Analyzing the Relationship between in Vivo Oxidized Low Density Lipoprotein and Low Density Lipoprotein Immune Complexes
Jun Wang
Abstract
Jun Wang
Abstract
Aim To investigate the possible relationship between oxidized low density lipoprotein (ox-LDL) and LDL-immune complexes (IC) level. Methods We developed a ELISA for measuring plasma LDL-IC level using anti-human IgG (Fab) as the capture antibody and quantitating with monoclonalanti-apoB enzyme conjugate. Oxidixed LDL was also detected by a sandwich ELISA method using monoclonal antibodies against ox-LDL as the capture antibody and quantitating with anti-apoB enzyme conjugate. Their levels were studied in 60 patients with coronary heart disease (CHD) and 50 control subjects. Results Plasma concentrations of TG, lipoprotein (a) and apolipoprotein B in CHD patients were all significantly increased whereas HDLC and apolipoprotein AI levels were decreased. Plasma LDL-IC (2.74 ± 0.73 AU vs 1.38 ± 0.78 AU, P 0.001) and ox-LDL (595.5 ±194.8 μg/L vs 440.3 ± 175.0 μg/L, P0.001) concentrations in the patients with CHD were both significantly higher than those of control. The relationships between LDL-IC ox-LDL levels and other lipid traits in all the studied subjects ( n = 110) were carried out. LDL-IC levels were positively correlated with TC, TG, LDLC, lipoprotein(a) and apolipoprotein B concentrations while negatively correlated with apolipoprotein AI concentrations respectively. Similarly ox-LDL levels were also found positively correlated with TC, LDLC, or apolipoprotein B concentrations respectively. Furthermore a significantly positive relation between ox-LDL and LDL-IC levels was found (r = 0.313, P 0.005). Conclusions Increased oxidized LDL and LDL immune complexes levels are risk factors for atherosclerosis.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Aim To investigate the possible relationship between oxidized low density lipoprotein (ox-LDL) and LDL-immune complexes (IC) level. Methods We developed a ELISA for measuring plasma LDL-IC level using anti-human IgG (Fab) as the capture antibody and quantitating with monoclonalanti-apoB enzyme conjugate. Oxidixed LDL was also detected by a sandwich ELISA method using monoclonal antibodies against ox-LDL as the capture antibody and quantitating with anti-apoB enzyme conjugate. Their levels were studied in 60 patients with coronary heart disease (CHD) and 50 control subjects. Results Plasma concentrations of TG, lipoprotein (a) and apolipoprotein B in CHD patients were all significantly increased whereas HDLC and apolipoprotein AI levels were decreased. Plasma LDL-IC (2.74 ± 0.73 AU vs 1.38 ± 0.78 AU, P 0.001) and ox-LDL (595.5 ±194.8 μg/L vs 440.3 ± 175.0 μg/L, P0.001) concentrations in the patients with CHD were both significantly higher than those of control. The relationships between LDL-IC ox-LDL levels and other lipid traits in all the studied subjects ( n = 110) were carried out. LDL-IC levels were positively correlated with TC, TG, LDLC, lipoprotein(a) and apolipoprotein B concentrations while negatively correlated with apolipoprotein AI concentrations respectively. Similarly ox-LDL levels were also found positively correlated with TC, LDLC, or apolipoprotein B concentrations respectively. Furthermore a significantly positive relation between ox-LDL and LDL-IC levels was found (r = 0.313, P 0.005). Conclusions Increased oxidized LDL and LDL immune complexes levels are risk factors for atherosclerosis.
Key concepts: Apolipoprotein B, Chemistry, Low-density lipoprotein, Lipoprotein, Internal medicine, Endocrinology, Antibody, Immune system