心理复原力对运动神经元疾病患者的认知退化具有保护作用。

Andrea Rosano, Manuel Bicaj, Marta Cillerai, Marta Ponzano, Corrado Cabona, Chiara Gemelli, Claudia Caponnetto, Matteo Pardini, Alessio Signori, Antonio Uccelli, Angelo Schenone, Pilar M Ferraro
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摘要

目的:最近的研究表明,心理复原力(PR)与健康受试者(HS)更完好的认知能力有关,但对运动神经元疾病(MND)患者的这种现象仍缺乏调查。因此,我们的研究旨在评估 PR 及其与 MNDs 基线认知/行为和情绪症状的关系,以及纵向认知功能。采用康纳-戴维森复原力量表(CD-RISC)对复原力进行评估。使用爱丁堡认知和行为 ALS 筛选(ECAS)对患者的认知/行为障碍进行基线评估,使用医院焦虑和抑郁量表(HADS)对患者的情绪症状进行评估,并每 6 个月进行一次评估。采用曼-惠特尼U检验比较患者和HS的CD-RISC得分,并应用回归模型评估CD-RISC得分在预测MND患者基线认知/行为和情绪测量以及纵向认知表现方面的作用:结果:与 HS 相比,MND 病例的 PR 明显更高(p 从 0.01 到 0.05),纵向情绪症状更轻(p 从 0.001 到 0.04):PR是防止MND认知/情绪障碍发生和演变的重要保护因素,这表明增强复原力的心理干预措施有助于预防或延缓这些神经退行性疾病的认知和情绪障碍。
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Psychological resilience is protective against cognitive deterioration in motor neuron diseases.

Objectives: Recent studies suggest that psychological resilience (PR) is associated with more well-preserved cognition in healthy subjects (HS), but an investigation of such phenomenon in patients with motor neuron diseases (MNDs) is still lacking. The aim of our study was therefore to evaluate PR and its relationship with baseline cognitive/behavioral and mood symptoms, as well as longitudinal cognitive functioning, in MNDs.

Methods: 94 MND patients and 87 demographically matched HS were enrolled. PR was assessed using the Connor-Davidson Resilience Scale (CD-RISC). Patients were further evaluated both at baseline and every 6 months for cognitive/behavioral disturbances using the Edinburgh Cognitive and Behavioral ALS Screen (ECAS), and for mood symptoms using the Hospital Anxiety and Depression Scale (HADS). CD-RISC scores were compared between patients and HS using the Mann-Whitney U test, and regression models were applied to evaluate the role of CD-RISC scores in predicting baseline cognitive/behavioral and mood measures, as well as longitudinal cognitive performances, in MND patients.

Results: MND cases showed significantly greater PR compared to HS (p from <0.001 to 0.02). In MNDs, higher PR levels were significant predictors of both greater cognitive performance (p from 0.01 to 0.05) and milder mood symptoms (p from <0.001 to 0.04) at baseline, as well as less severe memory decline (p from 0.001 to 0.04) longitudinally.

Conclusions: PR is an important protective factor against the onset and evolution of cognitive/mood disturbances in MNDs, suggesting the usefulness of resilience enhancement psychological interventions to prevent or delay cognitive and mood disorders in these neurodegenerative conditions.

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