The quality of elastic fibers reflects a hallmark of cardiovascular aging and can be affected by the deposition of interstitial collagen, calcification, lipid peroxidation and glycoxidation. The latter are induced by advanced glycation end products (AGEs) which are generated by non-enzymatic glycation and oxidation of protein and reducing sugars 1. Their formation is increased in the blood and tissues of diabetic subjects as a result of hyperglycemia and is implicated in diabetes-associated vascular stiffening 12. N^ε-Carboxymethyllysine (CML) is the major non-cross linking AGE, which acts via the receptor of AGE (RAGE), thereby stimulating proinflammatory action 3. In atherosclerotic lesions CML is present in infiltrating cells, suggesting a role of CML in the development of vascular lesions potentially by glycoxidation of elastin fibers 2.

Circulating levels of AGEs have been measured and related to the degree of coronary arteriosclerosis in both diabetic 4 and non-diabetic 5 patients with coronary artery disease and also to impaired left ventricular function in patients with type 1 diabetes. Recently McNulty et al. observed that the concentration of plasma AGEs is significantly higher in hypertensive than in normotensive subjects and related to aortic stiffness independent of age and blood pressure 6. Therefore they suggested that plasma AGEs may play a blood pressure independent role in vascular remodeling in essential hypertension, in particular as vascular remodeling is associated with inflammation 78 which reflects a major action of AGEs 9. However, latter results needed to be confirmed in a strict normoglycemic group and furthermore need to be extended to carotid artery properties. Based on these observations we studied the relationship between plasma CML, carotid and aortic properties, in normoglycemic subjects. To investigate in how far CML is associated with vascular inflammatory processes fetuin-A was investigated as biomarker for vascular inflammation 1011. In this context we furthermore investigated whether fetuin-A explains carotid diameter changes. Additionally, we investigated the presence of CML in carotid arteries with atherosclerotic lesions to link systemic measures with local function and local CML deposition.

Hundred-two subjects of the FLEMish study of ENvironment, Genes and Health Outcomes (FLEMENGHO) 12 involving a random sample of families living in a defined geographical area in northern Belgium were included in this study. The Ethics Committee of the University of Leuven and Munich approved the study, respectively. All participants gave informed written consent. The inclusion criteria for the Flemish cohort were participation in a prospective substudy, the age of at least 18 years, no antihypertensive or antihypertensive treatment and normoglycemia defined as fasting blood sugar below 6.7 mmol/l. The inclusion criteria for the immunohistochemistry were atheromatous alteration of the carotid artery in context with the clinical need of carotidectomy.

For at least 3 h before being examined, the participants refrained from heavy exercise, smoking, alcohol or caffeine-containing beverages. Trained nurses measured blood pressure and anthropometric characteristics. They administered a questionnaire to collect information about each subject's medical history, smoking and drinking habits, and intake of medications. Each participant's office blood pressure was the average of five consecutive readings. Elevated blood pressure was a systolic blood pressure above 140 mmHg and/or 90 mmHg diastolic or use of antihypertensive treatment. Body mass index (BMI) was weight in kilograms divided by the square of height in metres. N^ε-Carboxymethyllysine (CML) plasma level of free CML and protein-bound CML was measured using an ELISA kit (Microcoat, Bernried, Germany), following the instructions of the manufacturer. Intra- and interassay variability were below 5%. The entire cohort was grouped according to the median of plasma CML (median: 200.8, 25^th percentile: 181.6, 75^th percentile: 226.1). The values below median are referred to as "low" and these above median as "high" CML, respectively. Blood glucose, total cholesterol, HDL, LDL, triglycerides, and serum creatinine were also measured in all subjects by routine laboratory methods. Fetuin-A was measured by commercially available ELISA according to the manufacturer protocol 13.

By means of a pulsed ultrasound wall-tracking system (Wall Track System; Pie Medical, Maastricht, The Netherlands), 3 trained researchers obtained vascular measurements at the common carotid artery 2 cm proximal of the carotid bulb. During the ultrasound examination, an automated oscillometric device (Dinamap 845; Critikon Inc, Tampa, FL, USA) recorded blood pressure at the upper arm at 5-minute intervals. As for the conventional auscultatory measurements, cuff size was adjusted to the circumference of the upper arm. Standard cuffs had an inflatable bladder of 12 × 24 cm 14. As described elsewhere, the observers used applanation tonometry with a pencil-shaped probe (Millar Instruments Inc, Houston, TX, USA) and calibration to mean arterial pressure and diastolic blood pressure at the brachial artery to derive the local pulse pressure at the carotid artery. We computed cross-sectional compliance (CC) and the distensibility coefficient (DC) from the diastolic cross-sectional area (A), the systolic increase in cross-sectional area (ΔA), and the local pulse pressure (PP): CC=ΔA/PP and DC = (ΔA/A)/PP. A and ΔA were calculated from diameter (D) and the change in diameter (ΔD) as A=π(Δ(D/2)² and ΔA=πX[(D+ΔD)/2)²-πX(D/2), respectively. The intraobserver intrasession variability was <10% for the carotid measurements. The intraobserver intersession and interobserver intrasession variability were of the same order of magnitude.

The observers also determined carotid-femoral pulse wave velocity (PWV) from the length of the carotid-femoral segment and the transit time of the pulse wave. The carotid-femoral segment was the difference of the distances between the site of the carotid ultrasound measurement and the suprasternal notch and between the suprasternal notch and the site of the femoral measurement. We measured PWV using a high-fidelity SPC-301 micromanometer (Millar Instruments, Inc.) interfaced with a laptop computer running the SphygmoCor software, version 6.31 (AtCor Medical Pty Ltd, Sydney, Australia).

Immunohistochemical CML staining of a carotid artery with atherosclerotic lesions was performed in human material after carotidectomy 15. Twenty six paraformaldehyde-fixed, paraffin-embedded tissue sections were cut (4 μm), dewaxed and rehydrated. After endogenous peroxidase blocking (endogenous enzyme block, Dakocytomation, Glostrup, Denmark), slides were incubated with a 1:100 dilution of CML biotine 0.34 mg/ml antibody, which was a kind gift by Dr. C. Schalkwijk (University Maastricht). This was followed by incubation with a 1:400 diluted secondary rabbit anti- mouse IgG HRP antibody (Serotec, Wiesbaden, Germany) and developed in diaminobenzidine tetrahydrochloride (DAB substrate kit for peroxidase SK-4100; Vector Laboratories, Burlingame, CA, USA) and counterstained with hematoxylin.

Statistical analyses were performed using SPSS software version 15.0 (SPSS, Chicago, IL, USA). Comparison between subjects with above and below the median of CML was performed by unpaired t-test or the χ²-test. The Spearman correlation coefficient was assessed for CML and the clinical properties in the whole cohort and the subgroup of normotensive and hypertensive subjects. Results are expressed as mean ± SD. A p value of less than 0.05 was considered to be statistically significant.

Baseline characteristics of the Flemish cohort and according to the median plasma CML level of the cohort (median: 200.8, 25^th percentile: 181.6, 75^th percentile: 226.1) are given in Table 1. Apart from plasma CML values no significant difference was present between the "low" and "high" CML group, in particular no differences in fasting blood glucose and lipid profile. Thirty-three subjects had elevated blood pressure level, including 20 with "low" CML and 13 with "high" CML.

Arterial properties according to the total cohort and according to the median plasma CML level of the cohort are given in Table 2. Carotid diameter was significantly larger in the "high" CML group (P < 0.05). PWV was not different between the "low" and "high" CML group. The bivariate Spearman association of CML and carotid diameter is for the normotensive cohort r = -0.01 (P = 0.92) and for subjects with elevated blood pressure r = 0.42 (P < 0.01; Table 3 and Figure 1). Additionally, the role of vascular inflammation was investigated with fetuin-A. CML is positively associated with fetuin-A (r = 0.28; P < 0.01). However Fetuin-A is in not associated with carotid diameter in any group (Figure 1).

Comparing subjects with normal and elevated blood pressure, no difference was apparent with respect to CML and carotid diameter. However, PWV was significantly elevated in the group with elevated blood pressure (6.5 ± 2.1 versus 7.5 ± 2.4 m/s; P < 0.05; Table 4).

Subdividing the normotensive subjects according to the CML median no significant differences were apparent for carotid and aortic properties (data not shown). In contrast, subdividing the group with elevated blood pressure according to the CML median resulted in an increased carotid diameter in the 13 subjects with "high" CML (514.5 ± 151.6 μm) as compared to the 20 subjects with "low" CML (377.9 ± 122.2 μm, P < 0.001; Figure 2), while the elastic properties as cross-sectional compliance ("high" CML: 0.94 ± 0.33 versus "low" CML: 0.72 ± 0.29 mm²/kPa; P = 0.07) and distensibility ("high" CML: 21.2 ± 7.1 versus "low" CML: 18.0 ± 7.3 10^-3/kPa; P = 0.20) were comparable between these two subgroups.

The characteristics of the patients with carotidectomy are summarized in Table 5. Immunohistochemical staining of CML in the human carotid artery is shown in Figure 3. The magnification of 2A (100×) and 2B (400×) reveal CML positive cells in the subendothelial space. CML staining is present in atheromatous lesions and colocalizes with inflammatory cells.

The main finding of this study is that carotid enlargement is apparent in context with elevated CML plasma levels which are still in the normal range. Moreover, the effect of CML on carotid enlargement is predominantly present in subjects with elevated blood pressure without changes in cross-sectional compliance or distensibility. Finally, CML was associated with fetuin-A as vasculo-inflammatory marker and was present in the subendothelial space of human carotid arteries.

CML is involved in vascular stiffening of type 1 diabetics as well as of hypertensive subjects 616. Our study demonstrates that carotid enlargement is apparent in this cohort of normoglycemic subjects. This is particularly striking in subjects with hypertensive blood pressure values, where CML demonstrated an independent association with carotid diameter. Moreover, the shown effect is already present at a CML range below levels obtained in diabetes or renal insufficiency 1718.

Although no prospective data exist on carotid diameter, Kawamoto et al. showed that the carotid artery diameter correlates with conventional cardiovascular risk factors including alcohol consumption 19, these findings suggest that the carotid artery diameter may reflect the ability of adaptive remodeling to the atherosclerosis before plaque formation. Moreover, increased carotid artery diameter as consequence of arterial stiffness limits the deterioration of the buffering capacity of the central artery 20. Thus, CML can be an important factor during the development of atherosclerosis and may be relevant in clinical risk assessment. As atherosclerosis is driven by inflammation, we additionally assessed fetuin-A as marker for vascular inflammation 2122. In this context, we observed and association between fetuin-A and CML throughout the whole cohort. This suggests that CML potentially reflects the state of vascular inflammation 23. This is further strengthened by our observation of CML in the subendothelial space of atherosclerotic human carotid artery material which is in line with previous descriptions in human aortic valves 24.

The mechanisms underlying this CML-related effect on carotid diameter cannot primarily be explained by an enhanced cross linking by AGEs as CML may affect the properties of the AGE-modified proteins but does not cause cross-linking in or between proteins 2526. Therefore, our findings suggest that the effect of CML on arterial diameter involves mechanisms other than cross-linking, such as ligation of the receptor for AGE (RAGE) 27. RAGE is highly expressed in the endothelium of activated vessels 28. Furthermore, CML is a ligand for RAGE 29. Binding of circulating CML modified proteins to RAGE activates extracellular-regulated kinase 1/2 (ERK1/2), nuclear factor κ-B, secretion of proinflammatory cytokines, and modulates gene expression in several cell types, such as monocytes, endothelial cells, and vascular smooth muscle cells 30. This may lead to changes in the production of extracellular matrix proteins, such as collagen and elastin structure, and alterations in vascular elasticity 3132, as obtained by glycoxidation, and lipid peroxidation 24. Because CML can be formed by glycoxidation and lipid peroxidation 2, the association of carotid diameter with CML may reflect the involvement of increased oxidative stress in arterial remodelling 33 which is further strengthened by the association with fetuin-A. However, as the serum concentration of soluble RAGE is in the picomolar range 34 whereas the CML molaritiy is in the micromolar range, it is questionable that sRAGE/CML binding occurs in vivo and has any biological effect. In this respect, serum CML is more likely an indicator of a dysfunctional cellular metabolism in the vascular wall in particular as we demonstrated CML deposition in atheromatous lesions of the carotid artery.

CML had no effect on carotid enlargement in subjects with normotensive blood pressure values. By contrast, in subjects with elevated blood pressure the CML plasma level characterized the extent of carotid enlargement without adaptive changes of the elastic artery properties. This may in turn lead to increased circumferential wall stress and consecutively result in a potentially defective mechanotransduction, that is, the control of smooth muscle cell growth and migration, and production of extracellular matrix in response to diameter enlargement 35. Furthermore, a direct effect on elastin may be considered as CML co-localizes with elastin 36 and results in fenestration of elastic laminae 37.

In this cohort no effect of CML on PWV was observed. Therefore this study contrasts a recent observation describing CML as blood pressure independent factor in aortic stiffness 6. However, there are important differences between both studies. Firstly, in the latter study AGE measurement was performed using a non-selective ELISA detecting other AGEs than CML as well, while in our study a specific ELISA for CML was used 38. Secondly, blood glucose levels were elevated in the hypertensive group of McNulty et al., suggesting a more general glucose effect on both CML level and stiffness complicating the detection of the effects of AGEs alone. By contrast, our study excluded subjects with a fasting blood sugar of >6.7 mmol/l.

In summary, normoglycemic subjects with higher CML plasma levels are characterized by carotid enlargement without changes in elastic properties, in particular in elevated blood pressure. This may be associated with a qualitative change of elastic fibers and may lead to a defective mechanotransduction both explainable by local glycoxidation and lipid peroxidation induced inflammation.

The authors declare that they have no competing interests.

MB designed, coordinated and wrote the manuscript. TR, TK and JS generated the data of the Flemish cohort. JP and HE provided the human carotid arteries. DS and UH coordinated and wrote the manuscript. All authors read and approved the final manuscript.