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. 2014 Oct 28;2014:234316. doi: 10.1155/2014/234316

Proatherogenic Oxidized Low-Density Lipoprotein/β2-Glycoprotein I Complexes in Arterial and Venous Disease

Jeffrey S Berger 1,2, Caron B Rockman 2, Kirk E Guyer 3, Luis R Lopez 4,*
PMCID: PMC4227323  PMID: 25405208

Abstract

OxLDL/β2GPI complexes have been implicated in the initiation and progression of atherosclerosis and associated with disease severity and adverse outcomes. We investigate the significance of anti-oxLDL/β2GPI antibodies and oxLDL/β2GPI complexes in patients with arterial and idiopathic venous disease. A cohort of 61 arterial disease patients, 32 idiopathic venous disease patients, and 53 healthy controls was studied. Because statins influence oxLDL/β2GPI, these complexes were analyzed on subjects not taking statins. Arterial and venous groups expressed higher levels of IgG anti-oxLDL/β2GPI antibodies than controls without any other significant clinical association. OxLDL/β2GPI complexes were significantly elevated in arterial (0.69 U/mL, P = 0.004) and venous disease (0.54 U/mL, P = 0.025) than controls (0.39 U/mL). Among arterial diseases, oxLDL/β2GPI was 0.85 U/mL for carotid artery disease, 0.72 U/mL for peripheral artery disease, and 0.52 U/mL for abdominal aortic aneurysm. There was a significant association with male gender, age, hypertension, and history of thrombosis. Subjects with oxLDL/β2GPI above the median (0.25 U/mL) were more likely to have arterial (OR 4.5, P = 0.004) or venous disease (OR 4.1, P = 0.008). Multivariate regression indicated that males (P = 0.021), high cholesterol (P = 0.011), and carotid disease (P = 0.023) were significant predictors of oxLDL/β2GPI. The coexistence of oxLDL/β2GPI in arterial and venous disease may suggest a common oxidative mechanism that independently predicts carotid artery disease.

1. Introduction

Atherosclerosis is a progressive disease of the arterial wall associated with an underlying systemic immune-inflammatory background that promotes dyslipidemia and arterial prothrombotic phenotypes. The oxidative modification of low-density lipoprotein (oxLDL) is one of the key events in the initiation and progression of atherosclerotic lesions [1]. OxLDL is highly inflammatory and immunogenically capable of further promoting endothelial dysfunction and enhanced secretion of chemotactic and proinflammatory cytokines including a proatherogenic immune response [2]. OxLDL interacts with the lipid binding plasma protein β2-glycoprotein I (β2GPI) to form oxLDL/β2GPI complexes [3], implicated as proatherothrombotic autoantigens [4, 5]. Further, the coexistence of oxLDL/β2GPI complexes and autoantibodies to these complexes in systemic lupus erythematosus (SLE) and antiphospholipid syndrome patients suggested a pathogenic role in both venous and arterial thromboembolic events [6, 7].

In some nonautoimmune patients positive for antiphospholipid antibodies and suffering from acute coronary syndromes, anti-β2GPI and anti-oxLDL/β2GPI antibodies were most prevalent [8]. In addition, circulating oxLDL/β2GPI complexes in these patients were associated with disease severity and with a 3.5-fold risk of 2-year adverse cardiovascular outcomes [9]. A recent report clearly demonstrated that rosuvastatin significantly reduced serum levels of oxLDL/β2GPI complexes in patients with diabetes, an effect that was independent of LDL levels but likely dependent on an antioxidant inhibition of nitric oxide metabolites [10]. The presence and significance of anti-oxLDL/β2GPI antibodies and oxLDL/β2GPI complexes have not been evaluated in nonautoimmune subjects with venous disease.

2. Methods

2.1. Patient Samples

We enrolled 146 subjects from the vascular surgery outpatient clinic at a tertiary medical center as follows: 61 with arterial disease, 32 with idiopathic venous disease, and 53 healthy controls. Since statins are known to lower oxLDL/β2GPI, we excluded subjects taking statins [10]. The demographic and clinical characteristics of 100 subjects not taking statins included in the study (27 arterial disease, 25 IVD, and 48 healthy controls) are summarized in Table 1. Of the 27 patients with arterial disease, 7 had carotid artery disease (CarAD), 11 peripheral artery disease (PAD), and 9 abdominal aortic aneurysm (AAA). Serum samples were obtained at study entry and were blind tested for IgG anti-oxLDL/β2GPI antibodies and oxLDL/β2GPI complexes.

Table 1.

Demographic and clinical characteristics of 100 study subjects by vascular disease phenotype.

  Controls 
(n = 48) 		Arterial∗ 
(n = 27) 		Venous 
(n = 25) 		P value∗∗
Age (yrs, mean ± SD) 35.4 ± 12.5 71.0 ± 11.6 54.2 ± 12.4 <0.0001
Sex (F/M) 34 F/14 M 9 F/18 M 16 F/9 M 0.005
Smoking (%) 17.0 8.3 8.0 0.422
DM (%) 0 22.2 0 0.0002
High cholesterol (%) 14.6 62.9 24.0 <0.0001
HTN (%) 8.3 55.6 24.0 <0.0001
BMI (kg/m2, mean ± SD) 26.3 ± 6.3 27.7 ± 5.7 30.1 ± 5.8 0.005
Fam Hx BC (%) 2.1 7.7 0 0.240
Fam Hx MI (%) 14.6 25.9 16.0 0.450
Fam Hx stroke (%) 4.2 7.4 0 0.394
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*Arterial disease = CarAD, PAD, AAA.

∗∗Wilcoxon/Kruskal-Wallis Rank Sum or Pearson's Chi-square.

2.2. ELISA for IgG Antibodies to oxLDL/β2GPI Complexes

IgG anti-oxLDL/β2GPI antibodies were measured by commercial ELISA (Corgenix, Inc., Broomfield, Colorado) following the manufacturer instructions. Diluted serum samples were incubated in microwells with immobilized oxLDL/β2GPI antigen complex to capture anti-oxLDL/β2GPI antibodies. Horseradish peroxidase (HRP) conjugated anti-human IgG antibodies were added to detect bound IgG anti-oxLDL/β2GPI antibodies followed by tetramethylbenzidine/H2O2 (TMB) as chromogenic substrate. Color development was stopped with 0.36 N sulphuric acid and optical density (OD) read at 450 nm (640 nm reference). IgG anti-oxLDL/β2GPI antibody concentration was calculated against a reference curve and results were expressed in G units.

2.3. ELISA for oxLDL/β2GPI Complexes

Serum oxLDL/β2GPI complexes were measured as previously described [10]. Briefly, IgG2b murine monoclonal antibody (3H3) specific for human β2GPI was coated onto 96-microwell plates and used to capture oxLDL/β2GPI complexes via its reactivity with β2GPI. Diluted patient serum was added to the appropriate microwells for incubation at room temperature for 1 hour. After washing, biotinylated 2E10 antibody (IgG murine monoclonal anti-human Apo B-100) was added to the microwells and incubated for 30 minutes, followed by Streptavidin-HRP for 30 minutes. Color was developed with tetramethylbenzidine/H2O2 (TMB) for 30 minutes and the reaction stopped with 0.36 N sulphuric acid. Optical density (OD) was read at a wavelength of 450 nm (650 nm reference). Serum oxLDL/β2GPI complex concentration (expressed in U/mL) was calculated against a reference curve built with threefold serial dilutions of a reference serum.

2.4. Statistical Analysis

For categorical variables, Chi-squared test or Fisher's exact test was used; for continuous variables paired t-test and Wilcoxon Signed Rank Sum test (when applicable) were used. Association between variables was assessed by univariate analysis (Pearson's rho) and the assumptions of the univariate analysis were tested by multiple regression. Cochran-Armitage Trend test was used to determine the trend between oxLDL/β2GPI quartiles and odds ratio (OR). Statistical analysis was performed using the JMP 9.0.0 program from SAS Institute Inc., NC, USA.

3. Results

The mean IgG anti-oxLDL/β2GPI antibody level for the arterial group was 15.3 ± 6.1 G units with 15.4% positive (above cut-off of the assay established at 20 G units) and 14.9 ± 4.3 G units with 12.1% positives for the venous group. These levels were not statistically different when compared to the healthy controls (13.4 ± 4.7 G units and 7.5% positives). Interestingly, the mean of the arterial and venous disease groups combined (15.2 ± 5.5 G units) was statistically higher than the controls (P = 0.037). No other association of IgG anti-oxLDL/β2GPI antibodies with demographic, serologic, or clinical variables was found.

The mean oxLDL/β2GPI complex level of 100 subjects not taking statins was significantly elevated in arterial (0.69 ± 0.50 U/mL, P = 0.004) and venous groups (0.54 ± 0.37 U/mL, P = 0.025) compared to healthy controls (0.39 ± 0.33 U/mL) (Figure 1), and oxLDL/β2GPI levels between the arterial and venous disease groups were not different (P = 0.394). However, the association between the three groups was statistically significant (P = 0.006). Among patients with arterial disease, mean oxLDL/β2GPI levels for CarAD (0.85 ± 0.59 U/mL, P = 0.013) and PAD (0.72 ± 0.54 U/mL, P = 0.033) were significantly higher than healthy controls, but AAA (0.52 ± 0.38 U/mL, P = 0.255) was not. The association between the arterial disease subgroups was not statistically significant (P = 0.466) (Figure 2).

Figure 1.

Figure 1

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Distribution of serum levels of oxLDL/β2GPI complexes measured by ELISA in 48 healthy controls and 25 patients with venous and 27 with arterial diseases (n = 27). Subjects taking statins were excluded. Mean oxLDL/β2GPI levels in arterial (0.69 ± 0.50 U/mL, P = 0.004) and venous diseases (0.54 ± 0.37 U/mL, P = 0.025) were significantly higher than healthy controls (0.39 ± 0.33 U/mL). Mean levels in arterial (0.69 ± 0.50 U/mL) versus venous diseases (0.54 ± 0.37 U/mL) were not statistically different (P = 0.394). OxLDL/β2GPI levels among the three groups were statistically significant (P = 0.006, Wilcoxon/Kruskal-Wallis Rank Sum test). Boxes represent 75/25 percentiles with the horizontal line the median for the group and whiskers the 90/10 percentile bars.

Figure 2.

Figure 2

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Distribution of serum levels of oxLDL/β2GPI complexes measured in 27 patients with arterial disease. Mean oxLDL/β2GPI levels of CarAD (0.85 ± 0.59 U/mL, P = 0.013) and PAD (0.72 ± 0.54 U/mL, P = 0.033) were significantly higher compared to healthy controls (0.38 ± 0.33 U/mL), while AAA (0.52 ± 0.38 U/mL, P = 0.255) were not. The trend among the arterial disease groups was not statistically significant (P = 0.466, Wilcoxon/Kruskal-Wallis Rank Sum test). Boxes represent 75/25 percentiles with the horizontal line the median for the group and whiskers the 90/10 percentile bars.

Subjects with oxLDL/β2GPI in the upper quartiles (above control median of 0.25 U/mL) were more likely to have arterial (OR 4.5, 1.54–13.14, P = 0.004) and/or venous diseases (OR 4.1, 1.38–11.99, P = 0.008) (Table 2). In unadjusted analysis, there was a significant association between oxLDL/β2GPI with male gender (0.55 versus 0.26 U/mL, P = 0.005), age (r = 0.299, P = 0.002), hypertension (0.54 versus 0.27 U/mL, P = 0.024), and history of thrombotic disease (0.95 versus 0.37 U/mL, P = 0.035). BMI was not associated with oxLDL/β2GPI levels. Multivariate regression models with oxLDL/β2GPI as a dependent variable indicated that male gender (t = 2.34, P = 0.021), high cholesterol (t = −2.58, P = 0.011), and CarAD phenotype (t = 2.32, P = 0.023) were significant predictors of oxLDL/β2GPI levels. Excluding venous disease, CarAD remained the only significant independent predictor of oxLDL/β2GPI levels (t = 2.30, P = 0.024). These results indicate a stronger proatherogenic role of oxLDL/β2GPI complexes in CarAD over the other arterial and venous vascular phenotypes studied.

Table 2.

Odds ratio (OR) for arterial or venous disease by oxLDL/β2GPI quartiles.

OxLDL/β2GPI quartiles∗ Arterial Venous
OR (95% CI)∧ P value∗∗ OR (95% CI)∧ P value∗∗
Q2 1.25 (0.213–7.354) 0.805 6.25 (0.641–60.938) 0.085
Q3 4.44 (0.931–21.218) 0.053 18.3 (2.016–166.725) 0.002
Q4 5.42 (1.249–23.489) 0.018 10.0 (1.093–91.441) 0.020
Q1 + 2 versus Q3 + 4 4.50 (1.541–13.140) 0.004 4.10 (1.382–11.996) 0.008
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*OxLDL/β2GPI quartiles: Q1 = 0–0.17; Q2 = 0.18–0.25; Q3 = 0.26–0.57; Q4 = 0.58–1.4 U/mL. The association increased significantly with oxLDL/β2GPI quartiles for arterial (P = 0.006) and venous disease (P = 0.015) (Cochran-Armitage Trend test).

∧Odds ratio (95% confidence interval).

∗∗Pearson's Chi-square against Q1.

4. Discussion

IgG anti-oxLDL/β2GPI antibodies in patients with arterial and venous diseases were higher than controls. This is consistent with current concepts for immune participation in atherothrombotic vascular disease. The relatively low prevalence and weak association of IgG anti-oxLDL/β2GPI antibodies with vascular phenotypes in this nonautoimmune patient population appear consistent with previous reports [8]. These results demonstrate significantly higher oxLDL/β2GPI complex levels in patients with arterial and venous diseases. This is the first report of high oxLDL/β2GPI in venous disease. In addition to statins, the clinical determinants that influenced serum levels of oxLDL/β2GPI were male gender, hypercholesterolemia, and carotid artery disease phenotype. Patients with oxLDL/β2GPI in the upper quartiles were equally more likely to have arterial (OR 4.5) and/or venous diseases (OR 4.1). The arterial disease results were consistent with a previous report that oxLDL/β2GPI complexes were associated with more severe coronary disease and poor outcomes [9]. Because patients with venous disease exhibited high oxLDL/β2GPI levels we hypothesize that arterial and venous thrombotic diseases share a similar underlying oxidative inflammatory mechanism. In arterial disease, lipid (LDL) peroxidation and oxLDL/β2GPI complexes promote the transmigration, localization, and activation of immune-inflammatory cells within the arterial wall, favoring the excessive intracellular accumulation of lipids by macrophages [11]. In venous disease, systemic oxidative inflammation and an intravascular phospholipid-β2GPI mediated pathway likely promote an endothelial prothrombotic dysfunction and the activation of coagulation factors. The simultaneous occurrence of these two events may have important clinical implications in cardiovascular disease.

The association between asymptomatic atherosclerosis and spontaneous venous thrombosis has been previously reported suggesting that these 2 diseases shared common risk factors [12–14]. A meta-analysis of 21 studies and 63,552 patients showed that cardiovascular risk factors were associated with venous thromboembolism (VTE) [15]. More recent reports indicate that patients with symptomatic atherosclerosis had increased risk for VTE [16] and that statins, in a dose dependent manner, decreased the incidence of VTE in 1,100 atherosclerosis patients from 22.3% to 6.3% [17]. The exact mechanism for this association remains unclear but the clinical relevance of the association has been emphasized with respect to individual screening, risk factor modification, and primary or secondary prevention of VTE. As we previously demonstrated the effect of statins on oxidative inflammation (oxLDL/β2GPI complexes) [10], however, the influence of statins on venous disease outcomes has not been fully evaluated. In conclusion, our results point to a possible common or overlapping risk factor for arterial and venous diseases, suggesting that high serum levels of oxLDL/β2GPI complexes may be used as a modifiable biomarker for evaluation and management of atherothrombotic CVD.

5. Conclusions

  1. Elevated serum levels of oxLDL/β2GPI complexes were associated with arterial and venous diseases.

  2. Male gender, dyslipidemia, and carotid disease were independent predictors of oxLDL/β2GPI complexes.

  3. Among the vascular phenotypes studied, oxLDL/β2GPI complexes were highest in carotid artery disease and peripheral artery disease.

  4. The presence of oxLDL/β2GPI complexes in arterial and venous diseases suggests a common oxidative mechanism among the different vascular phenotypes.

Conflict of Interests

Luis R. Lopez is medical director of Corgenix, Inc. Kirk E. Guyer has received consulting fees from Corgenix, Inc. The other authors state that they have no conflict of interests.

References

  • 1.Meisinger C., Baumert J., Khuseyinova N., Loewel H., Koenig W. Plasma oxidized low-density lipoprotein, a strong predictor for acute coronary heart disease events in apparently healthy, middle-aged men from the general population. Circulation. 2005;112(5):651–657. doi: 10.1161/CIRCULATIONAHA.104.529297. [DOI] [PubMed] [Google Scholar]
  • 2.Matsuura E., Kobayashi K., Tabuchi M., Lopez L. R. Oxidative modification of low-density lipoprotein and immune regulation of atherosclerosis. Progress in Lipid Research. 2006;45(6):466–486. doi: 10.1016/j.plipres.2006.05.001. [DOI] [PubMed] [Google Scholar]
  • 3.Kobayashi K., Matsuura E., Liu Q., Furukawa J.-I., Kaihara K., Inagaki J., Atsumi T., Sakairi N., Yasuda T., Voelker D. R., Koike T. A specific ligand for β2-glycoprotein I mediates autoantibody-dependent uptake of oxidized low density lipoprotein by macrophages. Journal of Lipid Research. 2001;42(5):697–709. [PubMed] [Google Scholar]
  • 4.Kobayashi K., Kishi M., Atsumi T., Bertolaccini M. L., Makino H., Sakairi N., Yamamoto I., Yasuda T., Khamashta M. A., Hughes G. R. V., Koike T., Voelker D. R., Matsuura E. Circulating oxidized LDL forms complexes with β 2-glycoprotein I: implication as an atherogenic autoantigen. Journal of Lipid Research. 2003;44(4):716–726. doi: 10.1194/jlr.M200329-JLR200. [DOI] [PubMed] [Google Scholar]
  • 5.Lopez L. R., Simpson D. F., Hurley B. L., Matsuura E. OxLDL/β2GPI complexes and autoantibodies in patients with systemic lupus erythematosus, systemic sclerosis, and antiphospholipid syndrome: Pathogenic implications for vascular involvement. Annals of the New York Academy of Sciences. 2005;1051:313–322. doi: 10.1196/annals.1361.073. [DOI] [PubMed] [Google Scholar]
  • 6.Bassi N., Ghirardello A., Iaccarino L., Zampieri S., Rampudda M. E., Atzeni F., Sarzi-Puttini P., Shoenfeld Y., Doria A. OxLDL/β 2GPI-anti-oxLDL/β 2GPI complex and atherosclerosis in SLE patients. Autoimmunity Reviews. 2007;7(1):52–58. doi: 10.1016/j.autrev.2007.06.003. [DOI] [PubMed] [Google Scholar]
  • 7.Pengo V., Bison E., Ruffatti A., Iliceto S. Antibodies to oxidized LDL/β2-glycoprotein I in antiphospholipid syndrome patients with venous and arterial thromboembolism. Thrombosis Research. 2008;122(4):556–559. doi: 10.1016/j.thromres.2007.12.028. [DOI] [PubMed] [Google Scholar]
  • 8.Greco T. P., Conti-Kelly A. M., Greco T., Jr., Doyle R., Matsuura E., Anthony J. R., Lopez L. R. Newer antiphospholipid antibodies predict adverse outcomes in patients with acute coronary syndrome. American Journal of Clinical Pathology. 2009;132(4):613–620. doi: 10.1309/AJCP2FJUT2YZGITK. [DOI] [PubMed] [Google Scholar]
  • 9.Greco T. P., Conti-Kelly A. M., Anthony J. R., Greco T., Jr., Doyle R., Boisen M., Kojima K., Matsuura E., Lopez L. R. Oxidized-LDL/β 2-glycoprotein I complexes are associated with disease severity and increased risk for adverse outcomes in patients with acute coronary syndromes. American Journal of Clinical Pathology. 2010;133(5):737–743. doi: 10.1309/AJCP88WVRDRDFBAS. [DOI] [PubMed] [Google Scholar]
  • 10.Ames P. R., Ortiz-Cadenas A., Garcia-De La Torre I., Nava A., Oregon-Miranda A., Batuca J. R., Kojima K., Lopez L. R., Matsuura E. Rosuvastatin treatment is associated with a decrease of serum oxidised low-density lipoprotein/beta2-glycoprotein i complex concentration in type 2 diabetes. British Journal of Diabetes and Vascular Disease. 2010;10(6):292–299. doi: 10.1177/1474651410388057. [DOI] [Google Scholar]
  • 11.Matsuura E., Lopez L. R., Shoenfeld Y., Ames P. R. J. β2-glycoprotein I and oxidative inflammation in early atherogenesis: a progression from innate to adaptive immunity? Autoimmunity Reviews. 2012;12(2):241–249. doi: 10.1016/j.autrev.2012.04.003. [DOI] [PubMed] [Google Scholar]
  • 12.Prandoni P., Bilora F., Marchiori A., Bernardi E., Petrobelli F., Lensing A. W. A., Prins M. H., Girolami A. An association between atherosclerosis and venous thrombosis. The New England Journal of Medicine. 2003;348(15):1435–1441. doi: 10.1056/NEJMoa022157. [DOI] [PubMed] [Google Scholar]
  • 13.Prandoni P. P., Ghirarduzzi A., Prins M. H., Pengo V., Davidson B. L., Sørensen H., Pesavento R., Iotti M., Casiglia E., Iliceto S., Pagnan A., Lensing A. W. A. Venous thromboembolism and the risk of subsequent symptomatic atherosclerosis. Journal of Thrombosis and Haemostasis. 2006;4(9):1891–1896. doi: 10.1111/j.1538-7836.2006.02058.x. [DOI] [PubMed] [Google Scholar]
  • 14.Prandoni P. Venous thromboembolism and atherosclerosis: is there a link? Journal of Thrombosis and Haemostasis. 2007;5(1):270–275. doi: 10.1111/j.1538-7836.2007.02467.x. [DOI] [PubMed] [Google Scholar]
  • 15.Ageno W., Becattini C., Brighton T., Selby R., Kamphuisen P. W. Cardiovascular risk factors and venous thromboembolism: a meta-analysis. Circulation. 2008;117(1):93–102. doi: 10.1161/CIRCULATIONAHA.107.709204. [DOI] [PubMed] [Google Scholar]
  • 16.Piazza G., Goldhaber S. Z., Lessard D. M., Goldberg R. J., Emery C., Spencer F. A. Venous thromboembolism in patients with symptomatic atherosclerosis. Thrombosis and Haemostasis. 2011;106(6):1095–1102. doi: 10.1160/TH11-07-0469. [DOI] [PubMed] [Google Scholar]
  • 17.Khemasuwan D., Chae Y. K., Gupta S., Carpio A., Yun J. H., Neagu S., Lucca A. B., Valsecchi M. E., Mora J. I. Dose-related effect of statins in venous thrombosis risk reduction. The American Journal of Medicine. 2011;124(9):852–859. doi: 10.1016/j.amjmed.2011.04.019. [DOI] [PubMed] [Google Scholar]

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