Plasma levels of soluble receptor for advanced glycation end products and coronary artery disease in nondiabetic men

被引:333
作者
Falcone, C
Emanuele, E
D'Angelo, A
Buzzi, MP
Belvito, C
Cuccia, M
Geroldi, D
机构
[1] Univ Pavia, Univ Hosp IRCCS San Mateo, Dept Cardiol, I-27100 Pavia, Italy
[2] Univ Pavia, Univ Hosp IRCCS San Mateo, Mol Med Lab, I-27100 Pavia, Italy
[3] Univ Pavia, Univ Hosp IRCCS San Mateo, Dept Internal Med & Med Therapeut, I-27100 Pavia, Italy
[4] Univ Pavia, Dept Genet & Microbiol, I-27100 Pavia, Italy
关键词
coronary artery disease; risk factor; soluble receptor for advanced glycation end products;
D O I
10.1161/01.ATV.0000160342.20342.00
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - The receptor for advanced glycation end products ( RAGE) is a cell surface receptor whose signaling pathway has been implicated in atherogenesis. RAGE has an endogenous secretory receptor form, called soluble RAGE (sRAGE), that could exert antiatherogenic effects by acting as a decoy. We sought to determine whether a decreased plasma level of sRAGE could be independently associated with the prevalence of coronary artery disease ( CAD) in nondiabetic men. Methods and Results - Plasma levels of sRAGE were determined in 328 nondiabetic male patients with angiographically proved CAD and in 328 age-matched healthy controls. The concentration of sRAGE in plasma was significantly lower ( P < 0.0001) in CAD cases [ median (interquartile range): 966 ( 658 - 1372) pg/mL] than in control subjects [ 1335 ( 936 - 1954) pg/mL]. In logistic regression analysis, the multivariate-adjusted odds ratio for the presence of CAD was 6.719 (95% confidence interval, 3.773 to 11.964; P < 0.0001) when the lowest quartile of the sRAGE level was compared with the highest quartile. Conclusions - Our findings indicate that low levels of sRAGE in plasma are independently associated with the presence of CAD in nondiabetic men and suggest that sRAGE is one of the clinically important molecules associated with atherosclerosis.
引用
收藏
页码:1032 / 1037
页数:6
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