Impact of sphingomyelin levels on coronary heart disease and left ventricular systolic function in humans

被引:19
作者
Chen, Xueying [1 ]
Sun, Aijun [1 ]
Zou, Yunzeng [1 ]
Ge, Junbo [1 ]
Lazar, Jason M. [2 ]
Jiang, Xian-Cheng [3 ]
机构
[1] Fudan Univ, Inst Cardiol, Zhongshan Hosp, Shanghai 200433, Peoples R China
[2] Suny Downstate Med Ctr, Div Cardiovasc Med, Brooklyn, NY 11203 USA
[3] Suny Downstate Med Ctr, Dept Cell Biol, Brooklyn, NY 11203 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
sphingomyelin left ventricular ejection fraction; coronary heart disease; lipids; NECROSIS-FACTOR-ALPHA; ADULT-RAT CARDIOMYOCYTES; TO-RETENTION HYPOTHESIS; E-KNOCKOUT MICE; PLASMA SPHINGOMYELIN; ATHEROGENIC LIPOPROTEINS; SUBENDOTHELIAL RETENTION; ARTERY-DISEASE; DEFICIENT MICE; RISK-FACTOR;
D O I
10.1186/1743-7075-8-25
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Sphingomyelin (SM) is an abundant phospholipid in cell membranes and in lipoproteins. In human plasma, SM is mainly found in atherogenic lipoproteins; therefore, higher levels of SM may promote atherogenesis. We investigated the relations between plasma SM levels and the presence of angiographic coronary heart disease (CHD) and left ventricular systolic dysfunction. We studied 732 patients referred for coronary angiography. Median SM levels were higher among patients with CHD and in those with LV systolic dysfunction (LVEF<50%) than in patients without CHD or LV dysfunction. SM levels were significantly correlated with fibrinogen levels, diabetes, apoB, and triglyceride levels. On multivariate analyses, higher median SM levels were associated with a higher risk of CHD and lower LV ejection fraction. The pro-atherogenic property of plasma SM might be related to 1) CHD; 2) LV systolic dysfunction; and 3) metabolism of apoB-containing or triglyceride-rich lipoproteins.
引用
收藏
页数:6
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