Suppr超能文献

运动神经元病中的睡眠呼吸障碍

Sleep disordered breathing in motor neurone disease.

作者信息

D'Cruz Rebecca F, Murphy Patrick B, Kaltsakas Georgios

机构信息

Lane Fox Respiratory Unit, Guy's and St. Thomas' NHS Foundation Trust, London, UK.

National Institute for Health Research (NIHR) Biomedical Research Centre, Guy's and St. Thomas' NHS Foundation Trust and King's College London, London, UK.

出版信息

J Thorac Dis. 2018 Jan;10(Suppl 1):S86-S93. doi: 10.21037/jtd.2017.12.19.

Abstract

Motor neurone disease (MND) is a neurodegenerative disease defined by axonal loss and gliosis of upper and lower motor neurones in the motor cortex, lower brainstem nuclei and ventral horn of the spinal cord. MND is currently incurable and has a poor prognosis, with death typically occurring 3 to 5 years after disease onset. The disease is characterised by rapidly progressive weakness leading to paralysis, fasciculations, bulbar symptoms (including dysarthria and dysphagia) and respiratory compromise. Respiratory complications arise as a result of weakness of upper airway (pharyngeal and laryngeal) muscles and respiratory muscles (diaphragm, intercostal and accessory muscles) leading to respiratory failure. Due to early involvement of respiratory muscles in MND, sleep disordered breathing (SDB) occurs at a higher frequency than compared to the general population. SDB usually precedes daytime respiratory symptoms and chronic respiratory failure. It significantly impacts upon patients' quality of life and survival and its presence may predict prognosis. Managing SDB in MND with non-invasive ventilation (NIV) improves quality of life and survival. Early identification and management of SDB in MND patients is therefore crucial. This update will review assessments of respiratory muscle function, types of SDB and the effects of NIV in patients with MND.

摘要

运动神经元病(MND)是一种神经退行性疾病,其定义为运动皮层、脑桥下部核团及脊髓腹角的上下运动神经元轴突丢失和胶质增生。MND目前无法治愈,预后较差,通常在疾病发作后3至5年死亡。该疾病的特征是迅速进展的肌无力,导致瘫痪、肌束震颤、延髓症状(包括构音障碍和吞咽困难)及呼吸功能不全。呼吸并发症是由于上呼吸道(咽和喉)肌肉及呼吸肌(膈肌、肋间肌和辅助肌)无力导致呼吸衰竭所致。由于MND中呼吸肌早期受累,睡眠呼吸障碍(SDB)的发生率高于普通人群。SDB通常先于日间呼吸症状和慢性呼吸衰竭出现。它对患者的生活质量和生存有显著影响,其存在可能预示预后。采用无创通气(NIV)管理MND中的SDB可改善生活质量和生存。因此,早期识别和管理MND患者的SDB至关重要。本综述将回顾MND患者呼吸肌功能评估、SDB类型及NIV的效果。

相似文献

1
Sleep disordered breathing in motor neurone disease.
J Thorac Dis. 2018 Jan;10(Suppl 1):S86-S93. doi: 10.21037/jtd.2017.12.19.
2
Sleep-Disordered Breathing in Patients with Motor Neurone Disease: One Size Does Not Fit all.
Neurodegener Dis. 2020;20(4):131-138. doi: 10.1159/000513887. Epub 2021 Mar 18.
4
Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort.
J Neurol Neurosurg Psychiatry. 2016 Mar;87(3):280-6. doi: 10.1136/jnnp-2014-310055. Epub 2015 Apr 9.
5
Respiratory failure and sleep-disordered breathing in late-onset Pompe disease: a narrative review.
J Thorac Dis. 2020 Oct;12(Suppl 2):S235-S247. doi: 10.21037/jtd-cus-2020-007.
6
7
The Benefit of Non-invasive Ventilation in Motor Neuron Disease.
Open Respir Med J. 2020 Dec 15;14:53-61. doi: 10.2174/1874306402014010053. eCollection 2020.
8
Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease.
Cochrane Database Syst Rev. 2013 Mar 28(3):CD004427. doi: 10.1002/14651858.CD004427.pub3.
10
Motor neurone disease: a practical update on diagnosis and management.
Clin Med (Lond). 2010 Jun;10(3):252-8. doi: 10.7861/clinmedicine.10-3-252.

引用本文的文献

1
Sleep Disturbances in Amyotrophic Lateral Sclerosis and Prognostic Impact-A Retrospective Study.
Life (Basel). 2024 Oct 11;14(10):1284. doi: 10.3390/life14101284.
2
Na+/K+-ATPase: ion pump, signal transducer, or cytoprotective protein, and novel biological functions.
Neural Regen Res. 2024 Dec 1;19(12):2684-2697. doi: 10.4103/NRR.NRR-D-23-01175. Epub 2024 Jan 31.
3
Hypothalamus and amyotrophic lateral sclerosis: potential implications in sleep disorders.
Front Aging Neurosci. 2023 Jul 3;15:1193483. doi: 10.3389/fnagi.2023.1193483. eCollection 2023.
4
Quality of life in patients with chronic respiratory failure on home mechanical ventilation.
Eur Respir Rev. 2023 May 3;32(168). doi: 10.1183/16000617.0237-2022. Print 2023 Jun 30.
5
Motor neuron disease mimics in practice: a case series.
BMJ Case Rep. 2022 Jul 11;15(7):e247441. doi: 10.1136/bcr-2021-247441.
6
Sleep quality in COPD patients: correlation with disease severity and health status.
J Bras Pneumol. 2022 Apr 29;48(3):e20210340. doi: 10.36416/1806-3756/e20210340. eCollection 2022.
7
Respiratory Muscle Function Tests and Diaphragm Ultrasound Predict Nocturnal Hypoventilation in Slowly Progressive Myopathies.
Front Neurol. 2021 Oct 14;12:731865. doi: 10.3389/fneur.2021.731865. eCollection 2021.
8
Effects of nasal high flow on nocturnal hypercapnia, sleep, and sympathovagal balance in patients with neuromuscular disorders.
Sleep Breath. 2021 Sep;25(3):1441-1451. doi: 10.1007/s11325-020-02263-2. Epub 2020 Dec 2.

本文引用的文献

1
Sleep-Disordered Breathing in Neuromuscular Disease: Diagnostic and Therapeutic Challenges.
Chest. 2017 Oct;152(4):880-892. doi: 10.1016/j.chest.2017.03.023. Epub 2017 Mar 31.
3
The Prognostic Role of Obstructive Sleep Apnea at the Onset of Amyotrophic Lateral Sclerosis.
Neurodegener Dis. 2017;17(1):14-21. doi: 10.1159/000447560. Epub 2016 Sep 6.
4
Respiratory Muscle Strength as a Predictive Biomarker for Survival in Amyotrophic Lateral Sclerosis.
Am J Respir Crit Care Med. 2017 Jan 1;195(1):86-95. doi: 10.1164/rccm.201604-0848OC.
5
Prevalence of Amyotrophic Lateral Sclerosis - United States, 2012-2013.
MMWR Surveill Summ. 2016 Aug 5;65(8):1-12. doi: 10.15585/mmwr.ss6508a1.
6
Noninvasive ventilation in amyotrophic lateral sclerosis: effects on sleep quality and quality of life.
Acta Clin Belg. 2016 Dec;71(6):389-394. doi: 10.1080/17843286.2016.1173941. Epub 2016 Apr 26.
10
Sniff nasal inspiratory pressure as a prognostic factor of tracheostomy or death in amyotrophic lateral sclerosis.
J Neurol. 2015 Mar;262(3):593-603. doi: 10.1007/s00415-014-7613-3. Epub 2014 Dec 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验