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The role of matrix metalloproteinases in patients with pulmonary hypertension: data from a prospective study

BMC Cardiovascular Disorders volume 21, Article number: 607 (2021) Cite this article

Abstract

Background

Despite several therapies, pulmonary hypertension (PH) is still a severe disease which can lead to right heart failure. Matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) are involved in cardiac and vascular remodeling in PH. Therefore, these biomarkers play an important role in PH patients. This study investigated whether TIMP-4, MMP-2, and N-terminal Pro-B-Type Natriuretic Peptide (NT-proBNP) plasma levels are useful in assessing the severity of PH and other clinical or echocardiographic parameters.

Methods

The concentrations of MMP-2, TIMP-4, and NT-proBNP in 68 PH patients were compared with those of 12 controls without PH. All patients underwent a physical examination, echocardiography, and were checked for the presence of cardiovascular risk factors; also, plasma concentrations of MMP-2, TIMP-4, NT-proBNP, total cholesterol, and triglycerides were determined.

Results

In PH patients, significantly elevated plasma levels of TIMP-4 (PH: 2877.99 ± 1363.78 pg/ml, control: 2028.38 ± 762.67 pg/ml, p = 0.0068) and NT-proBNP ( PH: 2405.00 pg/ml—5423.47 ± 6703.38 pg/ml, control: 411.0000 pg/ml—421.75 ± 315.37 pg/ml, p = 0.01) were detected. We also observed that MMP-2 and NT-proBNP were significantly increased in patients with higher WHO functional class (p = 0.001 for MMP-2, p = 0.008 for NT-proBNP), higher pressure in the pulmonary artery (p = 0.002 for MMP-2, p = 0.001 for NT-proBNP), and more severe tricuspid regurgitation (p = 0.001 for MMP-2, p = 0.009 for NT-proBNP). TIMP-4 was elevated in patients with more severe pressure in the pulmonary artery (p = 0.006).

Conclusions

The plasma levels of TIMP-4 and NT-proBNP are higher in PH patients. MMP-2 and NT-proBNP correlates with different PH parameters severity (WHO functional class, sPAP severity, TV regurgitation severity). Therefore, plasmatic levels of MMP-2 and NT-proBNP at this kind of patients reflect disease severity and may have a prognostic role. MMP-2 can help assess the beneficial effects of PH pharmacotherapy on tissue remodeling. These remodeling biomarkers may not have a diagnostic value but they have the potential to predict survival. Nevertheless, a greater understanding of the involvement of MMPs in PH is mandatory to further explore the prognostic role and the possibilities of therapeutic MMP inhibition in PH.

Peer Review reports

Background

Right ventricle (RV) dysfunction, defined as changes in the structure or function of the RV, is associated with poor clinical evolution regardless of the underlying disease mechanism. Right heart failure (RHF) frequently results from a gradual increase in RV afterload, caused by PH, which is commonly due to left heart failure. Chronic volume overload due to right heart diseases such as Tricuspid Valve (TV) Regugitation can also lead to RHF [1].

Pulmonary Hypertension (PH) is not a disease per se but rather a pathophysiological parameter defined by increased pressure in the pulmonary artery (with over 25 mmHg at rest) [2]. It occurs in various clinical situations and is associated with a wide range of pathophysiological changes [3]. Further, it is classified into five major groups based on their similar clinical presentation, pathological findings, hemodynamic characteristics, and treatment management [4]. PH is a severe disease in advances stages and can lead to right heart failure [5].

Several studies have found that pulmonary endothelial cell dysfunction is key to not only initiation but also progression of PH. The advanced PH stages involve the formation of intimal and plexiform lesions, endothelial apoptosis, medial and adventitial thickening of pulmonary arteries, and increased extracellular matrix (ECM) turnover, with the accumulation of ECM proteins. The ECM offers mechanical structure, elasticity, and compressibility to the vessels [6,7,8].

ECM Turnover is controlled by a balance between some proteolytic enzymes, such as MMPs and serine elastase, and their endogenous inhibitors [9]. The MMPs’ activity is regulated by tissue inhibitors of metalloproteinases (TIMPs) and membrane-type MMPs (MT-MMPs) [10]. Some studies have shown that MMPs and TIMPs are involved in cardiac and vascular remodelling in PH [2]. The expression of MMP2 and MT-1-MMP was detected in endothelial cells and proliferating myofibroblasts from the pulmonary arteries in the lungs of PH patients [11]. Other studies have shown that, in idiopathic PH, both in situ and in vitro, the pulmonary arteries reveal an imbalance between matrix metalloproteinases and TMP-1 and an increase in active MMP-2, leading to extracellular matrix accumulation. MMP-2 was increased in patients with idiopathic PH and may also be involved in other processes such as smooth muscle cell migration and proliferation [12, 13]. Tiede et al. have shown that plasma levels of MMP2 and TIMP2 in patients with PH correlate with disease severity and are prognostic factors. Although not diagnostic, elevated plasma levels are associated with an increased risk in these patients [14]. Schuman et al. discovered that patients with PH have increased MMP2 and TIMP4 plasma levels and that higher TIMP4 levels correlate with higher NYHA functional class and higher right ventricular hypertrophy [15].

This study aims is to investigate whether MMP2 and TIMP4 plasma concentrations correlate with disease severity, functional class (WHO), and ultrasound parameters and whether they play a prognostic role in patients with PH. These biomarkers could help monitor patients with PH and right heart failure and quantify different therapies’ effects.

Materials and methods

Study design

Eligible’ patients were those older than 18 years who were admitted to the Cardiology Department between January 2019 and December 2020 for dyspnea with the suspicion of PH. PH was classified according to the current guidelines and the diagnosis was set per the 2015 guidelines of the European Society of Cardiology [4]. Patients whose PH was measured echocardiographically, with systolic PAP (sPAP) over 40 mmHg, were included in the PH group of this study, and those with sPAP < 25 mmHg were included in the control group. We focused on the patients who belonged to these PH groups: PH due to left heart disease— PHLHD (we included patients who had the ejection fraction of left ventricle by more then 40%), PH due to lung diseases and/or hypoxia (PHCOPD), and chronic thromboembolic PH (CTEPH). We excluded patients with severe valvular heart disease or left heart inflow and outflow obstruction and congenital cardiomyopathies, sleep apnea, alveolar hypoventilation disorders, and developmental abnormalities of the lung. We also excluded group1 and group 5 PH patients according to the currernt guidelines [4]. We checked patients’ clinical history, conducted physical examination, and determined cardiovascular risk factors, echocardiography, plasma concentrations of MMP-2, TIMP-4, and NT-proBNP, total cholesterol, and triglycerides. Plasma was collected and centrifuged at 4000 rotation/min, for 12 min; samples were then frozen at -80 ºC prior to analysis. All patients were informed about the study protocol, after which they gave their, informed consent. The study was approved by the Ethics Committee of Emergency County Hospital Baia MARE, Romania (decision number 3085) as well as by the Ethics Committee of ‘Iuliu Hatieganu’ University of Medicine and Pharmacy (decision number 306).

Analysis of biomarkers

We determined the plasma concentration of MMP-2 (Human Elisa Kit, Thermo Fisher Scientific) and TIMP-4 (Human Elisa Kit, Thermo Fisher Scientific) per the recommendations of the manufacturer. We needed 40% dilution in order for TIMP-4 to fit the kit range.

The NT-pro-BNP levels were determined at the admission to the hospital using a Roche Cardiac Reader point-of-care instrument, which calculates the levels of NT-pro-BNP from venous blood. The results ranged between 60 and 30,000 pg/ml.

Echocardiography

We performed transthoracic 2D and colour Doppler echocardiography using the echocardiography device with a 2.5-MHz transducer on an ESAOTE MyLabClass C machine. The patients were advised to lie in the left lateral semi-recumbent or supine position during the test, per the criteria of the European Association of Echocardiography [16]. We measured right atrial and ventricular diameters, as well as sPAP, using the echo-Doppler estimation of tricuspid regurgitant wave velocity.

Statistical packages

MedCalc version 10.3.0.0 (MedCalc Software, Ostend, Belgium) and SPSS for Windows (v16.0, IBM Corporation, Armonk, NY, USA) were used for statistical analysis. Numerical data were checked for normal distribution. Correlation between plasma biomarker concentrations and functional or morphological parameters was evaluated using Pearson and Spearman coefficients. The results of categorical variables were presented as numbers, and percentages were compared using the χ2 test. Student and Mann–Whitney U tests were used for numerical data, calculating the mean, standard deviation, and median. ANOVA or Kruskal–Wallis test were used for evaluation of the groups’ differences. A value of p < 0.05 was considered significant; p < 0.001 was considered highly significant.

Results

The patients’ general characteristics are summarized in Table 1.

Table 1 Baseline characteristics of the studied population
Full size table

A total of 80 patients were enrolled, 68 with PH, 48 with PHLHD, 10 with CTEPH, 10 with PHCOPD, and 12 controls. The age of patients with PH was comparable to that of the control group (see Table 1).

We included 55 women (68.7%) and 25 men (31.2%). Regarding the metabolic profile, in the PH group, the total cholesterol level had a median of 155.03 ± 48.66 mg/dl and, in the control group, 182.01 ± 45.75 mg/dl (p = 0.065). The level of triglycerides was 109.39 ± 46.84 mg/dl in the PH group and 149.08 ± 79.95 mg/dl (p = 0.06) in the control group.

We calculated several echocardiographic parameters such as the right atrium area, left atrium area, right ventricle size, tricuspid annular plane systolic excursion (TAPSE), and systolic pulmonary arterial pressure (sPAP). We observed significant differences between the groups in terms of the right atrium area (26.91 ± 11.15 cm2 in PH group vs 19.9 ± 4.51 cm2 in the control group, p = 0.0006) and left atrium area (38.06 ± 31.42 cm2 in PH group vs 24.15 ± 5.36 cm2 in the control group, p = 0.0007). The base diameter of the right ventricle also differed between the two groups (49.31 ± 7.58 mm in PH group vs 43.00 ± 7.75 mm in the control group, p = 0.009); TAPSE was also measured and was 20.39 ± 4.36 mm in PH group vs 24.00 ± 3.71 mm in the control group with a significant p = 0.008.

Plasma TIMP-4 concentrations

Plasma TIMP-4 levels were highly increased in PH patients compared to the control group (Fig. 1a) (PH: 2877.99 ± 1363.78 pg/ml, control: 2028.38 ± 762.67 pg/ml, p = 0.0068). Plasma levels of TIMP-4 were different between patients with higher WHO classification but without a significant difference between the functional classes (Fig. 2a). On the other hand, in terms of the sPAP value, the TIMP-4 level was significantly different between groups, depending on the sPAP value (p = 0.006) (Fig. 2b). We also followed the TIMP-4 levels related to the TV regurgitation, with no significant differences detected (p = 0.18) (Fig. 2c). Plasma TIMP-4 concentration was not dependent on gender, age (Fig. 3a), or sex (global median value ± SD men 2438.98 ± 1399.26 vs women 2853.38 ± 1323.22 pg/ml, p = 0.2184).

Fig. 1
figure 1

Comparison of plasma biomarker levels. Box plots show plasma biomarker concentrations in pulmonary hypertension (PH) patients (n = 68) and controls (n = 12). a Tissue inhibitor of matrix metalloproteinase’s (TIMP-4), b Matrix metalloproteinase (MMP-2), and c N-terminal B-type natriuretic peptide (NT-proBNP)

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Fig. 2
figure 2

Correlation between disease severity and TIMP-4 concentration. We have box plots showing biomarker levels in different patient subpopulations. Patients were grouped based on disease severity determined as a WHO classification, b systolic arterial pressure (sPAP), and c the severity of TV regurgitation

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Fig. 3
figure 3

Linear regression analyses. No relationship between TIMP-4, MMP-2, NT-proBNP, and age has been found. a Tissue inhibitor of matrix metalloproteinases (TIMP-4), b Matrix metalloproteinase (MMP-2), and c N-terminal B-type natriuretic peptide (NT-proBNP)

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Plasma MMP-2 concentration

Plasma MMP-2 concentrations were increased in the PH group compared to the control (96.76 ± 14.10 ng/ml vs 92.47 ± 16.76) but without significant differences (Fig. 1b) (p = 0.34). The MMP-2 level was highly significantly increased in patients according to WHO functional class (Fig. 4a) (p = 0.001). MMP-2 concentrations were increased in patients with highly elevated sPAP (Fig. 4b) (p = 0.002) and highly significantly increased proportional to the severity of TV regurgitation (Fig. 4c) (p = 0.001). Plasma MMP-2 concentrations were not dependent on gender, age (Fig. 3b), or sex (global median value ± SD men 97.44 ± 13.76 vs women 95.52 ± 14.89 ng/ml, p = 0.5751).

Fig. 4
figure 4

Correlation between disease severity and MMP-2 concentration. We have box plots that show biomarker levels in different patient subpopulations. Patients were grouped based on disease severity determined as a WHO classification, b systolic arterial pressure (sPAP), and c the severity of TV regurgitation

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Plasma NT-proBNP concentration

We also measured the level of this marker of heart failure. Plasma levels of NT-proBNP were significantly higher in PH group compared to the control 2405.00 (5423.47 ± 6703.38) pg/ml vs 411.0000 (421.75 ± 315.37) pg/ml) (Fig. 1c) (p = 0.01). Further, the NT-proBNP level was highly significantly increased in patients according to the WHO functional class (Fig. 5a) (p = 0.008). NT-proBNP concentrations were significantly increased in patients with highly elevated sPAP (Fig. 5b) (p = 0.001) and significantly increased proportional to the severity of TV regurgitation (Fig. 5c) (p = 0.009). Plasma NT-proBNP concentrations were not dependent on gender, age (Fig. 3c), or sex (global median value ± SD men 1585 ± 7160.637 vs women 2344 ± 6139.716 ng/ml, p = 0.893).

Fig. 5
figure 5

Correlation between disease severity and NT-proBNP concentration. We have box plots showing biomarker levels in different patient subpopulations. Patients were grouped based on disease severity determined by a WHO classification, b systolic arterial pressure (sPAP), and c the severity of TV regurgitation

Full size image

We found no relationship between TIMP-4 (p = 0.47), MMP-2 (p = 0.14), and age. The NT-proBNP level tended to be age-dependent but did not reach statistical significance (p = 0.08, Fig. 3c).

Discussion

Structural remodelling of the pulmonary vessels and cardiopulmonary tissue is controlled mostly by the balance of MMP-TIMP. In the areas of vascular remodelling, increased expression and activation of MMPs were observed [17].

We could not obtain organ specificity, but several studies showed an increased level of MMP-2 in PH patients. We referred to a meta-analysis with several studies that highlighted their role in PH patients [2]. Some studies showed an increased MMP-2 activity in lung tissue in patients with idiopathic PAH (IPAH); increased levels of proMMP-2 in the urine of patients with associated PAH; higher plasma concentrations of MMP-2 in PH patients with SVR < 1440 dyn·s·cm−5; activation of MMP-2 in patients with plexogenic pulmonary arteriopathy.

There are also studies with experimental models of PH that showed an elevated MMP-2 expression in monocrotaline-induced PH in rats; increased levels of MMP-2 in lungs in monocrotaline-treated group; increased expression of MMP-2/TIMP-2 ratio in the lungs of monocrotaline PH rats; monocrotaline-induced PH lungs with increased MMP-2 and MMP-9 activity and tumor necrosis factor expression.

Previous studies conducted on rats have shown that the plasma levels of MMP-2 and TIMP-1 reflect heart failure associated with haemodynamic, functional, and morphological changes [18]. Schumann et al. found that plasma concentrations of TIMP-4 and MMP-2 are elevated in different groups of PH (IPAH, CTEPH, and APAH-associated pulmonary arterial hypertension) patients compared to the healthy control individuals [15]. In our group, the MMP-2 level was not significantly increased in the PH group compared to the control, but, when we followed the levels of MMP-2 between milder and more severe forms of PH patients, we found MMP-2 levels to be significantly different between patients assigned as WHO I/II/III/IV and related to TV regurgitation severity. The plasma levels of MMP-2 were significantly increased in patients with highly elevated sPAP. We did not find any correlation between age or gender and the plasma MMP-2 levels.

Even organ specificity it can’t be done, TIMP-4, a cardiac inhibitor of metalloproteinases, was found to be expressed mostly in the heart, and much lower expression was detected in the kidney, pancreas, and colon. Green et al. also found that TIMP-4 may function as an acute response to tissue remodelling [19]. In our group, the TIMP-4 plasma level is significantly increased in PH patients and correlates with the sPAP value. We did not observe other significant correlations between other parameters of PH severity. Schumann et al. found that TIMP-4 levels are significantly increased in PH patients (IPAH, APAH, and CTEPH) and correlate with disease severity (different parameters such as RV hypertrophy and elevated sPAP) [15]. However, we lack knowledge about the TIMP-4 level in secondary PH patients. We found that plasma TIMP-4 concentration was neither gender nor age-dependent.

The NT-proBNP effects in heart failure patients are well-known. BNP is released at the ventricular and atrial levels as a response to the stretching of myocytes and pressure overload [20, 21]. The BNP levels are elevated in patients with valvular disease [22]. Some studies show that NTproBNP plasma level is increased in mitral regurgitation [23]. In mitral regurgitation, the BNP level correlates with mortality and the onset of chronic heart failure irrespective of the severity of mitral regurgitation on echocardiogram [24]. The level of NT-proBNP correlates with symptoms and echocardiographic severity of mitral stenosis [25]. The NT-proBNP levels are elevated in patients with COPD but not as much as in chronic heart failure [26]. In our group, the NT-proBNP level is significantly increased in PH patients and highly correlates with the sPAP value. The NT-proBNP levels are significantly different between patients assigned as WHO I/II/III/IV and between TV regurgitation severity. Once again, we confirmed the role of this important biomarker widely used in left ventricular heart failure that can also be used in PH patients.

Overall, we found that the level of TIMP-4 is elevated in PH patients proportional to the sPAP value. Although the MMP-2 level in this study was not significantly higher in patients with PH, its plasma level was a marker of PH severity, considering several parameters (WHO functional class, the sPAP level, and the severity of TV regurgitation). The expression and activity of MMP-2 have been also described as increase in idiopathic PH and it could provide data about the status of tissue remodelling or for monitoring the response to treatment with different target molecules for PH treatment: e.g. administration of the bosentan (dual endothelin receptor agonist) attenuated the monocrotaline-induced up regulation of MMP-2, TIMP-1 and endothelial NO synthase expression. [12, 27]. Also, everolimus or alagebrium in combination with sildenafil demonstrate supplementary regulatory effects on MMPs 2 and 9, as well as functional responses on pulmonary artery pressure [28]. Several vasoselective dihydropyridine calcium channel blocker have been shown to improve PH via regulation of MMP/TIMPs: lercanidipine, showed improvement in PAH subjects by reducing serum MMP-9 levels with no modification of proMMP-2 activity or TIMP-1 level; amlodipine, administered to the monocrotaline induced PH rats was shown to inhibit MMP-2 activity, platelet activation, and plexogenic proliferation [29, 30]. Different studies showed that MMP-2 and TIMP-1 levels in PH patients reflect disease severity and could predict outcome. They are not being of diagnostic value, but elevated levels are significantly associated with increased risk in patients with PH [14, 31]. Therefore, monitoring plasma levels of MMP-2 and TIMP-4 could bring complementary data, which can be added to NT-proBNP utilization. The NT-proBNP role in heart failure is well-known. We know that its level increases in valvulopathies [22, 24, 25] and in the presence of lung diseases, especially COPD [29, 32, 33] and in pulmonary thromboembolism [34, 35] but also with the degree of right ventricular dysfunction [36]. In this study, we found that NT-proBNP level statistically significantly differs among different patient subpopulations: in terms of functional WHO class, sPAP level, and the severity of TV regurgitation, confirming its prognostic and severity role in this PH category and right heart failure. However, these biomarkers need reassessment before being used prognostically or guiding specific treatment.

Our study has several potential limitations. We used a relatively small and heterogeneous group of patients with different causes of PH, and no analysis was undertaken concerning PH etiology. We determined the biomarker levels only at a single time point, and they might need longitudinal evaluation and correlation with medical management. Important limitations concerning the diagnostic of PH that was made in our study by echocardiography. In the current guidelines, the right heart catheterization (RHC) is mandatory in confirming PH diagnosis for groups 1 and 4 (CTEPH) of PH patients [4]. Group 1 (especially IPAH) patients were excluded from our study as they had good anamnesis and clinical correlations. For group 2 of PH (PHLHD), the indication for RHC is IIb and, for group 3 of PH (PHCOPD), RHC is not recommended (class III) unless therapeutic consequences are to be expected. Also, there are new comparative data—echocardiography versus RHC, which showed that hemodynamic changes found in transthoracic echocardiography, like sPAP, can be estimated with acceptable precision given an adequate TRV envelope [37, 38]. These are the reasons why we considered only the echocardiographic data instead of invasive RHC.

Conclusions

We found that plasma levels of TIMP-4 and NT-proBNP are higher in PH patients. MMP-2 and NT-proBNP correlates with different PH parameters severity (WHO functional class, sPAP severity, TV regurgitation severity). Therefore, plasmatic levels of MMP-2 and NT-proBNP at this kind of patients reflect disease severity and they have a prognostic role. MMP-2 can help assess the beneficial effects of PH pharmacotherapy on tissue remodeling.

These remodeling biomarkers may not have a diagnostic value but may have the potential to predict survival. Nevertheless, a greater understanding of the involvement of MMPs in PH is mandatory to further explore the prognostic role and the possibilities of therapeutic MMP inhibition in PH.

Availability of data and materials

All data generated or analysed during this study are included in this published article. The data are available from the corresponding author on reasonable request.

Abbreviations

PH:

Pulmonary hypertension

sPAP:

Pressure in the pulmonary artery

MMPs:

Matrix metalloproteinases

TIMPs:

Tissue inhibitors of metalloproteinases

NT-proBNP:

N-terminal Pro-B-Type natriuretic peptide

TV:

Tricuspid valve

ECM:

Extracellular matrix

PHLHD:

PULMONARY hypertension due to left heart disease

CTEPH:

Chronic thromboembolic pulmonary hypertension

PHCOPD:

Pulmonary hypertension due to lung diseases and/or hypoxia

TAPSE:

Tricuspid annular plane systolic excursion

References

  1. Konstam MA, Kiernan MS, Bernstein D, Bozkurt B, Jacob M, Kapur NK, Kociol RD, Lewis EF, Mehra MR, Pagani FD, Raval AN, Ward C. Evaluation and management of right-sided heart failure: a scientific statement from the american heart association. Circulation. 2018;137:e578–622. https://doi.org/10.1161/CIR.0000000000000560.

    Article  PubMed  Google Scholar 

  2. Chelladurai P, Seeger W, Pullamsetti SS. Matrix metalloproteinases and their inhibitors in pulmonary hypertension. Eur Respir J. 2012;40:766–82. https://doi.org/10.1183/09031936.00209911.

    CAS  Article  PubMed  Google Scholar 

  3. Badesch DB, Champion HC, Gomez Sanchez MA, Hoeper MM, Loyd JE, Manes A, McGoon M, Naeije R, Olschewski H, Oudiz RJ, Torbicki A. Diagnosis and assessment of pulmonary arterial hypertension. J Am Coll Cardiol. 2009;54:S55–66. https://doi.org/10.1016/j.jacc.2009.04.011.

    Article  PubMed  Google Scholar 

  4. Galiè N, Humbert M, Vachiery JL, Gibbs S, Lang I, Torbicki A, Simonneau G, Peacock A, Vonk Noordegraaf A, Beghetti M, Ghofrani A, Gomez Sanchez MA, Hansmann G, Klepetko W, Lancellotti P, Matucci M, McDonagh T, Pierard LA, Trindade PT, Zompatori M, Hoeper M; ESC Scientific Document Group. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Heart J. 2016;37(1):67–119. https://doi.org/10.1093/eurheartj/ehv317.

  5. Simonneau G, Gatzoulis MA, Adatia I, Celermajer D, Denton C, Ghofrani A, Gomez Sanchez MA, Krishna Kumar R, Landzberg M, Machado RF, Olschewski H, Robbins IM, Souza R. Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol. 2013;62:D34-41. https://doi.org/10.1016/j.jacc.2013.10.029.

    Article  PubMed  Google Scholar 

  6. Stenmark KR, Meyrick B, Galie N, Mooi WJ, McMurtry IF. Animal models of pulmonary arterial hypertension: the hope for etiological discovery and pharmacological cure. Am J Physiol Lung Cell Mol Physiol. 2009;297:L1013–32. https://doi.org/10.1152/ajplung.00217.2009.

    CAS  Article  PubMed  Google Scholar 

  7. Jones PL, Cowan KN, Rabinovitch M. Tenascin-C, proliferation and subendothelial fibronectin in progressive pulmonary vascular disease. Am J Pathol. 1997;150:1349–60.

    CAS  PubMed  PubMed Central  Google Scholar 

  8. Meyrick B. Structure function correlates in the pulmonary vasculature during acute lung injury and chronic pulmonary hypertension. Toxicol Pathol. 1991;19:447–57. https://doi.org/10.1177/0192623391019004-113.

    CAS  Article  PubMed  Google Scholar 

  9. Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function, and biochemistry. Circ Res. 2003;92:827–39. https://doi.org/10.1161/01.RES.0000070112.80711.3D.

    CAS  Article  PubMed  Google Scholar 

  10. Nagase H, Visse R, Murphy G. Structure and function of matrix metalloproteinases and TIMPs. Cardiovasc Res. 2006;69:562–73. https://doi.org/10.1016/j.cardiores.2005.12.002.

    CAS  Article  PubMed  Google Scholar 

  11. Matsui K, Takano Y, Yu ZX, Hi JE, Stetler-Stevenson WG, Travis WD, Ferrans VJ. Immunohistochemical study of endothelin-1 and matrix metalloproteinases in plexogenic pulmonary arteriopathy. Pathol Res Pract. 2002;198:403–12. https://doi.org/10.1078/0344-0338-00273.

    CAS  Article  PubMed  Google Scholar 

  12. Lepetit H, Eddahibi S, Fadel E, Frisdal E, Munaut C, Noel A, Humbert M, Adnot S, D’Ortho MP, Lafuma C. Smooth muscle cell matrix metalloproteinases in idiopathic pulmonary arterial hypertension. Eur Respir J. 2005;25:834–42. https://doi.org/10.1183/09031936.05.00072504.

    CAS  Article  PubMed  Google Scholar 

  13. Ricou B, Nicod L, Lacraz S, Welgus HG, Suter PM, Dayer JM. Matrix metalloproteinases and TIMP in acute respiratory distress syndrome. Am J Respir Crit Care Med. 1996;154:346–52. https://doi.org/10.1164/ajrccm.154.2.8756805.

    CAS  Article  PubMed  Google Scholar 

  14. Tiede SL, Wassenberg M, Christ K, Schermuly RT, Seeger W, Grimminger F, Ghofrani HA, Gall H. Biomarkers of tissue remodeling predict survival in patients with pulmonary hypertension. Int J Cardiol. 2016;223:821–6. https://doi.org/10.1016/j.ijcard.2016.08.240.

    Article  PubMed  Google Scholar 

  15. Schumann C, Lepper PM, Frank H, Schneiderbauer R, Wibmer T, Kropf C, Stoiber KM, Rüdiger S, Kruska L, Krahn T, Kramer F. Circulating biomarkers of tissue remodelling in pulmonary hypertension. Biomarkers. 2010;15:523–32. https://doi.org/10.3109/1354750X.2010.492431.

    CAS  Article  PubMed  Google Scholar 

  16. Steeds RP, Garbi M, Cardim N, Kasprzak JD, Sade E, Nihoyannopoulos P, Popescu BA, Stefanidis A, Cosyns B, Monaghan M, Aakhus S, Edvardsen T, Flachskampf F, Galiuto L, Athanassopoulos G, Lancellotti P, Delgado V, Donal E, Galderisi M, Lombardi M, Muraru D, Haugaa K. EACVI appropriateness criteria for the use of transthoracic echocardiography in adults: a report of literature and current practice review. Eur Heart J Cardiovasc Imaging. 2017;18:1191–204. https://doi.org/10.1093/ehjci/jew333.

    Article  PubMed  Google Scholar 

  17. Patel MI, Melrose J, Ghosh P, Appleberg M. Increased synthesis of matrix metalloproteinases by aortic smooth muscle cells is implicated in the etiopathogenesis of abdominal aortic aneurysms. J Vasc Surg. 1996;24:82–92. https://doi.org/10.1016/s0741-5214(96)70148-9.

    CAS  Article  PubMed  Google Scholar 

  18. Kramer F, Sandner P, Klein M, Krahn T. Plasma concentrations of matrix metalloproteinase-2, tissue inhibitor of metalloproteinase-1 and osteopontin reflect severity of heart failure in DOCA-salt hypertensive rat. Biomarkers. 2008;13:270–81. https://doi.org/10.1080/13547500801903123.

    CAS  Article  PubMed  Google Scholar 

  19. Greene J, Wang M, Liu YE, Raymond LA, Rosen C, Shi YE. Molecular cloning and characterization of human tissue inhibitor of metalloproteinase 4. J Biol Chem. 1996;271:30375–80. https://doi.org/10.1074/jbc.271.48.30375.

    CAS  Article  PubMed  Google Scholar 

  20. Luchner A, Stevens TL, Borgeson DD, Redfield M, Wei CM, Porter JG, Burnett JC. Differential atrial and ventricular expression of myocardial BNP during evolution of heart failure. Am J Physiol. 1998;274:H1684–9. https://doi.org/10.1152/ajpheart.1998.274.5.H1684.

    CAS  Article  PubMed  Google Scholar 

  21. Luchner A, Muders F, Dietl O, Friedrich E, Blumberg F, Protter AA, Riegger GA, Elsner D. Differential expression of cardiac ANP and BNP in a rabbit model of progressive left ventricular dysfunction. Cardiovasc Res. 2001;51:601–7. https://doi.org/10.1016/s0008-6363(01)00316-9.

    CAS  Article  PubMed  Google Scholar 

  22. Eimer MJ, Ekery DL, Rigolin VH, Bonow RO, Carnethon MR, Cotts WG. Elevated B-type natriuretic peptide in asymptomatic men with chronic aortic regurgitation and preserved left ventricular systolic function. Am J Cardiol. 2004;94:676–8. https://doi.org/10.1016/j.amjcard.2004.05.043.

    CAS  Article  PubMed  Google Scholar 

  23. Burke MA, Cotts WG. Interpretation of B-type natriuretic peptide in cardiac disease and other comorbid conditions. Heart Fail Rev. 2007;12:23–36. https://doi.org/10.1007/s10741-007-9002-9.

    CAS  Article  PubMed  Google Scholar 

  24. Detaint D, Messika-Zeitoun D, Avierinos JF, Scott C, Chen H, Burnett JC, Enriquez-Sarano M. B-type natriuretic peptide in organic mitral regurgitation: determinants and impact on outcome. Circulation. 2005;111:2391–7. https://doi.org/10.1161/01.CIR.0000164269.80908.9D.

    CAS  Article  PubMed  Google Scholar 

  25. Arat-Ozkan A, Kaya A, Yigit Z, Balci H, Okçün B, Yazicioglu N, Küçükoglu S. Serum N-terminal pro-BNP levels correlate with symptoms and echocardiographic findings in patients with mitral stenosis. Echocardiography. 2005;22:473–8. https://doi.org/10.1111/j.1540-8175.2005.04085.x.

    Article  PubMed  Google Scholar 

  26. McCullough PA, Hollander JE, Nowak RM, Storrow AB, Duc P, Omland T, McCord J, Herrmann HC, Steg PG, Westheim A, Knudsen CW, Abraham WT, Lamba S, Wu AH, Perez A, Clopton P, Krishnaswamy P, Kazanegra R, Maisel AS. Uncovering heart failure in patients with a history of pulmonary disease: rationale for the early use of B-type natriuretic peptide in the emergency department. Acad Emerg Med. 2003;10:198–204. https://doi.org/10.1111/j.1553-2712.2003.tb01990.x.

    Article  PubMed  Google Scholar 

  27. Koo HS, Kim KC, Hong YM. Gene expressions of nitric oxide synthase and matrix metalloproteinase-2 in monocrotaline-induced pulmonary hypertension in rats after bosentan treatment. Korean Circ J. 2011;41:83–90. https://doi.org/10.4070/kcj.2011.41.2.83.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  28. Atlı Ö, Ilgın S, Ergun B, Burukoğlu D, Musmul A, Sırmagül B. Matrix metalloproteinases are possible targets in monocrotaline-induced pulmonary hypertension: investigation of anti-remodeling effects of alagebrium and everolimus. Anatol J Cardiol. 2017;17:8–17. https://doi.org/10.14744/AnatolJCardiol.2016.6891.

    Article  PubMed  Google Scholar 

  29. Tayebjee MH, Nadar S, Blann AD, Gareth Beevers D, MacFadyen RJ, Lip GY. Matrix metalloproteinase-9 and tissue inhibitor of metalloproteinase-1 in hypertension and their relationship to cardiovascular risk and treatment: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT). Am J Hypertens. 2004;17:764–9. https://doi.org/10.1016/j.amjhyper.2004.05.019.

    CAS  Article  PubMed  Google Scholar 

  30. Mawatari E, Hongo M, Sakai A, Terasawa F, Takahashi M, Yazaki Y, Kinoshita O, Ikeda U. Amlodipine prevents monocrotaline-induced pulmonary arterial hypertension and prolongs survival in rats independent of blood pressure lowering. Clin Exp Pharmacol Physiol. 2007;34:594–600. https://doi.org/10.1111/j.1440-1681.2007.04618.x.

    CAS  Article  PubMed  Google Scholar 

  31. Schäfer M, Ivy DD, Nguyen K, Boncella K, Frank BS, Morgan GJ, Miller-Reed K, Truong U, Colvin K, Yeager ME. Metalloproteinases and their inhibitors are associated with pulmonary arterial stiffness and ventricular function in pediatric pulmonary hypertension. Am J Physiol Heart Circ Physiol. 2021;321:H242–52. https://doi.org/10.1152/ajpheart.00750.2020.

    CAS  Article  PubMed  Google Scholar 

  32. Yap LB, Mukerjee D, Timms PM, Ashrafian H, Coghlan JG. Natriuretic peptides, respiratory disease, and the right heart. Chest. 2004;126:1330–6. https://doi.org/10.1378/chest.126.4.1330.

    CAS  Article  PubMed  Google Scholar 

  33. Leuchte HH, Baumgartner RA, Nounou ME, Vogeser M, Neurohr C, Trautnitz M, Behr J. Brain natriuretic peptide is a prognostic parameter in chronic lung disease. Am J Respir Crit Care Med. 2006;173:744–50. https://doi.org/10.1164/rccm.200510-1545OC.

    CAS  Article  PubMed  Google Scholar 

  34. Pieralli F, Olivotto I, Vanni S, Conti A, Camaiti A, Targioni G, Grifoni S, Berni G. Usefulness of bedside testing for brain natriuretic peptide to identify right ventricular dysfunction and outcome in normotensive patients with acute pulmonary embolism. Am J Cardiol. 2006;97:1386–90. https://doi.org/10.1016/j.amjcard.2005.11.075.

    CAS  Article  PubMed  Google Scholar 

  35. Krüger S, Graf J, Merx MW, Koch KC, Kunz D, Hanrath P, Janssens U. Brain natriuretic peptide predicts right heart failure in patients with acute pulmonary embolism. Am Heart J. 2004;147:60–5. https://doi.org/10.1016/s0002-8703(03)00528-3.

    Article  PubMed  Google Scholar 

  36. Nagaya N, Nishikimi T, Okano Y, Uematsu M, Satoh T, Kyotani S, Kuribayashi S, Hamada S, Kakishita M, Nakanishi N, Takamiya M, Kunieda T, Matsuo H, Kangawa K. Plasma brain natriuretic peptide levels increase in proportion to the extent of right ventricular dysfunction in pulmonary hypertension. J Am Coll Cardiol. 1998;31:202–8. https://doi.org/10.1016/s0735-1097(97)00452-x.

    CAS  Article  PubMed  Google Scholar 

  37. He J, Fang W, Lv B, He JG, Xiong CM, Liu ZH, He ZX. Diagnosis of chronic thromboembolic pulmonary hypertension: comparison of ventilation/perfusion scanning and multidetector computed tomography pulmonary angiography with pulmonary angiography. Nucl Med Commun. 2012;33:459–63. https://doi.org/10.1097/MNM.0b013e32835085d9.

    Article  PubMed  Google Scholar 

  38. Brugger N, Lichtblau M, Maeder MT, Müller H, Pellaton C, Yerly P. Two-dimensional transthoracic echocardiography at rest for the diagnosis, screening and management of pulmonary hypertension. Swiss Med Wkly. 2021;151: w20486. https://doi.org/10.4414/smw.2021.20486.

    Article  PubMed  Google Scholar 

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Acknowledgements

Not applicable.

Funding

This research was funded by “Iuliu Haţieganu University of Medicine and Pharmacy, Dept. of Cardiology, Cluj-Napoca, Romania”, Grant Number 1300/33/13.01.2017. It was a Grant offered by the University to all doctoral students. In my case, included the settlement of the kits for TMP-4 and MMP-2.

Author information

Authors and Affiliations

  1. Iuliu Haţieganu” University of Medicine and Pharmacy, 400012, Cluj-Napoca, Romania

    Adriana Marc & Dana Pop

  2. Department of Cardiology, Emergency County Hospital Baia Mare, 430031, Baia Mare, Romania

    Adriana Marc & Calin Pop

  3. Faculty of Medicine Arad, West Vasile Goldis University, 310025, Arad, Romania

    Calin Pop

  4. Clinical Rehabilitaton Hospital, Cardiology, 400437, Cluj-Napoca, Romania

    Dana Pop

  5. Internal Medicine Department, 4Th Medical Clinic “Iuliu Haţieganu” University of Medicine and Pharmacy, 400012, Cluj-Napoca, Romania

    Adela-Viviana Sitar-Taut

  6. Research Center for Functional Genomics, Biomedicine and Translational Medicine, Iuliu – Hatieganu University of Medicine and Pharmacy, 400337, Cluj-Napoca, Romania

    Liviuta Budisan & Ioana Berindan-Neagoe

Authors
  1. Adriana Marc
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  2. Calin Pop
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  3. Adela-Viviana Sitar-Taut
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  4. Liviuta Budisan
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  5. Ioana Berindan-Neagoe
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  6. Dana Pop
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Contributions

AM contributed to the conceptualization, investigation, methodology, writing the article; LB, IN performed biomarkers analysis formal analysis; A.V.S.T performed the writing, review and editing; D.P, C.P. contributed to validation, visualization, supervision of the article. All authors have read and agreed to the published version of the manuscript and agree to be accountable for all aspects of the research in ensuring that the accuracy or integrity of any part of the work are appropriately investigated and resolved. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Calin Pop.

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Ethics approval and consent to participate

This study was approved by the Ethic Committee of Emergency County Hospital Baia MARE, Romania (decision number 3085/28.11.2018) and also by the Ethic Committee of ‘Iuliu Hatieganu’ University of Medicine and Pharmacy (decision number 306/28.09.2020). Informed consent was obtained from all subjects involved in the study. This study was conducted with observance of the Declaration of Helsinki and our National Ethical Guidelines.

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The authors declare that they have no competing interests.

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Marc, A., Pop, C., Sitar-Taut, AV. et al. The role of matrix metalloproteinases in patients with pulmonary hypertension: data from a prospective study. BMC Cardiovasc Disord 21, 607 (2021). https://doi.org/10.1186/s12872-021-02424-5

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  • DOI: https://doi.org/10.1186/s12872-021-02424-5

Keywords

  • Biomarkers
  • Pulmonary hypertension
  • Right heart failure
  • Matrix metalloproteinase 2
  • Tissue inhibitor of matrix metalloproteinase 4
  • N-terminal pro-B-Type Natriuretic peptide

BMC Cardiovascular Disorders

ISSN: 1471-2261

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