2003Unpublished venueRequires access

Analyzing the Relationship between in Vivo Oxidized Low Density Lipoprotein and Low Density Lipoprotein Immune Complexes

Jun Wang

Open publisher page 0 citations

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.

About this research paper

What this paper is about

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.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Apolipoprotein B, Chemistry, Low-density lipoprotein, Lipoprotein, Internal medicine, Endocrinology, Antibody, Immune system

Related papers

Back to paper searchBrowse research topicsOriginal source
Analyzing the Relationship between in Vivo Oxidized Low Density Lipoprotein and Low Density Lipoprotein Immune Complexes — Research Paper | ScholarLens