主题11 -认知和心理评估与支持

IF 2.5 4区 医学 Q2 CLINICAL NEUROLOGY Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Pub Date : 2022-11-01 DOI:10.1080/21678421.2022.2120687
M. Metzger, V. Sirenko, E. Giglia, P. Mehra, Y. Tadjine, S. Bista, N. Pender, P. Ferraro, E. Gervino, G. Meo, M. Cillerai, M. Pardini, L. Roccatagliata, A. Schenone, C. Caponnetto
{"title":"主题11 -认知和心理评估与支持","authors":"M. Metzger, V. Sirenko, E. Giglia, P. Mehra, Y. Tadjine, S. Bista, N. Pender, P. Ferraro, E. Gervino, G. Meo, M. Cillerai, M. Pardini, L. Roccatagliata, A. Schenone, C. Caponnetto","doi":"10.1080/21678421.2022.2120687","DOIUrl":null,"url":null,"abstract":"Background: Stress and dysphoria often follow the diagnosis MND, with some adapting quickly and finding a new balance, while others struggle to come to terms with the diagnosis and continue experiencing high levels of emotional distress. As observed in our previous study in patients with MND and their partners, re-appraisal and finding meaning play a significant role in the process of psychological adjustment. Psychological counselling can be offered to those in need, but is often not available or not specifically enough. Meaning Centred Psychotherapy: Breitbart ’ s Meaning Centred Psychotherapy (BMCP) has been found to be well- accepted and effective in advanced cancer patients. BMCP is a time-limited, manualized group psychotherapy, focusing on sense of meaning and thereby relieving distress and promoting psychological well-being and it has been proven effective in multiple RCT ’ s, also in the Netherlands. Most themes addressed in BMCP seem in clinical practice also suitable for MND patients, who are faced with similar complex issues related to the prospect of progressive physical decline and early death. Patients are supported and guided in a directive manner to focus on what is meaningful to them - by reflect-ing on their life and to thereby gaining sharper focus on what is important to them in the remaining time ahead of them. To date, BMCP has not been studied in MND patients. Physical barriers can be overcome by offering this therapy individually and online, where patients follow the pro- gramme from home with e-mail coaching and face to face video-consulting with the psychologist. Methods: We have adapted the Dutch group protocol for the purpose of such an online approach specifically for individuals diagnosed with ALS or PMA patients and this resulted in the Making Sense training. At this moment we are testing acceptability, feasibility and patient satisfaction, while we document changes in distress over time. We hypothesize that offering 8-weeks the internet-based Making Sense training for distressed MND patients, is acceptable, feasible and helpful in reducing emotional MND related distress with sub-sequent improvement in quality of life. A mixed method approach, collecting both quantitative and qualitative data, is used. For pragmatic and ethical reasons, we chose the best alternative for the RCT design namely a randomized Single-Case Experimental (SCE) design that requires only a small sample (N ¼ 5). This study aims to answer the following questions: 1. Is the Making Sense training acceptable, feasible and appreciated by patients with MND? 2. What are the effects on emotional MND related distress (primary outcome), perceived quality of life and sense of meaning (second- ary outcomes)? Results: At this moment three patients are included and started the training. Two new participants will be included and randomised soon. We will be able to present our first results in December 2022. Background: ALS primarily affects motor functions, but cog- nitive functions, including social understanding, may also be impaired. Von Economo neurons (VENs) are part of the neur- onal substrate of social understanding and these cells are histopathologically altered in ALS. Objective: We investigated whether activity in areas including VENs is associated with an impairment of cognitive tasks that mirror social functioning. Methods: In this observational prospective study, ALS patients ( N ¼ 26) were tested for cognitive behavioural function, encompassing different aspects of empathetic under- standing (interpersonal reactivity index, IRI), social behaviour (ultimatum game), recognition of faux-pas situations, and general cognitive functioning (Edinburgh Cognitive and Behavioural ALS Screen, ECAS). For in vivo pathological stag- ing according to Brettschneider/Braak, DTI-MRI was performed to determine those ALS FDG PET in N 20 ALS patients and compared to N matched healthy controls. Volume of interest analysis was performed in the anterior cingulate cortex (ACC) and the anterior insular cortex (AIC), which contain high numbers of VENs. Results: Compared to those without expected pathological involvement of VENs (B/B ALS stages 1 þ 2), ALS patients with anticipated pathological involvement of VENs (B/B ALS stages 3 þ 4) presented with significantly reduced fantasy to understand the mindset of others (IRI) and, social behaviour was more selfish (ultimatum game) despite the fact that cognitive understanding of socially inappropriate behaviour of others (faux-pas) was unimpaired. 18F-FDG-PET showed hypometabolism in ACC and AIC in ALS patients with antici- pated pathological involvement of VENs compared to those without and this was significantly correlated to cognitive-behavioral functions in certain tasks. Discussion: Here, we present evidence of altered social behaviour in ALS patients associated with regional 18FDG- PET hypometabolism in areas with a high density of VENs, thereby suggesting a possible causal association. Background: Deficits in verbal fluency are among the most common non-motor impairments which occur in ALS. Such symptomatic changes can be quantified by the Boston Naming Task (BNT) (1). However, performance in this task may not capture early or subtle impairments in verbal fluency, despite underlying pathophysiology. Further, perform- ance in the BNT may be impaired by deficits in language/ speech-generating cortical networks, in addition to those required for executive functioning (2). Objectives: We aimed to design Background: Psychological resilience (PR) is defined as the human capacity to overcome adverse events using individual and social resources, and to use crises as an incentive for personal growth. Recent investigations have observed that PR is significantly associated with more well-preserved cogni- tive function in healthy subjects, but a specific investigation of such phenomenon in patients with motor neuron diseases (MNDs) is still lacking. Objectives: To evaluate PR in MNDs, and to explore its relationship with cognitive, behavioral and mood symptoms in order to test the hypothesis that greater PR might be pro- tective against extra-motor clinical manifestations of MND. Methods: 72 MND patients and 62 age and gender matched healthy controls (HCs) were included in the study. PR was assessed using the 10-items Italian version of the Connor-Davidson Resilience Scale (CD-RISC-10), patients were asked behavioral disturbances. Discussion: Our results suggest that PR is an important protective factor against cognitive deterioration in MNDs, and provide preliminary evidence for the potential usefulness of resilience enhancement psychological interventions as a future strategy to prevent or delay the onset of cognitive dis- turbances in these neurodegenerative conditions. Background: Deficits in recognition of emotions is part of the cognitive impairment which occurs in ALS. Such symptomatic changes in social cognition can be quantified by the Reading the Mind in the Eyes Task (RMET) (1). However, performance in this task may not capture early or subtle impairments in social cognition, despite underlying patho- physiology. It has previously been demonstrated that social cortical network engagement during the RMET can be quan- tified using electroencephalography (EEG) (2). Objectives: To determine if dysfunction in cortical networks driving social cognition can be directly captured and quanti- fied in ALS using EEG. Methods: A modified version of the RMET is performed during recording of 128-channel EEG. The average cortical acti- vation (event related potential, ERP) which occurs during correct recognition of individuals ’ emotional state is compared to that captured during recognition individuals ’ sex, as a non-social control. Recruitment is ongoing, with datasets from 4 controls and 14 people with ALS collected to date. Analyses based on datasets from 15 controls and 25 people with ALS will be presented at the 2022 MNDA Symposium. Results: Preliminary examination of ERPs collected to date and comparison to control data reported previously (2) the post-bereavement experiences and coping were screened in Endnote V R Version X9. Meta-analyses and meta-regressions were calculated for cross-sectional data using Rstudio V R . Studies were assigned to temporal and physical categories and Hedges ’ g was calculated for the respect-ive categories to provide an estimate of a cognitive course based on cross-sectional data. Due to low numbers and het- erogeneity in reporting, longitudinal studies were analysed descriptively. Results: A total of N ¼ 45 cross-sectional and N ¼ 13 longitudinal studies were included. Impairments in all cognitive domains, except verbal IQ, were found in ALS patients (PALS). PALS showed stable cognitive performances in cross- sectional and in most longitudinal studies. PALS with symptoms for 18 – 24 months and PALS who had an ALSFRS-R score of 40 – 36 were the most frequently reported subgroup regarding neuropsychology. Age was related to visuospatial functioning, and depressiveness to attention. In longitudinal studies, impact of site of onset and cognitive status at base-line on cognitive course was found. Discussion: Despite vast evidence for cognitive impairment at disease onset in different domains, evidence for evolution of these deficits is rather limited, suggesting that PALS pre- sent with cognitive impairment early in the course possibly in a sense of disease trait. Background: Social Cognition (SC) deficits may be a distinct- ive feature of Amyotrophic Lateral Sclerosis (ALS) patients since the early stages of the Conclusions: Our results show that bulbar-onset ALS-CN patients are more impaired in RMET-36 and SET-IA than spi-nal-onset ALS-CN patients, compared to controls. This differ- entiated pattern of impairment in affective and cognitive ToM (RMET-36 and SET-IA, respectively) related to the onset site, may be due to the presence of a subtle affective and/or co","PeriodicalId":7740,"journal":{"name":"Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration","volume":"23 1","pages":"167 - 175"},"PeriodicalIF":2.5000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Theme 11 - Cognitive and Psychological Assessment and Support\",\"authors\":\"M. Metzger, V. Sirenko, E. Giglia, P. Mehra, Y. Tadjine, S. Bista, N. Pender, P. Ferraro, E. Gervino, G. Meo, M. Cillerai, M. Pardini, L. Roccatagliata, A. Schenone, C. Caponnetto\",\"doi\":\"10.1080/21678421.2022.2120687\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Stress and dysphoria often follow the diagnosis MND, with some adapting quickly and finding a new balance, while others struggle to come to terms with the diagnosis and continue experiencing high levels of emotional distress. As observed in our previous study in patients with MND and their partners, re-appraisal and finding meaning play a significant role in the process of psychological adjustment. Psychological counselling can be offered to those in need, but is often not available or not specifically enough. Meaning Centred Psychotherapy: Breitbart ’ s Meaning Centred Psychotherapy (BMCP) has been found to be well- accepted and effective in advanced cancer patients. BMCP is a time-limited, manualized group psychotherapy, focusing on sense of meaning and thereby relieving distress and promoting psychological well-being and it has been proven effective in multiple RCT ’ s, also in the Netherlands. Most themes addressed in BMCP seem in clinical practice also suitable for MND patients, who are faced with similar complex issues related to the prospect of progressive physical decline and early death. Patients are supported and guided in a directive manner to focus on what is meaningful to them - by reflect-ing on their life and to thereby gaining sharper focus on what is important to them in the remaining time ahead of them. To date, BMCP has not been studied in MND patients. Physical barriers can be overcome by offering this therapy individually and online, where patients follow the pro- gramme from home with e-mail coaching and face to face video-consulting with the psychologist. Methods: We have adapted the Dutch group protocol for the purpose of such an online approach specifically for individuals diagnosed with ALS or PMA patients and this resulted in the Making Sense training. At this moment we are testing acceptability, feasibility and patient satisfaction, while we document changes in distress over time. We hypothesize that offering 8-weeks the internet-based Making Sense training for distressed MND patients, is acceptable, feasible and helpful in reducing emotional MND related distress with sub-sequent improvement in quality of life. A mixed method approach, collecting both quantitative and qualitative data, is used. For pragmatic and ethical reasons, we chose the best alternative for the RCT design namely a randomized Single-Case Experimental (SCE) design that requires only a small sample (N ¼ 5). This study aims to answer the following questions: 1. Is the Making Sense training acceptable, feasible and appreciated by patients with MND? 2. What are the effects on emotional MND related distress (primary outcome), perceived quality of life and sense of meaning (second- ary outcomes)? Results: At this moment three patients are included and started the training. Two new participants will be included and randomised soon. We will be able to present our first results in December 2022. Background: ALS primarily affects motor functions, but cog- nitive functions, including social understanding, may also be impaired. Von Economo neurons (VENs) are part of the neur- onal substrate of social understanding and these cells are histopathologically altered in ALS. Objective: We investigated whether activity in areas including VENs is associated with an impairment of cognitive tasks that mirror social functioning. Methods: In this observational prospective study, ALS patients ( N ¼ 26) were tested for cognitive behavioural function, encompassing different aspects of empathetic under- standing (interpersonal reactivity index, IRI), social behaviour (ultimatum game), recognition of faux-pas situations, and general cognitive functioning (Edinburgh Cognitive and Behavioural ALS Screen, ECAS). For in vivo pathological stag- ing according to Brettschneider/Braak, DTI-MRI was performed to determine those ALS FDG PET in N 20 ALS patients and compared to N matched healthy controls. Volume of interest analysis was performed in the anterior cingulate cortex (ACC) and the anterior insular cortex (AIC), which contain high numbers of VENs. Results: Compared to those without expected pathological involvement of VENs (B/B ALS stages 1 þ 2), ALS patients with anticipated pathological involvement of VENs (B/B ALS stages 3 þ 4) presented with significantly reduced fantasy to understand the mindset of others (IRI) and, social behaviour was more selfish (ultimatum game) despite the fact that cognitive understanding of socially inappropriate behaviour of others (faux-pas) was unimpaired. 18F-FDG-PET showed hypometabolism in ACC and AIC in ALS patients with antici- pated pathological involvement of VENs compared to those without and this was significantly correlated to cognitive-behavioral functions in certain tasks. Discussion: Here, we present evidence of altered social behaviour in ALS patients associated with regional 18FDG- PET hypometabolism in areas with a high density of VENs, thereby suggesting a possible causal association. Background: Deficits in verbal fluency are among the most common non-motor impairments which occur in ALS. Such symptomatic changes can be quantified by the Boston Naming Task (BNT) (1). However, performance in this task may not capture early or subtle impairments in verbal fluency, despite underlying pathophysiology. Further, perform- ance in the BNT may be impaired by deficits in language/ speech-generating cortical networks, in addition to those required for executive functioning (2). Objectives: We aimed to design Background: Psychological resilience (PR) is defined as the human capacity to overcome adverse events using individual and social resources, and to use crises as an incentive for personal growth. Recent investigations have observed that PR is significantly associated with more well-preserved cogni- tive function in healthy subjects, but a specific investigation of such phenomenon in patients with motor neuron diseases (MNDs) is still lacking. Objectives: To evaluate PR in MNDs, and to explore its relationship with cognitive, behavioral and mood symptoms in order to test the hypothesis that greater PR might be pro- tective against extra-motor clinical manifestations of MND. Methods: 72 MND patients and 62 age and gender matched healthy controls (HCs) were included in the study. PR was assessed using the 10-items Italian version of the Connor-Davidson Resilience Scale (CD-RISC-10), patients were asked behavioral disturbances. Discussion: Our results suggest that PR is an important protective factor against cognitive deterioration in MNDs, and provide preliminary evidence for the potential usefulness of resilience enhancement psychological interventions as a future strategy to prevent or delay the onset of cognitive dis- turbances in these neurodegenerative conditions. Background: Deficits in recognition of emotions is part of the cognitive impairment which occurs in ALS. Such symptomatic changes in social cognition can be quantified by the Reading the Mind in the Eyes Task (RMET) (1). However, performance in this task may not capture early or subtle impairments in social cognition, despite underlying patho- physiology. It has previously been demonstrated that social cortical network engagement during the RMET can be quan- tified using electroencephalography (EEG) (2). Objectives: To determine if dysfunction in cortical networks driving social cognition can be directly captured and quanti- fied in ALS using EEG. Methods: A modified version of the RMET is performed during recording of 128-channel EEG. The average cortical acti- vation (event related potential, ERP) which occurs during correct recognition of individuals ’ emotional state is compared to that captured during recognition individuals ’ sex, as a non-social control. Recruitment is ongoing, with datasets from 4 controls and 14 people with ALS collected to date. Analyses based on datasets from 15 controls and 25 people with ALS will be presented at the 2022 MNDA Symposium. Results: Preliminary examination of ERPs collected to date and comparison to control data reported previously (2) the post-bereavement experiences and coping were screened in Endnote V R Version X9. Meta-analyses and meta-regressions were calculated for cross-sectional data using Rstudio V R . Studies were assigned to temporal and physical categories and Hedges ’ g was calculated for the respect-ive categories to provide an estimate of a cognitive course based on cross-sectional data. Due to low numbers and het- erogeneity in reporting, longitudinal studies were analysed descriptively. Results: A total of N ¼ 45 cross-sectional and N ¼ 13 longitudinal studies were included. Impairments in all cognitive domains, except verbal IQ, were found in ALS patients (PALS). PALS showed stable cognitive performances in cross- sectional and in most longitudinal studies. PALS with symptoms for 18 – 24 months and PALS who had an ALSFRS-R score of 40 – 36 were the most frequently reported subgroup regarding neuropsychology. Age was related to visuospatial functioning, and depressiveness to attention. In longitudinal studies, impact of site of onset and cognitive status at base-line on cognitive course was found. Discussion: Despite vast evidence for cognitive impairment at disease onset in different domains, evidence for evolution of these deficits is rather limited, suggesting that PALS pre- sent with cognitive impairment early in the course possibly in a sense of disease trait. Background: Social Cognition (SC) deficits may be a distinct- ive feature of Amyotrophic Lateral Sclerosis (ALS) patients since the early stages of the Conclusions: Our results show that bulbar-onset ALS-CN patients are more impaired in RMET-36 and SET-IA than spi-nal-onset ALS-CN patients, compared to controls. This differ- entiated pattern of impairment in affective and cognitive ToM (RMET-36 and SET-IA, respectively) related to the onset site, may be due to the presence of a subtle affective and/or co\",\"PeriodicalId\":7740,\"journal\":{\"name\":\"Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration\",\"volume\":\"23 1\",\"pages\":\"167 - 175\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2022-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/21678421.2022.2120687\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/21678421.2022.2120687","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 1

摘要

背景:被诊断为MND后,通常会出现压力和烦躁不安,一些人会迅速适应并找到新的平衡,而另一些人则很难接受诊断并继续经历高水平的情绪困扰。我们在之前对MND患者及其伴侣的研究中发现,重新评估和寻找意义在心理调整过程中起着重要作用。心理咨询可以提供给那些有需要的人,但往往是不可用的或不够具体。意义中心心理治疗:布莱巴特的意义中心心理治疗(BMCP)已被发现在晚期癌症患者中被广泛接受和有效。BMCP是一种有时间限制的、手动的群体心理治疗,专注于意义感,从而缓解痛苦,促进心理健康,在多个随机对照试验中被证明是有效的,在荷兰也是如此。BMCP中涉及的大多数主题在临床实践中似乎也适用于MND患者,他们面临着与进行性身体衰退和早期死亡前景相关的类似复杂问题。通过对他们的生活进行反思,从而在他们剩下的时间里更敏锐地关注对他们重要的事情,以一种指导性的方式支持和引导患者关注对他们有意义的事情。迄今为止,BMCP尚未在精神病患者中进行研究。通过单独和在线提供这种治疗,可以克服物理障碍,患者可以在家接受电子邮件指导和与心理学家面对面的视频咨询。方法:我们改编了荷兰小组协议,专门为诊断为ALS或PMA患者的个人提供这种在线方法,这导致了Making Sense培训。目前,我们正在测试可接受性、可行性和患者满意度,同时记录痛苦随时间的变化。我们假设,为苦恼的MND患者提供为期8周的基于网络的Making Sense培训,是可接受的、可行的,并且有助于减少情绪性MND相关的痛苦,并随后改善生活质量。采用混合方法,收集定量和定性数据。出于实用和伦理原因,我们选择了RCT设计的最佳替代方案,即只需要小样本(N¼5)的随机单例实验(SCE)设计。本研究旨在回答以下问题:有意义的训练是可接受的,可行的和赞赏的患者的精神障碍?2. 对情绪性MND相关痛苦(主要结果)、感知生活质量和意义感(次要结果)的影响是什么?结果:此时3例患者入组,开始训练。两名新的参与者将很快被纳入并随机分配。我们将在2022年12月公布第一批结果。背景:ALS主要影响运动功能,但包括社会理解在内的认知功能也可能受损。Von Economo神经元(VENs)是社会理解的神经基质的一部分,这些细胞在ALS中发生组织病理学改变。目的:我们调查了包括VENs在内的区域的活动是否与反映社会功能的认知任务的损害有关。方法:在这项观察性前瞻性研究中,对ALS患者(n26)进行了认知行为功能测试,包括共情理解(人际反应指数,IRI)、社会行为(最后通牒游戏)、对失礼情况的识别和一般认知功能(爱丁堡认知和行为ALS筛查,ECAS)的不同方面。为了进行Brettschneider/Braak的体内病理分期,采用DTI-MRI测定n20例ALS患者的ALS FDG PET,并与N匹配的健康对照进行比较。在含有大量VENs的前扣带皮层(ACC)和前岛皮层(AIC)进行兴趣体积分析。结果:与没有预期的VENs病理参与的患者(B/B ALS阶段1 ~ 2)相比,预期的VENs病理参与的ALS患者(B/B ALS阶段3 ~ 4)表现出明显减少的理解他人心态的幻想(IRI),社会行为更自私(最后通牒游戏),尽管事实上对他人社交不当行为(失礼)的认知理解并未受损。18F-FDG-PET显示,与未出现VENs病理累及的ALS患者相比,预期有VENs病理累及的ALS患者ACC和AIC代谢降低,这与某些任务的认知行为功能显著相关。 讨论:在此,我们提出证据表明,在VENs密度高的地区,ALS患者的社会行为改变与区域性18FDG- PET低代谢有关,从而提示可能存在因果关系。背景:语言流畅性缺陷是ALS患者最常见的非运动障碍。这种症状变化可以通过波士顿命名任务(BNT)来量化(1)。然而,尽管存在潜在的病理生理因素,但在这项任务中的表现可能无法捕捉到语言流利性的早期或微妙损害。此外,除了执行功能所需的功能外,语言/言语生成皮层网络的缺陷可能会损害BNT的表现(2)。背景:心理弹性(PR)被定义为人类利用个人和社会资源克服不良事件的能力,并将危机作为个人成长的激励因素。最近的研究发现,在健康受试者中,PR与保存较好的认知功能显著相关,但对运动神经元疾病(MNDs)患者中这种现象的具体研究仍然缺乏。目的:评价脑障碍患者的PR水平,探讨其与认知、行为和情绪症状的关系,以验证PR水平高可能对脑障碍运动外临床表现有保护作用的假说。方法:将72例MND患者和62例年龄、性别匹配的健康对照(hc)纳入研究。采用10项意大利版康纳-戴维森弹性量表(CD-RISC-10)评估PR,并询问患者行为障碍。讨论:我们的研究结果表明,PR是一种重要的保护因素,可以防止心智障碍患者的认知退化,并为弹性增强心理干预作为预防或延缓这些神经退行性疾病中认知障碍发生的未来策略的潜在有效性提供初步证据。背景:情绪识别障碍是ALS患者认知障碍的一部分。这种社会认知的症状性变化可以通过“通过眼睛读心任务”(RMET)来量化(1)。然而,尽管存在潜在的病理生理学,但在这项任务中的表现可能无法捕捉到社会认知的早期或微妙损伤。先前已经证明,RMET期间的社会皮质网络参与可以使用脑电图(EEG)进行量化(2)。目的:确定是否可以使用脑电图直接捕获和量化ALS患者驱动社会认知的皮质网络功能障碍。方法:在记录128通道脑电图的同时进行改良版RMET。将正确识别个体情绪状态时的平均皮质激活(事件相关电位,ERP)与识别个体性别时捕获的皮质激活(作为非社会控制)进行比较。招募工作正在进行中,迄今收集了来自4名对照和14名ALS患者的数据集。基于15名对照和25名ALS患者数据集的分析将在2022年MNDA研讨会上发表。结果:对迄今收集的erp进行初步检查,并与之前报告的对照数据进行比较(2)在Endnote V R Version X9中筛选丧恸后的经历和应对。采用Rstudio V R对截面数据进行meta分析和meta回归。研究被分配到时间和物理类别,并为各自的类别计算Hedges ' g,以提供基于横截面数据的认知过程估计。由于报告的数量少且不均匀性,因此对纵向研究进行了描述性分析。结果:共纳入了n¼45的横断面研究和n¼13的纵向研究。ALS患者(PALS)除语言智商外,所有认知领域均存在损伤。在横断面研究和大多数纵向研究中,pal表现出稳定的认知表现。在神经心理学方面,症状持续18 - 24个月的PALS和ALSFRS-R评分为40 - 36的PALS是最常被报道的亚组。年龄与视觉空间功能有关,抑郁与注意力有关。在纵向研究中,发现发病部位和基线认知状态对认知过程的影响。讨论:尽管有大量证据表明,在不同领域的疾病发病时存在认知障碍,但这些缺陷的进化证据相当有限,这表明PALS在病程早期就表现出认知障碍,可能是一种疾病特征。 背景:社会认知(SC)缺陷可能是肌萎缩性侧索硬化症(ALS)患者早期的一个明显特征。结论:我们的研究结果表明,与对照组相比,球源性ALS- cn患者在RMET-36和SET-IA中受损程度高于脊髓源性ALS- cn患者。这种与发病部位相关的情感性和认知性ToM(分别为RMET-36和SET-IA)损伤的不同模式,可能是由于微妙的情感性和/或co的存在
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Theme 11 - Cognitive and Psychological Assessment and Support
Background: Stress and dysphoria often follow the diagnosis MND, with some adapting quickly and finding a new balance, while others struggle to come to terms with the diagnosis and continue experiencing high levels of emotional distress. As observed in our previous study in patients with MND and their partners, re-appraisal and finding meaning play a significant role in the process of psychological adjustment. Psychological counselling can be offered to those in need, but is often not available or not specifically enough. Meaning Centred Psychotherapy: Breitbart ’ s Meaning Centred Psychotherapy (BMCP) has been found to be well- accepted and effective in advanced cancer patients. BMCP is a time-limited, manualized group psychotherapy, focusing on sense of meaning and thereby relieving distress and promoting psychological well-being and it has been proven effective in multiple RCT ’ s, also in the Netherlands. Most themes addressed in BMCP seem in clinical practice also suitable for MND patients, who are faced with similar complex issues related to the prospect of progressive physical decline and early death. Patients are supported and guided in a directive manner to focus on what is meaningful to them - by reflect-ing on their life and to thereby gaining sharper focus on what is important to them in the remaining time ahead of them. To date, BMCP has not been studied in MND patients. Physical barriers can be overcome by offering this therapy individually and online, where patients follow the pro- gramme from home with e-mail coaching and face to face video-consulting with the psychologist. Methods: We have adapted the Dutch group protocol for the purpose of such an online approach specifically for individuals diagnosed with ALS or PMA patients and this resulted in the Making Sense training. At this moment we are testing acceptability, feasibility and patient satisfaction, while we document changes in distress over time. We hypothesize that offering 8-weeks the internet-based Making Sense training for distressed MND patients, is acceptable, feasible and helpful in reducing emotional MND related distress with sub-sequent improvement in quality of life. A mixed method approach, collecting both quantitative and qualitative data, is used. For pragmatic and ethical reasons, we chose the best alternative for the RCT design namely a randomized Single-Case Experimental (SCE) design that requires only a small sample (N ¼ 5). This study aims to answer the following questions: 1. Is the Making Sense training acceptable, feasible and appreciated by patients with MND? 2. What are the effects on emotional MND related distress (primary outcome), perceived quality of life and sense of meaning (second- ary outcomes)? Results: At this moment three patients are included and started the training. Two new participants will be included and randomised soon. We will be able to present our first results in December 2022. Background: ALS primarily affects motor functions, but cog- nitive functions, including social understanding, may also be impaired. Von Economo neurons (VENs) are part of the neur- onal substrate of social understanding and these cells are histopathologically altered in ALS. Objective: We investigated whether activity in areas including VENs is associated with an impairment of cognitive tasks that mirror social functioning. Methods: In this observational prospective study, ALS patients ( N ¼ 26) were tested for cognitive behavioural function, encompassing different aspects of empathetic under- standing (interpersonal reactivity index, IRI), social behaviour (ultimatum game), recognition of faux-pas situations, and general cognitive functioning (Edinburgh Cognitive and Behavioural ALS Screen, ECAS). For in vivo pathological stag- ing according to Brettschneider/Braak, DTI-MRI was performed to determine those ALS FDG PET in N 20 ALS patients and compared to N matched healthy controls. Volume of interest analysis was performed in the anterior cingulate cortex (ACC) and the anterior insular cortex (AIC), which contain high numbers of VENs. Results: Compared to those without expected pathological involvement of VENs (B/B ALS stages 1 þ 2), ALS patients with anticipated pathological involvement of VENs (B/B ALS stages 3 þ 4) presented with significantly reduced fantasy to understand the mindset of others (IRI) and, social behaviour was more selfish (ultimatum game) despite the fact that cognitive understanding of socially inappropriate behaviour of others (faux-pas) was unimpaired. 18F-FDG-PET showed hypometabolism in ACC and AIC in ALS patients with antici- pated pathological involvement of VENs compared to those without and this was significantly correlated to cognitive-behavioral functions in certain tasks. Discussion: Here, we present evidence of altered social behaviour in ALS patients associated with regional 18FDG- PET hypometabolism in areas with a high density of VENs, thereby suggesting a possible causal association. Background: Deficits in verbal fluency are among the most common non-motor impairments which occur in ALS. Such symptomatic changes can be quantified by the Boston Naming Task (BNT) (1). However, performance in this task may not capture early or subtle impairments in verbal fluency, despite underlying pathophysiology. Further, perform- ance in the BNT may be impaired by deficits in language/ speech-generating cortical networks, in addition to those required for executive functioning (2). Objectives: We aimed to design Background: Psychological resilience (PR) is defined as the human capacity to overcome adverse events using individual and social resources, and to use crises as an incentive for personal growth. Recent investigations have observed that PR is significantly associated with more well-preserved cogni- tive function in healthy subjects, but a specific investigation of such phenomenon in patients with motor neuron diseases (MNDs) is still lacking. Objectives: To evaluate PR in MNDs, and to explore its relationship with cognitive, behavioral and mood symptoms in order to test the hypothesis that greater PR might be pro- tective against extra-motor clinical manifestations of MND. Methods: 72 MND patients and 62 age and gender matched healthy controls (HCs) were included in the study. PR was assessed using the 10-items Italian version of the Connor-Davidson Resilience Scale (CD-RISC-10), patients were asked behavioral disturbances. Discussion: Our results suggest that PR is an important protective factor against cognitive deterioration in MNDs, and provide preliminary evidence for the potential usefulness of resilience enhancement psychological interventions as a future strategy to prevent or delay the onset of cognitive dis- turbances in these neurodegenerative conditions. Background: Deficits in recognition of emotions is part of the cognitive impairment which occurs in ALS. Such symptomatic changes in social cognition can be quantified by the Reading the Mind in the Eyes Task (RMET) (1). However, performance in this task may not capture early or subtle impairments in social cognition, despite underlying patho- physiology. It has previously been demonstrated that social cortical network engagement during the RMET can be quan- tified using electroencephalography (EEG) (2). Objectives: To determine if dysfunction in cortical networks driving social cognition can be directly captured and quanti- fied in ALS using EEG. Methods: A modified version of the RMET is performed during recording of 128-channel EEG. The average cortical acti- vation (event related potential, ERP) which occurs during correct recognition of individuals ’ emotional state is compared to that captured during recognition individuals ’ sex, as a non-social control. Recruitment is ongoing, with datasets from 4 controls and 14 people with ALS collected to date. Analyses based on datasets from 15 controls and 25 people with ALS will be presented at the 2022 MNDA Symposium. Results: Preliminary examination of ERPs collected to date and comparison to control data reported previously (2) the post-bereavement experiences and coping were screened in Endnote V R Version X9. Meta-analyses and meta-regressions were calculated for cross-sectional data using Rstudio V R . Studies were assigned to temporal and physical categories and Hedges ’ g was calculated for the respect-ive categories to provide an estimate of a cognitive course based on cross-sectional data. Due to low numbers and het- erogeneity in reporting, longitudinal studies were analysed descriptively. Results: A total of N ¼ 45 cross-sectional and N ¼ 13 longitudinal studies were included. Impairments in all cognitive domains, except verbal IQ, were found in ALS patients (PALS). PALS showed stable cognitive performances in cross- sectional and in most longitudinal studies. PALS with symptoms for 18 – 24 months and PALS who had an ALSFRS-R score of 40 – 36 were the most frequently reported subgroup regarding neuropsychology. Age was related to visuospatial functioning, and depressiveness to attention. In longitudinal studies, impact of site of onset and cognitive status at base-line on cognitive course was found. Discussion: Despite vast evidence for cognitive impairment at disease onset in different domains, evidence for evolution of these deficits is rather limited, suggesting that PALS pre- sent with cognitive impairment early in the course possibly in a sense of disease trait. Background: Social Cognition (SC) deficits may be a distinct- ive feature of Amyotrophic Lateral Sclerosis (ALS) patients since the early stages of the Conclusions: Our results show that bulbar-onset ALS-CN patients are more impaired in RMET-36 and SET-IA than spi-nal-onset ALS-CN patients, compared to controls. This differ- entiated pattern of impairment in affective and cognitive ToM (RMET-36 and SET-IA, respectively) related to the onset site, may be due to the presence of a subtle affective and/or co
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来源期刊
CiteScore
5.40
自引率
10.70%
发文量
64
期刊介绍: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration is an exciting new initiative. It represents a timely expansion of the journal Amyotrophic Lateral Sclerosis in response to the clinical, imaging pathological and genetic overlap between ALS and frontotemporal dementia. The expanded journal provides outstanding coverage of research in a wide range of issues related to motor neuron diseases, especially ALS (Lou Gehrig’s disease) and cognitive decline associated with frontotemporal degeneration. The journal also covers related disorders of the neuroaxis when relevant to these core conditions.
期刊最新文献
The correlation between social support, coping style, advance care planning readiness, and quality of life in patients with amyotrophic lateral sclerosis: a cross-sectional study. Effects of COVID-19 on motor neuron disease mortality in the United States: a population-based cross-sectional study SOD1 gene screening in ALS – frequency of mutations, patients’ attitudes to genetic information and transition to tofersen treatment in a multi-center program How to break the news in amyotrophic lateral sclerosis/motor neuron disease: practical guidelines from experts A nurse coaching intervention to improve support to individuals living with ALS.
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