PSG), brain imaging and genetic analysis, were used. Two male and three female patients were recruited in this study. Three of the five patients had more comprehensive family medical records. The most typical clinical manifestations in all 5 patients were sleep disturbances, including insomnia, laryngeal stridor, sleep breath disturbance, and sleep-related involuntary movements. PSG of all these five cases showed reduction in total sleep time, sleep fragmentation, abnormal short non-rapid eye movement - rapid eye movement (REM) cycling, REM sleep reduction or loss, and REM sleep instruction in wakefulness. Patient 2's emission tomography scan demonstrated a reduction in glucose uptake in the left thalamus and bilateral inferior parietal lobe. In summary, Chinese FFI patients are typically characterized by organic sleep related symptoms, rapidly progressive dementia and sympathetic symptoms. We propose that structural damages in the thalamus and cortex are mostly responsible for clinical manifestations of FFI. Nature Publishing Group UK 2017-06-15 /pmc/articles/PMC5472586/ /pubmed/28620158 http://dx.doi.org/10.1038/s41598-017-03817-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wu, Liyong
Lu, Hui
Wang, Xianling
Liu, Jia
Huang, Chaoyang
Ye, Jing
Li, Cuijiang
Lu, Jun
Wang, Yuping
Jia, Jianping
Zhan, Shuqin
Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia
title Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia
title_full Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia
title_fullStr Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia
title_full_unstemmed Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia
title_short Clinical Features and Sleep Analysis of Chinese Patients with Fatal Familial Insomnia
title_sort clinical features and sleep analysis of chinese patients with fatal familial insomnia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472586/
https://www.ncbi.nlm.nih.gov/pubmed/28620158
http://dx.doi.org/10.1038/s41598-017-03817-3
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