F37 Is social cognition in huntington’s disease more than just a marker for disease progression? – an exploration of social functioning in the day to day experiences of people with hd, their companions and friends

A. Fisher, Anna Lavis, S. Greenfield, H. Rickards
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Abstract

Background In HD, deducing what another person means through their facial emotions is thought to erode as the illness progresses. Emotional recognition data is now being collected in longitudinal studies (Henley, Novak et al. 2012). Aims Showing that the underlying skills of social cognition are impaired in HD through quantitative means leaves a large gap in our knowledge (Bora, Velakoulis et al. 2016). We do not know how the person with HD and those who live with them are experiencing this change, and how it is played out in the many spaces of mundane life. This project aims to capture this ‘social functioning’. Methods Ethnography which employs both participant observation and interacting with participants in a naturalist setting over an extended period will be used. Additionally, using a non-word based participatory method such as photo elicitation (Lorenz 2011) will optimise the views of people with HD who may have communication and cognitive problems. A social convoy map (Sherman et al (2015)) may also be used to establish changes over time. Results/conclusions A submission for the project to ethics review will be take place shortly following a consultation with the UK HDA Public Involvement group – HD Voice. Approximating the real world should allow for a more nuanced person-centred and in-depth portrait of how these concerns affect overall functioning in HD; allowing clinicians to develop more sensitive assessments to capture these issues in way that are meaningful to the community and developing interventions which are aimed at reducing the concerns raised in the context in which they occur. References . Bora E, Velakoulis D, Walterfang M. Social cognition in Huntington’s disease: A meta-analysis. Behavioural brain research2016;297:131. . Henley SM, Novak MJ, Frost C, King J, Tabrizi SJ, Warren JD. Emotion recognition in Huntington’s disease: a systematic review. Neuroscience & Biobehavioral Reviews2012;36(1):237–253. . Lorenz LS. A way into empathy: a ’case’ of photo- elicitation in illness research. Health2011 (London, England: 1997);15(3):259. . Sherman CW, Wan WH, Antonucci TC. Social convoy model. The Encyclopedia of Adulthood and Aging [SK Whitbourne (Ed.)]. 2015.
F37亨廷顿氏病的社会认知不仅仅是疾病进展的标志吗?-探索自闭症患者、他们的同伴和朋友在日常生活中的社会功能
在HD患者中,通过面部表情来推断他人的意思被认为随着疾病的进展而削弱。情绪识别数据现在被收集到纵向研究中(Henley, Novak et al. 2012)。通过定量手段显示HD患者社会认知的潜在技能受损,这在我们的知识中留下了很大的空白(Bora, Velakoulis et al. 2016)。我们不知道患有HD的人和与他们一起生活的人是如何经历这种变化的,以及它是如何在世俗生活的许多空间中发挥作用的。该项目旨在捕捉这种“社会功能”。方法人种学采用参与者观察和与参与者在自然环境中进行长时间的互动。此外,使用非基于单词的参与式方法,如照片引出(Lorenz 2011)将优化HD患者的观点,他们可能有沟通和认知问题。社交车队地图(Sherman等人(2015))也可以用来确定随时间的变化。结果/结论在与英国HDA公众参与小组- HD Voice协商后,将很快提交项目伦理审查。接近真实世界应该允许更细致入微的以人为本和深入的描述这些问题如何影响HD的整体功能;允许临床医生制定更敏感的评估,以对社区有意义的方式捕捉这些问题,并制定干预措施,旨在减少在这些问题发生的背景下引起的关注。参考文献张丽娟,张丽娟,张丽娟,等。亨廷顿舞蹈病患者社会认知的meta分析。行为脑研究2016;297:131。李建军,李建军,李建军,李建军,李建军。亨廷顿舞蹈病的情绪识别:系统回顾。中国生物医学工程学报,2012;36(1):237-253。洛伦茨LS。一种进入同理心的方式:疾病研究中照片启发的“案例”。《健康2011》(英国伦敦:1997年);15(3):259。谢尔曼CW,万WH,安东努奇TC。社会护卫队模式。成人与衰老百科全书[SK惠特伯恩(主编)]。2015.
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