HEMOGLOBIN-AGE - A CIRCULATING MARKER OF ADVANCED GLYCOSYLATION

被引:257
作者
MAKITA, Z
VLASSARA, H
RAYFIELD, E
CARTWRIGHT, K
FRIEDMAN, E
RODBY, R
CERAMI, A
BUCALA, R
机构
[1] ALTEON INC, NORTHVALE, NJ 07647 USA
[2] RUSH PRESBYTERIAN ST LUKES MED CTR, CHICAGO, IL 60612 USA
[3] SUNY DOWNSTATE MED CTR, BROOKLYN, NY 11203 USA
关键词
D O I
10.1126/science.1411574
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Advanced glycosylation end products (AGEs) form spontaneously from glucose-derived Amadori products and accumulate on long-lived tissue proteins. AGEs have been implicated in the pathogenesis of several of the complications of aging and diabetes, including atherosclerosis and renal disease. With the use of recently developed AGE-specific antibodies, an AGE-modified form of human hemoglobin has been identified. Termed hemoglobin-AGE (Hb-AGE), this modified species accounts for 0.42 percent of circulating hemoglobin in normal individuals but increases to 0.75 percent in patients with diabetes-induced hyperglycemia. In a group of diabetic patients treated with the advanced glycosylation inhibitor aminoguanidine, Hb-AGE levels decreased significantly over a 1-month period. Hemoglobin-AGE measurements may provide an index of long-term tissue modification by AGEs and prove useful in assessing the contribution of advanced glycosylation to a variety of diabetic and age-related complications.
引用
收藏
页码:651 / 653
页数:3
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