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多发性硬化症行为干预的生物学结果测量。

Biological outcome measurements for behavioral interventions in multiple sclerosis.

机构信息

Institute for Neuroimmunology and Clinical Multiple Sclerosis Research (inims), University Hospital Hamburg, Eppendorf, Germany.

出版信息

Ther Adv Neurol Disord. 2011 Jul;4(4):217-29. doi: 10.1177/1756285611405252.

DOI:10.1177/1756285611405252
PMID:21765872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3131172/
Abstract

Behavioral interventions including exercise, stress management, patient education, psychotherapy and multidisciplinary neurorehabilitation in general are receiving increasing recognition in multiple sclerosis (MS) clinical practice and research. Most scientific evaluations of these approaches have focused on psychosocial outcome measures such as quality of life, fatigue or depression. However, it is becoming increasingly clear that neuropsychiatric symptoms of MS are at least partially mediated by biological processes such as inflammation, neuroendocrine dysfunction or regional brain damage. Thus, successful treatment of these symptoms with behavioral approaches could potentially also affect the underlying biology. Rigidly designed scientific studies are needed to explore the potential of such interventions to affect MS pathology and biological pathways linked to psychological and neuropsychiatric symptoms of MS. Such studies need to carefully select outcome measures on the behavioral level that are likely to be influenced by the specific intervention strategy and should include biomarkers with evidence for an association with the outcome parameter in question. In this overview, we illustrate how biological and psychological outcome parameters can be combined to evaluate behavioral interventions. We focus on two areas of interest as potential targets for behavioral interventions: depression and fatigue.

摘要

行为干预措施,包括运动、压力管理、患者教育、心理治疗和一般的多学科神经康复,在多发性硬化症(MS)的临床实践和研究中越来越受到重视。这些方法的大多数科学评估都集中在心理社会结果测量上,如生活质量、疲劳或抑郁。然而,越来越明显的是,MS 的神经精神症状至少部分是由炎症、神经内分泌功能障碍或区域性脑损伤等生物学过程介导的。因此,通过行为方法成功治疗这些症状,也有可能影响潜在的生物学机制。需要严格设计的科学研究来探索这些干预措施对 MS 病理学和与 MS 的心理和神经精神症状相关的生物学途径的潜在影响。这些研究需要仔细选择行为层面的结果测量指标,这些指标很可能受到特定干预策略的影响,并且应该包括与所研究的结果参数具有关联证据的生物标志物。在本综述中,我们说明了如何将生物学和心理学结果参数结合起来评估行为干预措施。我们重点关注两个可能作为行为干预目标的感兴趣领域:抑郁和疲劳。

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本文引用的文献

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Demyelination causes synaptic alterations in hippocampi from multiple sclerosis patients.脱髓鞘导致多发性硬化症患者海马突触改变。
Ann Neurol. 2011 Mar;69(3):445-54. doi: 10.1002/ana.22337.
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Endocrine and immune substrates of depressive symptoms and fatigue in multiple sclerosis patients with comorbid major depression.多发性硬化症合并重性抑郁患者抑郁症状和疲劳的内分泌和免疫基础。
J Neurol Neurosurg Psychiatry. 2011 Jul;82(7):814-8. doi: 10.1136/jnnp.2010.230029. Epub 2011 Feb 4.
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Understanding suicide and disability through three major disabling conditions: Intellectual disability, spinal cord injury, and multiple sclerosis.通过三种主要致残状况了解自杀和残疾:智力残疾、脊髓损伤和多发性硬化症。
Disabil Health J. 2010 Apr;3(2):74-8. doi: 10.1016/j.dhjo.2009.09.001. Epub 2009 Nov 3.
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Discrimination between patients with melancholic depression and healthy controls: comparison between 24-h cortisol profiles, the DST and the Dex/CRH test.抑郁障碍患者与健康对照者的甄别:24 小时皮质醇谱、DST 和 Dex/CRH 试验的比较。
Psychoneuroendocrinology. 2011 Jun;36(5):691-8. doi: 10.1016/j.psyneuen.2010.10.002. Epub 2010 Oct 28.
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MS quality of life, depression, and fatigue improve after mindfulness training: a randomized trial.正念训练后 MS 生活质量、抑郁和疲劳得到改善:一项随机试验。
Neurology. 2010 Sep 28;75(13):1141-9. doi: 10.1212/WNL.0b013e3181f4d80d.
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Linking molecules to mood: new insight into the biology of depression.将分子与情绪联系起来:抑郁症生物学的新见解。
Am J Psychiatry. 2010 Nov;167(11):1305-20. doi: 10.1176/appi.ajp.2009.10030434. Epub 2010 Sep 15.
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Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.使用监督机器学习和荟萃分析在 12566 个人中对多发性硬化症的 CRHR1 进行研究。
Hum Mol Genet. 2010 Nov 1;19(21):4286-95. doi: 10.1093/hmg/ddq328. Epub 2010 Aug 10.
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Int MS J. 2010 Jan;17(1):28-34.
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The hippocampus in major depression: evidence for the convergence of the bench and bedside in psychiatric research?重度抑郁症中的海马体:精神科研究中从 bench to bedside 的证据?
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