Shahmoon Suzette, Georgiev Dejan, Jarman Paul, Bhatia Kailash, Limousin Patricia, Jahanshahi Marjan
Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London, UK.
Department of Neurology, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Mov Disord Clin Pract. 2025 Sep;12(9):1302-1312. doi: 10.1002/mdc3.70098. Epub 2025 Apr 29.
Loneliness is a state in which an individual feels socially isolated due to deficiencies in the quantity or quality of social relationships and interaction. To date very little is known about loneliness in Parkinson's disease (PD) and focal/segmental craniocervical dystonia (FSCD).
To explore whether level of loneliness is disease-specific by comparing PD, FCSD and healthy controls (HCs), and to define predictors of loneliness in both PD and FSCD.
Eighty-two people with PD, 63 people with FSCD and 50 HC were surveyed. The UCLA Loneliness Scale was used to assess loneliness. Various non-motor symptoms, psychosocial variables and measures of subjective well-being were assessed and used as potential predictors of loneliness.
There was no significant difference in reported levels of loneliness between people with PD and matched HCs, and between people with PD and people with FSCD, but people with FSCD reported higher levels of loneliness than HCs (p = 0.018). Perceived stigma predicted loneliness in both disease groups (p < 0.001). Additionally, non-motor symptoms (p = 0.006), lack of optimism (p = 0.015) and practical social support (p = 0.006) predicted loneliness in people with PD. Patients with PD and FSCD with higher perceived stigma levels felt lonelier (p < 0.001), as did female patients with PD (p = 0.004), younger patients with FSCD (p = 0.007) and older patients with PD (p = 0.023).
We identified important predictors of loneliness in PD and FSCD. The identified age- and gender-specific differences in loneliness in people with PD and FSCD contribute to our better understanding of this complex and not yet fully understood concept.
孤独是一种个体因社会关系和互动的数量或质量不足而感到社会孤立的状态。迄今为止,对于帕金森病(PD)和局限性/节段性颅颈肌张力障碍(FSCD)中的孤独感知之甚少。
通过比较帕金森病、局限性/节段性颅颈肌张力障碍患者和健康对照者,探讨孤独程度是否具有疾病特异性,并确定帕金森病和局限性/节段性颅颈肌张力障碍中孤独感的预测因素。
对82例帕金森病患者、63例局限性/节段性颅颈肌张力障碍患者和50名健康对照者进行了调查。使用加利福尼亚大学洛杉矶分校孤独量表评估孤独感。评估了各种非运动症状、心理社会变量和主观幸福感指标,并将其用作孤独感的潜在预测因素。
帕金森病患者与匹配的健康对照者之间、帕金森病患者与局限性/节段性颅颈肌张力障碍患者之间报告的孤独程度没有显著差异,但局限性/节段性颅颈肌张力障碍患者报告的孤独程度高于健康对照者(p = 0.018)。在两个疾病组中,感知到的耻辱感均预测了孤独感(p < 0.001)。此外,非运动症状(p = 0.006)、缺乏乐观情绪(p = 0.015)和实际社会支持(p = 0.006)预测了帕金森病患者的孤独感。帕金森病和局限性/节段性颅颈肌张力障碍患者中,感知到的耻辱感水平较高者感觉更孤独(p < 0.001),帕金森病女性患者(p = 0.004)、局限性/节段性颅颈肌张力障碍年轻患者(p = 0.007)和帕金森病老年患者(p = 0.023)也是如此。
我们确定了帕金森病和局限性/节段性颅颈肌张力障碍中孤独感的重要预测因素。在帕金森病和局限性/节段性颅颈肌张力障碍患者中确定的孤独感的年龄和性别特异性差异,有助于我们更好地理解这个复杂且尚未完全理解的概念。