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ORIGINAL ARTICLE
Year : 2012  |  Volume : 29  |  Issue : 2  |  Page : 143-146  

Evaluation of correlation between airway and serum inflammatory markers in asthmatic patients


1 Department of Pulmonary Medicine, Shaheed Sadoughi University of Medical Sciences and Health Services, Yazd, Iran
2 Department of Immunology, Shaheed Sadoughi University of Medical Sciences and Health Services, Yazd, Iran

Date of Web Publication24-Apr-2012

Correspondence Address:
Abolhasan Halvani
Department of Pulmonary Medicine, Shaheed Sadoughi University of Medical Sciences and Health Services, Yazd
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-2113.95317

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   Abstract 

Context: Asthma is one of the most common chronic diseases all over the world, resulting from a state of persistent sub-acute inflammation of the airways. Beside local inflammation, systemic inflammation is also present, which can be shown by increased levels of C-reactive protein (CRP). One of the most important cells in this disease is eosinophil, and sputum eosinophilia is used for its diagnosis. Aims: The purpose of the present study was to compare and evaluate the correlation between CRP level and sputum eosinophilia in asthmatic and control subjects. Materials and Methods: A total of 61 patients suffering from mild-to-moderate asthma participated in this study. They were divided into two groups based on whether they used inhaled steroid or not. Sputum was induced by ultrasonic nebulizer, and then samples of peripheral venous blood were collected to measure peripheral cell count and CRP by Enzyme-linked immunosorbent assay (ELISA). Thirty-seven healthy subjects were selected and their blood samples were taken. Thirty-seven healthy subjects were selected and their blood samples were taken. Results: Thirty asthmatic patients in user group (14 females/16 males) with the mean age of 39.4±9.37 years, 31 asthmatic patients in non-user group (13 females/18 males) with the mean age of 35.5±8.87 years, and 37 healthy controls (17 females/20 males) were included in our study. The mean serum concentration of CRP was 2.6 μg/mL, 3.32 μg/mL, and 1.16 μg/mL in user, non-user, and control groups, respectively. Compared to healthy controls, serum concentrations of high sensitivity-CRP (hs-CRP) significantly increased in the non-user group (P=0.0001), and user group as well. (P=0.016). The number of sputum eosinophils and peripheral blood eosinophils significantly increased in the non-users compared to the healthy controls (P=0.0001, P=0.003, respectively). In the non-user group, serum hs-CRP levels correlated negatively with FEV 1 and positively with numbers of sputum eosinophils, which was not statistically significant. Atopy status, age, and sex did not affect hs-CRP levels in both asthmatic groups. Conclusions: It was found that serum concentrations of hs-CRP significantly increased in asthmatic patients, and in the steroid-native group it partly correlated with FEV 1 and numbers of sputum eosinophils. It suggests that serum hs-CRP can indirectly indicate the degree of airway inflammation.

Keywords: Asthma, C-reactive protein, eosinophilia, forced expiratory volume in one second, sputum


How to cite this article:
Halvani A, Tahghighi F, Nadooshan HH. Evaluation of correlation between airway and serum inflammatory markers in asthmatic patients. Lung India 2012;29:143-6

How to cite this URL:
Halvani A, Tahghighi F, Nadooshan HH. Evaluation of correlation between airway and serum inflammatory markers in asthmatic patients. Lung India [serial online] 2012 [cited 2019 Nov 14];29:143-6. Available from: http://www.lungindia.com/text.asp?2012/29/2/143/95317


   Introduction Top


Asthma, one of the most common chronic diseases all over the world, currently affects 300 million people. [1] It is defined as a chronic inflammation of airways characterized by increased responsiveness of trachea and bronchial tree to a variety of stimuli. [2] Asthma results from a state of persistent sub-acute inflammation of the airways. The main pathogenesis of asthma is infiltration of such inflammatory cells as eosinophils, basophils, and CD4 + lymphocytes. [3],[4] C-reactive protein (CRP) is a well-known inflammatory marker synthesized by hepatocytes. This marker increases in systemic inflammations such as diabetes, cardiovascular diseases, collagen vascular diseases, malignancies, and also obesity. [5],[6],[7] CRP is a marker of inflammation that predicts incidence of myocardial infarction, stroke, peripheral arterial disease, and sudden cardiac death among healthy individuals without history of cardiovascular disease. [8] Recent population-based studies showed a correlation between increased levels of serum high sensitivity-CRP (hs-CRP) with a high frequency of airway hyper-responsiveness and low forced expiratory volume in one second (FEV 1 ) among subjects without heart disease. [9] In the present study, the serum levels of hs hs-CRP of asthmatic patients with and without inhaled corticosteroid (ICS) treatment were compared to those of healthy controls, and the correlation between serum CRP levels (systemic inflammatory marker) and sputum eosinophils (airway inflammatory marker) was evaluated as well.


   Materials and Methods Top


A comparative-descriptive cross-sectional study was conducted on 61 asthmatic patients (diagnosed according to American Thoracic Society criteria) [10] who visited the outpatient clinic. All patients suffered from mild-to-moderate persistent stage, according to GINA (the Global Initiative For Asthma) criteria. [2] Patients were divided into two groups: 30 patients receiving inhaled fluticasone (500 μg/day), named as the user group, and 31 patients who did not receive ICS, named as the non-user group. All of them were non-smokers without any history of respiratory tract infection or exacerbation of asthma during the previous 6 weeks. Subjects suffering from heart disease, diabetes mellitus, cancer, obesity (body mass index [BMI] ≥ 30kg/m 2 ) or systemic inflammatory disorders (such as collagen vascular diseases) were excluded from the study. Demographic data, duration of asthma, and history of asthma were recorded in questionnaires. Sputum was induced by ultrasonic nebulizer, so subjects were premedicated with inhaled salbutamol (two puffs), and inhaled hypertonic (5%) saline solution was administered to them for 10-20 min by an ultrasonic nebulizer (Shining World Health Co., Ltd. made by Taipei Taiwan), then they were asked to try to cough sputum into a plastic  Petri dish More Details. Then, smear of sputum was prepared and colored with Giemsa and cellular counts were performed. Thereafter, a group of healthy subjects (N=37) without history of smoking, ischemic heart disease, or other diseases, with normal pulmonary function tests, were selected as control group. These subjects were matched with asthmatic patients in terms of age and sex. Five cc of blood was taken from each person, poured into a clot tube, and then coagulated. Serum sample was separated by centrifugation and stored at -80°C. After collecting samples, ELISA test (DRG International, Inc.1167 US Highway 22 East, Mountainside, NJ 07092 USA) was performed. This kit showed CRP level as a quantitative measure and its sensitivity was 10 ng/mL. Data were analyzed by descriptive statistics (percentage, mean, and standard deviation) and comprehensive statistics (analysis of variance (ANOVA) and t test, Kruskal-Wallis test, and Mann-Whitney test) using SPSS (ver. 13.5).


   Results Top


This study was conducted on 30 patients in user group (14 females/16 males) and 31 patients in non-user group (13 females/18 males). Their mean age was 39.4±9.37 and 35.5±8.87 years, respectively. Thirty-seven healthy controls (17 females/20 males) and the subjects in case groups were matched in terms of age, sex, and BMI. The mean serum CRP concentration was 2.6 μg/mL, 3.32 μg/mL, and 1.16 μg/mL in user, non-user, and control groups, respectively. The difference was statistically significant between user and control groups (P=0.016) and non-user and control groups (P=0.0001), but was not significant between user and non-user groups (P=0.369). The number of sputum eosinophils and peripheral blood eosinophils significantly increased in the non-user group compared to users and healthy controls. In the non-user group, serum hs-CRP levels correlated negatively with FEV 1 and positively with numbers of sputum eosinophils, but this correlation was not statistically significant (P=0.072, P=0.437, respectively) [Table 1], [Figure 1]. Atopy, age, and sex indices did not affect hs-CRP levels in both asthmatic groups.
Figure 1: Serum high-sensitivity C-reactive protein (hs-CRP) levels (μg/mL) in a healthy control group (n=37) and two asthmatic groups (inhaled corticosteroid [ICS] + (n=31); ICS- (n=30)

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Table 1: Characteristics and outcomes of asthmatic and control subjects

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   Discussion Top


According to our findings, serum CRP level was higher in asthmatic patients (users and non-users) than in controls. However, mean blood and sputum eosinophil count was higher in non-users. CRP level had a positive correlation with eosinophil count of sputum and blood and negative correlation with FEV 1 , which was not significant statistically. On the other hand, there was no significant correlation between CRP and sex or history of atopy.

Besides chronic local inflammation of airways, systemic inflammation is also present in asthma, but there aren't enough studies about it. [11] Jousilaht reported higher level of amyloid A and plasma fibrinogen in asthmatic cases than in controls. [12] Buyukozturk et al. noted that although CRP level was higher in allergic rhinitis and asthma, mean CRP and fibrinogen level was not significantly higher than in healthy population. However, serum amyloid A level was significantly higher than in controls. [13] Takemura et al. showed that serum CRP level of non-user asthmatic patients was significantly higher than in controls. Although serum CRP level among user patients was more than in control group, this was not statistically significant. [11]

Previous studies have shown that FEV 1 decline is associated with increased serum CRP level. Mean FEV 1 among subjects of user group of this study was lower than in patients in the Takemura study, so discrepancy between two studies may be due to difference in disease stage.

Our findings showed positive correlation between serum CRP of non-users and blood and sputum eosinophil and negative correlation with FEV 1 , both of which were statistically insignificant. There was no such correlation among subjects of user group. Takemura findings confirmed this as well. [11]

Dahl et al. reported a negative correlation between plasma fibrinogen and FEV 1 . [14] Engstrom also showed a negative correlation between FVC and plasma inflammatory proteins such as fibrinogen, α1 AT, haptoglobulin, and ceruloplasmin in males. [15] Kauffman showed a negative correlation between FEV 1 and haptoglobulin level in men. [16] This relationship indicates that with increasing severity of disease and further reduction of FEV 1 , the inflammatory process and its serum markers will increase.

There was no statistically significant relationship between CRP and history of atopy. An epidemiologic study performed by Olafsdottir et al. showed a higher CRP level in non-allergic asthmatics than in healthy population but in allergic asthmatic patients, serum CRP was similar to that in healthy population. [17] Buyokoztu reported a higher level of CRP in allergic rhinitis and asthma groups than in the control group, which was statistically insignificant. [13] Takemura also didn't find any relationship between serum CRP level and atopy. [11] It seems that the correlation between atopy and CRP is not yet well understood and more research is needed. Our findings showed a lower CRP level in steroid users than in non-users, which was statistically insignificant either. Hashino and Nakamura reported that Beclomethasone Dipropionate suppressed cellular infiltration in airways and improved hyper-responsiveness in non-atopic asthma. [18] Takemura showed although serum CRP level of steroid users was higher than in control group, this difference was statistically insignificant. [11] Sin et al. studied the effect of steroid inhaler on systemic inflammatory markers in mild-to-moderate chronic obstructive pulmonary disease cases. They found that following discontinuation of inhaler fluticasone, serum CRP level increased and vice versa. [19] It seems that steroid inhalation decreases systemic inflammatory markers in asthma too, which should be studied more in cohort investigations. It should be noted that according to our findings, mean levels of sputum eosinophils in asthma group were significantly higher than upper limit of normal population in both user and non-user groups. Based on the European respiratory society (ERS) International Guidelines and other studies, a normal upper value of eosinophils of <3% or <2.5% has been reported. [20],[21],[22] Mean levels of sputum eosinophils were 6.3% and 9.96% in steroid user and non-user groups, respectively, which was more than upper limit of normal population. On the other hand, mean levels of sputum eosinophils were higher in non-users than user group, and this difference was statistically significant as well. In a similar study by Pin et al., sputum eosinophils and macrophages were significantly higher in asthmatics than controls, but no significant difference was seen between controlled and uncontrolled asthma groups. [23] Beasley and Kirby studies showed similar findings too. [24],[25] Takemura reported that sputum eosinophils of steroid users was significantly higher than controls and non-users, [11] which was against our findings. It seems that according to the topical anti-inflammatory effects of inhaled steroids, levels of sputum eosinophils in user group should be less than non-user group.

Our study showed that levels of eosinophils in peripheral blood smear (PBS) were higher than in normal population. In asthmatic cases on steroid inhalers, mean levels of eosinophils in PBS were lower than non-users. Gibson et al. studied 18 allergic asthmatic cases being exposed to inhaled allergens and found a rise in the level of eosinophils and basophils during 24 h after exposure in 13 of them. [26] Gauvreau et al. performed a study on normal and atopic asthma groups to show the rise of PBS eosinophils following exposure to an allergen in asthmatic patients. [27] Bousquet also reported a rise in PBS eosinophils and eosinophils in bronchoalveolar lavage (BAL) in chronic asthma, which correlated with severity of the disease. [28] Evans et al. also showed that steroid inhalation decreased PBS eosinophils in 10 mild asthmatic individuals. [29] These findings showed a rise in PBS eosinophils in asthma, which can be decreased by steroid inhalers. To prove this hypothesis, more studies are needed.

It is concluded that in asthma, besides airway inflammation, systemic inflammatory markers are increased as well, and steroid inhalers can decrease inflammation of airways and also systemic inflammation.

 
   References Top

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2.National Asthma Education and Prevention Program: Expert panel report III: Guidelines for the diagnosis and management of asthma. Bethesda, MD: National Heart, Lung, and Blood Institute; 2007. (NIH publication no. 08-4051). Available from: http://www.nhlbi.nih.gov/guidelines/asthma/asthgdln.htm [Last accessed on 2007 Sept 01].  Back to cited text no. 2
    
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7.Roberts WL, Moulton L, Law TC, Farrow G, Cooper-Anderson M, Savory J, et al. Evaluation of nine automated high sensitivity C-reactive protein methods: Implications for clinical and epidemiological applications. Part 2. Clin Chem 2001;47:418-25.  Back to cited text no. 7
    
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10.American Thoracic Society. Standards for the diagnosis and care of patients with chronic obstructive pulmonary disease (COPD) and asthma. Am Rev Respir Dis 1987;136:225-44.  Back to cited text no. 10
    
11.Takemura A, Matsumoto H, Niimi A, Ueda T, Matsuoka H, Yamaguchi M, et al. High sensitivity C-reactive protein in asthma. Eur Respir J 2006;27:908-12.  Back to cited text no. 11
    
12.Jousilahti P, Salomma V. The association of sensitive systemic inflammatory markers with bronchial asthma. Ann allergy asthma immunol 2002;89:381-5.  Back to cited text no. 12
    
13.Buyukozturk S, Gelincik AA, Genc S, Koçak H, Oneriyidogan Y, Erden S, et al. Acute phase reactants in allergic airway disease. Tohoku J Exp Med 2004;204:209-13.  Back to cited text no. 13
    
14.Dahl M, Tybjaerg-Hansen A, Vesto J, Lange P, Nordestgaard BG, et al. Elevated plasma fibrinogen associated with reduced pulmonary function and increased risk of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2001;164:1008-11.  Back to cited text no. 14
    
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17.Olafsdottir IS, Gislason T, Thjodleifsson B, Olafsson I, Gislason D, Jögi R, et al. C reactive protein levels are increased in non-allergic but not allergic asthma: A multicentre epidemiological study. Thorax 2005;60:451-4.  Back to cited text no. 17
    
18.Hoshino M, Nakamura Y. Anti-inflamattory effects of inhaled beclomathasone dipropionate in nonatopic asthmatics. Eur Respir J 1996;9:696-702.  Back to cited text no. 18
    
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20.American Thoracic Society; European Respiratory Society. ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005. Am J Respir Crit Care Med 2005;171:912-30.  Back to cited text no. 20
    
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23.Pin I, Gibson PG, Kolendowicz R, Girgis-Gabardo A, Denburg JA, Hargreave FE, et al. Use of induced sputum cell counts to investigate airway inflammation in asthma. Thorax 1992;47:25-9.  Back to cited text no. 23
    
24.Beasley R, Roche WR, Roberts JA, Holgate ST. Cellular events in the bronchi in mild asthma and after bronchial provocation. Am Rev Respir Dis 1989;139:806-17.  Back to cited text no. 24
    
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26.Gibson PG, Manning PJ, O'Byrne PM, Girgis-Gabardo A, Dolovich J, Denburg JA. Allergen-induced asthmatic responses. Relationship between increases in airway responsiveness and increases in circulating eosinophils, basophils, and their progenitors. Am Rev Respir Dis 1991;143:331-5.  Back to cited text no. 26
    
27.Gauvreau GM, O'Byrne PM, Moqbel R, Velazquez J, Watson RM, Howie KJ, et al. Enhanced Expression of GM-CSF in differentiating eosinophils of atopic and atopic asthmatic subjects. Am J Respir Cell Mol Biol 1998;19:55-62.  Back to cited text no. 27
    
28.Bousquet J, Chanez P, Lacoste JY, Barneon G, Ghavanian N, Enander I, et al. Eosinophilic inflammation in asthma. N Engl J Med 1990;11:1033-9.  Back to cited text no. 28
    
29.Evans PM, O'Connor BJ, Fuller RW, Barnes PJ, Chung KF. Effect of inhaled corticosteroids on peripheral blood eosinophil counts and density profiles in asthma. J Allergy Clin Immunol 1993;91:643-50.  Back to cited text no. 29
    


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