Relationships between glucose excursion and the activation of oxidative stress in patients with newly diagnosed type 2 diabetes or impaired glucose regulation

被引:120
作者
Zheng, Fenping [1 ]
Lu, Weina [1 ]
Jia, Chengfang [1 ]
Li, Hong [1 ]
Wang, Zhou [1 ]
Jia, Weiping [2 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Sir Run Run Shaw Hosp, Dept Endocrinol, 3 E Qingchun Rd, Hangzhou 310016, Zhejiang, Peoples R China
[2] Jiaotong Univ, Peoples Hosp 6, Shanghai Diabet Inst, Dept Endocrinol & Metab, Shanghai, Peoples R China
关键词
Glucose excursion; Oxidative stress; Diabetes; Impaired glucose regulation; URINARY; 8-HYDROXYDEOXYGUANOSINE; POSTPRANDIAL HYPERGLYCEMIA; PROTEIN DAMAGE; DNA-DAMAGE; IN-VIVO; COMPLICATIONS; ASSOCIATION; EXPRESSION; BIOMARKER; MELLITUS;
D O I
10.1007/s12020-009-9296-6
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The effect of glucose excursions on oxidative stress is an important topic in diabetes research. We investigated this relationship by analyzing markers of oxidative stress and glycemic data from a continuous glucose monitoring system (CGMS) in 30 individuals with normal glucose regulation (NGR), 27 subjects with impaired glucose regulation (IGR), and 27 patients with newly diagnosed type 2 diabetes (T2DM). We compared the mean amplitude of glycemic excursion (MAGE), mean postprandial glucose excursion (MPPGE), and mean postprandial incremental area under the curve (IAUC) with plasma levels of oxidative stress markers 8-iso-PGF2 alpha, 8-OH-dG, and protein carbonyl content in the study subjects. Patients with T2DM or IGR had significantly higher glucose excursions and plasma levels of oxidative stress markers compared to normal controls (P < 0.01 or 0.05). Multiple linear regression analyses showed significant relationships between MAGE and plasma 8-iso-PGF2 alpha, and between MPPGE and plasma 8-OH-dG in patients with IGR or T2DM (P < 0.01 or 0.05). Furthermore, 2h-postprandial glucose level and IAUC were related to plasma protein carbonyl content in the study cohort including T2DM and IGR (P < 0.01). We demonstrate that glucose excursions in subjects with IGR and T2DM trigger the activation of oxidative stress.
引用
收藏
页码:201 / 208
页数:8
相关论文
共 30 条
[1]
Glycated and oxidized protein degradation products are indicators of fasting and postprandial hyperglycemia in diabetes [J].
Ahmed, N ;
Babaei-Jadidi, R ;
Howell, SK ;
Thornalley, PJ ;
Beisswenger, PJ .
DIABETES CARE, 2005, 28 (10) :2465-2471
[2]
Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[3]
Postprandial glucose regulation and diabetic complications [J].
Ceriello, A ;
Hanefeld, M ;
Leiter, L ;
Monnier, L ;
Moses, A ;
Owens, D ;
Tajima, N ;
Tuomilehto, J .
ARCHIVES OF INTERNAL MEDICINE, 2004, 164 (19) :2090-2095
[4]
Role of hyperglycemia in nitrotyrosine postprandial generation [J].
Ceriello, A ;
Quagliaro, L ;
Catone, B ;
Pascon, R ;
Piazzola, M ;
Bais, B ;
Marra, G ;
Tonutti, L ;
Taboga, C ;
Motz, E .
DIABETES CARE, 2002, 25 (08) :1439-1443
[5]
Postprandial hyperglycaemia and cardiovascular complications of diabetes: An update [J].
Ceriello, Antonio ;
Davidson, Jamie ;
Hanefeld, Markolf ;
Leiter, Lawrence ;
Monnier, Louis ;
Owens, David ;
Tajima, Naoko ;
Tuomilehto, Jaakko .
NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES, 2006, 16 (07) :453-456
[6]
Diabet Control Complications Trial Res Grp, 1997, DIABETES, V46, P1829
[7]
Urinary 8-hydroxydeoxyguanosine levels in diabetic retinopathy patients [J].
Dong, Q. Y. ;
Cui, Y. ;
Chen, L. ;
Song, J. ;
Sun, L. .
EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2008, 18 (01) :94-98
[8]
Genuth Saul, 2006, Endocr Pract, V12 Suppl 1, P34
[9]
Oxidative DNA damage in diabetes mellitus: its association with diabetic complications [J].
Hinokio, Y ;
Suzuki, S ;
Hirai, M ;
Chiba, M ;
Hirai, A ;
Toyota, T .
DIABETOLOGIA, 1999, 42 (08) :995-998
[10]
Should minimal blood glucose variability become the gold standard of glycemic control? [J].
Hirsch, IB ;
Brownlee, M .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2005, 19 (03) :178-181