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顺铂神经病变中的神经元受累:前瞻性临床与神经生理学研究

Neuronal involvement in cisplatin neuropathy: prospective clinical and neurophysiological studies.

作者信息

Krarup-Hansen A, Helweg-Larsen S, Schmalbruch H, Rørth M, Krarup C

机构信息

Department of Oncology, Rigshospitalet, Copenhagen, Denmark.

出版信息

Brain. 2007 Apr;130(Pt 4):1076-88. doi: 10.1093/brain/awl356. Epub 2007 Feb 14.

Abstract

Although it is well known that cisplatin causes a sensory neuropathy, the primary site of involvement is not established. The clinical symptoms localized in a stocking-glove distribution may be explained by a length dependent neuronopathy or by a distal axonopathy. To study whether the whole neuron or the distal axon was primarily affected, we have carried out serial clinical and electrophysiological studies in 16 males with testicular cancer before or early and late during and after treatment with cisplatin, etoposide and bleomycin at limited (<400 mg/m2 cisplatin), conventional (approximately 400 mg/m2 cisplatin) or high (>400 mg/m2 cisplatin) doses. At cumulative doses of cisplatin higher than 300 mg/m2 the patients lost distal tendon and H-reflexes and displayed reduced vibration sense in the feet and the fingers. The amplitudes of sensory nerve action potentials (SNAP) from the fingers innervated by the median nerve and the dorsolateral side of the foot innervated by the sural nerve were 50-60% reduced, whereas no definite changes occurred at lower doses. The SNAP conduction velocities were reduced by 10-15% at cumulative doses of 400-700 mg/m2 consistent with loss of large myelinated fibres. SNAPs from primarily Pacinian corpuscles in digit 3 and the dorsolateral side of the foot evoked by a tactile probe showed similar changes to those observed in SNAPs evoked by electrical stimulation. At these doses, somatosensory evoked potentials (SEPs) from the tibial nerve had increased latencies of peripheral, spinal and central responses suggesting loss of central processes of large dorsal root ganglion cells. Motor conduction studies, autonomic function and warm and cold temperature sensation remained unchanged at all doses of cisplatin treatment. The results of these studies are consistent with degeneration of large sensory neurons whereas there was no evidence of distal axonal degeneration even at the lowest toxic doses of cisplatin.

摘要

虽然众所周知顺铂会导致感觉神经病变,但受累的主要部位尚未明确。局限于手套袜套样分布的临床症状,可能是由长度依赖性神经元病变或远端轴索性病变所解释。为了研究整个神经元还是远端轴索首先受到影响,我们对16例睾丸癌男性患者进行了系列临床和电生理研究,这些患者在接受顺铂、依托泊苷和博来霉素治疗之前、治疗期间及治疗后早期和晚期,接受的是低剂量(<400mg/m²顺铂)、常规剂量(约400mg/m²顺铂)或高剂量(>400mg/m²顺铂)治疗。当顺铂累积剂量高于300mg/m²时,患者失去远端腱反射和Hoffmann反射,并在足部和手指出现振动觉减退。由正中神经支配的手指及腓肠神经支配的足背外侧的感觉神经动作电位(SNAP)波幅降低了50 - 60%,而较低剂量时未出现明确变化。在顺铂累积剂量为400 - 700mg/m²时,SNAP传导速度降低了10 - 15%,这与大的有髓纤维丢失一致。用触觉探针刺激第三指主要的环层小体及足背外侧所引出的SNAP,显示出与电刺激引出的SNAP类似的变化。在这些剂量下,来自胫神经的体感诱发电位(SEP)外周、脊髓和中枢反应的潜伏期延长,提示大的背根神经节细胞的中枢突丢失。在所有顺铂治疗剂量下,运动传导研究、自主神经功能以及冷热温度觉均保持不变。这些研究结果与大感觉神经元变性一致,而即使在顺铂最低中毒剂量时,也没有远端轴索变性的证据。

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