Arslan Deniz, Merdin Alparslan, Tural Deniz, Temizel Mustafa, Akın Olgun, Gündüz Seyda, Tatlı Ali Murat, Avcı Fatma, Uysal Mükremin
Department of Internal Medicine, Ministry of Health Okmeydanı Training and Research Hospital, İstanbul, Turkey.
Department of Internal Medicine, Akdeniz University Hospital, Antalya, Turkey.
Med Sci Monit. 2014 Jul 10;20:1176-9. doi: 10.12659/MSM.890742.
Type 1 diabetes mellitus (DM) is an autoimmune disease with chronic complications that is becoming more frequent as life expectancy of diabetics has increased owing to improved methods of detection and better management. In this study, we investigated whether the presence of autoimmunity can be used in predicting the development time of microvascular complications.
Our study included 52 patients with type 1 diabetes mellitus (DM). The subjects had developed microvascular complications and they had been tested for anti-GAD (glutamic acid decarboxylase) antibodies and/or islet-cell antibodies (ICA). In the assessment of microvascular complications, we used ocular fundus examination, electromyography (EMG), and 24-h urine microalbuminuria tests.
Of the patients included in the study, 30 were female and 22 were male. Of all patients characterized for the existence of diabetic complications, 36 of 52 had both diabetic retinopathy and diabetic nephropathy, 5 patients had diabetic neuropathy, and 11 patients had diabetic retinopathy only. At the diagnosis of diabetes, 20 in 52 patients tested negative for autoantibodies (anti-GAD and anti-ICA), while 32 of 52 tested positive for anti-GAD and/or anti-ICA. The mean HbA1C level of autoantibody-negative patients was 7.7%, while antibody-positive patients had slightly higher HbA1c levels (7.9%). However, this difference was not statistically significant (p>0.05). The mean development time of microvascular complications in autoantibody-positive patients was calculated as 11: 40±6.46 years, and in patients with negative autoimmunity results it was 10.91±6.70 years.
The presence of diabetes-related autoantibodies (DRAs) in patients with type 1 diabetes mellitus does not have a significant effect on the development time of diabetic microvascular complications.
1型糖尿病(DM)是一种伴有慢性并发症的自身免疫性疾病,由于检测方法的改进和管理的改善,糖尿病患者的预期寿命增加,该疾病正变得越来越常见。在本研究中,我们调查了自身免疫的存在是否可用于预测微血管并发症的发生时间。
我们的研究纳入了52例1型糖尿病患者。这些受试者已出现微血管并发症,并已检测抗谷氨酸脱羧酶(GAD)抗体和/或胰岛细胞抗体(ICA)。在评估微血管并发症时,我们采用了眼底检查、肌电图(EMG)和24小时尿微量白蛋白尿检测。
纳入研究的患者中,30例为女性,22例为男性。在所有有糖尿病并发症的患者中,52例中有36例同时患有糖尿病视网膜病变和糖尿病肾病,5例患有糖尿病神经病变,11例仅患有糖尿病视网膜病变。在糖尿病诊断时,52例患者中有20例自身抗体(抗GAD和抗ICA)检测呈阴性,而52例中有32例抗GAD和/或抗ICA检测呈阳性。自身抗体阴性患者的平均糖化血红蛋白(HbA1C)水平为7.7%,而抗体阳性患者的HbA1c水平略高(7.9%)。然而,这种差异无统计学意义(p>0.05)。自身抗体阳性患者微血管并发症的平均发生时间计算为11.40±6.46年,自身免疫结果为阴性的患者为10.91±6.70年。
1型糖尿病患者中糖尿病相关自身抗体(DRA)的存在对糖尿病微血管并发症的发生时间没有显著影响。