应激、炎症和疼痛:单核细胞在纤维肌痛相关症状严重程度中的潜在作用

A. Taylor, T. G. Fischer-White, Joel G. Anderson, K. Adelstein, M. Murugesan, Janet E. Lewis, Michael M. Scott, R. Gaykema, L. Goehler
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引用次数: 19

摘要

免疫变化可能导致纤维肌痛(FM)症状严重程度的可能性促使这项概念验证研究确定与健康对照相比,FM患者中单核细胞亚群是否存在差异。通过比较FM患者的特定症状(n = 20)和与年龄匹配和性别匹配的健康对照(n = 20)的单核细胞亚群模式来评估相关性。在同一时间段内,所有参与者提供了血液样本,并完成了与疼痛、疲劳、睡眠障碍、感知压力、积极和消极影响以及抑郁情绪相关的测量(以及FM患者的纤维肌痛影响问卷)。流式细胞术评估单核细胞亚群。两组间循环单核细胞的总百分比无差异;然而,疼痛与FM组循环经典(r = -0.568, p = 0.011)和中间(r = -0.511, p = 0.025)单核细胞百分比呈负相关。应激与疼痛高度相关(r = 0.608, p = 0.004)。在FM组中发现的循环单核细胞亚群百分比变化的新模式伴随着更高的感知疼痛评分以及压力和疼痛之间的相关性,值得进一步研究。版权所有©2015 John Wiley & Sons, Ltd
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Stress, Inflammation and Pain: A Potential Role for Monocytes in Fibromyalgia-related Symptom Severity.
The possibility that immunological changes might contribute to symptom severity in fibromyalgia (FM) prompted this proof-of-concept study to determine whether differences in monocyte subpopulations might be present in persons with FM compared with healthy controls. Relationships were assessed by comparing specific symptoms in those with FM (n = 20) and patterns of monocyte subpopulations with healthy age-matched and gender-matched controls (n = 20). Within the same time frame, all participants provided a blood sample and completed measures related to pain, fatigue, sleep disturbances, perceived stress, positive and negative affect and depressed mood (and the Fibromyalgia Impact Questionnaire for those with FM). Monocyte subpopulations were assessed using flow cytometry. No differences were observed in total percentages of circulating monocytes between the groups; however, pain was inversely correlated with percentages of circulating classical (r = -0.568, p = 0.011) and intermediate (r = -0.511, p = 0.025) monocytes in the FM group. Stress and pain were highly correlated (r = 0.608, p = 0.004) in the FM group. The emerging pattern of changes in the percentages of circulating monocyte subpopulations concomitant with higher ratings of perceived pain and the correlation between stress and pain found in the FM group warrant further investigation. Copyright © 2015 John Wiley & Sons, Ltd.
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