INCREASED COLLAGEN-LINKED PENTOSIDINE LEVELS AND ADVANCED GLYCOSYLATION END-PRODUCTS IN EARLY DIABETIC NEPHROPATHY

被引:152
作者
BEISSWENGER, PJ
MOORE, LL
BRINCKJOHNSEN, T
CURPHEY, TJ
机构
[1] DARTMOUTH COLL SCH MED,DEPT MED,HANOVER,NH 03755
[2] DARTMOUTH COLL SCH MED,DEPT PATHOL,HANOVER,NH 03755
关键词
MAILLARD REACTION; DIABETIC RETINOPATHY; DIABETIC MICROANGIOPATHY; AMADORI REACTION; MICROALBUMINURIA;
D O I
10.1172/JCI116552
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Rationale: Advanced glycosylation end products (AGEs) may play an important role in the development of diabetic vascular sequelae. An AGE cross-link, pentosidine, is a sensitive and specific marker for tissue levels of AGEs. Objectives: To evaluate the role of AGEs in the development of diabetic nephropathy and retinopathy, we studied pentosidine levels and the clinical characteristics of 48 subjects with insulin-dependent diabetes mellitus. Diabetic nephropathy was classified as normal, microalbuminuria, or gross proteinuria, and retinopathy was graded as none, background, or proliferative. Newly observed findings: Significant elevation of pentosidine (P = 0.025) was found in subjects with microalbuminuria or gross proteinuria (73.03+/-9.47 vs 76.46+/-6.37 pmol/mg col) when compared with normal (56.96+/-3.26 pmol/mg col). Multivariate analysis to correct for age, duration of diabetes, and gender did not modify the results. Elevated pentosidine levels were also found in those with proliferative when compared with those with background retinopathy (75.86+/-5.66 vs 60.42+/-5.98 pmol/mg col) (P < 0.05). Conclusions: Microalbuminuria is associated with elevated levels of pentosidine similar to those found in overt diabetic nephropathy suggesting that elevated AGE levels are already present during the earliest detectable phase of diabetic nephropathy.
引用
收藏
页码:212 / 217
页数:6
相关论文
共 27 条
[1]   GLUCOSYLATED COLLAGEN IS ANTIGENIC [J].
BASSIOUNY, AR ;
ROSENBERG, H ;
MCDONALD, TL .
DIABETES, 1983, 32 (12) :1182-1184
[2]   AN OVERVIEW OF ROLE OF MATRIX COMPONENTS [J].
BROWN, DM ;
CHARONIS, AS ;
FURCHT, LT ;
KLEIN, DJ ;
MAUER, SM ;
STEFFES, MW ;
TSILIBARY, PEC .
DIABETES CARE, 1991, 14 (02) :157-159
[3]   COVALENT ATTACHMENT OF SOLUBLE-PROTEINS BY NONENZYMATICALLY GLYCOSYLATED COLLAGEN - ROLE IN THE INSITU FORMATION OF IMMUNE-COMPLEXES [J].
BROWNLEE, M ;
PONGOR, S ;
CERAMI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (05) :1739-1744
[4]  
BROWNLEE M, 1988, NEW ENGL J MED, V318, P1315
[5]   GLOMERULAR-LESIONS AND URINARY ALBUMIN EXCRETION IN TYPE-I DIABETES WITHOUT OVERT PROTEINURIA [J].
CHAVERS, BM ;
BILOUS, RW ;
ELLIS, EN ;
STEFFES, MW ;
MAUER, SM .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (15) :966-970
[6]  
Krolewski AJ, 1987, NEW ENGL J MED, V18, P267
[7]  
MAKITA Z, 1992, J BIOL CHEM, V267, P5133
[8]   ADVANCED GLYCOSYLATION END-PRODUCTS IN PATIENTS WITH DIABETIC NEPHROPATHY [J].
MAKITA, Z ;
RADOFF, S ;
RAYFIELD, EJ ;
YANG, Z ;
SKOLNIK, E ;
DELANEY, V ;
FRIEDMAN, EA ;
CERAMI, A ;
VLASSARA, H .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (12) :836-842
[9]   IMMUNOHISTOCHEMICAL DETECTION OF ADVANCED GLYCOSYLATION END-PRODUCTS IN DIABETIC TISSUES USING MONOCLONAL-ANTIBODY TO PYRRALINE [J].
MIYATA, S ;
MONNIER, V .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (04) :1102-1112
[10]   PREDICTION OF CLINICAL DIABETIC NEPHROPATHY IN IDDM PATIENTS - ALTERNATIVES TO MICROALBUMINURIA [J].
MOGENSEN, CE .
DIABETES, 1990, 39 (07) :761-767