Grus F H, Sabuncuo P, Dick H B, Augustin A J, Pfeiffer N
Dept. of Ophthalmology, University of Mainz, Germany.
BMC Ophthalmol. 2002 Oct 31;2:4. doi: 10.1186/1471-2415-2-4.
Previous studies have shown a significant increase in tear protein peaks in the tears of diabetic patients suffering from dry eye. The aim of this study was to analyze the tear protein patterns from patients with diabetes mellitus who do not suffer from ocular surface diseases (DIA).
A total of 515 patients were examined in this study (255 healthy subjects (controls) and 260 patients suffering from diabetes mellitus). Tear proteins were separated by sodium-dodecyl-sulfate polyacrylamide gel electrophoresis. After digital image analysis densitometric data files were created and subsequently used for multivariate statistical procedures.
A significant increase in the number of peaks was detected in diabetic patients compared to controls (P < 0.0003). The analysis of discriminance revealed a highly significant discrimination between diabetic patients and controls (Wilks lambda: 0.27; P < 0.000001). Furthermore, a significant difference in the protein pattern of diabetic patients could be detected between those suffering from dry eye or not (P < 0.002). The changes in protein patterns of diabetic patients increased with the duration of the diabetic disease. In diabetic patients with a disease duration longer than 10 years the changes were significantly more expressed than in patients with a shorter diabetic history (P < 0.003) and in healthy subjects (P < 0.0001).
The tear protein patterns of diabetic patients are very different in the number and intensity of spots from those of healthy subjects. Furthermore, it could be demonstrated that the differences found in the tear patterns of diabetic patients are not equal to those found in previous studies in patients suffering from dry-eye disease. The alterations in the diabetic tears were correlated with the duration of the diabetic disease. With longer disease, history changes in the tear protein patterns increased. With the course of the disease some protein peaks appeared that are not present in healthy persons. Our study shows that the analysis of electrophoretic tear protein patterns is a new non-invasive approach in the early diagnosis and analysis of the pathogenesis of diabetes induced ocular surface disease.
先前的研究表明,患有干眼症的糖尿病患者泪液中的蛋白质峰显著增加。本研究的目的是分析未患眼表疾病的糖尿病患者(糖尿病组)的泪液蛋白质图谱。
本研究共检查了515名患者(255名健康受试者(对照组)和260名糖尿病患者)。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳分离泪液蛋白质。经过数字图像分析后创建光密度数据文件,随后用于多变量统计程序。
与对照组相比,糖尿病患者的峰数量显著增加(P < 0.0003)。判别分析显示糖尿病患者与对照组之间存在高度显著的差异(威尔克斯λ:0.27;P < 0.000001)。此外,在患有或未患干眼症的糖尿病患者之间,可以检测到蛋白质图谱存在显著差异(P < 0.002)。糖尿病患者蛋白质图谱的变化随着糖尿病病程的延长而增加。糖尿病病程超过10年的患者,其变化比糖尿病病史较短的患者(P < 0.003)和健康受试者(P < 0.0001)更为明显。
糖尿病患者的泪液蛋白质图谱在斑点数量和强度上与健康受试者有很大不同。此外,可以证明,糖尿病患者泪液图谱中发现的差异与先前干眼症患者研究中发现的差异不同。糖尿病患者泪液的改变与糖尿病病程相关。病程越长,泪液蛋白质图谱的变化越大。随着疾病的发展,出现了一些健康人不存在的蛋白质峰。我们的研究表明,电泳泪液蛋白质图谱分析是糖尿病性眼表疾病早期诊断和发病机制分析的一种新的非侵入性方法。