Emily Beswick, Deborah Forbes, Kay Johnson, J. Newton, Rachel Dakin, Stella Glasmcher, Sharon Abrahams, Alan Carson, Siddharthan Chandran, S. Pal
{"title":"运动神经元疾病的非运动症状:发病率、评估和影响","authors":"Emily Beswick, Deborah Forbes, Kay Johnson, J. Newton, Rachel Dakin, Stella Glasmcher, Sharon Abrahams, Alan Carson, Siddharthan Chandran, S. Pal","doi":"10.1093/braincomms/fcad336","DOIUrl":null,"url":null,"abstract":"\n People with motor neuron disease often experience non-motor symptoms that may occur secondary to, or distinct from, motor degeneration, and that may significantly reduce quality of life, despite being under-recognised and evaluated in clinical practice. Non-motor symptoms explored in this population based study include: pain, fatigue, gastrointestinal issues, poor sleep, low mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction.\n People registered on the Clinical, Audit, Research and Evaluation of motor neuron disease platform, the Scottish motor neuron disease register, were invited to complete a questionnaire on non-motor symptoms and a self-reported Amyotrophic Lateral Sclerosis Functional Rating Scale. The questionnaire comprised a pre-defined list of 11 potential non-motor symptoms, with the opportunity to list additional symptoms.\n 120 individuals participated in this cross-sectional study, a 39% response rate of those sent questionnaires (n = 311). 99% of participants recruited (n = 120) experienced at least one non-motor symptom, with 72% (n = 120) reporting five or more. The symptoms most often reported were pain and fatigue (reported by 76% of participants respectively). The symptoms reported to be most impactful were gastrointestinal issues (reported as ‘severe’ by 54% of participants who experienced them), followed by pain and problematic saliva (51% respectively). Lower Amyotrophic Lateral Sclerosis Functional Rating Scale scores, indicating more advanced disease, and being a long survivor (diagnosed over 8 years ago [1]) were significantly associated with reporting more symptoms. 73% of respondents were satisfied with the frequency that non-motor symptoms were discussed in clinical care. 80% of participants indicated they believe evaluation of non-motor symptom is important to include as outcomes in trials, independent of their personal experience of these symptoms. The preferred method of assessment was completing questionnaires, at home.\n The overwhelming majority of people with motor neuron disease report non-motor symptoms and these frequently co-occur. Pain, fatigue, gastrointestinal issues, sleep, mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction are prevalent. People with motor neuron disease who had worse physical function and those who were long survivors were more likely to report more symptoms. Where reported, these symptoms are frequent, impactful and a priority for people with motor neuron disease in clinical care and trial design.","PeriodicalId":9318,"journal":{"name":"Brain Communications","volume":"118 19","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Non-motor symptoms in motor neuron disease: prevalence, assessment and impact\",\"authors\":\"Emily Beswick, Deborah Forbes, Kay Johnson, J. Newton, Rachel Dakin, Stella Glasmcher, Sharon Abrahams, Alan Carson, Siddharthan Chandran, S. Pal\",\"doi\":\"10.1093/braincomms/fcad336\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n People with motor neuron disease often experience non-motor symptoms that may occur secondary to, or distinct from, motor degeneration, and that may significantly reduce quality of life, despite being under-recognised and evaluated in clinical practice. Non-motor symptoms explored in this population based study include: pain, fatigue, gastrointestinal issues, poor sleep, low mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction.\\n People registered on the Clinical, Audit, Research and Evaluation of motor neuron disease platform, the Scottish motor neuron disease register, were invited to complete a questionnaire on non-motor symptoms and a self-reported Amyotrophic Lateral Sclerosis Functional Rating Scale. The questionnaire comprised a pre-defined list of 11 potential non-motor symptoms, with the opportunity to list additional symptoms.\\n 120 individuals participated in this cross-sectional study, a 39% response rate of those sent questionnaires (n = 311). 99% of participants recruited (n = 120) experienced at least one non-motor symptom, with 72% (n = 120) reporting five or more. The symptoms most often reported were pain and fatigue (reported by 76% of participants respectively). The symptoms reported to be most impactful were gastrointestinal issues (reported as ‘severe’ by 54% of participants who experienced them), followed by pain and problematic saliva (51% respectively). Lower Amyotrophic Lateral Sclerosis Functional Rating Scale scores, indicating more advanced disease, and being a long survivor (diagnosed over 8 years ago [1]) were significantly associated with reporting more symptoms. 73% of respondents were satisfied with the frequency that non-motor symptoms were discussed in clinical care. 80% of participants indicated they believe evaluation of non-motor symptom is important to include as outcomes in trials, independent of their personal experience of these symptoms. The preferred method of assessment was completing questionnaires, at home.\\n The overwhelming majority of people with motor neuron disease report non-motor symptoms and these frequently co-occur. Pain, fatigue, gastrointestinal issues, sleep, mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction are prevalent. People with motor neuron disease who had worse physical function and those who were long survivors were more likely to report more symptoms. Where reported, these symptoms are frequent, impactful and a priority for people with motor neuron disease in clinical care and trial design.\",\"PeriodicalId\":9318,\"journal\":{\"name\":\"Brain Communications\",\"volume\":\"118 19\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/braincomms/fcad336\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/braincomms/fcad336","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Non-motor symptoms in motor neuron disease: prevalence, assessment and impact
People with motor neuron disease often experience non-motor symptoms that may occur secondary to, or distinct from, motor degeneration, and that may significantly reduce quality of life, despite being under-recognised and evaluated in clinical practice. Non-motor symptoms explored in this population based study include: pain, fatigue, gastrointestinal issues, poor sleep, low mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction.
People registered on the Clinical, Audit, Research and Evaluation of motor neuron disease platform, the Scottish motor neuron disease register, were invited to complete a questionnaire on non-motor symptoms and a self-reported Amyotrophic Lateral Sclerosis Functional Rating Scale. The questionnaire comprised a pre-defined list of 11 potential non-motor symptoms, with the opportunity to list additional symptoms.
120 individuals participated in this cross-sectional study, a 39% response rate of those sent questionnaires (n = 311). 99% of participants recruited (n = 120) experienced at least one non-motor symptom, with 72% (n = 120) reporting five or more. The symptoms most often reported were pain and fatigue (reported by 76% of participants respectively). The symptoms reported to be most impactful were gastrointestinal issues (reported as ‘severe’ by 54% of participants who experienced them), followed by pain and problematic saliva (51% respectively). Lower Amyotrophic Lateral Sclerosis Functional Rating Scale scores, indicating more advanced disease, and being a long survivor (diagnosed over 8 years ago [1]) were significantly associated with reporting more symptoms. 73% of respondents were satisfied with the frequency that non-motor symptoms were discussed in clinical care. 80% of participants indicated they believe evaluation of non-motor symptom is important to include as outcomes in trials, independent of their personal experience of these symptoms. The preferred method of assessment was completing questionnaires, at home.
The overwhelming majority of people with motor neuron disease report non-motor symptoms and these frequently co-occur. Pain, fatigue, gastrointestinal issues, sleep, mood, anxiety, problematic saliva, apathy, emotional lability, cognitive complaints and sexual dysfunction are prevalent. People with motor neuron disease who had worse physical function and those who were long survivors were more likely to report more symptoms. Where reported, these symptoms are frequent, impactful and a priority for people with motor neuron disease in clinical care and trial design.