[儿童和青少年1型糖尿病患者体内胱抑素C水平是否为糖尿病肾病的早期标志?]

Jadwiga Peczyńska, Mirosława Urban, Barbara Głowińska, Bozena Florys
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引用次数: 0

摘要

背景:1型糖尿病病程中最重要的并发症是糖尿病肾病。目前,除了评估尿液中白蛋白的增加量外,我们无法足够早地识别这些可能因肾病而危及健康的患者。寻找其他可以标记肾脏损害/肾功能障碍早期症状的生化指标似乎是合理的。目的:1。儿童和青少年1型糖尿病患者体内胱抑素C的浓度是多少?其水平是否与患者年龄、患者发病年龄、病程长短、代谢代偿、糖尿病控制和是否存在微血管病变有关?2. 胱氨酸抑素C、微量白蛋白尿和肾效率之间是否存在相互依赖关系?材料:学习小组。研究对象为1 ~ 17岁的青少年糖尿病患者130例(女孩60例,男孩70例,年龄从7岁到20岁不等)。对照组为健康青少年,年龄和性别匹配,无任何/负担/病史。方法:对所有患者进行以下检查:测量人体测量,定义BMI (kg/m2),估计基于HbA1c(%)的代谢代偿。进行眼科检查和动脉血压昼夜监测。在24小时尿液收集中测定微量白蛋白尿。在内源性肌酐清除率和胱抑素C浓度的帮助下,评估两组肾小球滤过率。结果要进行统计分析。结果:全组患者平均年龄15+/-3岁,平均病程6、85+/-3岁,36岁。糖尿病患者胱抑素C浓度高于对照组(0.75+/-0.13 vs. 0.68+/-0.12 mg/l)。我们还发现,胱氨酸抑制素C的浓度随着病程的延长而增加,在患病时间超过10年的患者组中达到最高水平(0.52+/-0.11 vs. 0.67+/-0.13 vs. 0.93+/-0.13 mg/l),同样具有统计学意义。糖尿病控制不充分的患者胱抑素C浓度较高(0.765+/-0.12 mg/l vs. 0.71+/-0.12 pg/ml)。讨论:结合初步结果,可以得出以下结论:只有进一步的长期研究才能为我们提供可靠的数据,评估儿童和青少年糖尿病患者血清胱抑素C浓度水平是否可以成为比微量白蛋白尿更早的肾功能障碍标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[If the level of cystatin C in children and adolescents with type 1 diabetes an early marker for diabetic nephropathy?].

Background: The most important complication in the course of diabetes mellitus type I is diabetic nephropathy. Nowadays, apart from assessing the increased amount of albumins in urine, we are not able to identify early enough these patients whose health might be endangered by nephropathy. Looking for other biochemical indicators which could mark the early symptoms of kidney damage/renal malfunction seems to be justified.

Objectives: 1. What is the concentration of cystatin C among children and teenagers suffering from diabetes mellitus type 1 and whether its level depends on the age of patient, the age in which the patient was affected with the disease, the length of the disease, metabolic compensation, diabetes control and the presence of microangiopathy? 2. Is there any interdependence between cystatin C and microalbuminuria and the renal efficiency rates?

Material: Study group. A group of 130 patients (60 girls and 70 boys aged from 7 and 20,8) who have been suffering from juvenile diabetes from 1 to 17 years was examined. The control group were healthy youngsters, matched for age and sex, without any /burdening/ medical history.

Methods: All the patients were examined in the following way: anthropometric measurements were taken, BMI in kg/m2 was defined, metabolic compensation based on HbA1c (%) was estimated. Ophthalmological examination and a circadian monitoring of arterial blood pressure were carried out. Microalbuminuria in a 24-hour urine collection was determined. In both groups glomerular filtration rate with the help of endogenous creatinine clearance and the concentration of cystatin C were evaluated. The results were subject to statistical analysis.

Results: The average age of the whole examined group was 15+/-3,0 the average disease length 6,85+/-3,36 years. The concentration of cystatin C among diabetic patients was higher in comparison with the control group (0.75+/-0.13 vs. 0.68+/-0.12 mg/l). It was also discovered that the concentration of cystatin C was increasing along with the length of the disease reaching the highest level in the group of patients suffering from this disease longer than 10 years (0.52+/-0.11 vs. 0.67+/-0.13 vs. 0.93+/-0.13 mg/l), which is again statistically significant. Moreover the concentration of cystatin C is higher among patients with insufficient diabetes control (0.765+/-0.12 mg/l vs. 0.71+/-0.12 pg/ml, p<0.05). These patients who additionally developed vascular complications (retinopathy, nephropathy, arterial hypertension) had significantly higher condensation of cystatin C (0.75+/-0.13 vs. 0.69+/-0.11 mg/l, p<0.05).

Discussion: Having considered the initial results, the following conclusion can be reached: only further, long-term research can supply us with the reliable data whether assessing the level of cystatin C concentration in children's and teenagers' serum in diabetic patients could become the earlier marker of renal malfunction than microalbuminuria.

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