|Year : 2014 | Volume
| Issue : 2 | Page : 115-120
Serum uric acid as a biomarker for prediction of outcomes of patients hospitalized for acute exacerbation of chronic obstructive pulmonary disease
Sameh Embarak MD 1, Ashraf E Sileem1, Maged Abdrabboh1, Ahmed Mokhtar2
1 Department of Chest, Faculty of Medicine, Zagazig University, Zagazig, Egypt
2 Department of Clinical Pathology, Faculty of Medicine, Zagazig University, Zagazig, Egypt
|Date of Submission||05-Jul-2014|
|Date of Acceptance||15-Aug-2014|
|Date of Web Publication||29-Nov-2014|
Chest Department, Faculty of Medicine, Zagazig University, Zagazig
Source of Support: None, Conflict of Interest: None
Background Serum uric acid, the final product of purine degradation, has been shown to be increased in the hypoxic state as well as in systemic inflammation including patients with chronic obstructive pulmonary disease (COPD). The aim of this study was to assess the possible role of serum uric acid as a biomarker for the prediction of outcome of patients hospitalized for acute exacerbation of COPD (AECOPD).
Patients and methods Serum uric acid levels were measured in 115 eligible AECOPD patients on admission. The primary end-point was all-cause mortality at 30 days. The secondary outcomes included the length of hospital stay, need for noninvasive ventilation, or ICU admission within 30 days.
Results Serum uric acid presented an area under the receiver operating characteristic curve of 0.721 (95% confidence interval: 0.63-0.80) for the prediction of 30-day mortality in patients with AECOPD, with a sensitivity of 0.82 and a specificity of 0.61 for the cutoff point greater than 6.9 mg/dl (P = 0.021). Also, patients with higher serum uric acid levels required longer hospitalization and more often required the use of noninvasive ventilation and ICU admission at 30 days. In addition, serum uric acid levels were higher in patients with more severe airflow limitation, patients with cardiovascular comorbidity, and among frequent exacerbators.
Conclusion High serum uric acid levels on admission were associated with increased 30-day mortality in patients with AECOPD. The results of this work suggest a possible role for serum uric acid in the identification of COPD patients at an increased risk of adverse outcomes who may need early intensive management. Egypt J Broncho 2014 8:115-120
2014 Egyptian Journal of Bronchology.
Keywords: acute exacerbation, chronic obstructive pulmonary disease, serum uric acid
|How to cite this article:|
Embarak S, Sileem AE, Abdrabboh M, Mokhtar A. Serum uric acid as a biomarker for prediction of outcomes of patients hospitalized for acute exacerbation of chronic obstructive pulmonary disease. Egypt J Bronchol 2014;8:115-20
|How to cite this URL:|
Embarak S, Sileem AE, Abdrabboh M, Mokhtar A. Serum uric acid as a biomarker for prediction of outcomes of patients hospitalized for acute exacerbation of chronic obstructive pulmonary disease. Egypt J Bronchol [serial online] 2014 [cited 2021 Mar 2];8:115-20. Available from: http://www.ejbronchology.eg.net/text.asp?2014/8/2/115/145703
| Introduction|| |
Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality worldwide and results in an economic and social burden that is both substantial and increasing  . An acute exacerbation of COPD (AECOPD) is an acute event characterized by a worsening of the patient's respiratory symptoms that is beyond normal day-to-day variations and leads to a change in medication  .
Serum uric acid, the final product of purine degradation, has been shown to be increased in the hypoxic state, including in patients with COPD ,, . Importantly, serum uric acid has been proposed as a marker for impaired oxidative metabolism and an independent predictor of impaired prognosis in several processes such as congestive heart failure  , pulmonary thromboembolism  , primary pulmonary hypertension  , Eisenmenger syndrome  , or acute myocardial infarction-related future adverse effects  .
In COPD, Garcia-Pachon et al.  assessed the association of serum uric acid and serum uric acid to creatinine ratio with clinical and functional characteristics in stable patients with COPD. However, few data exist on the significance of serum uric acid in patients with AECOPD. Thus, the aim of this study was to evaluate the possible role of serum uric acid as a biomarker for the prediction of outcome of patients hospitalized with AECOPD.
| Patients and methods|| |
This study was carried out at the Respiratory ICU and Chest Department, Zagazig University Hospitals, during the period from January 2012 to January 2014. It included 115 AECOPD patients. AECOPD was diagnosed according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria  , supported by spirometric evidence of airflow obstruction [forced expiratory volume in 1 s (FEV 1 )/forced vital capacity<0.70] when clinically stable, with clinical criteria of exacerbation including increased dyspnea, increased sputum volume, or sputum purulence. Criteria for exclusion were as follows: previous inclusion in the study; a primary reason for admission other than AECOPD; a history of respiratory disorders other than COPD; patients without available spirometry data; refusal to participate in the study; or patients with chronic comorbidities that significantly influence uric acid levels (i.e. chronic renal failure, severe liver dysfunction, or malignancies).
All the patients studied were subjected to the following:
(1) Thorough assessment of medical history.
(2) Full clinical examination (general and local examination).
(3) Plain chest radiography.
(4) Blood samples were collected from each patient on admission and before the initiation of any treatment for serum uric acid and other routine laboratory investigations including:
(a) Complete blood count.
(b) Liver functions.
(c) Kidney functions.
(d) Serum electrolytes (Na, K, Cl).
(e) C-reactive protein (CRP).
(5) Stable-state dyspnea was assessed using the modified Medical Research Council dyspnea scale  ; this has scores from 0 to 4 according to the patient's severity of dyspnea.
(6) Arterial blood gases analysis.
(7) The primary end-point was all-cause mortality at 30 days. The secondary outcomes included the length of hospital stay, need for noninvasive ventilation (NIV), or ICU admission for AECOPD within 30 days.
Decisions on treatment and discharge were made by attending physicians not involved in this study according to the GOLD guidelines  . The diagnosis and classification of airflow limitation were based on postbronchodilator spirometry in a stable condition, that is, in the previous 6 months and at least 4 weeks before admission from the patients' records or 4-8 weeks after discharge, according to GOLD guidelines (patients were classified as GOLD stages 1-4 as follows: GOLD 1, FEV 1 ≥80% predicted; GOLD 2, 50% ≤FEV 1 <80% predicted; GOLD 3, 30% ≤FEV 1 <50% predicted; GOLD 4, FEV 1 <30% predicted)  .
Statistical analysis was carried out using Epi Info, version 7 and the SPSS version 19 statistical software package (SPSS Inc., Chicago, Illinois, USA). Epi InfoTM version 7 (available at: https://wwwn.cdc.gov/epiinfo/html/downloads.htm). P-value less than 0.05 was considered significant.
| Results|| |
This study included 115 patients with AECOPD who were eligible for inclusion. Patients were divided into two groups according to the presence of serum uric acid levels below or equal to and above the median value (≤6.9 mg/dl n = 65 or >6.9 mg/dl n = 50, respectively). The demographic data of both groups are presented in [Table 1], which showed that patients with high serum uric acid levels had more comorbidity (i.e. cardiovascular disease and arterial hypertension) compared with patients with low serum uric acid levels.
[Table 2] shows that patients with high serum uric acid levels had more hospital admissions in previous year, more number of AECOPD in the previous year, more severe airflow obstruction, more dyspnea, more acidemia, more hypercapnia, more hypoxemia, and higher CRP levels compared with patients with low serum uric acid levels.
The median (range) serum uric acid levels on admission were higher in patients with more severe airflow limitation [6.4 (5.9-7.3), 6.6 (5.9-7.5), 7.6 (6.1-10.3), and 7.9 (6.5-11.1) mg/dl for GOLD stages 1-4, respectively; P < 0.001] ([Figure 1]). Also, serum uric acid levels were higher in frequent (n = 66) compared with nonfrequent (n = 49) exacerbators [7.4 (6.1-11.1) vs. 6.4 (5.9-7.4) mg/dl, respectively; P < 0.001] ([Figure 2]).
|Figure 1: Serum uric acid levels on admission in all studied patients according to airflow limitation severity [Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage 1-4].|
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|Figure 2: Serum uric acid levels on admission in all studied patients according to exacerbation frequency (nonfrequent = 0-1 events/year vs. frequent ≥2 events/year).|
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[Figure 3] shows that serum uric acid levels had a significant negative correlation with FEV 1 % predicted (rs = −0.57, P < 0.001). [Figure 4] shows that serum uric acid levels presented a positive correlation with length of hospitalization in all study population (rs = 0.69, P < 0.001).
|Figure 3: Correlation between serum uric acid levels and FEV1% of predicted in the study population. FEV1, forced expiratory volume in 1 s.|
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|Figure 4: Correlation between serum uric acid levels and length of hospital stay in the study population.|
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[Table 3] shows a comparison of clinical outcomes at 30 days in patients with low and high serum uric acid levels on admission. Patients with high serum uric acid levels required more prolonged hospitalization and presented higher rates of 30-day mortality compared with patients with low serum uric acid levels. Moreover, patients with high serum uric acid levels required NIV and ICU admission at 30 days more than patients with low serum uric acid levels.
|Table 3 Comparison of clinical outcomes at 30 days with low and high serum uric acid levels |
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[Figure 5] shows the receiver operating characteristic curve evaluating the diagnostic performance of serum uric acid as a predictor of 30-day mortality. In receiver operating characteristic curve analysis, serum uric acid presented an area under the curve of 0.721 (95% confidence interval: 0.63-0.80) for the prediction of 30-day mortality, with a sensitivity of 0.82 and a specificity of 0.61 for the cutoff point greater than 6.9 mg/dl.
|Figure 5: Receiver operating characteristic curve evaluating the diagnostic performance of serum uric acid as a predictor of 30-day mortality. AUC = 0.721 (95% confidence interval: 0.63-0.80). AUC, area under the curve.|
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| Discussion|| |
In the current study, it has been shown that high serum uric acid levels on admission were associated with increased 30-day mortality in patients with AECOPD. Also, patients with increased uric acid levels required more prolonged hospitalization and more often required the use of NIV and ICU admission at 30 days. In addition, serum uric acid levels were higher in patients with more severe airflow limitation, patients with cardiovascular comorbidity, and in frequent exacerbators. These results are comparable and in agreement with those obtained by Bartziokas et al.  , who assessed serum uric acid, the widely available and rapidly measured biomarker, as a predictor of clinically important outcomes in a prospective cohort of patients with AECOPD. Also in agreement with the results of the present work, Lopez  evaluated serum uric acid levels among 110 patients with COPD and found a significant correlation between hypoxemia and serum uric acid levels (in stable and exacerbated patients) and between severity of COPD and serum uric acid.
An increase in serum uric acid occurs as a result of purine catabolism secondary to tissue hypoxia , . It is to be expected that patients with worse pulmonary function and more dyspnea represent a group of COPD patients with a higher risk of hypoxia and impaired oxidative metabolism  , especially during acute exacerbation. Serum uric acid has been studied in several conditions associated with hypoxic states, and results consistently show that this parameter reflects a worse situation or a worse prognosis. Epidemiologic studies have shown that uric acid may be a risk factor for cardiovascular diseases and a negative prognostic marker for mortality in patients with pre-existing heart failure  . In patients with pulmonary thromboembolism, serum uric acid increases in proportion to the severity of the embolism  . In patients with pulmonary hypertension, serum uric acid has an independent association with long-term mortality  . Serum uric acid increases in proportion to hemodynamic severity in adult patients with Eisenmenger syndrome and is associated independently with long-term mortality  . Also, serum uric acid level is a suitable marker for predicting acute myocardial infarction-related future adverse effects  .
Several mechanisms may be involved in the presence of high uric acid levels in AECOPD. First, prolonged hypoxemia that is further increased during AECOPD may result in increased pulmonary artery pressures, leading to increased right ventricular afterload, which promotes purine degradation through increased xanthine oxidase activity  . The presence of more hypoxemia in patients with high serum uric acid levels in this study ([Table 2]) lends support for this mechanism. Also, a considerable proportion of patients with COPD have comorbid cardiovascular disease that may be related to elevated uric acid  . This is further supported by the more common cardiovascular disease in patients with increased uric acid levels in our study. Finally, COPD is characterized by systemic inflammation  , and elevated uric acid levels have been associated with increased levels of inflammatory markers (e.g. CRP and interleukin-6)  that may be important in the outcomes of COPD patients , .
Previous studies have attempted to identify biomarkers that predict clinically relevant outcomes during hospitalization for AECOPD. In a previous study carried out by Koutsokera et al.  , the measurement of several serum biomarkers, including CRP, serum amyloid-A, tumor necrosis factor-a, interleukin-6, and fibrinogen, failed to identify patients with early or late recovery from hospitalization for AECOPD. Stolz et al.  showed that plasma proadrenomedullin and proendothelin levels were associated with the length of hospitalization, but only proadrenomedullin is a predictor of long-term survival. In addition, in another study by the same investigators, CRP and procalcitonin failed to predict short-term mortality, but increased levels of copeptin were associated with an increased risk of death during hospitalization  . In this study, high serum uric acid levels were associated with increased 30-day mortality, suggesting that this easy-to-obtain biomarker may be used to identify high-risk patients with AECOPD who require more intensive treatment. On the basis of these data, serum uric acid may be evaluated as a useful biomarker in a multicomponent score in future studies  .
In agreement with the current study, uric acid levels have been associated previously with clinical and functional characteristics in patients with COPD in cross-sectional studies ,, . Significant associations between serum uric acid/creatinine ratio and FEV 1 , forced vital capacity and Medical Research Council dyspnea scale were reported by Garcia-Pachon et al.  , but they included a small sample of stable COPD patients and no data on the outcomes of those patients were reported. Another study that included 91 COPD outpatients receiving home oxygen therapy has suggested that serum uric acid/creatinine ratio is related to the survival of such patients  . In contrast, a population-based cross-sectional study by Nicks et al.  has shown reduced uric acid levels in patients with severe COPD. This discrepancy may be related to the fact that serum uric acid was measured at the time of hospitalization for an AECOPD, in contrast to the stable condition of the patients studied by Nicks et al.  .
Cardiovascular disease is associated with increased morbidity and mortality in COPD , . Elevated uric acid levels were a strong independent marker of impaired prognosis in patients with cardiovascular disease [5,28]. A recent study showed that hyperuricemia is associated with poor outcomes in heart failure patients without chronic kidney disease, but not in those with chronic kidney disease, suggesting that hyperuricemia may predict poor outcomes when it is related to increased xanthine oxidase activity, but not because of impaired renal excretion of uric acid  . The exclusion of patients with chronic renal failure in the present study suggests that the elevated serum uric acid levels may be associated with increased uric acid production in our study population. Some of the patients with cardiovascular comorbidities were receiving medication known to influence uric acid levels, including aspirin or diuretics  . However, serum uric acid levels continued to be associated with increased 30-day mortality, even after adjustment for the presence of cardiovascular disease. This further supports the possible role of uric acid as a clinically relevant biomarker in COPD  .
As in other studies ,, , no correlation was found, in this study, between serum uric acid and arterial oxygen saturation. Tissue hypoxia is determined by the balance between arterial oxygen transport and oxygen demands in tissue, and the lack of correlation between arterial oxygen saturation and markers of tissue hypoxia is not surprising. Oxygen transport is determined not only by oxygen saturation but also by the concentration of hemoglobin, the hemoglobin dissociation curve, cardiac output, the distribution of tissue blood flow, and other factors  .
It should be taken into consideration that serum uric acid is the end-product of purine degradation, which increases in a very sensitive but nonspecific manner in several forms of tissue damage and inflammation, all of which are very dynamic processes in COPD patients , . Uric acid levels are influenced by several factors including cardiovascular disease  , food intake  , alcohol consumption  , renal dysfunction, and genetic disorders of purine metabolism  . There are also genetic influences in the way in which COPD patients react to inflammation  , which could play an important role in serum uric acid levels. In the present study, patients with chronic renal failure were excluded, but we cannot exclude other possible confounders that may have influenced the results of this study. However, despite these possible limitations, data from this work provide evidence for a possible role of serum uric acid as a biomarker that is associated with disease severity and may identify patients with worse prognosis in hospitalized patients with AECOPD.
| Conclusion|| |
High serum uric acid levels on admission were associated with increased 30-day mortality in patients with AECOPD. The results of the present study, combined with the fact that serum uric acid is a widely and rapidly available, easy to interpret, low-cost biomarker, suggest a possible role for serum uric acid in the identification of COPD patients at an increased risk of adverse outcomes who may need early intensive management.
| Acknowledgements|| |
Conflicts of interest
| References|| |
Vestbo J, Hurd SS, Agustý´ AG, et al.
Global strategy for the diagnosis, management and prevention of chronic obstructive pulmonary disease, GOLD executive summary. Am J Respir Crit Care Med
Braghiroli A, Sacco C, Erbetta M, et al.
Overnight urinary acid/creatinine ratio for detection of sleep hypoxemia: validation study in chronic obstructive pulmonary disease and obstructive sleep apnea before and after treatment with nasal continuous positive airway pressure. Am Rev Respir Dis
Lewis JG, Gardner JE. The relation of serum uric acid to haemoglobin level in patients with cardiac and respiratory disease. J Clin Pathol
Saito H, Nishimura M, Shibuya E, et al.
Tissue hypoxia in sleep apnea syndrome assessed by uric acid and adenosine. Chest
Anker SD, Doehner W, Rauchhaus M, et al.
Uric acid and survival in chronic heart failure: validation and application in metabolic, functional, and hemodynamic staging. Circulation
Shimizu Y, Nagaya N, Satoh T, et al.
Serum acid uric level increases in proportion to the severity of pulmonary thromboembolism. Circ J
Nagaya N, Uematsu M, Satoh T, et al.
Serum uric acid levels correlate with the severity and the mortality of primary pulmonary hypertension. Am J Respir Crit Care Med
Oya H, Nagaya N, Satoh T, et al.
Haemodynamic correlates and prognostic significance of acid uric in adult patients with Eisenmenger syndrome. Heart
Kojima S, Sakamoto T, Ishihara M, et al.
Prognostic usefulness of serum uric acid after acute myocardial infarction. The Japanese Acute Coronary Syndrome Study. Am J Cardiol
Garcia-Pachon E, Padilla-Navas I, Shum C. Serum uric acid to creatinine ratio in patients with chronic obstructive pulmonary disease. Lung
Bartziokas K, Papaioannou AI, Loukides S, et al.
Serum uric acid as a predictor of mortality and future exacerbations of COPD. Eur Respir J
Lopez IH. Serum uric acid levels among patients with chronic obstructive pulmonary disease. Chest
Elsayed NM, Nakashima JM, Poslethwait EM. Measurement of uric acid as a marker of oxygen tension in the lung. Arch Biochem Biophys
Mateos AF, Garcia PJ, Gomez FP, et al.
Degradation of purine nucleotides in patients with chronic airflow obstruction. Med Clin (Barc)
Pascual-Figal DA, Hurtado-Martýnez JA, Redondo B, et al.
Hyperuricaemia and long-term outcome after hospital discharge in acute heart failure patients. Eur J Heart Fail
Ruggiero C, Cherubini A, Miller E3rd, et al.
Usefulness of uric acid to predict changes in C-reactive protein and interleukin-6 in 3-year period in Italians aged 21 to 98 years. Am J Cardiol
Fabbri LM, Rabe KF. From COPD to chronic systemic inflammatory syndrome? Lancet
Celli BR, Locantore N, Yates J, et al.
Inflammatory biomarkers improve clinical prediction of mortality in chronic obstructive pulmonary disease. Am J Respir Crit Care Med
Dahl M, Vestbo J, Lange P, et al.
C-reactive protein as a predictor of prognosis in chronic obstructive pulmonary disease. Am J Respir Crit Care Med
Koutsokera A, Kiropoulos TS, Nikoulis DJ, et al.
Clinical, functional and biochemical changes during recovery from COPD exacerbations. Respir Med
Stolz D, Christ-Crain M, Morgenthaler NG, et al.
Plasma pro-adrenomedullin but not plasma pro-endothelin predicts survival in exacerbations of COPD. Chest
Stolz D, Christ-Crain M, Morgenthaler NG, et al.
Copeptin, C-reactive protein, and procalcitonin as prognostic biomarkers in acute exacerbation of COPD. Chest
Aida Y, Shibata Y, Osaka D, et al.
The relationship between serum uric acid and spirometric values in participants in a health check: the Takahata study. Int J Med
Sci 2011; 8
Sato N, Kurashima K, Ubukata M, et al.
Prognostic significance of serum uric acid in patients with chronic obstructive pulmonary disease receiving home oxygen therapy [article in Japanese]. Nihon Kokyuki Gakkai Zasshi
Nicks ME, O'Brien MM, Bowler RP. Plasma antioxidants are associated with impaired lung function and COPD exacerbations in smokers. COPD
Hunninghake DB. Cardiovascular disease in chronic obstructive pulmonary disease. Proc Am Thorac Soc
Sin DD. Man SF. Why are patients with chronic obstructive pulmonary disease at increased risk of cardiovascular diseases? The potential role of systemic inflammation in chronic obstructive pulmonary disease. Circulation
So A, Thorens B. Uric acid transport and disease. J Clin Invest
Filippatos GS, Ahmed MI, Gladden JD, et al.
Hyperuricaemia, chronic kidney disease, and outcomes in heart failure: potential mechanistic insights from epidemiological data. Eur Heart J
Demartini FE. Hyperuricemia induced by drugs. Arthritis Rheum
Gan WQ, Man SF, Senthilselvan A, et al.
Association between chronic obstructive pulmonary disease and systemic inflammation: a systematic review and a meta-analysis. Thorax
Holme I, Aastveit AH, Hammar N, et al.
Uric acid and risk of myocardial infarction, stroke and congestive heart failure in 417 734 men and women in the Apolipoprotein MOrtality RISk study (AMORIS). J Intern Med
Feig DI, Kang DH, Johnson RJ. Uric acid and cardiovascular risk. N Engl J Med
Choi HK, Liu S, Curhan G. Intake of purine-rich foods, protein, and dairy products and relationship to serum levels of uric acid: the Third National Health and Nutrition Examination Survey. Arthritis Rheum
Choi HK, Curhan G. Beer, liquor, and wine consumption and serum uric acid level: the Third National Health and Nutrition Examination Survey. Arthritis Rheum
Yanbaeva DG, Dentener MA, Creutzberg EC, et al.
Systemic inflammation in COPD: is genetic susceptibility a key factor? COPD
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
[Table 1], [Table 2], [Table 3]