School of Kinesiology, Faculty of Health Science, London, Ontario, Canada.
Department of Clinical Neurological Sciences, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada.
Clin Anat. 2020 Jan;33(1):77-84. doi: 10.1002/ca.23473. Epub 2019 Oct 30.
Neuropathic features of chronic inflammatory demyelinating polyneuropathy (CIDP) have been well documented, however very little is known about the implication of this neuropathy on skeletal muscle, and whether nerve lesions in CIDP lead to uniform disruptions in skeletal muscles. In this study, we assessed the triceps surae complex, using magnetic resonance imaging (MRI) in a group (n = 10) of CIDP patients compared with a healthy age-matched control group (n = 9). MRI (T1 and T2) of the leg musculature as well as plantar flexion strength measurements were obtained from both groups. CIDP patients compared with controls had ∼28% lower plantar flexion strength and ∼19% less total muscle volume (T1) of the triceps surae. When strength was normalized to fat corrected triceps surae volume CIDP patients were ∼30% weaker than controls. Relaxation times from the T2 scans were significantly longer in CIDP with the soleus, medial head of gastrocnemius and lateral head of gastrocnemius showing ∼37%, ∼38% and ∼26% longer relaxation times, respectively. CIDP patients were significantly weaker compared to controls and despite normalizing strength to total triceps surae contractile tissue volume this difference remained. CIDP patients had significantly longer T2 times, reflecting increased noncontractile tissue infiltration. These results indicate reduced muscle quantity and quality as a result of alterations in axonal function. Furthermore, when present study results are considered together with a prior report on the anterior compartment (Gilmore et al. 2016, Muscle Nerve 3:413-420), it is clear that both anterior and posterior leg compartments are affected similarly in CIDP despite different terminal nerve innervation and functional properties. Clin. Anat. 32:77-84, 2019. © 2019 Wiley Periodicals, Inc.
慢性炎症性脱髓鞘性多发性神经病(CIDP)的神经病变特征已得到充分证实,然而,对于这种神经病变对骨骼肌的影响,以及 CIDP 中的神经病变是否导致骨骼肌的一致性破坏,我们知之甚少。在这项研究中,我们使用磁共振成像(MRI)评估了一组 CIDP 患者(n = 10)和健康年龄匹配对照组(n = 9)的比目鱼肌复合体。我们从两组中获得了腿部肌肉的 MRI(T1 和 T2)以及跖屈力量测量结果。与对照组相比,CIDP 患者的跖屈力量低 28%,比目鱼肌的总肌肉体积(T1)低 19%。当将力量与脂肪校正的比目鱼肌体积进行归一化时,CIDP 患者比对照组弱约 30%。T2 扫描的弛豫时间在 CIDP 中显著延长,其中比目鱼肌、腓肠肌内侧头和外侧头的弛豫时间分别延长了约 37%、38%和 26%。与对照组相比,CIDP 患者明显较弱,尽管将力量与比目鱼肌总收缩组织体积归一化,但这种差异仍然存在。CIDP 患者的 T2 时间明显更长,反映出非收缩组织浸润增加。这些结果表明,由于轴突功能的改变,导致肌肉数量和质量减少。此外,当将本研究结果与之前关于前间隔(Gilmore 等人,2016 年,《肌肉神经》3:413-420)的报告一起考虑时,很明显,尽管前侧和后侧腿部间隔具有不同的末端神经支配和功能特性,但 CIDP 中这两个间隔都受到类似的影响。临床解剖学 32:77-84,2019。©2019 威利期刊公司。