Folkhälsan Research Center, Biomedicum Helsinki, Haartmaninkatu 8, FIN-00290, Helsinki, Finland.
Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.
Cardiovasc Diabetol. 2024 Sep 28;23(1):350. doi: 10.1186/s12933-024-02427-4.
Hyperglycemia-induced oxidative stress is a well-established pathological mediator of vascular complications in diabetes. We assessed plasma oxidant and antioxidant levels in response to acute and chronic hyperglycemia in relation to vascular stiffness and varying degrees of kidney disease in type 1 diabetes individuals.
The acute hyperglycemia study included 22 type 1 diabetic individuals with normal albumin excretion rate (AER) and 13 non-diabetic controls. These individuals received an acute glucose challenge during a 120-minute hyperglycemic clamp. The chronic hyperglycemia study included 118 type 1 diabetic individuals with chronically low (n = 60) or high (n = 58) HbA1c concentrations and varying degrees of diabetic kidney disease (DKD) classified as normal, moderate, or severe albuminuria (AER). Levels of malondialdehyde (MDA), reactive oxygen metabolites (ROMs), total antioxidant capacity (TAC), biological antioxidant potential (BAP) and superoxide dismutase (SOD) were measured from plasma or serum samples in the FinnDiane study.
Levels of MDA (p < 0.01) and ROMs (p < 0.01) were elevated in type 1 diabetes individuals compared to non-diabetic controls at baseline. Acute hyperglycemia further increased MDA levels (p < 0.05) and sustained the elevation of ROMs in type 1 diabetes individuals. Acute hyperglycemic challenge impaired TAC in both non-diabetic (p < 0.05) and type 1 diabetes (p < 0.01) individuals compared to baseline whereas BAP was increased (p < 0.05) with no difference observed in non-diabetic controls. There was a positive association between high circulating MDA and AIx (r2 = 0.611, p = 0.05), and between delta ROMs and delta AIx (r2 = 0.955, p = 0.014) in combined analysis of individuals with type 1 diabetes and non-diabetic controls. Type 1 diabetes individuals with varying status of DKD, showed elevated levels of ROMs in those with high HbA1c compared to their counterpart with low HbA1c (p < 0.05). Individuals with severe albuminuria showed elevated ROM levels (p < 0.01) and depressed antioxidant capacity (p < 0.01) compared to those with normal AER of comparable HbA1c concentrations.
Biomarkers of oxidative stress are associated with vascular stiffness and DKD following acute and chronic hyperglycemic exposure and may provide added value to HbA1c in understanding disease pathology, predicting risk and assessing the status of secondary complications of type 1 diabetes.
高血糖诱导的氧化应激是糖尿病血管并发症的一种公认的病理介质。我们评估了 1 型糖尿病个体在急性和慢性高血糖反应中血浆氧化剂和抗氧化剂水平与血管僵硬和不同程度肾脏疾病的关系。
急性高血糖研究包括 22 名正常白蛋白排泄率(AER)的 1 型糖尿病个体和 13 名非糖尿病对照者。这些个体在 120 分钟高血糖钳夹期间接受急性葡萄糖挑战。慢性高血糖研究包括 118 名慢性低(n=60)或高(n=58)HbA1c 浓度的 1 型糖尿病个体和不同程度的糖尿病肾病(DKD),分为正常、中度或重度白蛋白尿(AER)。在 FinnDiane 研究中,从血浆或血清样本中测量了丙二醛(MDA)、活性氧代谢物(ROMs)、总抗氧化能力(TAC)、生物抗氧化潜力(BAP)和超氧化物歧化酶(SOD)的水平。
与非糖尿病对照组相比,1 型糖尿病个体在基线时 MDA(p<0.01)和 ROMs(p<0.01)水平升高。急性高血糖进一步增加 MDA 水平(p<0.05)并维持 1 型糖尿病个体 ROMs 的升高。与基线相比,急性高血糖挑战降低了非糖尿病个体(p<0.05)和 1 型糖尿病个体(p<0.01)的 TAC,而 BAP 增加(p<0.05),非糖尿病对照组无差异。在 1 型糖尿病和非糖尿病对照组个体的联合分析中,高循环 MDA 与 AIx 呈正相关(r2=0.611,p=0.05),delta ROMs 与 delta AIx 呈正相关(r2=0.955,p=0.014)。在不同 DKD 状态的 1 型糖尿病个体中,与低 HbA1c 个体相比,HbA1c 较高的个体中 ROMs 水平升高(p<0.05)。与具有可比 HbA1c 浓度的正常 AER 的个体相比,严重白蛋白尿个体的 ROM 水平升高(p<0.01),抗氧化能力降低(p<0.01)。
在急性和慢性高血糖暴露后,氧化应激的生物标志物与血管僵硬和 DKD 相关,并且在了解疾病病理、预测风险和评估 1 型糖尿病的继发性并发症状态方面,可能比 HbA1c 更具价值。