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Circulating microparticles and central blood pressure according to antihypertensive strategy

Abstract

OBJECTIVES:

This prospective, randomized, open-label study aimed to compare the effects of antihypertensive treatment based on amlodipine or hydrochlorothiazide on the circulating microparticles and central blood pressure values of hypertensive patients.

METHODS:

The effects of treatments on circulating microparticles were assessed during monotherapy and after the consecutive addition of valsartan and rosuvastatin followed by the withdrawal of rosuvastatin. Each treatment period lasted for 30 days. Central blood pressure and pulse wave velocity were measured at the end of each period. Endothelial, monocyte, and platelet circulating microparticles were determined by flow cytometry. Central blood pressure values and pulse wave velocity were recorded at the end of each treatment period.

RESULTS:

No differences in brachial blood pressure were observed between the treatment groups throughout the study. Although similar central blood pressure values were observed during monotherapy, lower systolic and diastolic central blood pressure values and early and late blood pressure peaks were observed in the amlodipine arm after the addition of valsartan alone or combined with rosuvastatin. Hydrochlorothiazide-based therapy was associated with a lower number of endothelial microparticles throughout the study, whereas a higher number of platelet microparticles was observed after rosuvastatin withdrawal in the amlodipine arm.

CONCLUSIONS:

Despite similar brachial blood pressure values between groups throughout the study, exposure to amlodipine was associated with lower central blood pressure values after combination with valsartan, indicating a beneficial interaction. Differences between circulating microparticles were modest and were mainly influenced by rosuvastatin withdrawal in the amlodipine arm.

Endothelial Microparticles; Monocyte Microparticles; Platelet Microparticles; Central Blood Pressure; Hydrochlorothiazide; Amlodipine


INTRODUCTION

Arterial hypertension is responsible for high morbidity and mortality rates around the world. After the publication of the 2017 American College of Cardiology (ACC)/American Heart Association (AHA) blood pressure guidelines, a substantial increase in the number of hypertensive adults eligible for drug therapy is expected (11. Khera R, Lu Y, Lu J, Saxena A, Nasir K, Jiang L, et al. Impact of 2017 ACC/AHA guidelines on prevalence of hypertension and eligibility for antihypertensive treatment in United States and China: nationally representative cross sectional study. BMJ. 2018;362:k2357. https://doi.org/10.1136/bmj.k2357.
https://doi.org/10.1136/bmj.k2357...
).

Hypertension is a progressive and complex disease that is associated with anatomical and functional changes in blood vessels, such as endothelial dysfunction, inflammation, and disturbance in adaptive and innate immunity (2. Chistiakov DA, Orekhov AN, Bobryshev YV. Endothelial Barrier and Its Abnormalities in Cardiovascular Disease. Front Physiol. 2015;6:365. https://doi.org/10.3389/fphys.2015.00365.
https://doi.org/10.3389/fphys.2015.00365...
3. Belo VA, Guimarães DA, Castro MM. Matrix Metalloproteinase 2 as a Potential Mediator of Vascular Smooth Muscle Cell Migration and Chronic Vascular Remodeling in Hypertension. J Vasc Res. 2015;52(4):221-31. https://doi.org/10.1159/000441621.
https://doi.org/10.1159/000441621...
2-44. Barbaro NR, Fontana V, Modolo R, De Faria AP, Sabbatini AR, Fonseca FH, et al. Increased arterial stiffness in resistant hypertension is associated with inflammatory biomarkers. Blood Press. 2015;24(1):7-13. https://doi.org/10.3109/08037051.2014.940710.
https://doi.org/10.3109/08037051.2014.94...
). Indeed, antihypertensive drugs have been widely used to achieve appropriate blood pressure levels and prevent comorbidities (5. Brandão SA, Izar MC, Fischer SM, Santos AO, Monteiro CM, Póvoa RM, et al. Early increase in autoantibodies against human oxidized low-density lipoprotein in hypertensive patients after blood pressure control. Am J Hypertens. 2010;23(2):208-14. https://doi.org/10.1038/ajh.2009.214.
https://doi.org/10.1038/ajh.2009.214...
6. Schiffrin EL. Vascular remodeling in hypertension: mechanisms and treatment. Hypertension. 2012;59(2):367-74. https://doi.org/10.1161/HYPERTENSIONAHA.111.187021.
https://doi.org/10.1161/HYPERTENSIONAHA....
7. Sakamoto M, Suzuki H, Hayashi T, Iuchi H, Isaka T, Sakamoto N, et al. Effects of candesartan in hypertensive patients with type 2 diabetes mellitus on inflammatory parameters and their relationship to pulse pressure. Cardiovasc Diabetol. 2012;11:118. https://doi.org/10.1186/1475-2840-11-118.
https://doi.org/10.1186/1475-2840-11-118...
5-88. Fonseca HA, Fonseca FA, Lins LC, Monteiro AM, Bianco HT, Brandão SA, et al. Antihypertensive therapy increases natural immunity response in hypertensive patients. Life Sci. 2015;143:124-30. https://doi.org/10.1016/j.lfs.2015.10.030.
https://doi.org/10.1016/j.lfs.2015.10.03...
).

Blood pressure monitoring is essential for the treatment of hypertension. However, the assessment of peripheral blood pressure may be insufficient to achieve better control of this complex disease. Thus, the measurement of vascular compliance and central blood pressure can provide important information to expand the possibilities of clinical treatment (9. Laurent S, Boutouyrie P. Recent advances in arterial stiffness and wave reflection in human hypertension. Hypertension. 2007;49(6):1202-6. https://doi.org/10.1161/HYPERTENSIONAHA.106.076166.
https://doi.org/10.1161/HYPERTENSIONAHA....
10. Sarafidis PA, Loutradis C, Karpetas A, Tzanis G, Piperidou A, Koutroumpas G, et al. Ambulatory Pulse Wave Velocity Is a Stronger Predictor of Cardiovascular Events and All-Cause Mortality Than Office and Ambulatory Blood Pressure in Hemodialysis Patients. Hypertension. 2017;70(1):148-57. https://doi.org/10.1161/HYPERTENSIONAHA.117.09023.
https://doi.org/10.1161/HYPERTENSIONAHA....
9-1111. Omboni S, Posokhov IN, Rogoza AN. Relationships between 24-h blood pressure variability and 24-h central arterial pressure, pulse wave velocity and augmentation index in hypertensive patients. Hypertens Res. 2017;40(4):385-91. https://doi.org/10.1038/hr.2016.156.
https://doi.org/10.1038/hr.2016.156...
).

In addition to these measurements, endothelium-, platelet-, and monocyte-derived microparticles have been proposed as novel vascular biomarkers because they have been related to endothelial erosion, thrombosis, and atherosclerosis (12. Nomura S. Microparticle and Atherothrombotic Diseases. J Atheroscler Thromb. 2016;23(1):1-9. https://doi.org/10.5551/jat.32326.
https://doi.org/10.5551/jat.32326...
13. França CN, Pinheiro LF, Izar MC, Brunialti MK, Salomão R, Bianco HT, et al. Endothelial progenitor cell mobilization and platelet microparticle release are influenced by clopidogrel plasma levels in stable coronary artery disease. Circ J. 2012;76(3):729-36. https://doi.org/10.1253/circj.CJ-11-1145.
https://doi.org/10.1253/circj.CJ-11-1145...
12-1414. da Silva EF, Fonseca FA, França CN, Ferreira PR, Izar MC, Salomão R, et al. Imbalance between endothelial progenitor cells and microparticles in HIV-infected patients naive for antiretroviral therapy. AIDS. 2011;25(13):1595-601. https://doi.org/10.1097/QAD.0b013e32834980f4.
https://doi.org/10.1097/QAD.0b013e328349...
). Some differences in microparticle concentrations have been described in relation to the use or withdrawal of statins (1515. Pinheiro LF, França CN, Izar MC, Barbosa SP, Bianco HT, Kasmas SH, et al. Pharmacokinetic interactions between clopidogrel and rosuvastatin: effects on vascular protection in subjects with coronary heart disease. Int J Cardiol. 2012;158(1):125-9. https://doi.org/10.1016/j.ijcard.2012.04.051.
https://doi.org/10.1016/j.ijcard.2012.04...
). Thus, considering the high cardiovascular risk of many hypertensive individuals, the analysis of the concomitant use of statins, even in patients with adequate blood pressure control, seems relevant.

In the ACCOMPLISH study (1616. Jamerson K, Weber MA, Bakris GL, Dahlöf B, Pitt B, Shi V, et al. Benazepril plus amlodipine or hydrochlorothiazide for hypertension in high-risk patients. N Engl J Med. 2008;359(23):2417-28. https://doi.org/10.1056/NEJMoa0806182.
https://doi.org/10.1056/NEJMoa0806182...
), subjects with similar blood pressure control received combined antihypertensives based on two different strategies, and the difference in cardiovascular outcomes highlighted the relevance of the effects of these drugs on vascular biology (1717. Weber MA, Bloch M, Bakris GL, Weir MR, Zappe DH, Dahlof B, et al. Cardiovascular Outcomes According to Systolic Blood Pressure in Patients With and Without Diabetes: An ACCOMPLISH Substudy. J Clin Hypertens. 2016;18(4):299-307. https://doi.org/10.1111/jch.12816.
https://doi.org/10.1111/jch.12816...
,1818. Brook RD, Kaciroti N, Bakris G, Dahlöf B, Pitt B, Velazquez E, et al. Prior Medications and the Cardiovascular Benefits From Combination Angiotensin-Converting Enzyme Inhibition Plus Calcium Channel Blockade Among High-Risk Hypertensive Patients. J Am Heart Assoc. 2018;7(1). pii: e006940. https://doi.org/10.1161/JAHA.117.006940.
https://doi.org/10.1161/JAHA.117.006940...
). Furthermore, central blood pressure responses to therapy may differ from peripheral blood pressure responses, thus explaining some differences in cardiovascular outcomes, as described in the Conduit Artery Function Evaluation (CAFE) study (1919. Williams B, Lacy PS, Thom SM, Cruickshank K, Stanton A, Collier D, et al. Differential impact of blood pressure-lowering drugs on central aortic pressure and clinical outcomes: principal results of the Conduit Artery Function Evaluation (CAFE) study. Circulation. 2006;113(9):1213-25. https://doi.org/10.1161/CIRCULATIONAHA.105.595496.
https://doi.org/10.1161/CIRCULATIONAHA.1...
,2020. Williams B, Lacy PS, Cruickshank JK, Collier D, Hughes AD, Stanton A, et al. Impact of statin therapy on central aortic pressures and hemodynamics: principal results of the Conduit Artery Function Evaluation-Lipid-Lowering Arm (CAFE-LLA) Study. Circulation. 2009;119(1):53-61. https://doi.org/10.1161/CIRCULATIONAHA.108.785915.
https://doi.org/10.1161/CIRCULATIONAHA.1...
).

The present study aimed to compare the effects of an antihypertensive treatment based on amlodipine or hydrochlorothiazide on circulating endothelium-, monocyte-, and platelet-derived microparticles and central blood pressure parameters. Thus, new aspects of antihypertensive therapy that might be related to different clinical outcomes are described here, as reported in the ASCOT and ACCOMPLISH studies.

MATERIALS AND METHODS

Ethics

This prospective, randomized, open-label trial with blinded endpoints complied with the Declaration of Helsinki and was approved by the Ethics Committee of UNIFESP. Patients were invited to participate and were included in the trial after they agreed to the study protocol and signed a written informed consent form.

Study population

Adult hypertensive patients (aged 40-75 years, of both sexes) were enrolled if they had systolic blood pressure (SBP) or diastolic blood pressure (DBP) in the ranges of 160-179 and/or 100-119 mmHg, respectively, without pharmacological treatment; or 140-159 and/or 90-99 mmHg, respectively, or appropriate blood pressure levels (<140 and/or <90 mm Hg) with the use of two antihypertensive drugs. The key exclusion criteria were as follows: secondary hypertension, prior coronary heart disease or stroke, estimated glomerular filtration rate less than 30 mL/min per 1.73 m2 of body-surface area, history of neoplasm in the last five years, or active liver disease.

The trial was designed to compare the effects of antihypertensive treatments (strategy: 30 successive days) based on hydrochlorothiazide (Clorana®; Sanofi Aventis Pharma, 25 mg daily) or amlodipine (Amlocor®, Torrent Pharma, 5 mg daily) on circulating microparticles. At baseline, all subjects received nutritional counseling, and those using lipid-lowering drugs suspended their use. The first period of monotherapy (hydrochlorothiazide or amlodipine) was followed by the addition of valsartan (Brasart®, Torrent Pharma; 160 mg daily) and rosuvastatin (Rosucor®, Torrent Pharma; 20 mg daily), and the withdrawal of rosuvastatin with the maintenance of the antihypertensive drugs was performed in the last 30 days of treatment. Central blood pressure and pulse wave velocity (PWV) were also measured at the end of each 30-day treatment (Figure 1).

Figure 1
Study design. Eligible hypertensive subjects were randomized to receive amlodipine (5 mg daily) or hydrochlorothiazide (25 mg daily) for 4 weeks (V1), followed by three consecutive 4-week periods of treatment with the addition of valsartan (V2) and rosuvastatin (V3) and the withdrawal of rosuvastatin (V4) in both study arms. Blood samples for measurement of circulating microparticle concentrations and central blood pressure levels were obtained at the end of each treatment period. The use of antihypertensive and lipid-lowering drugs was suspended in V1 when monotherapy with either hydrochlorothiazide or amlodipine was initiated.

Circulating microparticles

Circulating endothelium-, monocyte- and platelet-derived microparticles were measured as previously reported (2121. Lins LC, França CN, Fonseca FA, Barbosa SP, Matos LN, Aguirre AC, et al. Effects of ezetimibe on endothelial progenitor cells and microparticles in high-risk patients. Cell Biochem Biophys. 2014;70(1):687-96. https://doi.org/10.1007/s12013-014-9973-9.
https://doi.org/10.1007/s12013-014-9973-...
,2222. Camargo LM, França CN, Izar MC, Bianco HT, Lins LS, Barbosa SP, et al. Effects of simvastatin/ezetimibe on microparticles, endothelial progenitor cells and platelet aggregation in subjects with coronary heart disease under antiplatelet therapy. Braz J Med Biol Res. 2014;47(5):432-7. https://doi.org/10.1590/1414-431X20143628.
https://doi.org/10.1590/1414-431X2014362...
). In brief, blood samples were collected and centrifuged (160g; 20-22°C; 10 min) to obtain platelet-rich plasma (PRP). The PRP was centrifuged (1500g; 20-22°C; 6 min) to obtain platelet-poor plasma (PPP). Furthermore, PPP (50 µL) was labeled (20 min; room temperature) with CD51FITC, CD42FITC and CD31 PE, and CD14FITC (BD Biosciences) for the identification of endothelial, platelet, and monocytic microparticles, respectively. Isotypes (BD Biosciences) were used as controls. Microparticles were quantified per microliter of PPP injected into the cytometer, according to the standard protocol. TruCOUNT (BD Biosciences) tubes containing a known number of beads were used to quantify the number of microparticles per microliter of PPP.

Pulse wave velocity and peripheral and central blood pressure

Ambulatory blood pressure, central blood pressure, and PWV were recorded for 24h at the end of each treatment period using a Dyna-MAPA Plus (Cardios, Brazil) (2323. Jardim PC, Souza WK, Lopes RD, Brandão AA, Malachias MV, Gomes MM, et al. I RBH - First Brazilian Hypertension Registry. Arq Bras Cardiol. 2016;107(2):93-8. https://doi.org/10.5935/abc.20160120.
https://doi.org/10.5935/abc.20160120...
).

Statistical Analysis

Data are expressed as the mean (± standard deviation) or median (and interquartile range) for continuous variables, and n (%) is used for categorical variables. The Kolmogorov-Smirnov test was used to evaluate normality. Continuous variables that were normally distributed were evaluated by ANOVA-GLM. Microparticles were compared (within group and between groups) using the Friedman and Mann-Whitney (nonparametric) tests, respectively. SPSS software (v. 18.0) was used for statistical analysis. A significance level of an alpha risk less than 5% was adopted for all tests.

RESULTS

Population

Female, elderly, and overweight individuals (n=46) were more prevalent in the sample. Table 1 shows the major baseline characteristics of the study population. The pharmacological therapies were well tolerated, and no serious adverse events were recorded in either group. Both groups had similar blood pressure values at baseline and after 4 weeks of monotherapy with amlodipine (AMLO) or hydrochlorothiazide (HCTZ) (Table 2).

Table 1
Baseline characteristics of the study population receiving treatment based on amlodipine (AMLO) or hydrochlorothiazide (HCTZ).
Table 2
Brachial systolic and diastolic blood pressure levels (mmHg; median and interquartile range) as measured at the visits after treatment with hydrochlorothiazide (HCTZ, 25 mg) or amlodipine (AMLO, 5 mg).

Biochemical parameters

No changes in glucose or creatinine serum levels were observed throughout the study. After a 4-week exposure to rosuvastatin (V4), a significant and similar decrease was observed in serum levels of total cholesterol and LDL-C in both groups (p<0.0001 vs. V2, V3, and V5) (Table 3).

Table 3
Biochemical characteristics (mean ± standard error) by visit and treatment based on hydrochlorothiazide (HCTZ, 25 mg) and amlodipine (AMLO, 5 mg).

Brachial blood pressure

Brachial blood pressure was measured in both groups (AMLO and HCTZ) and showed similar values for SBP and DBP at each medical visit. However, higher values were observed at V2 in both arms. Differences within and between groups can be calculated from the data shown in Table 2.

Central blood pressure

Central blood pressure was monitored for 24h from V2 to V5 in eight patients in the AMLO and HCTZ groups. The mean values obtained were similar to those obtained at V2. In the HCTZ arm, no difference between medical visits was observed in the central SBP or DBP values throughout the study. However, lower central blood pressure was recorded beginning at V3 in the AMLO arm. PWV values did not change during the study, and similar results were recorded in both groups at each visit from V2 to V5. Central blood pressure values are shown in Table 4.

Table 4
Central blood pressure levels (mmHg; median and interquartile range) and pulse wave velocity (PWV, m/s; median and interquartile range) by visit and treatment based on hydrochlorothiazide (HCTZ, 25 mg) and amlodipine (AMLO, 5 mg).

Circulating microparticles

The AMLO-based treatment did not change plasma concentrations of monocyte-derived microparticles (MMP) or endothelium-derived microparticles (EMP) throughout the study. However, more platelet-derived microparticles (PMP) were observed at visit 5 after rosuvastatin withdrawal (Friedman test; p=0.045). Regarding the HCTZ-based treatment, no difference was observed in the amount of circulating PMP or MMP throughout the study, except for a lower number of EMP at V5 (Friedman test; p=0.001). Higher levels of MMP (visit 2) and PMP (visit 5) were observed in the AMLO group (Mann-Whitney test; p=0.011 and p=0.003, respectively). Table 5 shows the number of circulating microparticles at each visit and differences between treatment groups. Figure 2 shows the effects of amlodipine- or hydrochlorothiazide-based therapies on the circulating levels of microparticles throughout the study.

Table 5
Levels of circulating microparticles (MPs; mg/dL; median and interquartile range) by visit and treatment based on hydrochlorothiazide (HCTZ, 25 mg) or amlodipine (AMLO, 5 mg).
Figure 2
Box plots of microparticle concentrations by treatment period (visits, V) and study arm. *indicates significant differences. Monocytic (A), endothelial (B), and platelet (C) microparticle concentrations after the hydrochlorothiazide-based treatment. Monocytic (D), endothelial (E), and platelet (F) microparticle concentrations after the amlodipine-based treatment. The concentration of endothelial microparticles decreased after exposure to hydrochlorothiazide (p=0.001; Friedman test). The concentration of platelet microparticles increased after withdrawal of rosuvastatin in the amlodipine-based arm (p=0.045; Friedman test).

DISCUSSION

The study revealed that amlodipine- or hydrochlorothiazide-based antihypertensive therapies may have different effects on circulating microparticles. Furthermore, although central blood pressure values were similar during monotherapy, differences in central blood pressure parameters were noted after the addition of valsartan and/or rosuvastatin (not detected by brachial blood pressure measurements).

Circulating microparticles, also called extracellular vesicles or shedding vesicles, are released from the endothelium, platelets, and many other cells and may have physiological or pathological effects (2424. Anderson HC, Mulhall D, Garimella R. Role of extracellular membrane vesicles in the pathogenesis of various diseases, including cancer, renal diseases, atherosclerosis, and arthritis. Lab Invest. 2010;90(11):1549-57. https://doi.org/10.1038/labinvest.2010.152.
https://doi.org/10.1038/labinvest.2010.1...
). The diameters of circulating microparticles are usually in the range of 100-500 nm, and an elevated number of circulating microparticles has been reported in many pathological conditions and in subjects with uncontrolled hypertension (2525. Sansone R, Baaken M, Horn P, Schuler D, Westenfeld R, Amabile N, et al. Release of endothelial microparticles in patients with arterial hypertension, hypertensive emergencies and catheter-related injury. Atherosclerosis. 2018;273:67-74. https://doi.org/10.1016/j.atherosclerosis.2018.04.012.
https://doi.org/10.1016/j.atherosclerosi...
), acute myocardial infarction (2626. Christersson C, Thulin Å, Siegbahn A. Microparticles during long-term follow-up after acute myocardial infarction. Association to atherosclerotic burden and risk of cardiovascular events. Thromb Haemost. 2017;117(8):1571-81. https://doi.org/10.1160/TH16-11-0837.
https://doi.org/10.1160/TH16-11-0837...
), or chronic kidney disease (2727. Jalal D, Renner B, Laskowski J, Stites E, Cooper J, Valente K, et al. Endothelial Microparticles and Systemic Complement Activation in Patients With Chronic Kidney Disease. J Am Heart Assoc. 2018;7(14). pii: e007818. https://doi.org/10.1161/JAHA.117.007818.
https://doi.org/10.1161/JAHA.117.007818...
).

The first interesting finding of the study was related to MMP. During monotherapy, the four-week exposure to amlodipine was associated with higher levels of MMP than those associated with hydrochlorothiazide exposure, although in both groups, the brachial blood pressure values were higher than the recommended value range, which was expected because the majority of participants in both arms were previously treated by two antihypertensive agents. Elevated MMP values were previously reported in hypertensive subjects with type 2 diabetes, particularly among those with high SBP (2828. Nomura S, Inami N, Shouzu A, Urase F, Maeda Y. Correlation and association between plasma platelet-, monocyte- and endothelial cell-derived microparticles in hypertensive patients with type 2 diabetes mellitus. Platelets. 2009;20(6):406-14. https://doi.org/10.1080/09537100903114545.
https://doi.org/10.1080/0953710090311454...
). In addition, the higher titers of MMP in the amlodipine arm may be related to harmful effects on endothelial cells because MMP contains interleukin 1-beta (IL-1β), a cytokine that activates the inflammatory cascade related to cardiovascular disease (2929. Wang JG, Williams JC, Davis BK, Jacobson K, Doerschuk CM, Ting JP, et al. Monocytic microparticles activate endothelial cells in an IL-1β-dependent manner. Blood. 2011;118(8):2366-74. https://doi.org/10.1182/blood-2011-01-330878.
https://doi.org/10.1182/blood-2011-01-33...
,3030. Ridker PM, Everett BM, Thuren T, MacFadyen JG, Chang WH, Ballantyne C, et al. Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease. N Engl J Med. 2017;377(12):1119-31. https://doi.org/10.1056/NEJMoa1707914.
https://doi.org/10.1056/NEJMoa1707914...
). Hydrochlorothiazide decreases blood pressure but not the levels of high-sensitivity C-reactive protein, even when combined with valsartan, an angiotensin II blocker (ARB) with anti-inflammatory properties (3131. Ridker PM, Danielson E, Rifai N, Glynn RJ; Val-MARC Investigators. Valsartan, blood pressure reduction, and C-reactive protein: primary report of the Val-MARC trial. Hypertension. 2006;48(1):73-9. https://doi.org/10.1161/01.HYP.0000226046.58883.32.
https://doi.org/10.1161/01.HYP.000022604...
). Interestingly, hydrochlorothiazide seems to neutralize the benefits of renin-angiotensin system blockade in the context of experimental atherosclerosis (3232. Fonseca FA, Ihara SS, Izar MC, Silva EP, Kasinski N, Lopes IE, et al. Hydrochlorothiazide abolishes the anti-atherosclerotic effect of quinapril. Clin Exp Pharmacol Physiol. 2003;30(1):779-85. https://doi.org/10.1046/j.1440-1681.2003.03911.x.
https://doi.org/10.1046/j.1440-1681.2003...
). The amounts of circulating EMP were similar in both antihypertensive therapy arms, but lower levels were observed throughout the study in the HCTZ group. Conversely, a marginal increase in the levels of PMP was observed in the AMLO group after discontinuation of rosuvastatin, even without a change in the values of central or brachial arterial blood pressures. A similar finding was observed after discontinuation of rosuvastatin in subjects with stable coronary heart disease (1414. da Silva EF, Fonseca FA, França CN, Ferreira PR, Izar MC, Salomão R, et al. Imbalance between endothelial progenitor cells and microparticles in HIV-infected patients naive for antiretroviral therapy. AIDS. 2011;25(13):1595-601. https://doi.org/10.1097/QAD.0b013e32834980f4.
https://doi.org/10.1097/QAD.0b013e328349...
), with an increase in the amount of PMP despite the continuous use of antiplatelet therapy. Interestingly, not only blood pressure control but also lipid-lowering therapy may influence the amount of circulating PMP. Overall, the effects of amlodipine and hydrochlorothiazide on circulating microparticles seem to be affected differently by concomitant therapies.

Regarding central blood pressure, our study also showed differences between the AMLO- and HCTZ-based therapies, with lower SBP and DBP values in the AMLO-based arm. Indeed, these differences became apparent only after the addition of valsartan, suggesting a beneficial interaction between amlodipine and valsartan, an effect not observed with hydrochlorothiazide. A recent study showed that despite similar brachial blood pressure values, ARBs were more effective than atenolol for reducing central blood pressure, indicating their potential benefit for the prevention of cerebrovascular events (3333. Choi MH, Lee JS, Lee SE, Lee SJ, Yoon D, Park RW, et al. Central and cerebral haemodynamic changes after antihypertensive therapy in ischaemic stroke patients: A double-blind randomised trial. Sci Rep. 2018;8(1):1556. https://doi.org/10.1038/s41598-018-19998-4.
https://doi.org/10.1038/s41598-018-19998...
). Furthermore, a meta-analysis examining the effects of combined therapies on brachial and central blood pressures showed that betablockers and diuretics were less effective in reducing central blood pressure (3434. Manisty CH, Hughes AD. Meta-analysis of the comparative effects of different classes of antihypertensive agents on brachial and central systolic blood pressure, and augmentation index. Br J Clin Pharmacol. 2013;75(1):79-92. https://doi.org/10.1111/j.1365-2125.2012.04342.x.
https://doi.org/10.1111/j.1365-2125.2012...
). However, the combined treatment with chlorthalidone and amiloride was effective in reducing central blood pressure, suggesting possible differences in effectiveness between diuretics in terms of vascular benefits (3535. Fernandes LA, Cestario ED, Cosenso-Martin LN, Vilela-Martin JF, Yugar-Toledo JC, Fuchs FD. Chlorthalidone Plus Amiloride Reduces the Central Systolic Blood Pressure in Stage 1 Hypertension Patients. Cardiol Res. 2016;7(6):196-201. https://doi.org/10.14740/cr481w.
https://doi.org/10.14740/cr481w...
,3636. Yugar LBT, Moreno B, Moreno H, Vilela-Martin JF, Yugar-Toledo JC. Do thiazide diuretics reduce central systolic blood pressure in hypertension? J Clin Hypertens. 2018;20(1):133-5. https://doi.org/10.1111/jch.13134.
https://doi.org/10.1111/jch.13134...
).

Aortic augmentation index (AIx) has been recognized as an indicator of arterial stiffness and wave reflection. Changes in these parameters and PWV may require long-term exposure to therapies and seem to be related to the choice of antihypertensive therapy (3737. Lieber A, Millasseau S, Mahmud A, Bourhis L, Mairesse S, Protogerou A, et al. Cardiovascular prevention: relationships between arterial aging and chronic drug treatment. J Hum Hypertens. 2011;25(9):524-31. https://doi.org/10.1038/jhh.2011.28.
https://doi.org/10.1038/jhh.2011.28...
). In fact, a meta-analysis exploring the effects of antihypertensives on AIx and PWV revealed lower AIx values associated with ARBs compared to the effects of other antihypertensives. However, the authors failed to demonstrate a lesser decrease in PWV, probably due to other concomitant medications, comorbidities, age, and time of drug exposure (3838. Chen X, Huang B, Liu M, Li X. Effects of different types of antihypertensive agents on arterial stiffness: a systematic review and meta-analysis of randomized controlled trials. J Thorac Dis. 2015;7(12):2339-47.). In our study, the exposure to combined therapies was only 12 weeks, which was possibly insufficient for changes involving vascular remodeling. Differences in AIx values were not observed in either group, but the wave pressures were lower in the AMLO group after the addition of valsartan.

Limitations

Our prospective randomized study should be considered a pilot study. First, we enrolled a relatively small number of patients and examined the effects of therapies on short-term outcomes. In addition, we were unable to compare the effects of the treatments with baseline visits (V1) due to the need to homogenize treatments via the withdrawal of antihypertensives and statins. However, after 4 weeks of monotherapy with amlodipine or hydrochlorothiazide, the central and brachial blood pressures were similar, and changes in circulating microparticles and central blood pressure were observed shortly after the addition of ARB or ARB/statin. These findings may contribute to explaining some intriguing differences in cardiovascular outcomes in trials of combined therapies, such as the ACCOMPLISH study, despite similar brachial blood pressure values achieved, especially among diabetic patients (3939. Weber MA, Bakris GL, Jamerson K, Weir M, Kjeldsen SE, Devereux RB, et al. Cardiovascular events during differing hypertension therapies in patients with diabetes. J Am Coll Cardiol. 2010;56(1):77-85. https://doi.org/10.1016/j.jacc.2010.02.046.
https://doi.org/10.1016/j.jacc.2010.02.0...
).

Our observations are promising, although they are preliminary and require confirmation in larger prospective studies. Exploratory analysis of central parameters and PWV suggest that new technologies, which allow for the registry of central blood pressure, vascular compliance, and other hemodynamic data, are essential for establishing new targets beyond brachial blood pressure for the long-term treatment of patients with cardiovascular hypertensive disease.

CONCLUSIONS

The amlodipine- or hydrochlorothiazide-based antihypertensive therapy had different effects on circulating microparticles and central blood pressure parameters. Despite similar brachial arterial blood pressures and biochemical parameters throughout the study, exposure to amlodipine was associated with lower central blood pressure values after combination with valsartan, indicating a beneficial interaction. Differences in the amount of circulating microparticles were modest but were mainly influenced by rosuvastatin withdrawal in the amlodipine group.

ACKNOWLEDGMENTS

We acknowledge Cardio System SP for assistance with central blood pressure measurements and Torrent pharma for providing the drugs used in the study. This study was supported by a grant from the National Council for Scientific and Technological Development and São Paulo Research Foundation (FAPESP) INCT/FCx (2008/57685-7). NDM was the recipient of a grant from Coordination for the Improvement of Higher Education Personnel (CAPES).

References

  • 1
    Khera R, Lu Y, Lu J, Saxena A, Nasir K, Jiang L, et al. Impact of 2017 ACC/AHA guidelines on prevalence of hypertension and eligibility for antihypertensive treatment in United States and China: nationally representative cross sectional study. BMJ. 2018;362:k2357. https://doi.org/10.1136/bmj.k2357
    » https://doi.org/10.1136/bmj.k2357
  • 2
    Chistiakov DA, Orekhov AN, Bobryshev YV. Endothelial Barrier and Its Abnormalities in Cardiovascular Disease. Front Physiol. 2015;6:365. https://doi.org/10.3389/fphys.2015.00365
    » https://doi.org/10.3389/fphys.2015.00365
  • 3
    Belo VA, Guimarães DA, Castro MM. Matrix Metalloproteinase 2 as a Potential Mediator of Vascular Smooth Muscle Cell Migration and Chronic Vascular Remodeling in Hypertension. J Vasc Res. 2015;52(4):221-31. https://doi.org/10.1159/000441621
    » https://doi.org/10.1159/000441621
  • 4
    Barbaro NR, Fontana V, Modolo R, De Faria AP, Sabbatini AR, Fonseca FH, et al. Increased arterial stiffness in resistant hypertension is associated with inflammatory biomarkers. Blood Press. 2015;24(1):7-13. https://doi.org/10.3109/08037051.2014.940710
    » https://doi.org/10.3109/08037051.2014.940710
  • 5
    Brandão SA, Izar MC, Fischer SM, Santos AO, Monteiro CM, Póvoa RM, et al. Early increase in autoantibodies against human oxidized low-density lipoprotein in hypertensive patients after blood pressure control. Am J Hypertens. 2010;23(2):208-14. https://doi.org/10.1038/ajh.2009.214
    » https://doi.org/10.1038/ajh.2009.214
  • 6
    Schiffrin EL. Vascular remodeling in hypertension: mechanisms and treatment. Hypertension. 2012;59(2):367-74. https://doi.org/10.1161/HYPERTENSIONAHA.111.187021
    » https://doi.org/10.1161/HYPERTENSIONAHA.111.187021
  • 7
    Sakamoto M, Suzuki H, Hayashi T, Iuchi H, Isaka T, Sakamoto N, et al. Effects of candesartan in hypertensive patients with type 2 diabetes mellitus on inflammatory parameters and their relationship to pulse pressure. Cardiovasc Diabetol. 2012;11:118. https://doi.org/10.1186/1475-2840-11-118
    » https://doi.org/10.1186/1475-2840-11-118
  • 8
    Fonseca HA, Fonseca FA, Lins LC, Monteiro AM, Bianco HT, Brandão SA, et al. Antihypertensive therapy increases natural immunity response in hypertensive patients. Life Sci. 2015;143:124-30. https://doi.org/10.1016/j.lfs.2015.10.030
    » https://doi.org/10.1016/j.lfs.2015.10.030
  • 9
    Laurent S, Boutouyrie P. Recent advances in arterial stiffness and wave reflection in human hypertension. Hypertension. 2007;49(6):1202-6. https://doi.org/10.1161/HYPERTENSIONAHA.106.076166
    » https://doi.org/10.1161/HYPERTENSIONAHA.106.076166
  • 10
    Sarafidis PA, Loutradis C, Karpetas A, Tzanis G, Piperidou A, Koutroumpas G, et al. Ambulatory Pulse Wave Velocity Is a Stronger Predictor of Cardiovascular Events and All-Cause Mortality Than Office and Ambulatory Blood Pressure in Hemodialysis Patients. Hypertension. 2017;70(1):148-57. https://doi.org/10.1161/HYPERTENSIONAHA.117.09023
    » https://doi.org/10.1161/HYPERTENSIONAHA.117.09023
  • 11
    Omboni S, Posokhov IN, Rogoza AN. Relationships between 24-h blood pressure variability and 24-h central arterial pressure, pulse wave velocity and augmentation index in hypertensive patients. Hypertens Res. 2017;40(4):385-91. https://doi.org/10.1038/hr.2016.156
    » https://doi.org/10.1038/hr.2016.156
  • 12
    Nomura S. Microparticle and Atherothrombotic Diseases. J Atheroscler Thromb. 2016;23(1):1-9. https://doi.org/10.5551/jat.32326
    » https://doi.org/10.5551/jat.32326
  • 13
    França CN, Pinheiro LF, Izar MC, Brunialti MK, Salomão R, Bianco HT, et al. Endothelial progenitor cell mobilization and platelet microparticle release are influenced by clopidogrel plasma levels in stable coronary artery disease. Circ J. 2012;76(3):729-36. https://doi.org/10.1253/circj.CJ-11-1145
    » https://doi.org/10.1253/circj.CJ-11-1145
  • 14
    da Silva EF, Fonseca FA, França CN, Ferreira PR, Izar MC, Salomão R, et al. Imbalance between endothelial progenitor cells and microparticles in HIV-infected patients naive for antiretroviral therapy. AIDS. 2011;25(13):1595-601. https://doi.org/10.1097/QAD.0b013e32834980f4
    » https://doi.org/10.1097/QAD.0b013e32834980f4
  • 15
    Pinheiro LF, França CN, Izar MC, Barbosa SP, Bianco HT, Kasmas SH, et al. Pharmacokinetic interactions between clopidogrel and rosuvastatin: effects on vascular protection in subjects with coronary heart disease. Int J Cardiol. 2012;158(1):125-9. https://doi.org/10.1016/j.ijcard.2012.04.051
    » https://doi.org/10.1016/j.ijcard.2012.04.051
  • 16
    Jamerson K, Weber MA, Bakris GL, Dahlöf B, Pitt B, Shi V, et al. Benazepril plus amlodipine or hydrochlorothiazide for hypertension in high-risk patients. N Engl J Med. 2008;359(23):2417-28. https://doi.org/10.1056/NEJMoa0806182
    » https://doi.org/10.1056/NEJMoa0806182
  • 17
    Weber MA, Bloch M, Bakris GL, Weir MR, Zappe DH, Dahlof B, et al. Cardiovascular Outcomes According to Systolic Blood Pressure in Patients With and Without Diabetes: An ACCOMPLISH Substudy. J Clin Hypertens. 2016;18(4):299-307. https://doi.org/10.1111/jch.12816
    » https://doi.org/10.1111/jch.12816
  • 18
    Brook RD, Kaciroti N, Bakris G, Dahlöf B, Pitt B, Velazquez E, et al. Prior Medications and the Cardiovascular Benefits From Combination Angiotensin-Converting Enzyme Inhibition Plus Calcium Channel Blockade Among High-Risk Hypertensive Patients. J Am Heart Assoc. 2018;7(1). pii: e006940. https://doi.org/10.1161/JAHA.117.006940
    » https://doi.org/10.1161/JAHA.117.006940
  • 19
    Williams B, Lacy PS, Thom SM, Cruickshank K, Stanton A, Collier D, et al. Differential impact of blood pressure-lowering drugs on central aortic pressure and clinical outcomes: principal results of the Conduit Artery Function Evaluation (CAFE) study. Circulation. 2006;113(9):1213-25. https://doi.org/10.1161/CIRCULATIONAHA.105.595496
    » https://doi.org/10.1161/CIRCULATIONAHA.105.595496
  • 20
    Williams B, Lacy PS, Cruickshank JK, Collier D, Hughes AD, Stanton A, et al. Impact of statin therapy on central aortic pressures and hemodynamics: principal results of the Conduit Artery Function Evaluation-Lipid-Lowering Arm (CAFE-LLA) Study. Circulation. 2009;119(1):53-61. https://doi.org/10.1161/CIRCULATIONAHA.108.785915
    » https://doi.org/10.1161/CIRCULATIONAHA.108.785915
  • 21
    Lins LC, França CN, Fonseca FA, Barbosa SP, Matos LN, Aguirre AC, et al. Effects of ezetimibe on endothelial progenitor cells and microparticles in high-risk patients. Cell Biochem Biophys. 2014;70(1):687-96. https://doi.org/10.1007/s12013-014-9973-9
    » https://doi.org/10.1007/s12013-014-9973-9
  • 22
    Camargo LM, França CN, Izar MC, Bianco HT, Lins LS, Barbosa SP, et al. Effects of simvastatin/ezetimibe on microparticles, endothelial progenitor cells and platelet aggregation in subjects with coronary heart disease under antiplatelet therapy. Braz J Med Biol Res. 2014;47(5):432-7. https://doi.org/10.1590/1414-431X20143628
    » https://doi.org/10.1590/1414-431X20143628
  • 23
    Jardim PC, Souza WK, Lopes RD, Brandão AA, Malachias MV, Gomes MM, et al. I RBH - First Brazilian Hypertension Registry. Arq Bras Cardiol. 2016;107(2):93-8. https://doi.org/10.5935/abc.20160120
    » https://doi.org/10.5935/abc.20160120
  • 24
    Anderson HC, Mulhall D, Garimella R. Role of extracellular membrane vesicles in the pathogenesis of various diseases, including cancer, renal diseases, atherosclerosis, and arthritis. Lab Invest. 2010;90(11):1549-57. https://doi.org/10.1038/labinvest.2010.152
    » https://doi.org/10.1038/labinvest.2010.152
  • 25
    Sansone R, Baaken M, Horn P, Schuler D, Westenfeld R, Amabile N, et al. Release of endothelial microparticles in patients with arterial hypertension, hypertensive emergencies and catheter-related injury. Atherosclerosis. 2018;273:67-74. https://doi.org/10.1016/j.atherosclerosis.2018.04.012
    » https://doi.org/10.1016/j.atherosclerosis.2018.04.012
  • 26
    Christersson C, Thulin Å, Siegbahn A. Microparticles during long-term follow-up after acute myocardial infarction. Association to atherosclerotic burden and risk of cardiovascular events. Thromb Haemost. 2017;117(8):1571-81. https://doi.org/10.1160/TH16-11-0837
    » https://doi.org/10.1160/TH16-11-0837
  • 27
    Jalal D, Renner B, Laskowski J, Stites E, Cooper J, Valente K, et al. Endothelial Microparticles and Systemic Complement Activation in Patients With Chronic Kidney Disease. J Am Heart Assoc. 2018;7(14). pii: e007818. https://doi.org/10.1161/JAHA.117.007818
    » https://doi.org/10.1161/JAHA.117.007818
  • 28
    Nomura S, Inami N, Shouzu A, Urase F, Maeda Y. Correlation and association between plasma platelet-, monocyte- and endothelial cell-derived microparticles in hypertensive patients with type 2 diabetes mellitus. Platelets. 2009;20(6):406-14. https://doi.org/10.1080/09537100903114545
    » https://doi.org/10.1080/09537100903114545
  • 29
    Wang JG, Williams JC, Davis BK, Jacobson K, Doerschuk CM, Ting JP, et al. Monocytic microparticles activate endothelial cells in an IL-1β-dependent manner. Blood. 2011;118(8):2366-74. https://doi.org/10.1182/blood-2011-01-330878
    » https://doi.org/10.1182/blood-2011-01-330878
  • 30
    Ridker PM, Everett BM, Thuren T, MacFadyen JG, Chang WH, Ballantyne C, et al. Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease. N Engl J Med. 2017;377(12):1119-31. https://doi.org/10.1056/NEJMoa1707914
    » https://doi.org/10.1056/NEJMoa1707914
  • 31
    Ridker PM, Danielson E, Rifai N, Glynn RJ; Val-MARC Investigators. Valsartan, blood pressure reduction, and C-reactive protein: primary report of the Val-MARC trial. Hypertension. 2006;48(1):73-9. https://doi.org/10.1161/01.HYP.0000226046.58883.32
    » https://doi.org/10.1161/01.HYP.0000226046.58883.32
  • 32
    Fonseca FA, Ihara SS, Izar MC, Silva EP, Kasinski N, Lopes IE, et al. Hydrochlorothiazide abolishes the anti-atherosclerotic effect of quinapril. Clin Exp Pharmacol Physiol. 2003;30(1):779-85. https://doi.org/10.1046/j.1440-1681.2003.03911.x
    » https://doi.org/10.1046/j.1440-1681.2003.03911.x
  • 33
    Choi MH, Lee JS, Lee SE, Lee SJ, Yoon D, Park RW, et al. Central and cerebral haemodynamic changes after antihypertensive therapy in ischaemic stroke patients: A double-blind randomised trial. Sci Rep. 2018;8(1):1556. https://doi.org/10.1038/s41598-018-19998-4
    » https://doi.org/10.1038/s41598-018-19998-4
  • 34
    Manisty CH, Hughes AD. Meta-analysis of the comparative effects of different classes of antihypertensive agents on brachial and central systolic blood pressure, and augmentation index. Br J Clin Pharmacol. 2013;75(1):79-92. https://doi.org/10.1111/j.1365-2125.2012.04342.x
    » https://doi.org/10.1111/j.1365-2125.2012.04342.x
  • 35
    Fernandes LA, Cestario ED, Cosenso-Martin LN, Vilela-Martin JF, Yugar-Toledo JC, Fuchs FD. Chlorthalidone Plus Amiloride Reduces the Central Systolic Blood Pressure in Stage 1 Hypertension Patients. Cardiol Res. 2016;7(6):196-201. https://doi.org/10.14740/cr481w
    » https://doi.org/10.14740/cr481w
  • 36
    Yugar LBT, Moreno B, Moreno H, Vilela-Martin JF, Yugar-Toledo JC. Do thiazide diuretics reduce central systolic blood pressure in hypertension? J Clin Hypertens. 2018;20(1):133-5. https://doi.org/10.1111/jch.13134
    » https://doi.org/10.1111/jch.13134
  • 37
    Lieber A, Millasseau S, Mahmud A, Bourhis L, Mairesse S, Protogerou A, et al. Cardiovascular prevention: relationships between arterial aging and chronic drug treatment. J Hum Hypertens. 2011;25(9):524-31. https://doi.org/10.1038/jhh.2011.28
    » https://doi.org/10.1038/jhh.2011.28
  • 38
    Chen X, Huang B, Liu M, Li X. Effects of different types of antihypertensive agents on arterial stiffness: a systematic review and meta-analysis of randomized controlled trials. J Thorac Dis. 2015;7(12):2339-47.
  • 39
    Weber MA, Bakris GL, Jamerson K, Weir M, Kjeldsen SE, Devereux RB, et al. Cardiovascular events during differing hypertension therapies in patients with diabetes. J Am Coll Cardiol. 2010;56(1):77-85. https://doi.org/10.1016/j.jacc.2010.02.046
    » https://doi.org/10.1016/j.jacc.2010.02.046

Publication Dates

  • Publication in this collection
    11 Nov 2019
  • Date of issue
    2019

History

  • Received
    2 Apr 2019
  • Accepted
    18 Aug 2019
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