Disease Markers

Disease Markers / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 1821596 | https://doi.org/10.1155/2016/1821596

Angelo Zinellu, Salvatore Sotgia, Arduino A. Mangoni, Elisabetta Sotgiu, Sara Ena, Dionigia Arru, Stefano Assaretti, Angela Baralla, Andrea E. Satta, Ciriaco Carru, "Effects of Ramipril and Telmisartan on Plasma Concentrations of Low Molecular Weight and Protein Thiols and Carotid Intima Media Thickness in Patients with Chronic Kidney Disease", Disease Markers, vol. 2016, Article ID 1821596, 7 pages, 2016. https://doi.org/10.1155/2016/1821596

Effects of Ramipril and Telmisartan on Plasma Concentrations of Low Molecular Weight and Protein Thiols and Carotid Intima Media Thickness in Patients with Chronic Kidney Disease

Academic Editor: Manfredi Rizzo
Received18 May 2016
Revised28 Jun 2016
Accepted29 Jun 2016
Published02 Nov 2016


Hypertension, a common feature in chronic kidney disease (CKD), is an independent risk factor for CKD progression and cardiovascular disease. Although inhibitors of the renin-angiotensin system (RAS) exert salutary effects on blood pressure control and proteinuria in CKD patients, their activity towards traditional and novel oxidative markers is largely unknown. We studied the effects of 6-month treatment with telmisartan versus a combination of telmisartan and ramipril on plasma concentrations of low molecular mass (LMW, including homocysteine and cysteine) and protein thiols (PSH) plasma concentration and their relationships with carotid intima media thickness (IMT), in 24 hypertensive CKD patients (age years, 8 females and 16 males). Pretreatment PSH concentrations were independently associated with IMT (, ). Neither treatment affected plasma LMW thiols, in both reduced and total form. By contrast, both treatments increased PSH plasma concentrations and reduced IMT, although significant differences were only observed in the combined treatment group. Our results suggest that the beneficial effects of combined RAS inhibitor treatment on IMT in hypertensive CKD patients may be mediated by a reduction of oxidative stress markers, particularly PSH.

1. Introduction

Hypertension is present in more than 80% of patients with chronic kidney disease (CKD) and contributes to progression towards end stage renal disease (ESRD) as well as an increased risk of cardiovascular events such as myocardial infarction and stroke [1], leading to non-CKD-related causes of death in this group. Moreover, there is good evidence that the presence of hypertension in CKD is associated with structural alterations of the arterial wall, in particular an increased thickness of the intima media layers [2]. Carotid IMT has been shown to independently predict adverse clinical outcomes in CKD [3]. Although a prolonged increase in blood pressure might be directly responsible for the development and the progression of IMT [4], other factors are likely to be involved. For example, a recent study has identified the role of oxidative stress in the development of carotid IMT in young CKD [5]. Evidence from a large number of clinical trials has clearly demonstrated that adequate blood pressure control is key to preventing adverse outcomes in CKD [6]. Inhibitors of the renin-angiotensin system (RAS), such as angiotensin converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs), have been found to slow the progression of CKD to ESRD [7, 8]. Recent studies have also compared the effects of different RAS inhibitors. For example, in the ONTARGET study the ARB telmisartan had similar cardiovascular and renal protective effects to the ACEI ramipril in patients at high cardiovascular risk but was better tolerated [9]. Despite the established beneficial effects of RAS inhibitors in reducing proteinuria and in slowing the rate of CKD progression, direct mechanistic comparisons between ARBs and ACEIs, including possible effects on carotid IMT, have been poorly addressed. Although recent reports support the hypothesis that RAS inhibition by either ramipril or telmisartan suppresses inflammatory and lipid peroxidation markers in nonhypertensive diabetic patients [10], there is little information about other important markers of oxidation and cardiovascular risk such as LMW thiols, for example, homocysteine (Hcy) or cysteine (Cys), and their redox status modification during therapy. The highly reactive sulphur-containing amino acid Hcy has long been shown to exert detrimental effects on vascular homeostasis by inhibiting nitric oxide synthesis and promoting oxidative stress and inflammation [11]. Several studies have shown that higher plasma/serum homocysteine concentrations independently predict adverse cardiovascular outcomes [12]. Similar results have also been reported for cysteine [13, 14]. In CKD patients both Hcy and Cys plasma concentrations are commonly increased thus contributing, at least in part, to the high cardiovascular risk in this group [15]. Plasma LMW thiols also include cysteinylglycine (CysGly), glutathione (GSH), and glutamylcysteine (Glucys). These LMW thiols interact via redox disulfide exchange reactions and reduced, free-oxidized, and protein-bound forms of these species form a dynamic system referred to as thiols redox status that also comprises the free –SH groups of proteins (PSH) [16]. Since CKD patients are normally characterized by an increased oxidative stress and RAS inhibitors are reported to be able to reduce oxidative markers in diabetic mice [17], evaluation of total –SH groups in plasma may provide a more comprehensive assessment of the possible beneficial effects of RAS inhibition on oxidative status as well as carotid IMT. Thus, the aim of our study was to assess and compare the effects of 6-month treatment with telmisartan (80 mg day), a relatively new ARB with better tolerability, and relatively long duration of action in virtue of its longer half-life, versus a combination of telmisartan and ramipril (40/5 mg day) on LMW and PSH plasma concentrations and carotid IMT in patients with CKD. The objective was to evaluate whether the salutary effects of telmisartan on the outcomes of interest were augmented when combined with ramipril.

2. Methods

2.1. Subjects

Recruitment was performed as previously described [15]. In brief, 24 CKD hypertensive patients (age years, 8 females and 16 males) were identified at the Istituto di Patologia Medica, Azienda Ospedaliero Universitaria, with the following inclusion criteria: age > 18 years, blood pressure ≥ 140/90 mmHg, plasma LDL-cholesterol concentrations > 100 mg/dL (without concomitant hypolipidemic drugs), and presence of proteinuric CKD defined as creatinine clearance > 20 mL/min/1.73 m2 combined with urinary protein excretion rate > 0.3 g/24 h, without evidence of urinary tract infection or overt heart failure (New York Heart Association class III or more). Patients were of CKD stage 3 or 4, not receiving dialysis. None of the selected patients took any antihypertensive medications before the enrollment. Exclusion criteria were previous or concomitant treatment with steroids, anti-inflammatory and immunosuppressive agents, vitamin B6, vitamin B12, folate, or statin and evidence or clinical suspicion of renovascular disease, obstructive uropathy, type 1 diabetes, and vasculitis.

Enrolled patients were randomized to receive 6-month treatment with telmisartan (80 mg/day) versus a combination of telmisartan and ramipril (40/5 mg/day). Patients were assessed at baseline and at the end of treatment. Informed consent was obtained from each patient. The study was approved by our institution ethics committee and complied with the principles of the Helsinki Declaration.

2.2. Biochemical Analysis

Reduced and total LMW thiols were determined by capillary electrophoresis LIF detection as previously described [16, 18]. The LMW thiol redox status was calculated by measuring the ratio of the sum of reduced () and total () forms of thiols as follows: (CysGly + Cys + Hcy + GSH + GluCys)/(CysGly + Cys + Hcy + GSH + GluCys).

Plasma protein SH (PSH) determination was performed by spectrophotometry with 5,5′-dithiobis-2-nitrobenzoic acid (DTNB) as titrating agent by measuring the absorbance of conjugate at 405 nm [19]. Concentration in samples was determined from a GSH standard curve. Proteins –SH concentrations were normalized versus protein plasma quantity measured by Lowry’s method.

2.3. Blood Pressure Measurement

Blood pressure (BP) was measured at the Istituto di Patologia Medica, Azienda Ospedaliero Universitaria, by a trained research assistant using a calibrated and validated digital sphygmomanometer. BP measurements were taken with the patient in a seated position with the arm supported at heart level, after a 5 min rest and after abstaining from food, beverages containing caffeine, and smoking for at least 2 h prior to BP measurement. BP was recorded as three serial measurements at intervals of 30 sec on both arms. The mean of the six BP readings was used in the analysis. If a BP reading deviated by more than 10 mmHg from the average reading, the BP measurement on that arm was repeated.

2.4. Carotid IMT Measurement

The carotid artery was scanned by two trained and certified sonographers blinded to clinical information and treatment. All study subjects were examined in the supine position with the head tilted backward. Dedicated QIMT-Esaote software was used to measure the left and right IMT of the posterior wall of the common carotid, 1 cm distal to the bulb bifurcation, by ultrasound 2D exam. The IMT assessment was performed according to the recommendations of the Italian Society of Vascular Diagnostics [20] and the standardized criteria described by Mannheim Carotid Intima Media Thickness Consensus to ensure full reliability [21]. The manual image acquisition of carotid vessels was obtained before the automatic measurement of IMT using QIMT (Quality Intima Media Thickness) software, integrated into the instrument (Esaote MyLab 30 gold), and QIMT software, using the RF (Radio Frequency Data Processing). Two readings from both common carotid arteries were averaged to calculate the mean IMT. A thickness of >0.8 mm indicated increased IMT.

2.5. Statistical Analysis

All results are expressed as mean values (mean ± SD) or median values (median and interquartile range). The variables distribution was assessed by the Shapiro-Wilk test. Homogeneity of variance was checked by -test and differences between groups were compared by nonparametric Mann-Whitney test or by parametric independent -test, with or without Welch’s correction for unequal variances, as appropriate. Nonnormally distributed variables were -transformed prior assessment with parametric tests, and the normal distribution of the residuals was checked to assess the goodness of fit of the transformations. Correlation analysis between variables was performed by Pearson’s correlation or Spearman’s correlation. Multiple linear regression analysis was used to assess the association between different variables and IMT at baseline. The effect of treatment was evaluated by ANOVA.

Statistical analyses were performed using MedCalc for Windows, 12.5 64-bit version (MedCalc Software, Ostend, Belgium), and SPSS for Windows, 14.0 32-bit version (IBM Corporation, Armonk, NY, USA).

3. Results

Clinical characteristics of CKD patients at baseline are described in Table 1. After randomization, no significant differences were found among the two treatment groups in the clinical characteristics (Table 1). As expected, more than 60% of CKD subjects were hyperhomocysteinemic (Hcy >15 μmol/L) versus 10% normally found in healthy population. As reported in Figure 1, baseline IMT was inversely related to PSH concentrations (, ). In multiple linear regression analysis, with IMT as dependent variable and age, gender, GFR, creatinine, PSH, SBP, and LMW red/ox ratio as independent variables, only PSH (, ) was independently associated with baseline IMT.

CKD ()Group 1 ()
40/5 mg/day
Group 2 ()
80 mg/day
Mean ± SD
or median (IQR)
Mean ± SD
or median (IQR)
Mean ± SD
or median (IQR)

Sex, F/M (% F)8/16 (33%)4/8 (33%)4/8 (33%)
Age, years60 ± 1262 ± 1258 ± 13
Systolic BP, mmHg133 ± 13132 ± 13133 ± 14
Diastolic BP, mmHg80 ± 982 ± 877 ± 9
Creatinine, mg/dL1.6 (1.1–2.1)1.6 (1.0–2.3)1.7 (1.3–2.0)
GFR, mL/min per 1.73 m248 (32–66)48 (22–71)48 (34–66)
Proteinuria, g/24 h0.95 (0.30–2.35)0.52 (0.28–2.49)1.28 (0.36–2.35)
IMT, mm0.90 (0.73–1.00)0.95 (0.72–1.05)0.88 (0.73–1.00)
Total LMW thiols
 t-CysGly, µmol/L30.2 ± 8.631.6 ± 8.828.8 ± 8.4
 t-Hcy, µmol/L17.0 (12.1–24.4)16.3 (12.1–26.3)19.2 (11.8–23.7)
 t-Cys, µmol/L381 ± 98391 ± 89370 ± 109
 t-GSH, µmol/L7.5 ± 2.67.4 ± 2.17.6 ± 3.2
 t-GluCys, µmol/L5.8 (3.9–6.5)5.7 (4.5–6.0)5.4 (3.5–7.6)
 Sum of total LMW thiols, µmol/L444 ± 112458 ± 106432 ± 122
Reduced LMW thiols
 r-Cys-Gly, µmol/L6.2 ± 2.25.8 ± 1.66.6 ± 2.6
 r-Hcy, µmol/L0.24 (0.15–0.37)0.20 (0.13–0.37)0.29 (0.18–0.37)
 r-Cys, µmol/L21.6 ± 4.120.9 ± 4.721.9 ± 3.5
 r-GSH, µmol/L1.09 (0.78–1.46)1.01 (0.74–1.31)1.11 (0.85–1.67)
 r-Glu-Cys, µmol/L0.36 (0.26–0.46)0.35 (0.22–0.58)0.37 (0.27–0.44)
 Sum of reduced LMW thiols, µmol/L29.4 ± 5.928.4 ± 5.930.5 ± 6.0
Thiols redox status
 LMW redox, %0.072 ± 0.0270.066 ± 0.0230.078 ± 0.030
 PSH, µmol/g prot3.95 (3.31–4.80)3.59 (3.23–4.15)4.61 (3.39–5.80)

As reported in Table 2, a reduction in blood pressure was observed in both groups; however it was statistically significant only in the telmisartan/ramipril group (). Creatinine and proteinuria showed a nonsignificant trend toward improvement in both groups after 6-month treatment. LMW thiols concentrations were unaffected by drug treatment both in the reduced and in the total form. In particular no differences were found in the cardiovascular risk factors homocysteine and cysteine plasma concentrations. As a result, the LMW red/ox ratio remained essentially unchanged at the end of treatment (Table 3).

Group 1 ()Group 2 ()
40/5 mg/day
80 mg/day
Mean ± SD
or median (IQR)
Mean ± SD
or median (IQR)
Mean ± SD
or median (IQR)
Mean ± SD
or median (IQR)

Systolic BP, mmHg132 ± 13122 ± 100.04133 ± 14123 ± 150.11
Diastolic BP, mmHg82 ± 875 ± 50.0277 ± 976 ± 100.80
Creatinine, mg/dL1.6 (1.0–2.3)1.5 (1.1–2.2)0.571.7 (1.3–2.0)1.5 (1.3–2.0)0.85
GFR, mL/min per 1.73 m248 (22–71)47 (23–61)0.7948 (34–66)55 (36–71)0.79
Proteinuria, g/24 h0.52 (0.28–2.49)0.49 (0.22–1.15)0.071.28 (0.36–2.35)0.67 (0.44–1.68)0.08

Group 1 ()Group 2 ()
40/5 mg/day
p valueBaselineTelmisartan
80 mg/day
p value
Mean ± SD
median (IQR)
Mean ± SD
median (IQR)
Mean ± SD
median (IQR)
Mean ± SD
median (IQR)

Total LMW thiols
 t-CysGly, µmol/L31.6 ± 8.831.1 ± 8.50.8928.8 ± 8.425.6 ± 7.90.35
 t-Hcy, µmol/L16.3 (12.1–26.3)17.3 (10.3–27.6)0.9019.2 (11.8–23.7)14.4 (11.2–19.2)0.27
 t-Cys, µmol/L391 ± 89404 ± 1220.77370 ± 109341 ± 940.49
 t-GSH, µmol/L7.4 ± 2.17.7 ± 1.80.717.6 ± 3.27.6 ± 4.61.00
 t-GluCys, µmol/L5.7 (4.5–6.0)5.7 (4.4–9.7)0.385.4 (3.5–7.6)4.4 (3.2–7.2)0.95
 Sum of total LMW thiols, µmol/L458 ± 106472 ± 1440.79432 ± 122400 ± 1120.51
Reduced LMW thiols
 r-CysGly, µmol/L5.8 ± 1.65.5 ± 1.60.656.6 ± 2.66.4 ± 1.70.83
 r-Hcy, µmol/L0.20 (0.13–0.37)0.17 (0.12–0.36)0.570.29 (0.18–0.37)0.23 (0.17–0.29)0.42
 r-Cys, µmol/L20.9 ± 4.719.7 ± 4.70.5421.9 ± 3.521.0 ± 4.40.58
 r-GSH, µmol/L1.01 (0.74–1.31)0.94 (0.47–1.37)0.911.11 (0.85–1.67)1.10 (0.71–1.60)0.34
 r-GluCys, µmol/L0.35 (0.22–0.58)0.41 (0.31–0.47)0.850.37 (0.27–0.44)0.43 (0.33–0.45)0.97
 Sum of reduced sLMW thiols, µmol/L28.4 ± 5.926.1 ± 5.10.3230.5 ± 6.029.3 ± 5.80.62
Thiols redox status
 LMW redox, %0.066 ± 0.0230.061 ± 0.0250.620.078 ± 0.0300.079 ± 0.0280.93

By contrast, as shown in Figure 2(a), PSH plasma concentrations significantly increased in the telmisartan/ramipril group (median: 3.59 μmol/g prot (3.31–4.80 μmol/g prot) at baseline versus 4.66 μmol/g prot (3.94–5.96 μmol/g prot) after treatment, ) whereas they remained essentially unchanged in the telmisartan group (median: 4.61 μmol/g prot (3.39–5.80 μmol/g prot) at baseline versus 4.43 μmol/g prot (4.16–7.27 μmol/g prot) after treatment). Carotid IMT decreased in both groups (Figure 2(b)). However, the reduction was statistically significant only in the telmisartan/ramipril group [telmisartan/ramipril: median 0.95 mm (0.72–1.05 mm) at baseline versus 0.68 mm (0.60–0.80 mm) after treatment, ; telmisartan: median 0.88 mm (0.73–1.00 mm) at baseline versus 0.68 mm (0.55–0.93) after treatment].

4. Discussion

A number of trials and meta-analyses have demonstrated that combined treatment with ACEIs and ARBs exerts greater effects on blood pressure lowering and proteinuria than agent alone [22, 23]. However, combination therapy may also result in a significant increased incidence of adverse effects, as demonstrated in the ONTARGET trial of 25,620 patients with preexisting vascular disease or diabetes. ONTARGET was designed to evaluate the effects of ramipril, telmisartan, or their combination on cardiovascular and renal endpoints during approximately 4.5 years of follow-up [24]. In this study, a small but significant increase in the incidence of ESRD, hyperkalemia, and hypotension was observed with the combination therapy [24]. Moreover, the combination treatment was not associated with better clinical outcomes when compared with each treatment alone [25].

In view of the ongoing debate on the efficacy and safety of combined RAS inhibitors treatment and the uncertainties regarding the putative mechanisms responsible for the beneficial effects of these drug class, we assessed and compared the effects of telmisartan administration alone (80 mg day) versus a combination of telmisartan/ramipril (40/5 mg day) on plasma LMW and protein thiols concentrations and carotid IMT in CKD patients. Our data confirm previous observations that dual RAS blockade has greater blood pressure effects if compared with telmisartan alone [24]. For the first time, we comprehensively evaluated the effect of RAS inhibitor therapy on low molecular mass thiols Hcy and Cys (two well known risk factors for cardiovascular disease) both in the total and in the reduced form. As expected, CKD was associated with relatively high plasma concentrations of both total Cys and Hcy. RAS treatment did not exert any significant effect on plasma low molecular mass thiols (for both reduced and total forms) so that LMW thiols redox status remains unchanged after therapy. Conversely, combined treatment significantly increased PSH concentrations. PSH values provide a comprehensive measure of total protein sulfhydryl groups in plasma. The most abundant reduced -SH group in plasma is that of human serum albumin (HSA), given its high concentrations. The single free cysteinyl thiol of HSA, Cys34, accounts for ~80% of reduced thiols in human plasma and is an important scavenger of reactive oxygen and nitrogen species in the vascular compartment, thus a quantitatively important redox buffer of blood [26]. Therefore, in the presence of reactive oxygen species the PSH concentrations decrease, whereas an increment in PSH concentrations indicates oxidative stress reduction. Our data on PSH are in agreement with previous reports showing that ramipril effectively decreased oxidative stress indices [17].

Notably, the salutary effects of RAS combination treatment were paralleled by a concomitant reduction in carotid IMT. As baseline PSH was the only parameter independently associated with IMT, we speculate that the changes in IMT during combination treatment may be mediated, at least in part, by the reduction of oxidative stress. This hypothesis is supported by previous studies showing an inverse association between IMT and plasma total antioxidant capacity [27].

There are some limitations in this study that deserve mention. The data were obtained from a relatively small study population and did not include a placebo group. Therefore, our results require confirmation in larger study cohorts. The treatment duration, 6 months, is relatively short if compared to previous studies, reporting follow-ups between 2 and 4 years. Finally, the applicability of our results to populations other than CKD remains to be established, in view of the peculiar proinflammatory and oxidative stress state of these patients.

5. Conclusion

We found that 6-month RAS inhibitor treatment in CKD with either telmisartan alone or in combination with ramipril did not significantly affect LMW plasma thiols in both the reduced and the total form, particularly Hcy and Cys. By contrast, a significant reduction in carotid IMT and a concomitant increase in PSH plasma concentrations were observed in the combination treatment group. These results provide novel information on the potential mechanistic effects of RAS inhibition on carotid IMT, a key marker of vascular remodeling and independent predictor of adverse events in hypertension and CKD. Further studies in larger cohorts with longer follow-ups and other established surrogate risk markers are required to confirm the hypothesis that the IMT improvement with RAS inhibition is mediated by oxidative stress decrease.


ACEIs:Angiotensin converting enzyme inhibitors
ARBs:Angiotensin II receptor blockers
CKD:Chronic kidney disease
LMW:Low molecular weight
PSH:Protein thiols
RAS:Renin-angiotensin system.

Competing Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


This study was supported by the “Fondazione Banco di Sardegna, Sassari, Italy,” and by the “Ministero dell’Università e della Ricerca,” Italy. Arduino A. Mangoni has participated in this work during a Visiting Professorship at the University of Sassari.


  1. R. D. Toto, “Treatment of hypertension in chronic kidney disease,” Seminars in Nephrology, vol. 25, no. 6, pp. 435–439, 2005. View at: Publisher Site | Google Scholar
  2. T. Ohara, Y. Kokubo, K. Toyoda et al., “Impact of chronic kidney disease on carotid atherosclerosis according to blood pressure category: the suita study,” Stroke, vol. 44, no. 12, pp. 3537–3539, 2013. View at: Publisher Site | Google Scholar
  3. S. Zoungas, J. D. Cameron, P. G. Kerr et al., “Association of carotid intima-medial thickness and indices of arterial stiffness with cardiovascular disease outcomes in CKD,” American Journal of Kidney Diseases, vol. 50, no. 4, pp. 622–630, 2007. View at: Publisher Site | Google Scholar
  4. A. Szarejko-Paradowska, A. Gluba-Brzózka, R. Pietruszyński, and J. Rysz, “Assessment of the relationship between selected cardiovascular risk factors and the indices of intima-media thickness and coronary artery calcium score in various stages of chronic kidney disease,” International Urology and Nephrology, vol. 47, no. 12, pp. 2003–2012, 2015. View at: Publisher Site | Google Scholar
  5. J. Kotur-Stevuljević, A. Peco-Antić, S. Spasić et al., “Hyperlipidemia, oxidative stress, and intima media thickness in children with chronic kidney disease,” Pediatric Nephrology, vol. 28, no. 2, pp. 295–303, 2013. View at: Publisher Site | Google Scholar
  6. F. Turnbull, “Effects of different blood-pressure-lowering regimens on major cardiovascular events: results of prospectively-designed overviews of randomised trials,” The Lancet, vol. 362, no. 9395, pp. 1527–1535, 2003. View at: Publisher Site | Google Scholar
  7. P. Ruggenenti, A. Perna, G. Gherardi, F. Gaspari, R. Benini, and G. Remuzzi, “Renal function and requirement for dialysis in chronic nephropathy patients on long-term ramipril: REIN follow-up trial,” The Lancet, vol. 352, no. 9136, pp. 1252–1256, 1998. View at: Publisher Site | Google Scholar
  8. P. Ruggenenti, A. Perna, G. Gherardi et al., “Renoprotective properties of ACE-inhibition in non-diabetic nephropathies with non-nephrotic proteinuria,” The Lancet, vol. 354, no. 9176, pp. 359–364, 1999. View at: Publisher Site | Google Scholar
  9. J. F. Mann, R. E. Schmieder, M. McQueen et al., “Renal outcomes with telmisartan, ramipril, or both, in people at high vascular risk (the ONTARGET study): a multicentre, randomised, double-blind, controlled trial,” The Lancet, vol. 372, no. 9638, pp. 547–553, 2008. View at: Publisher Site | Google Scholar
  10. S. Koulouris, P. Symeonides, K. Triantafyllou et al., “Comparison of the effects of Ramipril versus Telmisartan in reducing serum levels of high-sensitivity C-reactive protein and oxidized low-density lipoprotein cholesterol in patients with type 2 diabetes mellitus,” The American Journal of Cardiology, vol. 95, no. 11, pp. 1386–1388, 2005. View at: Publisher Site | Google Scholar
  11. W. K. C. Lai and M. Y. Kan, “Homocysteine-induced endothelial dysfunction,” Annals of Nutrition and Metabolism, vol. 67, no. 1, pp. 1–12, 2015. View at: Publisher Site | Google Scholar
  12. P. Ganguly and S. F. Alam, “Role of homocysteine in the development of cardiovascular disease,” Nutrition Journal, vol. 14, article 6, 2015. View at: Publisher Site | Google Scholar
  13. N. Jacob, E. Bruckert, P. Giral, M. J. Foglietti, and G. Turpin, “Cysteine is a cardiovascular risk factor in hyperlipidemic patients,” Atherosclerosis, vol. 146, no. 1, pp. 53–59, 1999. View at: Publisher Site | Google Scholar
  14. L. El-Khairy, P. M. Ueland, H. Refsum, I. M. Graham, and S. E. Vollset, “Plasma total cysteine as a risk factor for vascular disease: the European concerted action project,” Circulation, vol. 103, no. 21, pp. 2544–2549, 2001. View at: Publisher Site | Google Scholar
  15. A. Zinellu, G. Loriga, B. Scanu et al., “Increased low-density lipoprotein S-homocysteinylation in chronic kidney disease,” American Journal of Nephrology, vol. 32, no. 3, pp. 242–248, 2010. View at: Publisher Site | Google Scholar
  16. C. Carru, L. Deiana, S. Sotgia, G. M. Pes, and A. Zinellu, “Plasma thiols redox status by laser-induced fluorescence capillary electrophoresis,” Electrophoresis, vol. 25, no. 6, pp. 882–889, 2004. View at: Publisher Site | Google Scholar
  17. W. Liang, C. Y. R. Tan, L. Ang et al., “Ramipril improves oxidative stress-related vascular endothelial dysfunction in db/db mice,” The Journal of Physiological Sciences, vol. 58, no. 6, pp. 405–411, 2008. View at: Publisher Site | Google Scholar
  18. A. Zinellu, C. Carru, F. Galistu et al., “N-methyl-d-glucamine improves the laser-induced fluorescence capillary electrophoresis performance in the total plasma thiols measurement,” Electrophoresis, vol. 24, no. 16, pp. 2796–2804, 2003. View at: Publisher Site | Google Scholar
  19. G. L. Ellman, “Tissue sulfhydryl groups,” Archives of Biochemistry and Biophysics, vol. 82, no. 1, pp. 70–77, 1959. View at: Publisher Site | Google Scholar
  20. Società Italiana di Diagnostica Vascolare, “Operative procedures for vascular diagnostic investigations. Guidelines of the Italian Society of Vascular Diagnosis (GUIV),” Minerva Cardioangiologica, vol. 48, no. 9, pp. 303–355, 2000. View at: Google Scholar
  21. P.-J. Touboul, M. G. Hennerici, S. Meairs et al., “Mannheim intima-media thickness consensus,” Cerebrovascular Diseases, vol. 18, no. 4, pp. 346–349, 2004. View at: Publisher Site | Google Scholar
  22. P. Susantitaphong, K. Sewaralthahab, E. M. Balk, S. Eiam-Ong, N. E. Madias, and B. L. Jaber, “Efficacy and safety of combined vs. single renin-angiotensin-aldosterone system blockade in chronic kidney disease: a meta-analysis,” American Journal of Hypertension, vol. 26, no. 3, pp. 424–441, 2013. View at: Publisher Site | Google Scholar
  23. F. Catapano, P. Chiodini, L. De Nicola et al., “Antiproteinuric response to dual blockade of the renin-angiotensin system in primary glomerulonephritis: meta-analysis and metaregression,” American Journal of Kidney Diseases, vol. 52, no. 3, pp. 475–485, 2008. View at: Publisher Site | Google Scholar
  24. S. Yusuf, K. K. Teo, J. Pogue et al., “Telmisartan, ramipril, or both in patients at high risk for vascular events,” The New England Journal of Medicine, vol. 358, no. 15, pp. 1547–1559, 2008. View at: Publisher Site | Google Scholar
  25. S. W. Tobe, C. M. Clase, P. Gao et al., “Cardiovascular and renal outcomes with telmisartan, ramipril, or both in people at high renal risk: results from the ONTARGET and TRANSCEND studies,” Circulation, vol. 123, no. 10, pp. 1098–1107, 2011. View at: Publisher Site | Google Scholar
  26. R. Rossi, D. Giustarini, A. Milzani, and I. Dalle-Donne, “Cysteinylation and homocysteinylation of plasma protein thiols during ageing of healthy human beings,” Journal of Cellular and Molecular Medicine, vol. 13, no. 9, pp. 3131–3140, 2009. View at: Publisher Site | Google Scholar
  27. M. H. El Samahy, R. M. Matter, O. I. Youssef, M. A. Shams El Din El Telbany, and N. A. Kamal, “Relation between carotid intima media thickness and oxidative stress markers in type 1 diabetic children and adolescents,” Journal of Diabetes and Metabolic Disorders, vol. 12, no. 1, article 50, 2013. View at: Publisher Site | Google Scholar

Copyright © 2016 Angelo Zinellu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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