- Research article
- Open Access
- Open Peer Review
High circulating osteoprotegerin levels are associated with non-zero blood groups
© The Author(s). 2016
- Received: 26 September 2015
- Accepted: 14 May 2016
- Published: 26 May 2016
Osteoprotegerin (OPG) and von Willebrand factor (VWF) form complex within endothelial cells and following secretion. The nature of blood group antigens strongly influences the levels of circulating VWF, but there is no available data concerning its ascendancy on OPG levels. We aimed to assess the relationship of AB0 blood groups with OPG, VWF levels (VWF: Ag) and collagen binding activity (VWF: CB) in peripheral arterial disease (PAD) patients.
Functional and laboratory parameters of 105 PAD patients and 109 controls were examined. Results of OPG, VWF: Ag, VWF: CB (ELISA-s) were analysed by comparative statistics, together with clinical data.
OPG levels were higher in patients than in controls (4.64 ng/mL vs. 3.68 ng/mL, p < 0.001). Among patients elevation was marked in the presence of critical limb ischemia (5.19 ng/mL vs. 4.20 ng/mL, p = 0.011). The OPG in patients correlated positively with VWF: Ag and VWF: CB (r = 0.26, p = 0.008; r = 0.33, p = 0.001) and negatively with ankle-brachial pressure index (r = -0.22, p = 0.023). Furthermore, OPG was significantly elevated in non-0 blood groups compared to 0-groups both in patients and controls (4.95 ng/mL vs. 3.90 ng/mL, p = 0.012 and 4.09 ng/mL vs. 3.40 ng/mL, p = 0.002).
OPG levels are associated to blood group phenotypes and higher in non-0 individuals. Increased OPG levels in PAD characterize disease severity. The significant correlation between OPG and VWF:CB might have functional importance in an atherothrombosis-prone biological environment.
- Von Willebrand factor
- Peripheral arterial disease
- Endothelial dysfunction
- AB0 blood groups
- Critical ischemia
Peripheral arterial disease (PAD) is an occlusive manifestation of atherosclerosis involving most frequently the limbs. Persons with an increased risk are primarily the elderly, smokers, and patients with diabetes, hypertension and dyslipidaemia. The third important clinical manifestation of atherosclerosis presents significant clinical overlap with coronary artery disease (CAD) and carotid stenosis [1, 2]. Intermittent claudication is the leading symptom of PAD and a 10 year follow-up investigative branch of Framingham study showed that it has the lowest occurrence rate in individuals with blood group 0 .
Endothelial dysfunction is an early and important trigger of atherogenesis, emerging as a response to a number of various oxidative, infectious and mechanical injuries. Von Willebrand factor (VWF) and osteoprotegerin (OPG) are markers of these processes [4, 5].
VWF, a large multimeric glycoprotein that adheres to sub-endothelial collagen in order to catch bound platelets at high shear- and elongation forces . Osteoprotegerin (OPG) is a dimeric glycoprotein with a multifunctional cytokine role and highly expressed in a large number of tissues . They are associated in plasma, co-localized in, and co-secreted from the Weibel-Palade bodies of the endothelial cells [8, 9]. The up-regulation of OPG in severe forms of peripheral arterial disease has been described .
There is evidence that AB0 blood type is a major determinant of VWF [11-13] VWF level and activity were lower in 00, A0, B0, A20, A30 and rare genotypes than in AA, BB, and AB . The relationship between circulating OPG levels and AB0 blood groups has never been analysed. Little is known about the potential action of glycosyltransferases A and B on OPG levels, the effects of glycosylation sites D178 and D183 on the formation of disulphide bonds, the correct folding of the molecule and how OPG glycosylation could interfere with degradative pathways [15–17].
Our hypothesis is, that AB0 blood group type is determinant of OPG levels in blood, similar to its role on VWF.
The aim of our observational study was to investigate the association of OPG and PAD along with VWF level (VWF: Ag) and collagen binding activity (VWF: CB) in an AB0 group dependent manner. To achieve our target, we performed measurement of serum and plasma OPG, VWF: Ag and VWF: CB along with AB0 blood group determination; then we analysed the relationship between those parameters in PAD patient and control groups; we then analysed their clinical and biochemical correlations. Since some studies have measured OPG from sera, while others focus on the plasma fraction [18, 19] and as the sample for VWF is plasma, we compared OPG results from serum and plasma too in order to test the relevance of OPG in this aspect.
Patients, diagnosis, risk factors and comorbidities
One hundred fifteen patients – previously diagnosed with various stages of PAD- were selected for this study. After excluding 10 patients with malignancies, acute inflammatory disorders, infections, or autoimmune vascular disease, 84 males and 21 females (age 64.5 ± 0.98 years) remained. The control group consisted of 109 individuals (75 males, 34 females, age 57 ± 1.34 years), selected from the National Health Care Survey, Romania. Before admission, written consignment was obtained from each patient; the study was approved by the ethics committee of the Clinical Emergency Hospital of Târgu-Mureș and was carried out in accordance with the Declaration of Helsinki for experiments involving humans.
Diagnosis of PAD was stated on medical history, clinical examination and measurement of the ankle-brachial pressure index (ABI) and Duplex ultrasonography. For calculation of the ABI, systolic blood pressure measurements were performed on the brachial, dorsalis pedis, and posterior tibial arteries bilaterally. The higher ankle pressure of the dorsalis pedis artery and the posterior tibial artery measurements for each limb were divided by the higher of the two brachial values. Both the lower and the mean of the two indexes were used for statistical comparison.
Intermittent claudication was assessed using the Walking Impairment Questionnaire. Stages III and IV, the presence of rest pain and/or ulceration associated with an ankle systolic pressure of ≤50 Hgmm were considered as critical leg ischemia.
Coronary artery disease was assumed to be present in patients with clinical history of angina pectoris or documented myocardial infarction (MI), previous positive coronary angiography or angioplasty, and/or resting ECG changes suggestive for ischemia: ST-segment depression, Q-wave changes or T-wave changes, according to the Minnesota coding method.
A Colour Duplex carotid artery scan was performed using a GE Agilent Image Point HXB.1 Sonos 4500/5500B.1 ultrasound system. B-mode, colour- and pulsed-wave Doppler analyses were performed on both sides to identify arterial wall lesions and stenosis (expressed as the percentage decrease in artery diameter). Where no plaques were identified, carotid intima-media thickness (CIMT) was measured bilaterally at the far wall of the distal common carotid artery, immediately proximal to bifurcation, in the end diastole. Carotid artery atherosclerosis was defined as CIMT > 1.00 mm, or the presence of plaques at any levels.
The risk factors evaluated in this study included diabetes mellitus, hypertension, haemostatic, lipid and inflammatory factors. Hypertension was diagnosed according to JNC 7 protocols. Diabetes mellitus was defined as fasting glucose >6.94 mmol/L on at least two measurements, or evidence for current use of insulin or oral hypoglycaemic medication.
Blood samples were taken after overnight fasting into vacutainers with either no additive or 3.2 % trisodium citrate (Becton-Dickinson Vacutainer Systems, UK). Centrifugation was performed at 3000 rpm for 10 min, after which the serum and plasma aliquots were separated, submitted to routine biochemistry or deep-frozen at −70 °C. Serum fasting glucose, total cholesterol, high-density cholesterol and triglycerides were determined by enzymatic methods on an ABBOTT AEROSET automated biochemistry analyser (Abbott Diagnostics, USA). High-sensitivity CRP (hs CRP) was measured on a COBAS INTEGRA 400 analyser by an immunoturbidimetric method (Roche Diagnostics, Switzerland). Plasma fibrinogen was determined according to the Clauss method with Fibrinogen Reagent (Technoclone, Austria) and Behnk Thrombotimer (Germany). AB0 blood group antigens were determined by the direct Beth-Vincent method with anti-A, anti-B, anti-AB sera (DiaClon AB0, Bio-Rad Laboratories, Switzerland).
VWF: Ag was measured by ELISA according to a previously established protocol , VWF: CB was measured as Ag, but type III collagen (Sigma, USA) was used for coating high binding capacity plate (Greiner Bio-One, Austria). Infiniti 200 M (Tecan Trading AG, Männedorf, Switzerland) was used for optical reading and its Magellan software for data processing. All samples were determined in duplicate and calculations were based on four-parameter Marquardt standard curve fitting. A standard was purchased from Siemens, Germany, and results were expressed as %.
OPG levels were determined both from serum and plasma using the R&D Systems DuoSet ELISA kit (DY805, R&D Systems Europe, UK), according to the manufacturer’s instructions. Recombinant human OPG (Part No. 840371; R&D Systems) served as standard, and concentrations were expressed as ng/mL. There are controversial results with regards to the relation of OPG serum and plasma levels in the literature. Different anticoagulants, clot activator, anti-proteases, time between-collection, centrifugation and storage cause the main variations [18, 19]. Bland-Altman analysis did not reveal difference between our serum and plasma based OPG measurements (n = 181, bias = 0.055, SD = 0.39), for this reason we used the plasma values for further statistical analysis. Intra-observer coefficient of variation for OPG, VWF: Ag and VWF: CB, the outcome parameters were below 11, 10 and 12 %, respectively.
We used the IBM SPSS Statistics for Windows, Version 19.0 (IBM Corp., Armonk, NY, USA) and GraphPad Prism 6 (GraphPad Software Inc., USA) for the statistical calculations. Since the main parameters, OPG and VWF had a non-Gaussian distribution, we applied non-parametric statistical tests in our evaluation. The Kruskal-Wallis ANOVA was used for multiple group comparison; paired contrasts were carried out using the Mann-Whitney U test. Fisher’s exact test was applied to compare 2×2 or larger between-group distributions of discrete parameters. All correlations were performed by the Spearman rank-correlation test. Multiple linear regression models were applied to define the effect of clinical and laboratory variables on ln-transformed OPG levels.
The main characteristics of the patients and control groups
The main clinical and laboratory parameters of the patient and control groups
Patients (n = 105)
Controls (n = 109)
64.2 ± 0.98
57.0 ± 1.34
Myocardial infarction history
Critical limb ischemia
Significant carotid stenosis a
Multiple atherosclerotic involvement***
Rate of AB0 blood groups (0/non-0)
CIMT (lower) a
CIMT (mean) a
OPG [ng/mL] ***
VWF:CB [%] *
Fibrinogen [g/L] ***
Total cholesterol [mmol/L]
HDL–cholesterol [mmol/L] ***
The distribution of genders, incidence of diabetes, history of stroke and MI and the rate of 0/non-0 blood groups revealed no different between patients and controls. The age was higher; hypertension, CAD, multiple atherosclerotic involvement, antihypertensive, anticoagulant and statin usage were more frequent in the PAD group. ABI and CIMT were measured for diagnostic and staging purposes during hospitalization of PAD patients.
Results of the biochemical tests show that OPG levels [ng/mL] and VWF: CB [%] were significantly higher in patients than in controls (4.64 vs. 3.68, p < 0.001, and 123 vs. 107, p = 0.03). On the whole population, the relative risk of having PAD in the upper OPG quartile vs. the lower quartile was 1.75 (95 % CI: 1.17–2.60, p = 0.006). Fibrinogen levels were also significantly increased, while HDL-cholesterol levels were decreased in patients compared to controls, see Table 1.
Correlations of OPG and the main clinical and laboratory parameters
OPG proved to be dependent on age (r = 0.36, p < 0.001) but independent of gender: 4.02 (3.09–5.55) in males vs. 4.45 (3.48–6.55) in females (p = 0.093). Diabetic patients showed higher OPG values than non-diabetics with a borderline significance, 4.83 (4.09–7.80) vs. 4.48 (3.30–6.26), p = 0.052. OPG levels were significantly elevated in the whole population (patients and controls) with hypertension (p < 0.001), previous stroke (p = 0.005), CAD (p = 0.037), anti-hypertensive (p < 0.001) and fibrate (p = 0.033) users. OPG levels were elevated but not significantly in MI history positive individuals, anticoagulant and statin receivers. Among patients, those with critical limb ischemia (n = 30) had a significantly higher OPG and VWF: CB, than the rest of the group (5.19 vs. 4.20, p = 0.011, and 138 vs. 116, p = 0.031). In patients OPG showed significant negative correlations with the mean and lower ABI values (r= -0.22, p = 0.023 and r = -0.21, p = 0.032). OPG was unrelated to CIMT obtained on patients with no significant carotid stenosis (data not shown).
We did not test the effect of smoking on OPG, as at the time of admission no patients were active smokers.
Clinical and laboratory parameters of zero- and non-zero blood group patients and controls
Comparison of clinical and laboratory parameters for 0- and non-0 blood group patients and controls is given in Additional file 1: Table S1. Age, distribution of genders, incidence of diabetes, hypertension, stroke history, CAD, critical limb ischemia, carotid stenosis were not significantly different between groups. History of previous MI was assessed significantly more often in the non-0 group. The positive history for MI was significantly related to the presence of the non-0 blood groups: all 11 patients and 16 controls from 18 with a previous MI had an A, B or AB phenotype (difference in proportions p = 0.002 for the overall population and = 0.031 for both patients and controls). Intima-media thickness showed a mild, but non-significant increase in the 0 compared to non-0 group, the frequency of carotid stenosis in the two groups was similar. CIMT and ABI values, fibrinogen, total serum cholesterol, HDL-cholesterol, triglycerides, CRP levels showed no difference.
Moreover, we observed that the nature of blood groups markedly influenced the OPG-VWF: CB correlation. In the 65 patients and controls with group 0, the correlation was absent (r = 0.017, p = 0.891). In non-0 patients and controls (n = 149), OPG correlated significantly with VWF: CB (r = 0.28, p < 0.001).
Association between circulating OPG and ABzero blood groups
A number of 29 blood group 0 patients had been registered (27.6 %), while the non-0 group had the following composition: 46 group A (43.8 %), 18 group B (17.1 %), 12 group AB (11.4 %) see Additional file 2: Table S2. Among controls, the distribution of AB0 phenotypes was as follows: 36 (33 %) group 0, 32 (29.3 %) group A, 29 (26.6 %) group B, 12 (11 %) group AB. The OPG VWF levels and collagen binding activity by individual blood groups are detailed in Additional file 2: Table S2. OPG showed the highest levels at blood group AB in patients and at group A in controls, while VWF: Ag and CB were highest in group B and AB, respectively.
Due to the relatively small number of patients and controls included in each blood group, we weighed the effect of AB0 groups as 0- and non-0.
Multiple linear regression model for high OPG levels
Multiple linear regression model for ln-transformed OPG levels in the overall study population
SE of B
Presence of PAD
Despite the strong association with the non-0 blood groups, a positive history for MI did not prove to be a significant determinant of OPG levels.
The biological consequence of elevated OPG remains a subject of debate, while it is has been shown for several years that the circulating OPG concentration correlates with the severity of atherosclerotic conditions . Although the higher prevalence of PAD among non-0 blood group carriers has been recognized for a long time , association of OPG and AB0 blood groups has not been analysed until our present study.
In our design, known peripheral arterial disease patients were selected with a high frequency of multiple atherosclerotic involvement and comorbidities, such as hypertension and diabetes. The clinical and laboratory characteristics of this group were compared to a control group. Diabetes, hypertension, stroke history, myocardial infarction history and CAD occurred also in the control group that in contrast, did not express PAD.
Considering the mean ABI values, our patient group had advanced forms of atherosclerosis. OPG values showed significant negative correlation with the mean and lower ABI, which are measures of PAD severity. Corroborating previous results, we observed significantly higher values of OPG in patients compared to individuals without PAD [22–24]. The association of OPG with PAD is still controversial, since some authors have failed to prove it [25, 26].
We also elucidated a higher OPG in sufferers of critical limb ischemia and a negative correlation with the ABI scores. In the study of Ziegler et al., plasma OPG correlated with the ABI, however, the authors found no significant increase in patients compared to controls. It should be noted that they did not determine the AB0 blood groups, which, in the cases of their 67 patients and 94 controls, could have influenced the results. The incidence of diabetes, hypertension, the level of plasma fibrinogen, total and HDL-cholesterol were comparable to the characteristics of our group . Ali et al. documented the association between serum OPG and ABI . In this study, two separate cohorts were included: one consisting of Afro-Americans and another of non-Hispanian whites, predominantly women, with a 73–80 % incidence of hypertension, high BMI values, but low frequency of peripheral arterial disease (9 % overall).
There are some controversial results regarding the effect of diabetes and hyperglycaemic status on OPG levels: absence of relationship with the glycaemia status , significantly elevated OPG in diabetic nephropathy and in Japanese men with diabetes type 2 , slightly increased OPG values in gestational diabetes . In our observations, the accompanying diabetes had only a borderline effect on OPG levels.
OPG has been defined as an important mediator of vascular calcification and is influenced by the presence of arterial hypertension [7, 30]. In our whole population (but not in PAD patients) high OPG levels were associated with the presence of hypertension.
Our findings revealed an association between higher OPG levels and CAD in the whole studied population, which was not significant in the patients with the leading symptoms of PAD. A number of clinical studies mention that OPG correlates to the presence and the most important cardiovascular disease endpoints, such as long-term mortality in CAD patients . In our MI history patients, OPG was higher but the difference did not reach the threshold of statistical significance due to the reduced number of individuals in the subgroup. Acute coronary events were correlated with elevation of circulating OPG, however, some studied failed to link myocardial ischemia to high OPG . CAD also causes increased levels of OPG, however, in polyvascular disease with no acute myocardial events, this association might be masked by the advanced peripheral involvement and calcification. Patients with carotid stenosis show variable OPG levels, with elevations especially on diabetes type 2 backgrounds . In our study, the subgroup with considerable carotid stenosis showed no higher OPG levels than the rest of the patients. This was also found in cases with a previous stroke history. In both subgroups OPG proved to be higher than in those without significant stenosis or stroke, but due to their restricted size the difference did not reach significance.
We observed positive correlations between OPG, VWF: Ag and VWF: CB both in patients and controls. This significant relationship has not been described before. In our setting the VWF: CB shows slightly stronger association with OPG levels, than VWF: Ag. In endothelial cells, OPG resides in the Weibel-Palade bodies, together with VWF and P-selectin and is co-secreted in complex with VWF . Vinholt et al. recently developed an ELISA to measure it in plasma and found that only a small fraction of OPG circulates in complex, and this amount cannot be related to the severity of coronary calcification. This finding is important but does not rule out the functional importance of OPG-VWF complexes . According to our results, the correlation of OPG and VWF: CB activity is significant only in non-0 group individuals. The number of individuals in 0 blood groups is relatively small to result in a significant correlations. It is not known if OPG has ABH antigenic structure. VWF does have, but it is also not known if the A and B antigenic forms of it bind better OPG than H form. The presence of non-0 blood groups might confer to carriers an increased potential for atherothrombosis . Recently, further relationships of VWF and OPG were given by Rutten et al., who measured the “active VWF” fraction and highlighted that in 1026 first ST-segment elevation myocardial infarction (STEMI) cases the plasma medians of total VWF, “active VWF”, OPG and the ratio of VWF to “a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13” (ADAMTS-13) were at a significantly high risk for STEMI. After adjustments of these, only the “active VWF” remained significant. In this compilation out of the Chinese, Scottish and Italian cohort: only the latter displayed elevated OPG, and AB0 blood groups were not determined .
The most important finding of our study is that we evidenced a significant association of high OPG with the non-0 blood groups in PAD patients and controls. The A and AB blood group carriers presented the highest OPG values both in patients and controls (Additional file 1: Table S1). VWF: Ag and VWF: CB levels showed similar differences in favour of non-0 groups. The correlation between VWF: CB and the categories of AB0 group is noteworthy. Specifically VWF: CB is sensitive for the size of the VWF multimers , but we have not found any information concerning the relation of VWF multimer distribution and AB0 group.
The effects of blood group antigens on atherosclerosis manifestations, disease progression and outcomes have been extensively studied [12, 37]. The glycosylated residues present on VWF at position N1574 influence the cleavage of the multimers by ADAMTS-13 . Whether VWF glycosylation affects or not complex formation between OPG and VWF is a question for further study.
To our knowledge, we are the first to show the association of circulating OPG levels with AB0 antigens. In addition, our results show a statistically strong difference between the VWF: CB activity of 0 and non-0 group patients.
Ziegler et al. suggest a decreased OPG clearance in PAD, which seems feasible for the Fontaine III-IV stages . In the mirror of our results, we assume that non-0 blood group carbohydrate antigens present on the molecule might influence OPG levels, either by inhibition of protease cleavage or by an enhanced co-secretion along VWF from a triggered vessel-wall with endothelial dysfunction.
One of the limitation of our study was that the data presented here are descriptive in nature and the observed associations do not prove causal relationships. The other limitation was the relatively restricted number of patients enrolled, and the lack of AB0 genotyping possibilities, which could offer a more exact assessment of the correlations described. Although we found evidence for the association of OPG with 0 and non-0 blood group, further studies are needed to confirm this relationship in larger populations.
High OPG levels are characteristic of PAD, especially in patients with critical limb ischemia. Our study brings new data regarding the association of high OPG values with non-0 AB0 blood groups in PAD patients. While the relationship of high VWF with non-0 groups is well characterized and thought to have a causal role in the higher incidence of atherothrombotic events in comparison to 0 groups, we are the first to correlate high circulating OPG with these determinants. It is also new that VWF collagen binding activity is a strong predictor of OPG levels and that the OPG-VWF correlation is AB0 phenotype dependent. We think VWF and OPG are markers of endothelial perturbation or damage as a result of arterial disease. To elucidate whether elevated OPG represents an increased prothrombotic potential or, on the other hand, a protective, tackling actor in peripheral arterial disease with high atherosclerotic burden, needs further studies.
ABI, ankle-brachial index; ADAMTS-13, a disintegrin and metalloprotease with thrombospondin-1 repeats; AP, angina pectoris; CAD, coronary artery disease; CIMT, carotid intima-media thickness; hsCRP, high-sensitive C-reactive protein; MI, myocardial infarction; OPG, osteoprotegerin; PAD, peripheral arterial disease; STEMI, first ST-segment elevation myocardial infarction; VWF, Von Willebrand Factor; VWF: Ag, VWF antigen; VWF: CB, VWF collagen binding.
OMFB-00486/2006 Science and Technology grant of the Hungarian and Romanian Governments. Turchanyi research grant of Semmelweis University, Department of Biophysics and Radiation Biology, Budapest. Hungarian Research and Innovation Fund (KTIA_AIK_12-1-2013-0005); Hungarian Research, Develeopment and Innovation (VKSZ_14-1-2015-0052).
Availability of data and materials
The raw dataset supporting the conclusion of this article is available in the Research Group repository. Password is available from the corresponding author.
EEN designed, performed and analyzed the research, and wrote the paper. TV-F performed the measurements; AP, PK, ZB effected recruitment of the patients, performed clinical and functional examination; KSz-Cs was responsible for the quality control of the methods, collected patient data for statistical analysis. TG and MCsCs designed and performed part of the statistical approach and contributed to the preparation of the manuscript. JH initiated the work, financed the laboratory measurements and was involved in the preparation of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interest.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Caro J, Migliaccio-Walle K, Ishak KJ, Proskorovsky I. The morbidity and mortality following a diagnosis of peripheral arterial disease: long-term follow-up of a large database. BMC Cardiovasc Disord. 2005;5:5–14.View ArticleGoogle Scholar
- Criqui MH, Aboyans V. Epidemiology of peripheral artery disease. Circ Res. 2015;116:1509–26.View ArticlePubMedGoogle Scholar
- Garrison RJ, Havlik RJ, Harris RB, Feinleib M, Kannel WB, Padgett SJ. ABO blood group and cardiovacular disease: the Framingham study. Atherosclerosis. 1976;25:311–8.View ArticlePubMedGoogle Scholar
- Sonneveld MA, Cheng JM, Oemrawsingh RM, de Maat MP, Kardys I, Garcia-Garcia HM, van Geuns RJ, Regar E, Serruys PW, Boersma E, Akkerhuis KM, Leebeek FW. Von Willebrand factor in relation to coronary plaque characteristics and cardiovascular outcome. Results of the ATHEROREMO-IVUS study. Thromb Haemost. 2015;113:577–84.View ArticlePubMedGoogle Scholar
- Hosbond SE, Poulsen TS, Diederichsen ACP, Nybo M, Rasmussen LM, Mickley H. Osteoprotegerin as a marker of atherosclerosis: a systematic update. Scand Cardiovasc J. 2012;46:203–11.View ArticlePubMedGoogle Scholar
- Bryckaert M, Rosa JP, Denis CV, Lenting PJ. Of von Willebrand factor and platelets. Cell Mol Life Sci. 2015;72:307–26.View ArticlePubMedGoogle Scholar
- Evrard S, Delanaye P, Kamel S, Cristol JP, Cavalier E. Vascular calcification: from pathophysiology to biomarkers. Clin Chim Acta. 2015;438:401–14.View ArticlePubMedGoogle Scholar
- Zannettino AC, Holding CA, Diamond P, Atkins GJ, Kostakis P, Farrugia A, Gamble J, To LB, Findlay DM, Haynes DR. Osteoprotegerin (OPG) is localized to the Weibel-Palade bodies of human vascular endothelial cells and is physically associated with von Willebrand factor. J Cell Physiol. 2005;204:714–23.View ArticlePubMedGoogle Scholar
- Shahbazi S, Lenting PJ, Fribourg C, Terraube V, Denis CV, Christophe OD. Characterization of the interaction between von Willebrand factor and osteoprotegerin. J Thromb Haemost. 2007;5:1956–62.View ArticlePubMedGoogle Scholar
- Niu Y, Zhang W, Yang Z, Li X, Wen J, Wang S, Zhang H, Wang X, Zhou H, Fang W, Qin L, Su Q. Association of plasma osteoprotegerin levels with the severity of lower extremity arterial disease in patients with type 2 diabetes. BMC Cardiovasc Disord. 2015;15:86.Google Scholar
- Liumbruno GM, Franchini M. Beyond immunohaematology: the role of the ABO blood group in human diseases. Blood Transfus. 2013;11:491–9.PubMedPubMed CentralGoogle Scholar
- Franchini M, Mannucci PM. ABO blood group and thrombotic vascular disease. Thromb Haemost. 2014;112:1103–9.View ArticlePubMedGoogle Scholar
- Franchini M, Lippi G. The intriguing relationship between the ABO blood group, cardiovascular disease, and cancer. BMC Med. 2015;13:7.View ArticlePubMedPubMed CentralGoogle Scholar
- Sousa NC, Anicchino-Bizzacchi JM, Locatelli MF, Castro V, Barjas-Castro ML. The relationship between ABO groups and subgroups, factor VIII and von Willebrand factor. Haematologica. 2007;92:236–9.View ArticlePubMedGoogle Scholar
- Middleton-Hardie C, Zhu Q, Cundy H, Lin JM, Callon K, Tong PC, Xu J, Grey A, Cornish J, Naot D. Deletion of aspartate 182 in OPG causes juvenile Paget's disease by impairing both protein secretion and binding to RANKL. J Bone Miner Res. 2006;21:438–45.View ArticlePubMedGoogle Scholar
- Standal T, Seidel C, Hjertner O, Plesner T, Sanderson RD, Waage A, Borset M, Sundan A. Osteoprotegerin is bound, internalized, and degraded by multiple myeloma cells. Blood. 2002;100:3002–7.View ArticlePubMedGoogle Scholar
- Yasuhara R, Miyamoto Y, Takami M, Imamura T, Potempa J, Yoshimura K, Kamijo R. Lysine-specific gingipain promotes lipopolysaccharide- and active-vitamin D3-induced osteoclast differentiation by degrading osteoprotegerin. Biochem J. 2009;419:159–66.View ArticlePubMedPubMed CentralGoogle Scholar
- Chan BY, Buckley KA, Durham BH, Gallagher JA, Fraser WD. Effect of anticoagulants and storage temperature on the stability of receptor activator for nuclear factor-kappa B ligand and osteoprotegerin in plasma and serum. Clin Chem. 2003;49:2083–5.View ArticlePubMedGoogle Scholar
- Perez de Ciriza C, Lawrie A, Varo N. Influence of pre-analytical and analytical factors on osteoprotegerin measurements. Clin Biochem. 2014;47:1279–85.View ArticlePubMedGoogle Scholar
- Cejka J. Enzyme immunoassay for factor VIII-related antigen. Clin Chem. 1982;28:1356–8.PubMedGoogle Scholar
- Kingsbury KJ. Relation of ABO blood-groups to atherosclerosis. Lancet. 1971;1:199–203.View ArticlePubMedGoogle Scholar
- Ali Z, Ellington AA, Mosley Jr TH, Kullo IJ. Association of serum osteoprotegerin with ankle-brachial index and urine albumin: creatinine ratio in African-Americans and non-Hispanic whites. Atherosclerosis. 2009;206:575–80.View ArticlePubMedPubMed CentralGoogle Scholar
- O’Sullivan EP, Ashley DT, Davenport C, Kelly J, Devlin N, Crowley R, Leahy AL, Kelly CJ, Agha A, Thompson CJ, O'Gorman DJ, Fitzgerald P, Smith D. Osteoprotegerin is higher in peripheral arterial disease regardless of glycaemic status. Thromb Res. 2010;126:e423–7.Google Scholar
- Ye Z, Ali Z, Klee GG, Mosley Jr TH, Kullo IJ. Associations of candidate biomarkers of vascular disease with the ankle-brachial index and peripheral arterial disease. Am J Hypertens. 2013;26:495–502.View ArticlePubMedPubMed CentralGoogle Scholar
- Ziegler S, Kudlacek S, Luger A, Minar E. Osteoprotegerin plasma concentrations correlate with severity of peripheral artery disease. Atherosclerosis. 2005;182:175–80.View ArticlePubMedGoogle Scholar
- Hosbond SE, Diederichsen ACP, Saaby L, Rasmussen LM, Lambrechtsen J, Munkholm H, Sand NPR, Gerke O, Poulsen TS, Mickley H. Can osteoprotegerin be used to identify the presence and severity of coronary artery disease in different clinical settings? Atherosclerosis. 2014;236:230–6.View ArticlePubMedGoogle Scholar
- Rasmussen LM, Tarnow L, Hansen TK, Parving HH, Flyvbjerg A. Plasma osteoprotegerin levels are associated with glycaemic status, systolic blood pressure, kidney function and cardiovascular morbidity in type 1 diabetic patients. Eur J Endocrinol. 2006;154:75–81.View ArticlePubMedGoogle Scholar
- Yaturu S, Rains J, Jain SK. Relationship of elevated osteoprotegerin with insulin resistance, CRP, and TNF-alpha levels in men with type 2 diabetes. Cytokine. 2008;44:168–71.View ArticlePubMedGoogle Scholar
- Akinci B, Demir T, Celtik A, Baris M, Yener S, Ozcan MA, Yuksel F, Secil M, Yesil S. Serum osteoprotegerin is associated with carotid intima media thickness in women with previous gestational diabetes. Diabetes Res Clin Pract. 2008;82:172–8.View ArticlePubMedGoogle Scholar
- Blazquez-Medela AM, Garcia-Ortiz L, Gomez-Marcos MA, Recio-Rodriguez JI, Sanchez-Rodriguez A, Lopez-Novoa JM, Martinez-Salgado C. Osteoprotegerin is associated with cardiovascular risk in hypertension and/or diabetes. Eur J Clin Invest. 2012;42:548–56.View ArticlePubMedGoogle Scholar
- Omland T, Ueland T, Jansson AM, Persson A, Karlsson T, Smith C, Herlitz J, Aukrust P, Hartford M, Caidahl K. Circulating osteoprotegerin levels and long-term prognosis in patients with acute coronary syndromes. J Am Coll Cardiol. 2008;51:627–33.View ArticlePubMedGoogle Scholar
- Poulsen MK, Nybo M, Dahl J, Hosbond S, Poulsen TS, Johansen A, Hoilund-Carlsen PF, Beck-Nielsen H, Rasmussen LM, Henriksen JE. Plasma osteoprotegerin is related to carotid and peripheral arterial disease, but not to myocardial ischemia in type 2 diabetes mellitus. Cardiovasc Diabetol. 2011;10:76.View ArticlePubMedPubMed CentralGoogle Scholar
- Heymann MF, Herisson F, Davaine JM, Charrier C, Battaglia S, Passuti N, Lambert G, Goueffic Y, Heymann D. Role of the OPG/RANK/RANKL triad in calcifications of the atheromatous plaques: comparison between carotid and femoral beds. Cytokine. 2012;58:300–6.View ArticlePubMedGoogle Scholar
- Vinholt PJ, Overgaard M, Diederichsen AC, Mickley H, Poulsen TS, Sand NP, Nybo M, Rasmussen LM. An ELISA for the quantitation of von Willebrand factor: osteoprotegerin complexes in plasma. Thromb Res. 2013;131:396–400.View ArticlePubMedGoogle Scholar
- Rutten B, Maseri A, Cianflone D, Laricchia A, Cristell N, Durante A, Spartera M, Ancona F, Limite L, Hu D, Li H, Uren N, de Groot P, Mannucci P, Roest M. Plasma levels of active Von Willebrand factor are increased in patients with first ST-segment elevation myocardial infarction: A multicenter and multiethnic study. Eur Heart J Acute Cardiovasc Care. 2015;4:64–74.View ArticlePubMedGoogle Scholar
- Gerritsen HE, Turecek PL, Schwarz HP, Lammle B, Furlan M. Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: a tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP). Thromb Haemost. 1999;82:1386–9.PubMedGoogle Scholar
- Dentali F, Sironi AP, Ageno W, Crestani S, Franchini M. ABO blood group and vascular disease: an update. Semin Thromb Hemost. 2014;40:49–59.PubMedGoogle Scholar
- McKinnon TA, Chion AC, Millington AJ, Lane DA, Laffan MA. N-linked glycosylation of VWF modulates its interaction with ADAMTS13. Blood. 2008;111:3042–9.View ArticlePubMedGoogle Scholar