Myśliwiec Małgorzata, Balcerska Anna, Zorena Katarzyna, Myśliwska Jolanta, Nowacka Mirosława, Lipowski Paweł, Raczyńska Krystyna
Klinika Pediatrii, Hematologii, Onkologii i Endokrynologii AM w Gdańsku.
Endokrynol Diabetol Chor Przemiany Materii Wieku Rozw. 2006;12(4):269-73.
Despite that numerous investigations on the nature of diabetic microangiopathy were carried out, its pathomechanism remains unclear.
The aim of the study was to analyze the relation between early diabetic microangiopathy and the proinflammatory cytokines, NAG and its A and B isoforms in blood and urine in children diagnosed with diabetes mellitus type 1.
The study was carried out on the group of 56 children with diabetes mellitus 1 (age 13.6+/-3.74) and 35 healthy children selected as the controls. All the patients had 24 hrs albuminuria, HbA1c, C-peptide as well as the NAG enzyme and its A and B isoforms serum and urine activities measured. Additionally, all the children had TNF-a and IL6 level in serum measured. Each patient had 24 hrs blood pressure monitored and underwent ophthalmologic examination.
Children with long-standing diabetes mellitus and retinopathy (group 1, n=15) were older and were characterized by a statistically significant longer duration of the disease and higher HbA1c level in comparison with the patients who presented with no sign of diabetic retinopathy (group 2, n=41). In the group 1 statistically significant higher TNF-alpha serum level (p=0.01), NAG (p=0.002) and its isoforms A (p=0.007) and B (p=0.001) urine activities were measured in relation to the group 2. Additionally the level of IL-6 and NAG and its isoforms A and B serum activities were higher in group 1 than in group 2, however the differences were of no statistical significance. Moreover the children from group 2 in comparison with the healthy controls showed statistically significant higher TNF-alpha serum activity (p=0.016) and NAG (p<0.001) and its A (p<0.001) and B (p<0.001) isoforms both serum and urine activities.
The occurrence of the detectable serum TNF-alpha activity in children with diabetes mellitus type 1 showing no sign of diabetic retinopathy and nephropathy and no microalbuminuria with the concomitant increase of NAG and its isoforms serum and urine activities might point toward prompt occurrence of these changes in the eye and the kidneys.
尽管对糖尿病微血管病变的本质进行了大量研究,但其发病机制仍不清楚。
本研究旨在分析1型糖尿病患儿早期糖尿病微血管病变与血液及尿液中促炎细胞因子、N-乙酰-β-D-氨基葡萄糖苷酶(NAG)及其A和B同工型之间的关系。
对56例1型糖尿病患儿(年龄13.6±3.74岁)和35例健康儿童进行研究,将健康儿童作为对照组。所有患者均测定24小时尿白蛋白、糖化血红蛋白(HbA1c)、C肽以及NAG酶及其A和B同工型的血清和尿液活性。此外,所有儿童均测定血清中肿瘤坏死因子-α(TNF-α)和白细胞介素6(IL-6)水平。每位患者均监测24小时血压并接受眼科检查。
患有长期糖尿病和视网膜病变的儿童(第1组,n = 15)年龄较大,与无糖尿病视网膜病变迹象的患者(第2组,n = 41)相比,其疾病持续时间在统计学上显著更长,HbA1c水平更高。与第2组相比,第1组中TNF-α血清水平(p = 0.01)、NAG(p = 0.002)及其同工型A(p = 0.007)和B(p = 0.001)的尿液活性在统计学上显著更高。此外,第1组中IL-6水平以及NAG及其同工型A和B的血清活性高于第2组,但差异无统计学意义。此外,与健康对照组相比,第2组儿童的TNF-α血清活性(p = 0.016)、NAG(p < 0.001)及其A(p < 0.001)和B(p < 0.001)同工型的血清和尿液活性在统计学上显著更高。
在无糖尿病视网膜病变、肾病及微量白蛋白尿迹象的1型糖尿病患儿中,可检测到血清TNF-α活性,同时NAG及其同工型的血清和尿液活性增加,这可能表明眼部和肾脏会迅速出现这些变化。