Kittelson Andrew J, Thomas Abbey C, Kluger Benzi M, Stevens-Lapsley Jennifer E
Physical Therapy Program, Department of Physical Medicine and Rehabilitation, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA,
Exp Brain Res. 2014 Dec;232(12):3991-9. doi: 10.1007/s00221-014-4079-6. Epub 2014 Sep 3.
Deficits in voluntary activation of the quadriceps muscle are characteristic of knee osteoarthritis (OA), contributing to the quadriceps weakness that is also a hallmark of the disease. The mechanisms underlying this central activation deficit (CAD) are unknown, although cortical mechanisms may be involved. Here, we utilize transcranial magnetic stimulation (TMS) to assess corticospinal and intracortical excitability in patients with knee OA and in a comparably aged group of healthy older adults, to quantify group differences, and to examine associations between TMS measures and pain, quadriceps strength, and CAD. Seventeen patients with knee OA and 20 healthy controls completed testing. Motor evoked potentials were measured at the quadriceps by superficial electromyographic recordings. Corticospinal excitability was assessed by measuring resting motor threshold (RMT) to TMS stimulation of the quadriceps representation at primary motor cortex, and intracortical excitability was assessed via paired-pulse paradigms for short-interval intracortical inhibition (SICI) and intracortical facilitation (ICF). No statistically significant differences between patients with knee OA and healthy controls were found for RMT, SICI or ICF measures (p > 0.05). For patients with knee OA, there were significant associations observed between pain and RMT, as well as between pain and ICF. No associations were observed between CAD and measures of corticospinal or intracortical excitability. These data suggest against direct involvement of corticospinal or intracortical pathways within primary motor cortex in the mechanisms of CAD. However, pain is implicated in the neural mechanisms of quadriceps motor control in patients with knee OA.
股四头肌自主激活功能缺陷是膝骨关节炎(OA)的特征之一,导致股四头肌无力,而这也是该疾病的一个标志。尽管可能涉及皮质机制,但这种中枢激活缺陷(CAD)的潜在机制尚不清楚。在此,我们利用经颅磁刺激(TMS)来评估膝OA患者和年龄匹配的健康老年人的皮质脊髓和皮质内兴奋性,以量化组间差异,并检查TMS测量值与疼痛、股四头肌力量和CAD之间的关联。17名膝OA患者和20名健康对照完成了测试。通过表面肌电图记录在股四头肌处测量运动诱发电位。通过测量对初级运动皮层股四头肌代表区进行TMS刺激的静息运动阈值(RMT)来评估皮质脊髓兴奋性,通过配对脉冲范式评估短间隔皮质内抑制(SICI)和皮质内易化(ICF)来评估皮质内兴奋性。在RMT、SICI或ICF测量方面,膝OA患者与健康对照之间未发现统计学上的显著差异(p>0.05)。对于膝OA患者,疼痛与RMT之间以及疼痛与ICF之间存在显著关联。未观察到CAD与皮质脊髓或皮质内兴奋性测量值之间的关联。这些数据表明,初级运动皮层内的皮质脊髓或皮质内通路在CAD机制中没有直接参与。然而,疼痛与膝OA患者股四头肌运动控制的神经机制有关。