Urine 伪-Glutathione S-Transferase, systemic inflammation and arterial function in juvenile type 1 diabetes

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• 作者：Peter Holmquist^a ; ^{Peter.Holmquist@skane.se} ; Petru Liuba^b
• 关键词：伪-GST ; Vascular endothelial function ; Inflammation ; Type 1 diabetes
• 刊名：Journal of Diabetes and its Complications
• 出版年：2012
• 期刊代码：154_10568727
• 类别：med
• 出版时间：May-June, 2012
• 卷：26
• 期：3
• 页码：199-204
• 文件大小：349 K

摘要

Background

Despite marked improvement in therapy and monitoring of patients with insulin-dependent (type 1) diabetes, diabetic nephropathy remains a serious complication, with subsequent end-stage renal disease in about 20%of cases.

Objective

To investigate in young patients with type 1 diabetes whether urine 伪-Glutathione S-transferase to creatinine ratio (伪-GST:crea) relates to markers of systemic inflammation and subclinical vasculopathy.

Design

Children and adolescents (median age and diabetes duration 14 and 6 years, respectively) with type 1 diabetes screened in a previous study for proximal tubular (urine 伪-GST:crea ratio) and renal (plasma creatinine, cystatin C glomerular filtration rate (GFR), and timed urine albumin excretion rate (AER)) function were, within the same timeframe, also investigated for vascular (blood pressure, carotid artery intima-media thickness (IMT) and compliance (CAC), brachial artery flow-mediated dilatation (FMD) and plasma cyclic guanosine monophosphate (cGMP) and inflammatory (C-reactive protein (CRP), and tumor necrosis factor-alpha (TNF-伪)) profiles. Exposure to environmental tobacco smoke (ETS) was assessed through questionnaire (n = 67 respondents).

Results

None of the patients (n = 69) had overt renal insufficiency. AER correlated with age (p = 0.01, r = 0.3), diabetes duration (p = 0.02, r = 0.3), FMD (p = 0.04, r = 鈭?#xA0;0.3, n = 52), CAC (p = 0.03, r = 鈭?#xA0;0.3, n = 62) and cGMP (p = 0.01, r = 鈭?#xA0;0.3, n = 59). 伪-GST:crea was lower (p = 0.03) in patients than in controls. 伪-GST:crea appeared to be particularly lower in older patients (p = 0.004, r = 鈭?#xA0;0.34 vs age), in those with worse diabetic control (p = 0.03, r = 鈭?#xA0;0.26 vs HbA1c), and in those with lower carotid artery elasticity (p = 0.017, r = 0.3 vs CAC). Although ETS had no direct significant impact on 伪-GST:crea, 伪-GST:crea correlated with FMD only in patients with ETS (r = 0.5, p = 0.009, n = 13). 伪-GST:crea showed positive association with TNF-伪 (p = 0.01, r = 0.3).

Conclusion

In children and adolescents with type 1 diabetes, lower levels of urine excretion of 伪-GST:crea appear to be associated with decreasing elasticity and endothelial vasomotor function of peripheral arteries, especially in patients with ETS. In contrast, higher levels of 伪-GST:crea are more common in patients with elevated markers of systemic inflammation. Large scale prospective studies are needed to clarify the meaning and mechanisms of this association.