Ishibashi Fukashi, Kojima Rie, Taniguchi Miki, Kosaka Aiko, Uetake Harumi, Tavakoli Mitra
Ishibashi Clinic, Hiroshima, Japan.
University of Exeter Medical School, Exeter, UK.
J Diabetes Res. 2017;2017:6069730. doi: 10.1155/2017/6069730. Epub 2017 Mar 22.
The main aim of the present paper is to examine whether the pupillary light reflex (PLR) mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) is impaired in type 2 diabetic patients. One hundred and three diabetic patients without diabetic autonomic neuropathy (DAN) and 42 age-matched controls underwent a series of detailed neurological examinations. The patients were stratified into three groups: stage I, no neuropathy; stage II, asymptomatic neuropathy; stage III, symptomatic but without DAN. The PLR to 470 and 635 nm light at 20 cd/m was recorded. Small fiber neuropathy was assessed by corneal confocal microscopy and quantifying corneal nerve fiber (CNF) morphology. The 470 nm light induced a stronger and faster PLR than did 635 nm light in all subjects. The PLR to both lights was impaired equally across all of the diabetic subgroups. The postillumination pupil response (PIPR) after 470 nm light offset at ≥1.7 sec was attenuated in diabetic patients without differences between subgroups. Receiver operating characteristic analysis revealed that the PIPR mediated by ipRGCs in patients with stage II and stage III neuropathy was different from that of the control subjects. Clinical factors, nerve conduction velocity, and CNF measures were significantly correlated with PLR parameters with 470 nm light. PLR kinetics were more impaired by stimulation with blue light than with red light in diabetic patients without DAN.
本文的主要目的是研究由内在光敏性视网膜神经节细胞(ipRGCs)介导的瞳孔光反射(PLR)在2型糖尿病患者中是否受损。103例无糖尿病自主神经病变(DAN)的糖尿病患者和42例年龄匹配的对照者接受了一系列详细的神经学检查。患者被分为三组:I期,无神经病变;II期,无症状神经病变;III期,有症状但无DAN。记录了在20 cd/m下对470和635 nm光的PLR。通过角膜共聚焦显微镜和量化角膜神经纤维(CNF)形态来评估小纤维神经病变。在所有受试者中,470 nm光比635 nm光诱导出更强、更快的PLR。所有糖尿病亚组对两种光的PLR均同等受损。在≥1.7秒时470 nm光熄灭后的照明后瞳孔反应(PIPR)在糖尿病患者中减弱,各亚组之间无差异。受试者工作特征分析显示,II期和III期神经病变患者中由ipRGCs介导的PIPR与对照受试者不同。临床因素、神经传导速度和CNF测量值与470 nm光的PLR参数显著相关。在无DAN的糖尿病患者中,蓝光刺激比红光刺激对PLR动力学的损害更大。