• Users Online: 92
  • Print this page
  • Email this page

 
Table of Contents
ORIGINAL ARTICLE
Year : 2020  |  Volume : 9  |  Issue : 2  |  Page : 61-66

Relationship between serum CRP level and left ventricular function in patients with acute ST-elevation myocardial infarction: A cross-sectional study


1 Department of Cardiology, Shohada Hospital, Urmia University of Medical Science, Urmia, Iran
2 Cardiology Resident, Shohada Hospital, Urmia University of Medical Science, Urmia, Iran

Date of Submission16-Nov-2019
Date of Decision16-Mar-2020
Date of Acceptance19-Mar-2020
Date of Web Publication28-Mar-2020

Correspondence Address:
Roghaiyeh Afsargharehbagh
Department of Cardiology, Shohada Hospital, Urmia University of Medical Science, Urmia
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2221-6189.281319

Rights and Permissions
  Abstract 


Objective: To investigate the relationship between serum C-reactive protein (CRP) level and left ventricular function in patients with acute ST-elevation myocardial infarction.
Methods: This study is a descriptive-analytic study and was conducted on patients with ST-elevation myocardial infarction, who were admitted to the Urmia Hospital in Seyed Alshohada Hospital, and underwent primary percutaneous coronary intervention from October to March 2018. Demographic, angiographic, echocardiographic data were evaluated based on the patients’ records. All patients were evaluated for 90 min and CRP levels were measured during the first 6 h after the primary percutaneous coronary intervention.
Results: A total of 114 patients were studied, among whom 71.9% (82 patients) were male, and their mean age was (57.86±9.57) years old. The mean BMI was (26.1±3.8) kg/m2. Altogether 38.6% (44 patients) had a history of smoking, 17.5% (20 patients) of diabetes, 38.6% (44 patients) of hypertension, 5.3% (6 patients) of hyperlipidemia and 7.0% (8 patient) of coronary artery disease. The results showed a significantly negative correlation between ejection fraction and CRP, left atrial volume and CRP (P<0.05), and a significantly positive correlation between the global longitudinal strain level and CRP. The CRP level was significantly different at various diastolic grades (P=0.001). The level of CRP in patients with grade 2 diastolic dysfunction was higher than grade 1 diastolic dysfunction, while the level of CRP in diastolic grade 1 diastolic dysfunction was higher than the normal function.
Conclusions: High CRP levels are associated with ejection fraction, global longitudinal strain loss and left atrial volume.

Keywords: Coronary artery disease; ST elevation myocardial infarction; C-reactive protein; Myocardial infarction


How to cite this article:
Shariati A, Afsargharehbagh R, Isfandyari P. Relationship between serum CRP level and left ventricular function in patients with acute ST-elevation myocardial infarction: A cross-sectional study. J Acute Dis 2020;9:61-6

How to cite this URL:
Shariati A, Afsargharehbagh R, Isfandyari P. Relationship between serum CRP level and left ventricular function in patients with acute ST-elevation myocardial infarction: A cross-sectional study. J Acute Dis [serial online] 2020 [cited 2022 May 22];9:61-6. Available from: https://www.jadweb.org/text.asp?2020/9/2/61/281319




  1. Introduction Top


Today, cardiovascular disease (CVD) including acute myocardial infarction is the most common cause of death in the world [1]. According to the latest global study, more than 422 million people suffer from CVD, and the disease kills over 17 million deaths annually [2]. Diagnosis of acute myocardial infarction is based on the clinical symptoms, electrocardiographic changes, and elevated cardiac enzymes [3]. There are two types of myocardial infarction: ST-segment elevation myocardial infarction (STEMI) and non- ST elevation myocardial infarction (NSTEMI), and each one has a specific treatment strategy. Two treatment strategies are effective for STEMI. i.e., angiography and thrombolytic therapy [4]. According to the recent guidelines, primary percutaneous coronary intervention (PPCI) is the gold standard for the treatment of STEMI patients [3]. PPCI refers to PCI in the case of STEMI when patients do not receive fibrinolytic therapy within 12 h of symptom onset. Compared to fibrinolytic, PPCI is associated with high openness of the involved vein, reduction of ischemia recurrence, and reduction of complications such as re-infarction, death, intracerebral hemorrhage, etc. For patients who need PPCI, the pre-procedure measurement of C-reactive protein (CRP) can help to identify high- risk patients [5]. Identifying the risk factors for coronary heart disease such as hypertension, diabetes, insulin resistance, dyslipidemia, positive family history, smoking, fibrinogen restriction, lipoprotein, and inflammatory markers is important for managing this disease [6]. In recent decades, it is strongly advocated to regard atherosclerosis as an inflammatory disease, therefore, serum levels of inflammatory markers (including CRP) have been taken into consideration to determine the risk of cardiovascular cases [7],[8].

Numerous studies have shown that CRP markers are elevated in myocardial infarction patients and are associated with the severity and complications (such as heart failure or remodeling)[9],[10],[11]. CRP is an accelerating or exacerbating factor of acute coronary diseases such as myocardial infarction, and the underlying mechanisms are not exactly known. Some researchers have shown that CRP is likely to trigger inflammation in atheromatous plaque or cause rupture or bleeding in the plaque by activating the complement, and it is still unknown whether there is a direct relationship between CRP level and the severity of the injury [12],[13].

Some studies have suggested CRP as a predictor of vascular events such as stroke, myocardial infarction, and peripheral vascular obstruction among healthy people, the elderly people and smokers [14],[15]. In patients with acute coronary artery disease or post-myocardial infarction, elevated CRP levels may indicate re- instability. This marker may even serve as a sensitive predictor for future cardiovascular events in healthy individuals [16].

Prolonged inflammation in patients with STEMI can also cause many complications, including loss of myocytes, reduction in left ventricular systolic function, dilation of heart cavities, loss and even rupture of ventricular wall integrity. As noted by Zacho et al., activation of the innate immune system by acute-phase proteins such as CRP in patients with coronary artery disease can lead to cellular damage, activation of complement and the aforementioned injuries [17]. One study has shown that it also causes cardiac dysfunction in addition to increasing infarct size [18].

To date, many studies explored the impact of elevated CRP levels on patients undergoing PCI selectively (stable or unstable angina) or following NSTEMI [19]. However, only a few addressed the predicting role of CRP in patients with PPCI following STEMI. On the other hand, the presence of echocardiographic criteria, especially diastolic or systolic dysfunction of the left ventricular following myocardial infarction and elevated left ventricular filling pressure can lead to adverse clinical complications and decreased survival rate [20],[21]. The present study investigated the CRP level at the baseline and left ventricular dysfunction in patients with STEMI who underwent successful PPCI. It was assumed that patients with high CRP levels were more likely to suffer from ventricular dysfunction. The aim of the present study was to investigate the relationship between serum CRP level and left ventricular function in patients with STEMI and to investigate the role of inflammatory factors in STEMI patients undergoing PPCI.


  2. Materials and Methods Top


2.1. Design

This cross-sectional study was performed on 114 patients with STEMI who underwent PPCI at Seyyed al-Shohada Hospital, Urmia from October to March 2018. The sample size was estimated 100 individuals based on previous studies, taking into account a lower error rate of less than 0.05, test power of 90%, 95% confidence interval, total patients (n=3 000), STEMI prevalence of 2.5% in Iran. To increase data reliability, 114 individuals were included in the study.

2.2. Participants

All patients who met the inclusion criteria were included in the study using a convenience sampling method. Data were collected using checklists, including demographic, angiographic and echocardiographic data. STEMI diagnosis was made based on a typical history of chest pain, electrocardiographic changes (greater than 1 mm increase in the two adjacent leads) and elevated levels of cardiac biomarkers [22]. PPCI was carried out in all patients within 90 min and CRP levels were measured within the first 6 h [23].

The inclusion critera of this study included (1) Patients with STEMI and referred to the center; (2) Patients over 75 years of age (to avoid the effect of age-related diastolic disorder); (3) Patients with a history of previous myocardial infarction were included. The exclusion criteria were as follows: (1) Having history of STEMI; (2) Patients who were on cardiogenic shock at baseline (pressure less than 90 mmHg that does not respond to inotrope or fluid therapy); (3) Patients with creatinine level ≥1.2 mg/dL; (4) Liver problems with higher than 2-fold increase in liver enzymes; (5) Patients with advanced cancer; (6) Patients with a previous history of liver failure, rheumatologic diseases or infectious diseases.

2.3. Indexes measurement

CRP levels were measured using Bayer wide-range kits [24]. Echocardiography was also performed by echocardiographic devices, including Medison, Vidid 6, Siemens, and Vivid 3. All echocardiographic criteria mentioned in the table of variables [ejection fraction, mitral cellulitis, E/E' pulmonary hypertension, isovolumic relaxation time, global longitudinal strain, left ventricle (LV) volume, and left atrial (LA) volume] were measured. Finally, based on the CRP level all patients were divided into three groups: <2.6 mg/L, 2.6-7.9 mg/L, and >7.9 mg/L [25]. The data were recorded and CRP levels were checked for each patient individually.

2.4. Ethical consideration

This study was approved by the Ethics Committee of Urmia University of Medical Sciences and the Ethics Committee of the place where the research was conducted (Ethic code: IR.UMSU. REC.1397.370). The Strengthening the Reporting of Observational studies in Epidemiology (STROBE) checklist was used to report the study. Oral and written consent was obtained from all participants.

2.5. Data analysis

The data were analyzed using SPSS ver. 22. Measurement data were expressed as mean±SD, while categorical data were expressed as percentages. Categorical (qualitative) variables were analyzed using Chi-square test, and measurement data by one-way ANOVA followed by Duncan’s post hoc test. The significance level of the tests was set at α=0.05.


  3. Results Top


The present study was performed on 114 patients with STEMI. The mean age of participants was (57.86±9.57) years (range: 36-74 years). Most participants were male (71.9%) and the BMI of males was 26.14 and it was 27.1 for females. A total of 38.6%, 17.5%, 38.6%, 5.3%, 3.5%, 1.8% and 7.3% of patients had history of hypertension, diabetes, smoking, dyslipidemia, asthma, COPD, and CVD, respectively. Most participants had no diastolic disorder. The location of infarction in most participants was the anterior part of the heart (56.1%). The most involved artery was left anterior descending artery (LAD) (56.1%). The mean CRP level was (14.75±15.79) mg/L. The mean ejection fraction (EF) level was (39.35±8.96)%. Velocity of mitral valve level was 0.85±0.08. E/e level was 0.09±0.02. Pulmonary hypertension was (22.8±4.3) mm Hg. Isovolumic relaxation time (IVRT) ratio was (101.63±16.28) msec. LV volume level was (93.88±23.96) mL. LA level was (44.67±12.03) mL, and global longitudinal strain level was -12.85±3.23.

The results of the Pearson test showed a significant inverse relationship between EF and CRP level (R2=0.082, P<0.05) [Figure 1]; A significant positive relationship between GLS and CRP level (R2=0.106, P<0.05), so that any decrease in the GLS level (indicating a decrease in left ventricular function) leads to an decrease in CRP level [Figure 2]; A significant inverse relationship between LA volume and CRP (R2=0.011, P<0.05) [Figure 3]. The CRP level was significantly different at various diastolic grades (P=0.001). CRP level in the diastolic grade 2 (7.9 mg/L) is higher than the diastolic grade 1 (2.6-7.9 mg/L) and the normal (2.6 mg/L).
Figure 1: Relationship between cardiac pumping and C-reactive protein levels.

Click here to view
Figure 2: Relationship between left ventricular total dilation values and C-reactive protein levels.

Click here to view
Figure 3: Relationship between cardiac pumping and C-reactive protein levels.

Click here to view



  4. Discussion Top


CRP is an acute-phase protein that is produced primarily in the liver. For many years, CRP has been used as a marker for systemic inflammation. However, recent findings suggest CRP should serve more than an inflammatory marker [3]. CRP may trigger complement activation and poor cardiac remodeling in the cases of ischemic injury. This protein has been found on cells in following myocardial infarction [26]. Many animal studies have shown that CRP significantly increases the extent of myocardial infarction- induced injury in the ischemic region [18],[23],[27]. Most patients in the present study were male, with an average age of 58 years, which is similar to some studies [22],[25],[28],[29]. It may indicate that men over the age of 60 are at higher risk of coronary heart diseases so that we should pay more attention to this group of people.

The history of smoking, diabetes, hypertension, hyperlipidemia, and family history of coronary heart diseases are the most effective risk factors in most studies [28],[29],[30]. With regard to BMI, Jeong et al. reported that patients’ BMI was 24 kg/m2, and there was no significant relationship between CRP and BMI [24]. Further research is needed in this regard.

The most common location of infarction was anterior and posterior regions. LAD and right coronary artery (RCA) were also the commonly involved arteries. Stumpf et al. also proved that the common involved artery was LAD followed by RCA and left circumflex artery (LCX). The most common location of the infarction was the anterior and then posterior regions [28], while it is also reported as the anterior region of the heart in another study [25]. The high prevalence of anterior infarction and LAD involvement indicates the importance of this cardiac region.

The results of the present study showed no significant relationship between mitral inflow velocity, E/E ratio, pulmonary hypertension, IVRT, left ventricular volume or LA volume with CRP levels. In contrast, Shacham et al. showed that patients with higher CRP levels had a higher septal E/e ratio. Mean mitral E- and e/e wave velocity, and pulmonary arterial pressure were high, but the study also showed that there was no significant difference in atrial and left ventricular volume [25], which is consistent with our study. The results of Karpi ski et al. study showed a significant inverse relationship between CRP, EF, IVRT, and DT levels and a significant positive association between CRP and E/A and E/Ep [3l]. In contrast, the results of a study by Arruda-Olson et al. are consistent with our study. They showed no relationship between mitral flow velocity, pulmonary hypertension, and LA volume with CRP levels [32]. Different results may be achieved depending on the type of patients selected (patients with reduced or retained EF [23]). However, these inconsistencies indicate the need for extensive matched studies.

Our results demonstrated that the CRP level was significantly different in various diastolic grades. The CRP level was higher in grade 2 diastolic disorder than grade 1 diastolic disorder, and grade 1 diastolic disorder higher than the normal diastolic function. One study showed that patients with higher CRP levels presented more advanced diastolic dysfunction (higher ventricular filling pressure)[25]. Karpmski et al. also reported that elevated CRP levels were associated with more advanced diastolic dysfunction [3l]. In myocardial infarction patients, the extent of left ventricular relaxation and thus the extent of ventricular filling in the diastolic phase (even mitral valve function) may be impaired due to impaired movement of some walls under ischemia, elevated left ventricular filling pressure, and some physiological changes [25],[32]. Therefore, the result of diastolic dysfunction in the present study is justified, and increased CRP levels led to an increase in diastolic dysfunction. There was a significant inverse relationship between EF and CRP level, and a significant association between GLS with CRP level. It showed left ventricular function in different ways and emphasized that CRP levels increase with a decrease in the left ventricular function in the case of myocardial infarction. Many studies have also emphasized the above finding, but have not investigated the extent of left ventricular dilatation [22],[24],[29]. However, one study revealed no significant relationship between EF and CRP [23]. Most studies confirmed the association of high CRP levels with low EF, and this inconsistency needs further investigation. In addition, CRP levels predict the progression of heart failure, mortality rates, and rates of major adverse cardiovascular events, which can predict long-term mortality as an independent factor. This marker also demonstrates the potential of biomarkers and shows the severity and number of vessels involved in patients with myocardial infarction [3],[25],[28],[30],[33],[34].

The results of the present study showed that high CRP levels are associated with greater EF and GLS decline as well as higher grades of diastolic disorder, but are not related with other echocardiographic parameters such as mitral flow velocity, pulmonary artery pressure, IVRT, LA volume, and LV volume. However, considering the limited number of patients and the type of study, as well as the critical role of CRP in patients with myocardial infarction, further research is needed.

Conflict of interest statement

The authors report no conflict of interest.

Authors’ contribution

A.S. and R.A: concept and design, P.I. performed the data collection; A.S. analyzed the data; A.S, P.I and R.A. wrote the paper.



 
  References Top

1.
WHO. The top 10 causes of death. [Online] Available from: https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death [Accessed on Augest 1st 2019].  Back to cited text no. 1
    
2.
Roth GA, Johnson C, Abajobir A, Abd-Allah F, Abera SF, Abyu G, et al. Global, regional, and national burden of cardiovascular diseases for 10 causes, 1990 to 2015. J Am College Cardiol 2017; 70 (1): 1-25.  Back to cited text no. 2
    
3.
O’Gara PT, Kushner FG, Ascheim DD, Casey DE, Chung MK, De Lemos JA, et al. 2013 ACCF/AHA guideline for the management of ST-elevation myocardial infarction: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Am College Cardiol 2013; 61 (4): 485-510.  Back to cited text no. 3
    
4.
Zipes D, Libby P, Bonow R. The cardiomyopathies. Braunwald’s heart disease. 7th ed. Philadelphia: Elsevier saunders; 2005.  Back to cited text no. 4
    
5.
Levine GN, Bates ER, Blankenship JC, Bailey SR, Bittl JA, Cercek B, et al. 2015 ACC/AHA/SCAI focused update on primary percutaneous coronary intervention for patients with ST-elevation myocardial infarction: an update of the 2011 ACCF/AHA/SCAI guideline for percutaneous coronary intervention and the 2013 ACCF/AHA guideline for the management of ST-elevation myocardial infarction. J Am College Cardiol 2016; 67 (10): 1235-1250.  Back to cited text no. 5
    
6.
Mozaffarian D, Benjamin EJ, Go AS, Arnett DK, Blaha MJ, Cushman M, et al. Heart disease and stroke statistics-2016 update a report from the Am Heart Assoc Circulat 2016; 133 (4): e38-e48.  Back to cited text no. 6
    
7.
Pearson TA, Mensah GA, Alexander RW, Anderson JL, Cannon III RO, Criqui M, et al. Markers of inflammation and cardiovascular disease: application to clinical and public health practice: a statement for healthcare professionals from the Centers for Disease Control and Prevention and the American Heart Association. Circulation 2003; 107 (3): 499-511.  Back to cited text no. 7
    
8.
Blake G, Rifai N, Buring J, Ridker P. Blood pressure, C-reactive protein, and risk of future cardiovascular events. Circulation 2003; 108 (24): 29932999.  Back to cited text no. 8
    
9.
Maron D. Dyslipidemia, other risk factors and the prevention of CHD. Hurst Heart 2001; 1131-1160.  Back to cited text no. 9
    
10.
Ridker P, Hennekens C, Buring J, Rifai N. C-reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. New Engl J Med 2000; 342 (12): 836-843.  Back to cited text no. 10
    
11.
Parrinello CM, Lutsey PL, Ballantyne CM, Folsom AR, Pankow JS, Selvin E. Six-year change in high-sensitivity C-reactive protein and risk of diabetes, cardiovascular disease, and mortality. Am Heart J 2015 ; 170 (2): 380-389.  Back to cited text no. 11
    
12.
Chung MK, Martin DO, Sprecher D, Wazni O, Kanderian A, Carnes CA, et al. C-reactive protein elevation in patients with atrial arrhythmias: inflammatory mechanisms and persistence of atrial fibrillation. Circulation 2001; 104 (24): 2886-2891.  Back to cited text no. 12
    
13.
Libby P, Ridker PM. Inflammation and atherosclerosis: role of C-reactive protein in risk assessment. Am J Med 2004; 116 (6): 9-16.  Back to cited text no. 13
    
14.
Ridker PM, Everett BM, Thuren T, MacFadyen JG, Chang WH, Ballantyne C, et al. Antiinflammatory therapy with canakinumab for atherosclerotic disease. New Engl J Med 2017; 377 (12): 1119-1131.  Back to cited text no. 14
    
15.
Khera AV, Emdin CA, Drake I, Natarajan P, Bick AG, Cook NR, et al. Genetic risk, adherence to a healthy lifestyle, and coronary disease. New Engl J Med 2016; 375 (24): 2349-2358.  Back to cited text no. 15
    
16.
Group MR, Kuller LH, Tracy RP, Shaten J, Meilahn EN. Relation of C-reactive protein and coronary heart disease in the MRFIT nested case- control study. Am J Epidemiol 1996; 144 (6): 537-547.  Back to cited text no. 16
    
17.
Zacho J, Tybjrg-Hansen A, Jensen JS, Grande P, Sillesen H, Nordestgaard BG. Genetically elevated C-reactive protein and ischemic vascular disease. New Engl J Med 2008; 359 (18):1897-1908.  Back to cited text no. 17
    
18.
Pepys MB, Hirschfield GM, Tennent GA, Gallimore JR, Kahan MC, Bellotti V, et al. Targeting C-reactive protein for the treatment of cardiovascular disease. Nature 2006; 440 (7088): 1217.  Back to cited text no. 18
    
19.
Ndrepepa G, Braun S, Tada T, Guerra E, Schunkert H, Laugwitz KL, et al. Comparative prognostic value of low-density lipoprotein cholesterol and C-reactive protein in patients with stable coronary artery disease treated with percutaneous coronary intervention and chronic statin therapy. Cardiovasc Revascularizat Med 2014; 15 (3): 131-136.  Back to cited text no. 19
    
20.
M0ller JE, S0ndergaard E, Seward JB, Appleton CP, Egstrup K. Ratio of left ventricular peak E-wave velocity to flow propagation velocity assessed by color M-mode Doppler echocardiography in first myocardial infarction: prognostic and clinical implications. J Am College Cardiol 2000; 35 (2): 363-370.  Back to cited text no. 20
    
21.
M0ller JE, S0ndergaard E, Poulsen SH, Egstrup K. Pseudonormal and restrictive filling patterns predict left ventricular dilation and cardiac death after a first myocardial infarction: a serial color M-mode Doppler echocardiography study. J Am College Cardiol 2000; 36 (6): 1841-1846.  Back to cited text no. 21
    
22.
Liu D, Qi X, Li Q, Jia W, Wei L, Huang A, et al. Increased complements and high-sensitivity C-reactive protein predict heart failure in acute myocardial infarction. Biomed Report 2016; 5 (6): 761-765.  Back to cited text no. 22
    
23.
Barrett TD, Hennan JK, Marks RM, Lucchesi BR. C-reactive-protein- associated increase in myocardial infarct size after ischemia/reperfusion. J Pharmacol Experiment Therapeut 2002; 303 (3): 1007-1013.  Back to cited text no. 23
    
24.
Jeong HC, Ahn Y, Park K-H, Sim DS, Hong YJ, Kim JH, et al. Effect of statin treatment in patients with acute myocardial infarction and left ventricular systolic dysfunction according to the level of high-sensitivity C-reactive protein. Int Heart J 2014; 55 (2): 106-112.  Back to cited text no. 24
    
25.
Shacham Y, Topilsky Y, Leshem-Rubinow E, Arbel Y, Assa EB, Keren G, et al. Association between C-reactive protein level and echocardiography assessed left ventricular function in first ST-segment elevation myocardial infarction patients who underwent primary coronary intervention. J Cardiol 2014; 63 (6): 402-408.  Back to cited text no. 25
    
26.
Lagrand WK, Niessen HW, Wolbink GJ, Jaspars LH, Visser CA, Verheugt FW, et al. C-reactive protein colocalizes with complement in human hearts during acute myocardial infarction. Circulation 1997; 95 (1): 97-103.  Back to cited text no. 26
    
27.
Griselli M, Herbert J, Hutchinson W, Taylor K, Sohail M, Krausz T, et al. C-reactive protein and complement are important mediators of tissue damage in acute myocardial infarction. J Experiment Med 1999; 190 (12): 1733-1740.  Back to cited text no. 27
    
28.
Stumpf C, Sheriff A, Zimmermann S, Schaefauer L, Schlundt C, Raaz D, et al. C-reactive protein levels predict systolic heart failure and outcome in patients with first ST-elevation myocardial infarction treated with coronary angioplasty. Arch Med Sci 2017; 13 (5): 1086.  Back to cited text no. 28
    
29.
Kim KH, Kim W, Kang WY, Hwang SH, Cho SC, Kim W, et al. The impact of ischemic time on the predictive value of high-sensitivity C-reactive protein in ST-segment elevation myocardial infarction patients treated by primary percutaneous coronary intervention. Korean Circ J 2013; 43 (10): 664-673.  Back to cited text no. 29
    
30.
Mincu R-I, Janosi RA, Vinereanu D, Rassaf T, Totzeck M. Preprocedural C-reactive protein predicts outcomes after primary percutaneous coronary intervention in patients with ST-elevation myocardial infarction a systematic meta-analysis. Sci Rep 2017; 7: 41530.  Back to cited text no. 30
    
31.
Karpinski L, Plaksej R, Kosmala W, Witkowska M. Serum levels of interleukin-6, interleukin-10 and C-reactive protein in relation to left ventricular function in patients with myocardial infarction treated with primary angioplasty. Kardiol Pol 2008; 66 (12): 1279-1285.  Back to cited text no. 31
    
32.
Arruda-Olson AM, Enriquez-Sarano M, Bursi F, Weston SA, Jaffe AS, Killian JM, et al. Left ventricular function and C-reactive protein levels in acute myocardial infarction. Am J Cardiol 2010; 105 (7): 917-921.  Back to cited text no. 32
    
33.
Udeanu M, Guizzardi G, Di Pasquale G, Marchetti A, Romani F, Dalmastri V, et al. Relationship between coronary artery disease and C-reactive protein levels in NSTEMI patients with renal dysfunction: a retrospective study. BMC Nephrol 2014; 15 (1): 152.  Back to cited text no. 33
    
34.
Arbel Y, Eros Y, Rogowski O, Berliner S, Shapira I, Keren G, et al. Comparison of values of wide-range C-reactive protein to high-sensitivity C-reactive protein in patients undergoing coronary angiography. Am J Cardiol 2007; 99 (11): 1504-1506.  Back to cited text no. 34
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

  2. Materials and...
  In this article
Abstract
1. Introduction
3. Results
4. Discussion
References
Article Figures

 Article Access Statistics
    Viewed1344    
    Printed109    
    Emailed0    
    PDF Downloaded163    
    Comments [Add]    

Recommend this journal