Kalita J, Misra U K, Yadav R K
Department of Neurology, Sanjay Gandhi PGIMS, Lucknow, India.
Eur J Neurol. 2007 Jun;14(6):638-43. doi: 10.1111/j.1468-1331.2007.01798.x.
Diabetes mellitus (DM) is occasionally associated with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) raising the question of coexistence or etiological link. The study compares, neurophysiological and outcome of CIDP patients with and without DM. Consecutive CIDP patients were subjected to detailed clinical evaluation, haematology, serum chemistry, vasculitis profile, paraproteins, myeloma screening and cerebrospinal fluid (CSF) examination. Electrodiagnostic (EDx) tests included motor and sensory conduction and F-wave studies. The patients were treated with oral prednisolone 1 mg/kg/day with or without azathioprine 1-2 mg/kg and followed up for 6 months. The clinical and EDx finding in CIDP with and without DM were compared. Thirty-five CIDP patients were included and nine had DM. CIDP with diabetes (CIDP-D) had higher frequency of autonomic dysfunction. In CIDP-D, motor (38.9% vs. 16.7%) and sensory (40.7% vs. 14.1%) nerve conductions were more frequently unrecordable or had reduced compound muscle action potential (CMAP) amplitude. F-waves were also more frequently unrecordable in CIDP-D (28.8% vs. 12.8%) compared with idiopathic CIDP (I-CIDP). The degree of conduction block was more in I-CIDP. At 6-month follow up, I-CIDP patients improved better than CIDP-D. CIDP-D patients present with higher frequency of autonomic dysfunction, electrophysiological evidences of associated axonal loss and had a poorer outcome at 6 months compared with I-CIDP.
糖尿病(DM)偶尔与慢性炎症性脱髓鞘性多发性神经根神经病(CIDP)相关,这引发了两者共存或病因联系的问题。本研究比较了合并和未合并DM的CIDP患者的神经生理学及预后情况。连续纳入的CIDP患者接受了详细的临床评估、血液学检查、血清化学检查、血管炎指标检测、副蛋白检测、骨髓瘤筛查及脑脊液(CSF)检查。电诊断(EDx)测试包括运动和感觉传导以及F波研究。患者接受口服泼尼松龙1mg/kg/天治疗,加或不加硫唑嘌呤1 - 2mg/kg,并随访6个月。比较了合并和未合并DM的CIDP患者的临床和EDx检查结果。共纳入35例CIDP患者,其中9例患有DM。合并糖尿病的CIDP(CIDP - D)患者自主神经功能障碍的发生率更高。在CIDP - D患者中,运动神经传导(38.9%对16.7%)和感觉神经传导(40.7%对14.1%)更常无法记录或复合肌肉动作电位(CMAP)波幅降低。与特发性CIDP(I - CIDP)相比,CIDP - D患者中F波也更常无法记录(28.8%对12.8%)。I - CIDP患者的传导阻滞程度更严重。在6个月的随访中,I - CIDP患者的改善情况优于CIDP - D患者。与I - CIDP相比,CIDP - D患者自主神经功能障碍的发生率更高,有轴索丢失的电生理证据,且在6个月时预后较差。