Next Article in Journal
Influence of Perinatal Factors on Gene Expression of IAPs Family and Main Factors of Pluripotency: OCT4 and SOX2 in Human Breast Milk Stem Cells—A Preliminary Report
Next Article in Special Issue
Single-Cell Analysis in Immuno-Oncology
Previous Article in Journal
The Journey of Mitochondrial Protein Import and the Roadmap to Follow
Previous Article in Special Issue
Tumor Treating Fields (TTFields) Concomitant with Immune Checkpoint Inhibitors Are Therapeutically Effective in Non-Small Cell Lung Cancer (NSCLC) In Vivo Model
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 24
Issue 3
10.3390/ijms24032478
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Serum Amyloid A in Stable Patients with Chronic Obstructive Pulmonary Disease Does Not Reflect the Clinical Course of the Disease

by
Marta Maskey-Warzęchowska
*,
Renata Rubinsztajn
,
Tadeusz Przybyłowski
,
Krzysztof Karwat
,
Patrycja Nejman-Gryz
,
Magdalena Paplińska-Goryca
and
Ryszarda Chazan
Department of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Banacha 1a, 02-097 Warsaw, Poland
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(3), 2478; https://doi.org/10.3390/ijms24032478
Submission received: 30 November 2022 / Revised: 9 January 2023 / Accepted: 20 January 2023 / Published: 27 January 2023
(This article belongs to the Special Issue Immunogenic Cell Death, Immunogenic Surrender and Antitumor Immunity)
Browse Figures
Review Reports Versions Notes

Abstract

:
Serum amyloid A (SAA) is a good systemic marker of the exacerbations of chronic obstructive pulmonary disease (COPD), but the significance of SAA in stable patients with COPD has not been widely investigated. We aimed to evaluate the SAA level in peripheral blood from stable patients with COPD and to search for correlations between SAA and other inflammatory markers and clinical characteristics of the disease. Serum SAA, IL-6, IL-8, TNF-alpha, basic blood investigations, pulmonary function testing and a 6-min walk test were performed. The correlations between SAA and other inflammatory markers, functional performance and the number of disease exacerbations were evaluated. A total of 100 consecutive patients with COPD were analyzed. No correlations between SAA and inflammatory markers as well as pulmonary function were found. Hierarchical clustering identified two clusters incorporating SAA: one comprised SAA, PaO2 and FEV1 and the second was formed of SAA and nine other disease markers. The SAA level was higher in patients with blood eosinophils < 2% when compared to those with blood eosinophils ≥ 2% (41.8 (19.5–69.7) ng/mL vs. 18.9 (1.0–54.5) ng/mL, respectively, p = 0.04). We conclude that, in combination with other important disease features, SAA may be useful for patient evaluation in stable COPD.

1. Introduction

Serum amyloid A (SAA) belongs to the group of acute phase proteins which are released in response to various types of injury including infection, inflammation, trauma, severe stress and neoplasia [1,2,3]. SAA comprises a group of four proteins: SAA1, SAA2, SAA3 and SAA4. SAA1 and SAA2 are secreted by hepatocytes, bind with serum high density lipoprotein (HDL) replacing apolipoprotein-1 and are predominantly involved in the acute phase response [2,4]. These proteins mediate the production of numerous cytokines (IL-1, IL-6, IL-10, IL-17, TNF-alpha and colony stimulating factors) by different cell types [4,5] and may act as an opsonin for Gram-negative bacteria [4]. The role of SAA3, which may be present at very low concentrations in humans but presents high expression in other mammals, is obscure. SAA4 is constitutively present in blood and its level may rise during some conditions related to inflammation, however, its precise role in pathophysiology and homeostasis, as well as its significance in the immune pathways, has not been fully explained [4].
SAA has been implicated in different chronic inflammatory diseases, including chronic obstructive pulmonary disease (COPD) [2,4]. The role of SAA in COPD is not clear. Being an acute phase reactant, SAA has been studied mainly in the context of acute COPD exacerbations (AECOPD). Studies have shown that AECOPD is related to a significant increase in SAA levels which is followed by a rapid decrease upon recovery [6,7]. Therefore, SAA has been considered as a marker of exacerbation severity [6,8,9]. However, elevated levels of SAA have also been found in patients with stable COPD [6,7,10]. In this context, SAA has been regarded as one of the markers of systemic inflammation in this disease. In patients with COPD, a higher SAA level was associated with a more severe airway obstruction [7], a higher blood neutrophil count [11] and a higher level of anxiety [12], whereas in vitro models have shown that SAA may be involved in muscle waste and atrophy [13]. As with other inflammatory markers, it is not known whether the increase in SAA level in systemic circulation is a result of a general inflammatory response in COPD or a result of an “overspill” from the lungs and airways. There is a strong body of evidence showing that SAA is involved in the inflammatory response also at the local level. Lopez-Campos et al. reported an increased expression of SAA in the airways and lung parenchyma in patients with COPD as compared to healthy smokers [10]. In vitro models have shown that macrophage SAA expression increased upon exposure to cigarette smoke and that SAA was involved in macrophage polarization similar to the polarization observed in COPD [14]. Based on a murine model, Hansen et al. pointed to SAA as one of the potential candidates responsible for sustained airway inflammation after smoking cessation [15].
The correlations between SAA and other disease markers and, particularly, with the clinical features of the disease, are not so evident. While the majority of studies on SAA in stable COPD have focused on the cellular and molecular level, only a few reports refer to clinical and functional data [7,16,17]. We therefore undertook a study aimed at the evaluation of serum SAA in patients with stable COPD. The study specifically aimed to: (1) assess the relationship between SAA and selected inflammatory markers in serum; (2) look for potential correlations between serum SAA and pulmonary function; and (3) look for potential correlations between serum SAA and the COPD symptom level in these patients.

2. Results

2.1. Patient Characteristics

The study included 100 patients aged 69.0 (61.0–75.0) years with a median post-bronchodilator FEV1 55.2 (43.0–70.0)% of predicted value. The patient characteristics are listed in Table 1.
Fifty-two (52%) patients were treated with inhaled corticosteroids (ICS) with a median daily ICS dose of 800 (800-800) mcg of budesonide or equivalent. Four patients (4%) received long-term oxygen therapy (LTOT).

2.2. SAA and Other Markers of Inflammation in Peripheral Blood

The median serum SAA concentration in the investigated patients was 24.9 (1.0–59.1) ng/mL. The median values of other inflammatory parameters are presented in Table 2.
The SAA levels did not correlate with the levels of IL-6, IL-8 and TNF alpha. We did not find correlations between SAA and serum CRP, fibrinogen, blood white cell, neutrophil and eosinophil count. SAA was higher in patients with blood eosinophils < 2% when compared to those with blood eosinophils ≥ 2% (41.8 (19.5–69.7) ng/mL vs. 18.9 (1.0–54.5) ng/mL, respectively, p = 0.04).
The correlations between the selected inflammatory markers as well as the selected functional and anthropometric parameters are shown in a heat map in Figure 1.

2.3. SAA Concentrations and Functional/Clinical Features of COPD

We did not find correlations between SAA and FEV1, FVC, RV, TLC, 6MWD, mMRC and the annual FEV1 change. Such correlations were also not found for CRP, whereas the fibrinogen level correlated with FEV1(%) at baseline (r = −0.299, p = 0.006). The SAA concentration was not different in the COPD groups stratified according to the severity of airway obstruction.
The SAA levels did not differ between the patients who were treated with ICS and those who were not (31.7 (1.2–61.6) ng/mL vs. 19.7 (0.9–57.5) ng/mL, respectively, p = 0.27), neither did we find differences in SAA between current and ex-smokers (24.3 (3.1–48.4) ng/mL vs. 30.4 (1.0–61.3) ng/mL, respectively, p = 0.86) (Figure 2).
Serum SAA did not correlate with the median number of exacerbations in the following 12 months; however, the SAA level tended to be higher in the patients who experienced ≥ 2 exacerbations (n = 34) than in those who had undergone ≤ 1 exacerbation in the following year (n = 66) (37.1 (7.3–61.9) ng/mL vs. 19.7 (0.9–57.5) ng/mL, respectively, p = 0.06) (Figure 2).
A hierarchical clustering analysis revealed two clusters of SAA and the other analyzed parameters: one included FEV1 and PaO2, with a higher SAA level in patients with lower FEV1 and PaO2, and the second comprised SAA and RV(%), RV/TLC, blood neutrophil count, CRP, fibrinogen, BMI, TNF-alpha, IL-8, age and IL-6 (Figure 1) indicating air-trapping, higher inflammatory activity and lower body mass in patients with a higher SAA level. No other specific clusters of COPD patients formed by SAA and the investigated biomarkers as well as the clinical and functional indices could be identified.

3. Discussion

Our study showed that although SAA alone does not seem to be a good marker of COPD-related inflammation and disease severity, it may be useful in the assessment of patients with COPD when combined with other disease markers, notably with two of the most important COPD prognostic factors, FEV1 and PaO2. Stable patients with COPD and higher SAA levels in serum were characterized by lower blood eosinophilia and tended to have more exacerbations. These findings confirm the involvement of SAA in the inflammatory response in COPD and support its role in the course of the disease.
In contrast to the well-established relevance of SAA in acute COPD exacerbations, data on SAA and the clinical course of COPD in stable patients are not abundant. Arellano-Orden et al. showed that in patients with stable COPD, the expression of SAA in the lung parenchyma is higher than in the pulmonary artery and peripheral blood leukocytes, and SAA expression was higher in patients with COPD than in healthy smokers [18]. The same applied for SAA plasma levels, which were higher in COPD when compared to controls. Importantly, plasma SAA increased with the COPD I-III stage of severity [18], and although these results may have been biased by the potentially altered inflammatory status of the lung parenchyma (obtained from COPD patients undergoing surgery for lung cancer), these findings support the role of SAA as an inflammatory marker in stable COPD. This was also confirmed by a study by Smith et al., who found higher serum SAA levels in stable patients with COPD when compared to controls. Moreover, in these patients, there was an inverse correlation between SAA and FEV1 [7]. In that study, however, a multivariate regression analysis showed that SAA is not a predictor for COPD. Similarly, Fu et al. did not confirm the usefulness of SAA measurements in the prediction of COPD outcomes [19]. In our study, SAA did not correlate with FEV1 and the indices of air trapping or CAT score. Nevertheless, a cluster analysis confirmed that SAA may provide additional information on the disease when combined with different disease markers. Analogically, Arellano-Orden et al., who investigated different APRs in patients with COPD and healthy controls, found no relationships between SAA and other markers in either of the groups; however, these authors were able to identify a cluster of SAA, tissue plasminogen activator (tPA) and procalcitonin in COPD patients, also indicating the value of SAA assessment but in combination with other inflammatory markers [16]. Our study revealed two clusters which included SAA, one of them being a simple but promising set of SAA with two significant COPD prognostic factors, FEV1 and PaO2, and the second showing an interplay between SAA and nine inflammatory and clinical markers. The first cluster may indirectly confirm the mutual relationship between systemic inflammation and COPD severity, while the second seems to be too complex for potential future clinical applications.
Our results showed that serum SAA was significantly lower in patients with blood eosinophilia. Data on the interrelationship between eosinophils and SAA in stable patients with COPD are very scarce. Gao et al. showed that COPD patients with sputum eosinophilia during exacerbation had almost three-fold lower serum SAA levels in the stable phase of the disease when compared to those with neutrophilic phenotype during exacerbations [20]. This seems to concur with our findings and also supports the current knowledge that SAA is involved in neutrophil-mediated inflammation [21,22,23]. In contrast, in patients with asthma, serum SAA correlated with sputum eosinophilia but not neutrophilia; however, after anti-inflammatory treatment, serum SAA remained at a comparable level despite a significant decrease in sputum eosinophils [24]. Given the above, it may be hypothesized that SAA involvement in COPD and asthma is related to alternative inflammatory pathways.
Since the classic study by Bozinovsky et al. [6], SAA has been regarded as a good marker of COPD exacerbation and exacerbation severity [7,8,20]. However, the value of serum SAA in predicting future exacerbations in stable patients with COPD seems to be low, which was confirmed in the study by Sakurai et al. [11]. This is in line with the results of the analysis of two combined SPIROMICS and GeneCOPD cohorts, which showed that biomarkers are poor predictors of COPD exacerbations and are inferior to the clinical parameters in this regard [25]. In contrast, a recent study by Zhao et al. showed that SAA is associated with the COPD phenotype with frequent exacerbations [26]. In our cohort, a trend towards a higher SAA level in patients with more frequent COPD exacerbations was observed, but with unattained statistical significance.
There are some limitations of our study that need to be recognized. First, we did not include a control group. However, the primary aim of our study was the evaluation of SAA in relation to other markers of systemic inflammation and to clinical and functional disease characteristics in stable patients with COPD. Second, although relevant concomitant diseases affecting SAA level were mentioned in the exclusion criteria, we were not able to exclude patients with atherosclerosis and related cardiovascular disease, one of the most frequent concomitant inflammatory diseases in COPD [27,28,29] because, as mentioned earlier, this was a real-life study. Nevertheless, the median levels of total cholesterol and triglycerides were not significantly elevated and there was no correlation between these results and serum SAA. This was also the case with diabetes and the level of fasting glucose. We may therefore assume that the impact of these diseases on serum SAA in our patients, and thus on our results, is negligible.

4. Materials and Methods

4.1. Study Design

This was an observational prospective study. Consecutive patients with stable COPD were recruited from the outpatient clinic of the Central Teaching Hospital in Warsaw between 2010 and 2011. The inclusion criteria were as follows: (1) diagnosis of COPD in accordance with the GOLD report [30], (2) lack of exacerbation for at least 6 weeks prior to enrollment. The exclusion criteria comprised: (1) history of relevant concomitant diseases which could affect SAA concentration (including malignancy, connective tissue diseases, rheumatoid arthritis, amyloidosis and severe liver diseases); (2) acute respiratory infection or disease exacerbation within 6 weeks prior to inclusion in the study. The patient evaluation included a detailed medical history, spirometry with bronchial reversibility testing, body plethysmography, a 6-min walking test (6MWT) and blood sampling for basic laboratory investigations (including C-reactive protein and fibrinogen) and SAA, IL-6, IL-8 and TNF-alpha. Pulmonary function, the 6MWT and the number of exacerbations were also assessed after a 12-month period of observation. The correlations between SAA and other inflammatory markers, as well as the relationships between SAA and the clinical features of COPD (pulmonary function, symptom severity, anti-inflammatory treatment and the number of exacerbations within 12 months), were sought.

4.2. Symptom Severity and Functional Assessment

Dyspnea was assessed with use of the modified Medical Research Council scale (mMRC) [31]. Spirometry with bronchial reversibility testing (LungTest 1000, MES, Cracow, Poland) and body plethysmography (BodyBox, Medisoft, Sorinnes, Belgium and Vmax 6200 Autobox, SensorMedics, Yorba Linda, CA, USA) were performed in accordance with the European Respiratory Society/American Thoracic Society (ERS/ATS) guidelines [32,33,34]. Only the post-bronchodilator values from the spirometry and body plethysmography were taken for analyses. Pulmonary function testing was performed at baseline and after 12 months of observation.
The 6-min walking test was performed in accordance with the ATS guidelines [35]. The predicted values for the 6-min walking distance were calculated with the use of the reference equations proposed by Enright and Sherrill [36].

4.3. Blood Sampling and SAA, IL-6, IL-8 and TNF-Alpha Measurement

The measurements of SAA and the basic laboratory tests were performed in fasting venous blood samples. A cut-off point of 2% was set to define blood eosinophilia [37].
SAA was measured with ELISA (Serum amyloid A ELISA kit, IBL International GmbH, Hamburg, Germany). The range and sensitivity of the applied kit was 9.4–600 ng/mL and 4 ng/mL, respectively.
For IL-6, IL-8 and TNF-alpha measurements in serum, ELISA was also applied (Quantikinine ELISA Human IL-6, IL-8 and TNF-alpha Immunoassays, R&D Systems, Minneapolis, MN, USA). The range and the sensitivity of the applied kits were as follows: 3.1–300 pg/mL and 0.7 pg/mL for IL-6, 31.2–2000 pg/mL and 7.5 pg/mL for IL-8 and 15.6–1000 pg/mL and 5.5 pg/mL for TNF-alpha, respectively.

4.4. Statistical Analysis

The statistical analysis was performed with Statistica for Windows (StatSoft, Inc. version 10, Tulsa, OK, USA). The data distribution was assessed using the Shapiro–Wilk test. Depending on the distribution type of the analyzed variable, data are presented as mean ± standard deviation or median and interquartile range, while comparisons between the groups were made using the Student’s t test or the Mann–Whitney U test. To evaluate the significance of the correlation coefficient, Spearman’s correlation test was used. p < 0.05 was regarded as statistically significant.
Hierarchical clustering was performed on the Spearman’s correlation coefficients, using the complete method with Euclidean distance as the dissimilarity measure. Heatmaps and dendrograms were generated with the “gplots” package. The computations were performed in the R environment [38]. The heatmaps denoted the similarities in terms of a set of biomarkers in COPD patients.

5. Conclusions

Serum SAA concentration alone is not a good indicator of COPD-related systemic inflammation, however, it may be useful for patient evaluation in combination with other important disease features to assess COPD severity.

Author Contributions

Conceptualization, M.M.-W., R.R. and R.C.; Data curation, P.N.-G. and M.P.-G.; Formal analysis, M.M.-W., K.K. and M.P.-G.; Funding acquisition, R.R. and R.C.; Investigation, M.M.-W., R.R., T.P., K.K. and P.N.-G.; Methodology, R.R., T.P., P.N.-G. and M.P.-G.; Resources, R.R. and R.C.; Software, M.P.-G.; Supervision, R.C.; Validation, T.P.; Writing—original draft, M.M.-W.; Writing—review and editing, T.P., K.K., P.N.-G. and R.C. All authors have read and agreed to the published version of the manuscript.

Funding

The study was performed as a part of a multicenter project titled “Chronic obstructive pulmonary disease (COPD)—systemic disease, the biggest threat of the XXIst century” which had received financial support from the National Center for Research and Development in Poland (no. 13 0034 06/2009).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board (KB/207/2008).

Informed Consent Statement

Informed consent was obtained from all the subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Urieli-Shoval, S.; Linke, R.P.; Matzner, Y. Expression and function of serum amyloid A, a major acute-phase protein, in normal and disease states. Curr. Opin. Hematol. 2000, 7, 64–69. [Google Scholar] [CrossRef] [PubMed]
  2. Ye, R.D.; Sun, L. Emerging functions of serum amyloid A in inflammation. J. Leukoc. Biol. 2015, 98, 923–929. [Google Scholar] [CrossRef] [PubMed]
  3. Malle, E.; De Beer, F.C. Human serum amyloid A (SAA) protein: A prominent acute-phase reactant for clinical practice. Eur. J. Clin. Investig. 1996, 26, 427–435. [Google Scholar] [CrossRef] [PubMed]
  4. De Buck, M.; Gouwy, M.; Ming Wang, J.; Van Snick, J.; Opdenakker, G.; Struyf, S.; Van Damme, J. Structure and Expression of Different Serum Amyloid A (SAA) Variants and their Concentration-Dependent Functions during Host Insults. Curr. Med. Chem. 2016, 23, 1725–1755. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. He, R.L.; Zhou, J.; Hanson, C.Z.; Chen, J.; Cheng, N.; Ye, R.D. Serum amyloid A induces G-CSF expression and neutrophilia via Toll-like receptor 2. Blood 2009, 113, 429–437. [Google Scholar] [CrossRef] [Green Version]
  6. Bozinovski, S.; Hutchinson, A.; Thompson, M.; MacGregor, L.; Black, J.; Giannakis, E.; Karlsson, A.-S.; Silvestrini, R.; Smallwood, D.; Vlahos, R.; et al. Serum amyloid a is a biomarker of acute exacerbations of chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 2008, 177, 269–278. [Google Scholar] [CrossRef] [Green Version]
  7. Smith, D.J.; Yerkovich, S.T.; Towers, M.A.; Carroll, M.L.; Thomas, R.; Uphamet, J.W. Reduced soluble receptor for advanced glycation end-products in COPD. Eur. Respir. J. 2011, 37, 516–522. [Google Scholar] [CrossRef] [Green Version]
  8. Hutchinson, A.F.; Black, J.; Thompson, M.A.; Bozinovski, S.; Brand, C.A.; Smallwood, D.M.; Irving, L.B.; Anderson, G.P. Identifying viral infections in vaccinated Chronic Obstructive Pulmonary Disease (COPD) patients using clinical features and inflammatory markers. Influ. Other Respir. Viruses 2010, 4, 33–39. [Google Scholar] [CrossRef] [Green Version]
  9. Koutsokera, A.; Kiropoulos, T.S.; Nikoulis, D.J.; Daniil, Z.D.; Tsolaki, V.; Tanou, K.; Papaioannou, A.I.; Germenis, A.; Gourgoulianis, K.I.; Kostikas, K. Clinical, functional and biochemical changes during recovery from COPD exacerbations. Respir. Med. 2009, 103, 919–926. [Google Scholar] [CrossRef] [Green Version]
  10. López-Campos, J.L.; Calero, C.; Rojano, B.; López-Porras, M.; Saenz, J.; Blanco, A.I.; Sánchez-López, V.; Tobar, D.; Montes-Worboys, A.; Arellano, E. C-reactive protein and serum amyloid a overexpression in lung tissues of chronic obstructive pulmonary disease patients: A case-control study. Int. J. Med. Sci. 2013, 10, 938–947. [Google Scholar] [CrossRef] [Green Version]
  11. Sakurai, K.; Chubachi, S.; Irie, H.; Tsutsumi, A.; Kameyama, N.; Kamatani, T.; Koh, H.; Terashima, T.; Nakamura, H.; Asano, K.; et al. Clinical utility of blood neutrophil-lymphocyte ratio in Japanese COPD patients. BMC Pulm. Med. 2018, 18, 65. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Zilz, C.; Blaas, S.H.; Pfeifer, M.; Jorres, S.A.; Budweiser, S. Mental health, serum biomarkers and survival in severe COPD: A pilot study. Multidiscip. Respir. Med. 2016, 11, 3. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Passey, S.L.; Bozinovski, S.; Vlahos, R.; Anderson, G.P.; Hansen, M.J. Serum amyloid A induces Toll-Like receptor 2-dependent inflammatory cytokine expression and atrophy in C2C12 skeletal muscle myotubes. PLoS ONE 2016, 11, e0146882. [Google Scholar] [CrossRef] [PubMed]
  14. Lim, E.X.; Anthony, D.A.; Seow, H.J.; Anderson, G.P.; Bozinovski, S. Serum Amyloid A is a Candidate Mediator for Altered Macrophage Polarisation in Cigarette Smoke-Related Disease. Abstract. Proceedings of the Australian Physiological Society. Available online: http://aups.org.au/Proceedings/42/53P/53P.pdf (accessed on 5 March 2021).
  15. Hansen, M.J.; Chan, S.P.J.; Langenbach, S.Y.; Dousha, L.F.; Jones, J.E.; Yatmaz, S.; Seow, H.; Vlahos, R.; Anderson, G.P.; Bozinovski, S. IL-17A and serum amyloid A are elevated in a cigarette smoke cessation model associated with the persistence of pigmented macrophages, neutrophils and activated NK cells. PLoS ONE 2014, 9, e113180. [Google Scholar] [CrossRef] [Green Version]
  16. Arellano-Orden, E.; Calero-Acuña, C.; Cordero, J.A.; Abad-Arranz, M.; Sánchez-López, V.; Márquez-Martín, E.; Ortega-Ruiz, F.; López-Campos, J.L. Specific networks of plasma acute phase reactants are associated with the severity of chronic obstructive pulmonary disease: A case-control study. Int. J. Med. Sci. 2017, 14, 67–74. [Google Scholar] [CrossRef] [Green Version]
  17. Bizeto, L.; Mazzolini, A.B.; Ribeiro, M.; Stelmach, R.; Cukier, A.; Nunes, M.P. Interrelationship between serum and sputum inflammatory mediators in chronic obstructive pulmonary disease. Braz. J. Med Biol. Res. 2008, 41, 193–198. [Google Scholar] [CrossRef] [Green Version]
  18. Arellano-Orden, E.; Calero, C.; López-Ramírez, C.; Sánchez-López, V.; López-Villalobos, J.L.; Abad Arranz, M.; Blanco-Orozco, A.; Otero-Candelera, R.; López-Campos, J.L. Evaluation of lung parenchyma, blood vessels, and peripheral blood lymphocytes as a potential source of acute phase reactants in patients with COPD. Int. J. Chronic Obstr. Pulm. Dis. 2019, 14, 1323–1332. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Fu, J.; Gibson, P.G.; Simpson, J.L.; McDonald, V.M. Longitudinal in clinical outcomes in older patients with asthma, COPD and asthma-COPD overlap syndrome. Respiration 2014, 87, 63–74. [Google Scholar] [CrossRef]
  20. Gao, P.; Zhang, J.; He, X.; Hao, Y.; Wang, K.; Gibson, P.G. Sputum inflammatory cell-based classification of patients with acute exacerbation of chronic obstructive pulmonary disease. PLoS ONE 2013, 8, e57678. [Google Scholar] [CrossRef] [Green Version]
  21. Anthony, D.; Seow, H.J.; Uddin, M.; Thompson, M.; Dousha, L.; Vlahos, R.; Irving, L.B.; Levy, B.D.; Anderson, G.P.; Bozinovski, S. Serum amyloid A promotes lung neutrophilia by increasing IL-17A levels in the mucosa and γδ T cells. Am. J. Respir. Crit. Care Med. 2013, 188, 179–186. [Google Scholar] [CrossRef] [Green Version]
  22. Bozinovski, S.; Uddin, M.; Vlahos, R.; Thompson, M.; McQualter, J.L.; Merritt, A.-S.; Wark, P.A.B.; Hutchinson, A.; Irving, L.B.; Levy, B.D.; et al. Serum amyloid A opposes lipoxin A₄ to mediate glucocorticoid refractory lung inflammation in chronic obstructive pulmonary disease. Proc. Natl. Acad. Sci. USA 2012, 109, 935–940. [Google Scholar] [CrossRef] [Green Version]
  23. Ather, J.L.; Ckless, K.; Martin, R.; Foley, K.L.; Suratt, B.T.; Boyson, J.E.; Fitzgerald, K.A.; Flavell, R.A.; Eisenbarth, S.C.; Poynter, M.E. Serum amyloid A activates the NLRP3 inflammasome and promotes Th17 allergic asthma in mice. J. Immunol. 2011, 187, 64–73. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Ozseker, F.; Buyukozturk, S.; Depboylu, B.; Yilmazbayhan, D.; Karayigit, E.; Gelincik, A.; Genc, S.; Colakoglu, B.; Dal, M.; Issever, H. Serum amyloid A (SAA) in induced sputum of asthmatics: A new look to an old marker. Int. Immunopharmacol. 2006, 6, 1569–1576. [Google Scholar] [CrossRef] [PubMed]
  25. Keene, J.D.; Jacobson, S.; Kechris, K.; Kinney, G.L.; Foreman, M.G.; Doerschuk, C.M.; Make, B.J.; Curtis, J.L.; Rennard, S.I.; Barr, R.G.; et al. Biomarkers predictive of exacerbations in the SPIROMICS and COPDGene cohorts. Am. J. Respir. Crit. Care Med. 2017, 195, 473–481. [Google Scholar] [CrossRef] [PubMed]
  26. Zhao, D.; Abbasi, A.; Rossiter, H.B.; Su, X.; Liu, H.; Pi, Y.; Sang, L.; Zhong, W.; Yang, Q.; Guo, X.; et al. Serum Amyloid A in Stable COPD Patients is Associated with the Frequent Exacerbator Phenotype. Int. J. Chronic Obstr. Pulm. Dis. 2020, 15, 2379–2388. [Google Scholar] [CrossRef]
  27. Rabe, K.F.; Hurst, J.R.; Suissa, S. Cardiovascular disease and COPD: Dangerous liaisons? Eur. Respir. Rev. 2018, 27, 180057. [Google Scholar] [CrossRef]
  28. Rubinsztajn, R.; Przybyłowski, T.; Maskey-Warzęchowska, M.; Paplińska-Goryca, M.; Nejman-Gryz, P.; Karwat, K.; Chazan, R. Metabolic syndrome as a factor affecting systemic inflammation in patients with chronic obstructive pulmonary disease. Adv. Exp. Med. Biol. 2017, 1021, 55–62. [Google Scholar] [CrossRef]
  29. Hughes, M.J.; McGettrick, H.M.; Sapey, E. Shared mechanisms of multimorbidity in COPD, atherosclerosis and type-2 diabetes: The neutrophil as a potential inflammatory target. Eur. Respir. Rev. 2020, 29, 190102. [Google Scholar] [CrossRef] [Green Version]
  30. Rabe, K.F.; Hurd, S.; Anzueto, A.; Barnes, P.J.; Buist, S.A.; Calverley, P.; Fukuchi, Y.; Jenkins, C.; Rodriguez-Roisin, R.; van Weel, C.; et al. Global Initiative for Chronic Obstructive Lung Disease. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am. J. Respir. Crit. Care Med. 2007, 176, 532–555. [Google Scholar] [CrossRef] [Green Version]
  31. Fletcher, C.M.; Elmes, P.C.; Fairbairn, A.S.; Wood, C.H. The significance of respiratory symptoms and the diagnosis of chronic bronchitis in a working population. Br. Med. J. 1959, 2, 257–266. [Google Scholar]
  32. Miller, M.R.; Hankinson, J.A.; Brusasco, V.; Burgos, F.; Casaburi, R.; Coates, A.; Crapo, R.; Enright, P.; Van Der Grinten, C.P.; Gustafsson, P.; et al. ATS/ERS Task Force. Standardisation of spirometry. Eur. Respir. J. 2005, 26, 319–338. [Google Scholar] [CrossRef] [Green Version]
  33. Wanger, J.; Clausen, J.L.; Coates, A.; Pedersen, O.F.; Brusasco, V.; Burgos, F.; Casaburi, R.; Crapo, R.; Enright, P.; Van Der Grinten, C.P.M.; et al. ATS/ERS Task Force. Standardisation of the measurement of lung volumes. Eur. Respir. J. 2005, 26, 511–522. [Google Scholar] [CrossRef] [PubMed]
  34. Pellegrino, R.; Viegi, G.; Brusasco, V.; Crapo, R.O.; Burgos, F.; Casaburi, R.; Coates, A.; Van Der Grinten, C.P.M.; Gustafsson, P.; Hankinson, J.; et al. ATS/ERS Task Force. Interpretative strategies for lung function tests. Eur. Respir. J. 2005, 26, 948–968. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories. American Thoracic Society Statement: Guidelines for the six-minute walk test. Am. J. Respir. Crit. Care Med. 2002, 166, 111–117. [Google Scholar] [CrossRef] [PubMed]
  36. Enright, P.L.; Sherrill, D.L. Reference equations for the six-minute walk in healthy adults. Am. J. Respir. Crit. Care Med. 1998, 158 Pt 1, 1384–1387. [Google Scholar] [CrossRef] [Green Version]
  37. Ho, J.; He, W.; Chan, M.T.; Tse, G.; Liu, T.; Wong, S.H.; Leung, C.C.; Wong, W.T.; Tsang, S.; Zhang, L.; et al. Eosinophilia and clinical outcome of chronic obstructive pulmonary disease: A meta-analysis. Sci. Rep. 2017, 7, 13451. [Google Scholar] [CrossRef] [Green Version]
  38. The R Core Team. R: A Language and Environment for Statistical Computing. 2014. Available online: http://www.R-project.org/ (accessed on 29 January 2021).
Ijms 24 02478 g001 550
Figure 1. Hierarchical clustering of the clinical and inflammatory parameters of patients with COPD. The presented heat map shows the correlation between the selected inflammatory biomarkers and the selected functional and anthropometric indices. The color scale codes the correlation coefficient (R) with red corresponding to the lowest values, while light yellow/white denotes its highest values. The rows and columns are ordered based on the results of hierarchical clustering with dendrograms for the evaluated features shown on the horizontal and vertical axis. The number in each square indicates the p value; p < 0.05 is regarded as statistically significant. BMI—body mass index; SAA—serum amyloid A; CRP—C-reactive protein; RV—residual volume; TLC—total lung capacity; FEV1—forced expiratory volume at first second; PaO2—partial pressure of oxygen in arterial blood.
Figure 1. Hierarchical clustering of the clinical and inflammatory parameters of patients with COPD. The presented heat map shows the correlation between the selected inflammatory biomarkers and the selected functional and anthropometric indices. The color scale codes the correlation coefficient (R) with red corresponding to the lowest values, while light yellow/white denotes its highest values. The rows and columns are ordered based on the results of hierarchical clustering with dendrograms for the evaluated features shown on the horizontal and vertical axis. The number in each square indicates the p value; p < 0.05 is regarded as statistically significant. BMI—body mass index; SAA—serum amyloid A; CRP—C-reactive protein; RV—residual volume; TLC—total lung capacity; FEV1—forced expiratory volume at first second; PaO2—partial pressure of oxygen in arterial blood.
Ijms 24 02478 g001
Ijms 24 02478 g002 550
Figure 2. Comparison of serum amyloid A (SAA) concentration between (a) patients treated and not treated with inhaled corticosteroids (ICS/+/and ICS/-/, respectively), (b) ex-smokers and current smokers, (c) patients with ≤1 exacerbation and ≥2 exacerbations in the last year, (d) patients with and without blood eosinophilia.
Figure 2. Comparison of serum amyloid A (SAA) concentration between (a) patients treated and not treated with inhaled corticosteroids (ICS/+/and ICS/-/, respectively), (b) ex-smokers and current smokers, (c) patients with ≤1 exacerbation and ≥2 exacerbations in the last year, (d) patients with and without blood eosinophilia.
Ijms 24 02478 g002
Table
Table 1. Characteristics of the investigated patients.
Table 1. Characteristics of the investigated patients.
Variable Value
Age (years)69.0 (61.0–75.0)
Sex (M/F)62/38
BMI (kg/m2)26.6 (24.2–30.5)
Smoking history (packyears)41.0 (28.0–52.5)
Current/ex-/never smokers21/75/4
Pulmonary function (post-bronchodilator values)
FEV1 (% predicted)55.2 (43.0–70.0)
FVC (% predicted)86.6 (75.7–98.8)
FEV1/FVC (%)50.8 (40.8–59.1)
RV (% predicted)163.7 (136.0–202.8)
TLC (% predicted)121.1 (105.7–136.2)
RV/TLC (%)54.6 (50.6–61.9)
Exercise performance and symptom level
6 MWD (m)476.1 (435.7–527.5)
6 MWD (% predicted)92.0 (77.3–106.1)
mMRC (points)2.0 (1.0–3.0)
CAT (points)13.2 (5.6–21.4)
12 mo ΔFEV1 (mL) *0.06 [(−0.06)–0.16]
Number of exacerbations within 12 months 1.0 (0.0–2.0)
Arterial blood gases (room air)
PaO2 (mmHg)73.2 (65.3–80.4)
PaCO2 (mmHg)39.4 (36.9–42.3)
Biochemistry
Total cholesterol191.0 (158.0–221.0)
HDL52.0 (43.0–63.0)
Triglycerides97.0 (80.0–134.0)
Fasting glucose87.0 (78.0–97.0)
Data presented as median and IQR where applicable. BMI—body mass index; FEV1—forced expiratory volume at first second; FVC—forced vital capacity; 12 mo ΔFEV1—difference between FEV1 at baseline and after 12 months; RV—residual volume; TLC—total lung capacity; CAT—COPD Assessment Test; mMRC—modified Medical Research Council scale for dyspnea; 6MWD—6-min walk distance; HDL—high-density lipoprotein; LDL—low density lipoprotein. * n = 80.
Table
Table 2. Selected inflammatory parameters in peripheral blood.
Table 2. Selected inflammatory parameters in peripheral blood.
VariableValue
WBC (×109/L)6.3 (5.3–8.1)
Neutrophils (×109/L)3.36 (2.8–4.4)
Eosinophils (×109/L)0.21 (0.13–0.30)
Eosinophils (%)3.5 (2.3–5.2)
SAA (ng/mL)24.9 (1.0–59.1)
CRP (mg/L)3.0 (2.5–7.7)
Fibrinogen (mg/dL)373.0 (327.0–460.0)
IL-6 (pg/mL)2.6 (1.7–5.1)
IL-8 (pg/mL)8.6 (5.2–10.8)
TNF alpha (pg/mL)1.8 (1.5–2.2)
Data presented as median and IQR. WBC—white blood cells; SAA—serum amyloid A; CRP—C-reactive protein. In contrast to SAA, the CRP concentration correlated with IL-6 (r = 0.352, p < 0.001), IL-8 (r = 0.297, p = 0.004) and fibrinogen (r = 0.447, p < 0.001). There was also a correlation between IL-6 and IL-8 with fibrinogen (r = 0.318, p = 0.003 and r = 0.215, p = 0.047, respectively).
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Maskey-Warzęchowska, M.; Rubinsztajn, R.; Przybyłowski, T.; Karwat, K.; Nejman-Gryz, P.; Paplińska-Goryca, M.; Chazan, R. Serum Amyloid A in Stable Patients with Chronic Obstructive Pulmonary Disease Does Not Reflect the Clinical Course of the Disease. Int. J. Mol. Sci. 2023, 24, 2478. https://doi.org/10.3390/ijms24032478

AMA Style

Maskey-Warzęchowska M, Rubinsztajn R, Przybyłowski T, Karwat K, Nejman-Gryz P, Paplińska-Goryca M, Chazan R. Serum Amyloid A in Stable Patients with Chronic Obstructive Pulmonary Disease Does Not Reflect the Clinical Course of the Disease. International Journal of Molecular Sciences. 2023; 24(3):2478. https://doi.org/10.3390/ijms24032478

Chicago/Turabian Style

Maskey-Warzęchowska, Marta, Renata Rubinsztajn, Tadeusz Przybyłowski, Krzysztof Karwat, Patrycja Nejman-Gryz, Magdalena Paplińska-Goryca, and Ryszarda Chazan. 2023. "Serum Amyloid A in Stable Patients with Chronic Obstructive Pulmonary Disease Does Not Reflect the Clinical Course of the Disease" International Journal of Molecular Sciences 24, no. 3: 2478. https://doi.org/10.3390/ijms24032478

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop