Levenson Robert W, Merrilees Jennifer, Henry Maya L, Dronkers Nina F
Department of Psychology, University of California, Berkeley, CA, USA.
UCSF Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.
J Alzheimers Dis. 2025 Jul;106(1):206-217. doi: 10.1177/13872877251340578. Epub 2025 May 21.
BackgroundDementia is a significant public health issue globally. People with dementia (PWD) exhibit symptoms in multiple domains (e.g., cognition, emotion, motor, speech/language) that can vary in their impact on the caregiver and the PWD-caregiver relationship.ObjectiveWe assessed the relative impact of various dementia symptoms on caregiver health and well-being and on the PWD-caregiver relationship using a broad sampling of PWD symptoms and caregiver/relationship outcome measures.MethodsData were analyzed from 54 primary caregivers of PWDs who completed seven questionnaires assessing caregiver health and well-being and PWD-caregiver relationship quality. An exploratory factor analysis of these questionnaires revealed two primary factors: (a) General Distress (anxiety, burden, depression, general health, loneliness), and (b) Relationship Quality (interpersonal closeness, relationship satisfaction). Caregivers also rated nine categories of PWD symptoms (memory, executive functions, speech/language, visual/spatial, motor, changes in behavior, sleep, medical/sensory, activities of daily living).ResultsGreater caregiver General Distress was associated with greater PWD speech/language and sleep symptoms. Lower caregiver Relationship Quality was associated (at trend, < 0.10, levels) with greater PWD speech/language and activities of daily living symptoms. Correlations with the seven individual caregiver outcome measures revealed that speech/language symptoms were the most robust predictors (correlated with five measures), followed by sleep and activities of daily living symptoms (correlated with two measures), and memory, visual/spatial, and motor symptoms (correlated with one measure).ConclusionsFindings highlight the profound adverse effects that PWD speech and language deficits may have on caregivers and underscore the importance of addressing these deficits in dementia care.
背景
痴呆症是全球一个重大的公共卫生问题。患有痴呆症的人(PWD)在多个领域(如认知、情感、运动、言语/语言)表现出症状,这些症状对照顾者以及PWD与照顾者之间的关系的影响可能各不相同。
目的
我们使用广泛的PWD症状样本以及照顾者/关系结果测量方法,评估了各种痴呆症症状对照顾者健康和幸福感以及PWD与照顾者关系的相对影响。
方法
对54名PWD的主要照顾者的数据进行了分析,这些照顾者完成了七份问卷,评估照顾者的健康和幸福感以及PWD与照顾者关系的质量。对这些问卷进行的探索性因素分析揭示了两个主要因素:(a)一般困扰(焦虑、负担、抑郁、总体健康、孤独),以及(b)关系质量(人际亲密程度、关系满意度)。照顾者还对九类PWD症状(记忆、执行功能、言语/语言、视觉/空间、运动、行为变化、睡眠、医疗/感官、日常生活活动)进行了评分。
结果
照顾者更高的一般困扰与PWD更严重的言语/语言和睡眠症状相关。照顾者较低的关系质量与PWD更严重的言语/语言和日常生活活动症状相关(呈趋势性,<0.10水平)。与七项个体照顾者结果测量指标的相关性表明,言语/语言症状是最有力的预测因素(与五项指标相关),其次是睡眠和日常生活活动症状(与两项指标相关),以及记忆、视觉/空间和运动症状(与一项指标相关)。
结论
研究结果突出了PWD言语和语言缺陷可能对照顾者产生的深远不利影响,并强调了在痴呆症护理中解决这些缺陷的重要性。