Printer Friendly

Gene expression of adhesion molecules in endothelial cells from patients with peripheral arterial disease is reduced after surgical revascularization and pharmacological treatment.

1. Introduction

Atherosclerosis (ATH) is an inflammatory disease characterized by intense immunological activity [1] that involves the formation of lesions in the arteries and is characterized by lipid accumulation, inflammation, cell death, and fibrosis. Recruitment of monocytes and lymphocytes from the peripheral blood to the intima of the vessel wall represents the primary event in atherogenesis. Among the factors involved in ATH, the local presence of high amounts of low-density lipoproteins (LDL) has a key role [2]. Healthy endothelium is an important barrier to the free passage of LDL and immune cells to the underlying interstitium, and dysfunction of endothelial cells (EC) is considered an early step in atherogenesis. EC dysfunction results in increased activation of these cells [3], sustained by upregulation of adhesion molecules (AMs) such as vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1). VCAM-1 expression precedes lesion formation and correlates positively with the extent of exposure to plasma cholesterol [4]. Cells can then change their shape and migrate at the surface of the endothelium to reach the junctions. Recently, we have confirmed the occurrence of extensive alteration of endothelial layers in surgical specimens of patients submitted to carotid endarterectomy [5, 6]. In view of the role played by EC in the development, progression, and clinical complications of ATH, reduction of their activation represents a key point in the prevention of atherosclerotic plaque progression [7].

Lower-extremity peripheral artery disease (PAD) is a chronic arterial disease of atherosclerotic origin characterized by the occurrence of vascular obstruction in various districts. Although public awareness of PAD is extremely low [8], this condition is related to a very high short-term incidence of myocardial ischemia, stroke, and death [9]. Besides an aggressive treatment of cardiovascular risk factors, common femoral artery thrombendarterectomy (FEA) is among the treatments for PAD and represents a safe procedure in PAD with acceptable perioperative morbidity [10], as plaque debulking is considered safer than percutaneous transluminal angioplasty [11, 12]. Moreover, surgery treatment with a statin, aimed at reaching low LDL-cholesterol levels, is highly recommended [10].

No information exists so far about the modification of inflammatory parameters in PAD patients after surgery and/or pharmacological treatment. The first aim of the present study was therefore to investigate adhesion molecules expression in endothelial cells (ECs) of patients with PAD submitted to peripheral artery revascularization associated with pharmacological treatment. To this end, we longitudinally measured ICAM-1, VCAM-1, and [beta]1-integrin mRNA expression in EC isolated from venous blood (circulating EC, cEC) and purified from femoral plaques (pEC). In addition, as a secondary aim, we investigated in the same patients the expression of pro- and anti-inflammatory cytokines in peripheral blood mononuclear cells (PBMCs), in view of the pivotal role played by immune cell-derived cytokines in endothelial activation [13].

2. Materials and Methods

2. 1. Subjects. We enrolled 9 patients (2 F, 7M) with severe PAD scheduled for FEA and sent to the Lipid Clinic (Research Center on Dyslipidemia, University of Insubria, Varese, Italy) by the Department of Surgical and Morphological Sciences of our University Hospital. Only patients, who did not receive statins or steroids and had no ongoing clinical infection and/or the presence of infections in the previous three months, were enrolled. No patient had clinical contraindication for statin treatment. Clinical characteristics of the patients at enrollment are shown in Table 1.

After inclusion in the study, atorvastatin was prescribed to patients, according to established guidelines to reach recommended LDL-cholesterol levels [10](10 mg/day to 4 patients with LDL <130 mg/dL, and 80 mg/day to 5 patients with LDL > 130 mg/dL).

Patients were longitudinally studied at the following:

(i) the time of the decision for surgery before the institution of statin therapy (visit 1);

(ii) the day of surgery (visit 2) after at least 1 month of statin therapy, before pharmacological preparation for the surgical procedure;

(iii) 2 months (visit 3)

(iv) 5 months (visit 4) after surgery.

At each visit, a sample of peripheral venous blood was obtained for clinical evaluation and for PBMC and cEC isolation. AM mRNA expression on cEC was evaluated at each visit, whereas cytokine mRNA expression in PBMC was analyzed at visits 1 and 4. In addition, at visit 2, after surgery the femoral plaque specimens were collected and subsequently processed to isolate pEC (see below).

The study conforms to the principles outlined in the Declaration of Helsinki for use of human tissues or subjects and the study protocol was approved by the local Ethics Committee. All patients gave a written informed consent.

2. 2. Endothelial Cells (ECs) Purification. Venous blood was used to isolate cEC by means of immunomagnetic cell sorting. To this end, venous blood samples were divided in aliquots of 5 mL and each aliquot was washed with 5 mL of PBS/BSA 0. 1%. Antibodies targeted to CD146 (Dynal A. S.,

Oslo, Norway) were added to beads using a target-to-bead ratio 1: 4. After 30 min incubation, beads were washed and incubated for 20 min with 5 mL of blood aliquots. Cells were isolated from the mixture by placing the test tube in a magnetic particle concentrator. Medium was removed and cells were washed three times.

For the isolation of ECs from plaque (pEC), surgical specimens were placed in a solution of EDTA 0. 05 M for 5 min and then washed in PBS solution for 5 min. Subsequently, tissue was placed in HEPES containing collagenase type II 0. 2%, elastase 0. 01%, and trypsinase inhibitor 0. 1% and incubated under gentle stirring at 37[degrees]C for 90 min. Digested tissue was washed twice with PBS, filtered through a 70-micron cell strainer, and finally pECs were removed from the tissue mixture by immunomagnetic sorting (as above described for cEC).

ECs isolated from venous blood or from tissue were stained with Ab anti-CD45 and Ab anti-CD31 (specific marker for PECAM-1, which is highly expressed on EC) and visualized by fluorescence microscopy in order to test the absence of CD45+ positive cells. Typical preparations of CD146-sorted cells were negative for CD45 labelling and positive for CD31 labelling, confirming that immune cells were not present in our sample after cell sorting. A counting chamber was used to enumerate cells, which were finally frozen at -80[degrees]C until analysis.

2. 3. Isolation of Peripheral Blood Mononuclear Cells (PBMCs). PBMCs were separated by Ficoll-Paque Plus density gradient centrifugation from whole blood as previously described [14]. Cells were washed two times in NaCl 0.15M and finally resuspended in appropriate medium for subsequent experiments. Typical PBMC preparations contained about 80% lymphocytes and 16% monocytes, as assessed by flow cytometry. Cellviability, assessed by the trypan blue exclusion test, was always >99%. Isolated cells were finally stored at -80[degrees]C until real-time PCR assays.

2. 4. RNA Isolation and Real-Time Polymerase Chain Reaction (PCR) Analysis. Total mRNA was extracted from 1x 106 cells by Perfect RNA Eukaryotic Mini kit (Eppendorf, Hamburg, Germany) and the amount of RNA extracted was estimated by spectrophotometry at 260 nm. Total RNA was reverse transcribed using the high-capacity cDNA Archive Kit (Applied Biosystems, Foster City, CA, USA) according to the manufacturer's instructions.

Real-time PCR was performed by means of an ABI prism 7000 apparatus (Applied Biosystems, Foster City, CA, USA) using the assay-on-demand kits. Cycles included one 2 min hold (50[degrees]C), one 10 min (95[degrees]C), and 40 cycles according to the following steps: 15 s at 95[degrees]C (denaturation) and 1 min at 60[degrees]C (annealing and extension). Threshold cycle values (Ct1) for the genes of interest were calculated, normalized to 18S RNA (Ct2) (housekeeping) content, and finally expressed as [2.sup.-[DELTA]Ct], where [DELTA]Ct = Ct2 - Ctl. Primers were obtained from Applied Biosystems (Foster City, CA, USA), and are shown in

Table 2.

2. 5. Statistical Analysis. Data are presented as means [+ or -] standard error of the mean (SEM). Comparisons between independent measures were performed using the MannWhitney U test and comparisons between dependent measures were performed using the Wilcoxon test. Assessment of the statistical significance of correlations was performed by linear regression analysis. A commercial software was used for calculations (GraphPad Prism version 5. 00 for Windows, GraphPad Software, San Diego, CA, USA,

3. Results

3. 1. Clinical Evaluation. As described in Table 1, in the group of patients enrolled, 5 were smokers, 8 had hypertension, 7 had hypercholesterolemia, and 2 were subject with alcohol habitus. No change occurred during the study in all the clinical parameters evaluated (e. g. , blood pressure, BMI, and routine exams) or in habitus that could influence parameters measured (smoking, diet, etc. ).

All the patients had clinical symptoms referred to PAD and had monolateral (5 patients) or bilateral (4 patients) claudication and showed severe stenosis at angiographic evaluation. Severity of symptoms was evaluated according to Rutherford classification system as detailed in Table 1. Pharmacological treatments (Table 1) remained unchanged during the study with the only exception of the institution of atorvastatin therapy at the time of enrollment.

As expected, atorvastatin treatment and FEA significantly affected thelipid profile and hs-CRP of all the patients (Table 3) and no patient, either on 10 or 80 mg/die statin underwent any adverse event during the follow-up period.

3. 2. Adhesion Molecules mRNA Levels in EC. As shown in Figure 1(a), mRNA levels of AM in cEC progressively decreased from visit 1 to visit 4. In particular, both ICAM1and [beta]1-integrin were significantly reduced after 1 month, while reduction in expression for VCAM-1 was significant from visit 3. The % reduction for all molecule tested at visit 4 with respect to visit 1 varied from 41% to 50% (Figure 1(b)). No difference was observed in AM mRNA levels in EC between patients on atorvastatin 10 or 80mg/day and no relationship was found between AM mRNA expression and lipid profile or hs-CRP (data not shown).

AM mRNA levels in pEC at visit 2 (day of surgery) were always detectable and were significantly higher in comparison to those found in cEC isolated at the same visit (Table 4); however, no direct correlation between cEC and pEC mRNA levels was found for VCAM-1 ([r.sup.2] = 0.44; P = 0.051), ICAM-1 ([r.sup.2] = 0.005; P = 0.564), or [beta]1-integrin ([r.sup.2] = 0.08; P = 0.830).

No difference was observed in mRNA levels of AM in EC between patients on atorvastatin 10 or 80 mg/day (data not shown).

3. 3. Cytokine mRNA Levels in PBMC. As shown in Figure 2, cytokine mRNA expression in isolated PBMC was significantly affected by FEA and statin treatment. In particular, a significant increase in mRNA expression from visit 1 to visit 4 was observed for IFN-[gamma] and IL-4 while mRNA expression of IL-10 and TGF-[beta] remained unchanged. No difference was, however, observed in the ratio IFN-y/IL 4(0,229 [+ or -] 0,083 at visit 1 versus 0,420 [+ or -] 0,151 at visit 4, P = 0,237).

No significant relationship was found between cytokine mRNA levels in PBMC and AM mRNA levels in either cEC or pEC as well as between the mRNA levels of the different cytokines in PBMCs and all clinical parameters measured through the study (data not shown).

4. Discussion

The main finding of this study is the observation that in PAD patients, surgery and pharmacological treatment induce in cEC a profound reduction of the mRNA levels of ICAM-1, VCAM-1, and [beta]1-integrin. In addition, in circulating PBMCs of the same patients mRNA levels for IFN-[gamma] and IL-4 increase and mRNA levels for TGF-[beta] and IL-10 remain unchanged.

In patients with PAD, increased levels of soluble AM are associated with the presence, the severity, and the extent of ATH in the arteries of the lower limbs and are suggestive of a worse outcome [15]. Previous studies documented that PAD is associated with elevated levels of most inflammatory markers, such as CRP, CD40 ligand, fibrinogen, and others. Despite the potential benefits associated to the lowering of these molecule by therapeutic approaches, this is the first study showing that AM expression in cEC may be modified even in an advanced atherosclerotic stage. Our patients showed high levels of hs-CRP that were reduced 6 months after the beginning of the study. High hs-CRP level is commonly related to increased expression or circulating levels of different adhesion molecules [16] that can be considered as indicators of severity of peripheral ATH. Indeed, elevated levels of ICAM-1 in EC were found to be predictive of future development of PAD [17].

It has been shown that among drugs commonly used for managing cardiovascular disease, statins significantly improve endothelial function [18]. In particular a 4-week treatment with simvastatin was able to restore the vasodilator ability of endothelium, as assessed by increased vasodilatatory response to ACh, or contrasted L-NMMA-induced vasoconstriction, indicating that both stimulated and basal vasodilator function of the endothelium were enhanced [19]. The benefit of statin treatment in patients undergoing vascular surgery was documented by the reduced incidence of adverse cardiac outcome during the perioperative period and reduced adverse cardiac events after surgical procedures [20]. In our patients, statin treatment and surgical revascularization induced in cEC a decrease of mRNA expression of ICAM-1, VCAM-1, and [beta]1-integrins (evident after 1 month of therapy and much more marked 5 months after surgery). We failed to observe any correlation between AM mRNA levels in cEC and pEC (with the marginal exception of a weakly significant positive correlation for ICAM-1). Possible explanations may include less sensitivity of pEC to the effects of pharmacological treatment and need much more time to observe an effect (as indirectly suggested by the additional reduction of AM mRNA levels in cEC after 2 and 5 months). Moreover, we cannot exclude that the small number of patients could have masked any possible correlation.

Statins may affect cellular function in advanced atherosclerotic stage, such as in patients scheduled for femoral artery revascularization and therefore affected by marked atherosclerotic lesions. For example, recently we reported that FEA associated with statin treatment in PAD patients was able to reduce in circulating polymorphonuclear leukocytes Angiotensin II (Ang II) type 1 receptor expression (a receptor pathway extensively involved in the proinflammatory and proatherogenic effects of Ang II) [21].

It is well recognized that inflammation as well as its related immunological events positively correlate with the severity of the PAD disease [22] and regulate all the stages of the inflammatory cascade, from endothelial activation to immune cell adhesion and subsequent remodeling of the vascular environment [23]. Cytokines are key glycoproteins which modulate all the aspects of vascular inflammation; moreover, cytokine balance is involved in plaque morphology and stabilization and in determining the structure of the fibrous cap. In cardiovascular diseases, cytokines are usually classified into two categories: proatherogenic and protective, but recently it has been shown that this classification is not exhaustive, because of the complexity and overlapping of the biological roles. For example IL-4, a cytokine classically produced by Th2 cells, has been proposed as protective in ATH, but IL-4 also increases the expression of P-selectin [24], VCAM-1, and matrix metalloprotease 1 and 12, which are implicated in aortic aneurysm formation and in acute coronary syndrome [25]. IFN-[gamma], atypicalTh1cytokine, is directly related to ATH by contributing to all the events that induce disease progression. IFN-[gamma] is associated with increased levels of other proinflammatory cytokines, but it is also able to inhibit smooth muscle cells proliferation and collagen synthesis and to induce foam cells apoptosis within then lipid core, which could contribute to plaque stabilization resulting in beneficial effects in advanced stage of the disease [26]. In our patients' population, we observed that mRNA level of IL-4 and IFN-[gamma] increased throughout the study. Since plaque destabilization has been related to reduced IL-4 values and increased level of IFN-[gamma], the increase of both IFN-y and IL-4 might represent a protective effect [27]. No changes were observed in IL-10 and TGF-[beta] mRNA expression. We cannot exclude that the absence of effects on IL-10 and TGF/? may be interpreted as the results of polytherapy differentially affecting specific lymphocyte subsets. In addition, it must considered that these two cytokines are preferentially produced by a specific T-lymphocyte subset (the regulatory subset that represents a low percentage of PBMCs) while in this study we have investigated mononuclear cells as a whole; another possible explanation of lack of effect on these cytokines is that possibly 6 months are not enough to observe any effect on these parameters.

We acknowledge that a critical point of this study was the low number of patients and the absence of untreated patients; this latter point in particular is, however, difficult to address, as it is clearly unethical to withdraw drug treatments or delaying therapy in such a kind of patients at extremely high risk for vascular acute events, even for limited periods. As for the limited number of subjects, it was underlined that the strict selection criteria (absence of statin treatment before the study) used for the study did not allow the inclusion of a greater number of patients. In our opinion, this study should be considered a pilot study that aimed to point the attention to cellular aspects in this particular group of patients in a late stage of the atherosclerotic process. Indeed, very few studies so far addressed the possibility to modulate EC and/or immune cell function in the later phases of plaque progression.

In conclusion, this study supports the hypothesis that also in patients with an advanced ATH status, reduction of endothelial dysfunction and modulation of the immune response may be achieved by a combination of surgical procedures and appropriate pharmacological therapy. Future studies should address the possible relationship of such effects with the long-term clinical outcome of patients.


Conflict of Interests

The authors reported no conflict of interests.


The authors are grateful to Dr. Massimiliano Legnaro (Center of Research in Medical Pharmacology, University of Insubria) for his skilful technical assistance in performing the real-time PCR experiments. This work was supported by a Grant from the Italian Ministry of Instruction, University and Research (MIUR, PRIN 2005, Research project no. 2005060343. 005, University of Insubria, Varese, Italy).


[1] C. J. L. Murray and A. D. Lopez, "Global mortality, disability, and the contribution of risk factors: global burden of disease study, " The Lancet, vol. 349, no. 9063, pp. 1436-1442, 1997.

[2] J. A. Beckman, M. A. Creager, and P. Libby, "Diabetesand atherosclerosis epidemiology, pathophysiology, and management, " Journal of the American Medical Association, vol. 287, no. 19, pp. 2570-2581, 2002.

[3] U. Landmesser, B. Hornig, and H. Drexler, "Endothelial function: a critical determinant in atherosclerosis?" Circulation, vol. 109, supplement 1, no 21, pp II27-II33, 2004

[4] S. M. Lessner, H. L. Prado, E. K. Waller, and Z. S. Galis, "Atherosclerotic lesions grow through recruitment and proliferation of circulating monocytes in a murine model, " American Journal of Pathology, vol. 160, no. 6, pp. 2145-2155, 2002.

[5] T. Congiu, L. Schembri, M. Tozzi et al. , "Scanning electron microscopy examination of endothelium morphology in human carotid plaques, " Micron, vol. 41, no. 5, pp. 532-536, 2010.

[6] L. Schembri, T. Congiu, M. Tozzi, L. Guasti, M. Cosentino, and F. Marino, "Scanning electron microscopy examination and elemental analysis of atherosclerotic calcifications in a human carotid plaque, " Circulation, vol. 117, no. 23, pp. e479-e480, 2008.

[7] G. Giannotti and U. Landmesser, "Endothelial dysfunction as an early sign of atherosclerosis, " Herz, vol. 32, no. 7, pp. 568-572, 2007.

[8] A. T. Hirsch, T. P. Murphy, M. B. Lovell et al. , "Gaps in public knowledge of peripheral arterial disease: the first national PAD public awareness survey, " Circulation, vol. 116, no. 18, pp. 2086 2094, 2007.

[9] K. Watson, B. D. Watson, and K. S. Pater, "Peripheral arterial disease: a review of disease awareness and management, " American Journal Geriatric Pharmacotherapy, vol. 4, no. 4, pp. 365-379, 2006.

[10] W. R. Hiatt, "Medical treatment of peripheral arterial disease and claudication, " New England Journal of Medicine, vol. 344, no. 21, pp. 1608-1621, 2001.

[11] E. A. Prince, T. P. Murphy, R. Dhangana, G. M. Soares, S. H. Ahn, andG. J. Dubel, "Evaluation andmanagement of patients with peripheral artery disease by interventional radiologists: current practice, " Journal of Vascular and Interventional Radiology, vol. 19, no. 5, pp. 639-644, 2008.

[12] B. J. Arsenault, P. Barter, D. A. DeMicco et al. , "Prediction of cardiovascular events in statin-treated stable coronary patients by lipid and nonlipid biomarkers, " Journal of the American College of Cardiology, vol. 57, no. 1, pp. 63-69, 2010.

[13] C. Zhang, "The role of inflammatory cytokines in endothelial dysfunction, " Basic Research in Cardiology, vol. 103, no. 5, pp. 398-406, 2008.

[14] M. Cosentino, A. M. Fietta, M. Ferrari et al., "Human CD4+ CD25+ regulatory T cells selectively express tyrosine hydroxylase and contain endogenous catecholamines subserving an autocrine/paracrine inhibitory functional loop, " Blood, vol. 109, no. 2, pp. 632-642, 2007.

[15] G. Brevetti, V Schiano, and M. Chiariello, "Cellular adhesion molecules and peripheral arterial disease, " Vascular Medicine, vol. 11, no. 1, pp. 39-47, 2006.

[16] F. Montecucco, S. Steffens, F. Burger, G. Pelli, C. Monaco, and F. Mach, "C-reactive protein (CRP) induces chemokine secretion via CD11b/ICAM-1 interaction in human adherent monocytes, " Journal of Leukocyte Biology, vol. 84, no. 4, pp. 1109-1119, 2008.

[17] A. D. Pradhan, N. Rifai, and P. M. Ridker, "Soluble intercellular adhesion molecule-1, soluble vascular adhesion molecule-1, and the development of symptomatic peripheral arterial disease in men, " Circulation, vol. 106, no. 7, pp. 820-825, 2002.

[18] P. Balakumar, S. Kathuria, G. Taneja, S. Kalra, and N. Mahadevan, "Is targeting eNOS a key mechanistic insight of cardiovascular defensive potentials of statins?" Journal of Molecular and Cellular Cardiology, vol. 52, no. 1, pp. 83-92, 2012.

[19] G. O'Driscoll, D. Green, and R. R. Taylor, "Simvastatin, an HMG-coenzyme A reductase inhibitor, improves endothelial function within 1 month, " Circulation, vol. 95, no. 5, pp. 11261131, 1997.

[20] W. Pan, T. Pintar, J. Anton, V. Lee, W. K. Vaughn, andC. D. Collard, "Statinsareassociatedwithareducedincidence of perioperative mortality after coronary artery bypass graft surgery, " Circulation, vol. 110, supplement1, no. 11, pp. II45-II49, 2004.

[21] F. Marino, L. Guasti, M. Tozzi et al. , "Angiotensin type 1 receptor expression and interleukin-8 production in polymorphonuclear leukocytes of patients with peripheral arterial disease, " Journal of Cardiovascular Pharmacology, vol. 54, no. 6, pp. 520-525, 2009.

[22] S. S. Signorelli, M. C. Mazzarino, and D. A. Spandidos, "Malaponte G. Proinflammatory circulating molecules in peripheral arterial disease, " International Journal of Molecular Medicine, vol. 20, pp. 279-286, 2007.

[23] H. R. S. Girn, N. M. Orsi, and S. Homer-Vanniasinkam, "An overview of cytokine interactions in atherosclerosis and implications for peripheral arterial disease, " Vascular Medicine, vol. 12, no. 4,

pp. 299-309, 2007.

[24] Y. Khew-Goodall, C. Wadham, B. N. Stein, J. R. Gamble, and M. A. Vadas, "Stat6 activation is essential for interleukin 4 induction of P selectin transcription in human umbilical vein endothelial cells, " Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 19, no. 6, pp. 1421-1429, 1999.

[25] P. Szodoray, O. Timar, K. Veres et al., "Th1/Th2 imbalance, measured by circulating and intracytoplasmic inflammatory cytokines--immunological alterations in acute coronary syndrome and stable coronary artery disease, " Scandinavian Journal of Immunology, vol. 64, no. 3, pp. 336-344, 2006.

[26] E. J. Harvey andD. P. Ramji, "Interferon-y and atherosclerosis: pro- or anti-atherogenic?" Cardiovascular Research, vol. 67, no. 1, pp. 11-20, 2005.

[27] J. L. Young, P. Libby, and U. Schonbeck, "Cytokines in the pathogenesis of atherosclerosis, " Thrombosis and Haemostasis, vol. 88, no. 4, pp. 554-567, 2002.

Franca Marino, (1,2) Luigina Guasti, (2) Matteo Tozzi, (2) Laura Schembri, (2) Luana Castiglioni, (2) Elisabetta Molteni, (2) Gabriele Piffaretti, (2) Patrizio Castelli, (2) and Marco Cosentino (2)

(1) Department of Clinical and Experimental Medicine, University oflnsubria, Via Ottorino Rossi No. 9, 21100 Varese, Italy

(2) Center of Research in Medical Pharmacology, University of Insubria, Varese, Italy

Correspondence should be addressed to Franca Marino;

Received 8 October 2012; Revised 7 January 2013; Accepted 1 February 2013

Academic Editor: Robert M. Schainfeld

TABLE 1: Clinical characteristics of PAD patients
at enrollment. Values are means [+ or -] SD.

PAD patients: 9
  Sex: 2 females (22,3%); 7 males (77,7%)
  Age, years: 68,0 [+ or -] 8,5
Rutherford classification
  Stage 0-2: 0
  Stage 3: 3 (33,3%)
  Stage 4: 4 (44,4%)
  Stage 5: 2 (22,2%)
  Stage 6: 0
Pharmacological treatment
  Antiplatelet drugs: 8 (88,8%)
  ACE inhibitors: 5 (55,5%)
  [Ca.sup.++]-channel blockers: 7 (77,7%)
  Hypoglycaemic drugs: 1 (11,1%)
  Other drugs: 7 (77,7%)
Clinical notes
  Smokers: 5 (55,5%)
  Alcohol users: 2 (22,2%)
  Diabetes: 2 (22,2%)
  Hypertension *: 8 (88,8%)
  Hypercholesterolemia *: 7(77,7%)
  Atrial fibrillation: 1 (11,1%)
  Ictus: 1 (11,1%)

* Hypertension and hypercholesterolemia were defined
as indicated by National Committee on Prevention, Detection,
Evaluation, and Treatment of High Blood Pressure, National
High Blood Pressure Education Program Coordinating
Committee [8].

TABLE 2: Real-time PCR primers.

Gene       UniGene ID      Interrogated sequence      Translate
symbol                      RefSeq/GenBank mRNA        protein

ICAM-1   Hs.00277001.m1     NM00201.2/BC015969.2     NP_000192.2
VCAM-1   Hs.00365486_m1   NM001078.2/BC068490.1 o    NP.001069.1
ITGB1    Hs.00559595_m1   NM.00222211.3/BC020057.1   NP_002202.2
IL-4     Hs.00174122_m1    NM000589.2/BC066277.1     NP.000580.1
                                o BC067514 1
INFG     Hs.00174143_m1    NM.000619.2/BC070256.1    NP.000610.2
IL-10    Hs.00174086_m1      NM000572/BC04252.1      NP.000563.1
TGFB1    Hs.99999918.m1     NM004612.2/L11695.1      NP_004603.1

Gene        Exon         Assay
symbol    boundary     location
           RefSeq/      RefSeq/
           GenBank      GenBank
            mRNA        GenBank

ICAM-1     5-6/5-6     1502/1252
VCAM-1     7-8/7-8     1913/1012
                        o 1913
ITGB1    11-12/11-12   1688/1532
IL-4       3-4/3-4      733/427
                         o 428
INFG       1-2/1-2      244/246
IL-10      3-4/3-4      440/437
TGFB1      2-3/2-3      412/412

Gene       IMAGE     Amplicon
symbol   clone ID     length

ICAM-1    3506766       99
VCAM-1   30339170       84

ITGB1     3924411      102
IL-4      6971779       70
         o 6971780
INFG     304146644      79
IL-10    40035920      119
TGFB1       --          92

TABLE 3: Lipid, lipoprotein, and hs-CRP profile of patients
during the study. Values are expressed as mean [+ or -] standard
error (SEM). * P < 0,05 and ** p < 0,01 versus visit 1.

             TC         TG       HDL-c      LDL-c
          (mg/dL)    (mg/dL)    (mg/dL)    (mg/dL)

Visit 1    243.6      118.3      57.00     150.80
          [+ or -]   [+ or -]   [+ or -]   [+ or -]
           12.50      15.28       6.09       877
Visit 2    191.6      110.00      52.2      144.00
          [+ or -]   [+ or -]   [+ or -]   [+ or -]
          15.44 **    14.52       4.86       9.91
Visit 3    170.08     115.10     53.44      86.80
          [+ or -]   [+ or -]   [+ or -]   [+ or -]
          9.26 **     11.69       4.36      6.15 *
Visit 4    146.30     113.10     52.33      79.47
          [+ or -]   [+ or -]   [+ or -]   [+ or -]
          10.35 **    10.94       5.07      5.07 *

            ApoA       ApoB      hs-CRP
          (mg/dL)    (mg/dL)     (mg/L)

Visit 1    185.10     118.20      4.24
          [+ or -]   [+ or -]   [+ or -]
           22.75       6.20       0.82
Visit 2    179.30     110.80       --
          [+ or -]   [+ or -]
           16.10      10.12
Visit 3    165.80     86.78        --
          [+ or -]   [+ or -]
           12.66      5.26 *
Visit 4    169.10     78.44       2.12
          [+ or -]   [+ or -]   [+ or -]
           15.92     2.91 **     0.83 *

TC: total cholesterol; TG: triglycerides; HDL-c: high-density
lipoprotein cholesterol; LDL-c: low-density lipoprotein
cholesterol; ApoA: apolipoprotein A; ApoB: apolipoprotein
B; hs-CRP: high -sensitive C-reactive protein.

TABLE 4: Comparison between adhesion molecules mRNA levels in pEC
and cEC at visit 2. Values are expressed as mean [+ or -] standard
error (SEM).

Adhesion                  mRNA levels                     P
molecule           (2-[DELTA]Ct x [10.sup.4])

                   pEC                    cEC

ICAM-1     0.054 [+ or -] 0.013   0.032 [+ or -] 0.005   0.001
VCAM-1     0.013 [+ or -] 0.003   0.009 [+ or -] 0.003   0.026
[beta]1-   5.320 [+ or -] 1.160   3.100 [+ or -] 0.620   0.006
COPYRIGHT 2013 Hindawi Limited
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2013 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Clinical Study
Author:Marino, Franca; Guasti, Luigina; Tozzi, Matteo; Schembri, Laura; Castiglioni, Luana; Molteni, Elisab
Publication:International Journal of Vascular Medicine
Article Type:Report
Date:Jan 1, 2013
Previous Article:Diabetic foot: surgical approach in emergency.
Next Article:Our treatment strategy for critical limb ischemia.

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |