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首页> 外文期刊>Medicine. >Descending Control of Nociceptive Processing in Knee Osteoarthritis Is Associated With Intracortical Disinhibition: An Exploratory Study
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Descending Control of Nociceptive Processing in Knee Osteoarthritis Is Associated With Intracortical Disinhibition: An Exploratory Study

机译:降低对膝骨关节炎伤害性加工的控制与皮层内抑制相关:一项探索性研究。

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摘要

Based on the hypothesis that an imbalance in excitatory and inhibitory input is a central mechanism of knee osteoarthritis chronic pain (KOACP), this exploratory study had the following aims: to compare whether the function of the descending inhibitory pain pathway is associated with the state of inhibition in the corticospinal system indexed by the motor-evoked potential (MEP) and the cortical salient period (CSP) in patients with severe osteoarthritis (OA) and healthy controls; and to determine if there is correlation between the measures of intracortical inhibition (CSP, MEP) with changes on the numerical pain scale (NPS [0–10]) in KOACP during a conditioned pain modulation (CPM)-task considering the effect of self-reported function assessed by the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and analgesic use. In a cross-sectional study, we included females (n?=?21), with disability by pain or stiffness due to KOACP and healthy controls (n?=?10), aged 19 to 75 years. The motor cortex excitability parameters (MEP and CSP) were assessed using the transcranial magnetic stimulation. We assessed the pain and disability by the WOMAC, and change on NPS (0–10) during CPM-task. A Multivariate analysis of covariance revealed that the adjusted mean (SD) on the MEP amplitude was 13.53% higher in the OA than in healthy subjects (1.33 [0.49] vs 1.15 [0.13]), respectively (P?=?0.16). The adjusted mean (SD) on the CSP observed in OA patients was 23.43% lower than in healthy subjects (54.54 [16.10] vs 70.94 [22.87]), respectively (P?=?0.01). The function of the descending pain modulatory system assessed by change on NPS (0–10) during a CPM-task was negatively correlated with the cortical excitability parameter indexed by the CSP (P?=?0.001). Also, the CSP was negatively correlated with the pain and disability assessed by the WOMAC index. These findings support the hypothesis that the change in cortical plasticity in KOACP is associated with less intracortical inhibition, as measured by the CSP. These results show that the neural change in the motor cortex in KOACP is associated with pain and disability levels, and also with decreased activation of the endogenous pain-modulating system by a CPM-task.
机译:基于兴奋性和抑制性输入失衡是膝骨关节炎慢性疼痛(KOACP)的主要机制这一假说,该探索性研究的目的是:比较抑制性疼痛下行途径的功能是否与状态相关。在重度骨关节炎(OA)和健康对照患者中,以运动诱发电位(MEP)和皮质显着期(CSP)为指标的皮质脊髓系统抑制作用;并确定考虑到自我影响的条件性疼痛调节(CPM)任务期间KOACP的皮质内抑制措施(CSP,MEP)与数字疼痛量表(NPS [0-10])的变化之间是否存在相关性西部安大略省和麦克马斯特大学骨关节炎指数(WOMAC)评估的镇痛作用和止痛药的使用。在一项横断面研究中,我们纳入了19岁至75岁的女性(n = 21),因KOACP和健康对照组(n = 10)而导致的疼痛或僵硬残疾。使用经颅磁刺激评估运动皮层兴奋性参数(MEP和CSP)。我们通过WOMAC评估了疼痛和残疾,并在CPM任务期间改变了NPS(0-10)。协方差的多变量分析显示,OA中MEP幅度的调整均值(SD)分别比健康受试者高13.53%(P3 =?0.16)(1.33 [0.49]对1.15 [0.13])。在OA患者中观察到的CSP校正均值(SD)分别比健康受试者低23.43%(分别为54.54 [16.10]和70.94 [22.87])(P = 0.01)。通过在CPM任务过程中NPS(0-10)的变化评估的下行疼痛调节系统的功能与CSP索引的皮层兴奋性参数负相关(P <= 0.001)。而且,CSP与WOMAC指数评估的疼痛和残疾呈负相关。这些发现支持了以下假设:通过CSP测量,KOACP中皮质可塑性的变化与皮质内抑制作用较小相关。这些结果表明,KOACP中运动皮层的神经变化与疼痛和残疾水平有关,并且还与CPM任务对内源性疼痛调节系统的激活降低有关。

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