Asghar Omar, Petropoulos Ioannis N, Alam Uazman, Jones Wendy, Jeziorska Maria, Marshall Andrew, Ponirakis Georgios, Fadavi Hassan, Boulton Andrew J M, Tavakoli Mitra, Malik Rayaz A
Institute of Human Development, Centre for Endocrinology and Diabetes, University of Manchester and Central Manchester NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, U.K.
Department of Clinical Neurophysiology, Central Manchester NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, U.K.
Diabetes Care. 2014 Sep;37(9):2643-6. doi: 10.2337/dc14-0279. Epub 2014 Jun 26.
Impaired glucose tolerance (IGT) represents one of the earliest stages of glucose dysregulation and is associated with macrovascular disease, retinopathy, and microalbuminuria, but whether IGT causes neuropathy is unclear.
Thirty-seven subjects with IGT and 20 age-matched control subjects underwent a comprehensive evaluation of neuropathy by assessing symptoms, neurological deficits, nerve conduction studies, quantitative sensory testing, heart rate variability deep breathing (HRVdb), skin biopsy, and corneal confocal microscopy (CCM).
Subjects with IGT had a significantly increased neuropathy symptom profile (P < 0.001), McGill pain index (P < 0.001), neuropathy disability score (P = 0.001), vibration perception threshold (P = 0.002), warm threshold (P = 0.006), and cool threshold (P = 0.03), with a reduction in intraepidermal nerve fiber density (P = 0.03), corneal nerve fiber density (P < 0.001), corneal nerve branch density (P = 0.002), and corneal nerve fiber length (P = 0.05). No significant difference was found in sensory and motor nerve amplitude and conduction velocity or HRVdb.
Subjects with IGT have evidence of neuropathy, particularly small-fiber damage, which can be detected using skin biopsy and CCM.
糖耐量受损(IGT)是血糖调节异常的最早阶段之一,与大血管疾病、视网膜病变和微量白蛋白尿相关,但IGT是否会导致神经病变尚不清楚。
37例IGT患者和20例年龄匹配的对照受试者通过评估症状、神经功能缺损、神经传导研究、定量感觉测试、深呼吸心率变异性(HRVdb)、皮肤活检和角膜共焦显微镜检查(CCM)对神经病变进行了全面评估。
IGT患者的神经病变症状评分(P < 0.001)、麦吉尔疼痛指数(P < 0.001)、神经病变残疾评分(P = 0.001)、振动觉阈值(P = 0.002)、温觉阈值(P = 0.006)和冷觉阈值(P = 0.03)显著升高,表皮内神经纤维密度(P = 0.03)、角膜神经纤维密度(P < 0.001)、角膜神经分支密度(P = 0.002)和角膜神经纤维长度(P = 0.05)降低。感觉和运动神经振幅、传导速度或HRVdb无显著差异。
IGT患者有神经病变的证据,尤其是小纤维损伤,可通过皮肤活检和CCM检测到。