Abstract
BACKGROUND: Induced sputum is a noninvasive tool, aimed at collecting cellular and soluble materials from lung airways. Induced sputum sampling analysis has been validated in chronic obstructive lung diseases as well as in various diffuse interstitial lung disorders. Our objective was to evaluate the utility of induced sputum speciments of cellular and soluble materials noninvasively sampled from the lung airways of subjects with systemic sclerosis compared with healthy controls and determine possible correlation with disease manifestations.
METHODS: The study population included 20 consecutive subjects with systemic sclerosis and 16 healthy volunteers (controls). All of the participants underwent pulmonary function testing (PFT), single-breath diffusion capacity of carbon monoxide, and induced sputum cytology analysis.
RESULTS: The systemic sclerosis subjects' induced sputum samples contained a higher neutrophil count (P = .09) and lower lymphocyte count (P = .045) compared with the controls. Within the systemic sclerosis population, several clinical, PFT, and induced sputum findings were positively correlated: the modified Rodnan skin score score and CD3 (P = .044), modified Rodnan skin score and CD4 (P = .04), modified Rodnan skin score and percentage neutrophils (P = .059), and total lung capacity (TLC) and percentage lymphocytes (P = .02). Induced sputum neutrophil counts were inversely associated with TLC (P = .02) and FVC (P = .02). Induced sputum samples from the subgroup of systemic sclerosis subjects with PFT restrictive pattern contained a significantly lower percentage of lymphocytes (P = .004) and lower CD4/CD8 ratio (P = .03) compared with controls. In this subgroup, TLC also was negatively correlated with the neutrophil count (P = .043), and positive correlations were found between TLC and CD3 (P = .053), disease duration and CD4/CD8 ratio (P = .033), TLC and FVC and percentage macrophages (P = .033 and P = .052, respectively), diffusion per unit of alveolar volume, and percentage macrophages (P = .032), and C-reactive protein and percentage lymphocytes, percentage macrophages, and neutrophil count (P = .02, P = .008, and P = .006, respectively).
CONCLUSIONS: Induced sputum analysis of subjects with systemic sclerosis, including those with restrictive lung disease, shows changes in cellular pattern and correlation with several highly relevant clinical and PFT parameters.
Introduction
Systemic sclerosis is a relatively rare multisystem disease characterized by microvascular damage, autoimmunity, and massive collagen overproduction and deposition in the skin and internal organs.1 Interstitial lung disease is common among systemic sclerosis patients, with evidence of interstitial changes on high-resolution computed tomography in up to 90% of systemic sclerosis patients and clinically important lung fibrosis in approximately 25% of all patients with systemic sclerosis.2–4
Traditional pulmonary function tests (PFTs) and high-resolution computed tomography remain important tools in the diagnosis and monitoring of systemic sclerosis patients with interstitial lung disorder. Bronchoalveolar lavage is an invasive diagnostic tool that detects cellular infiltrate in the alveoli. The procedure is very unpleasant for the patients and requires expensive medical equipment while providing limited prognostic information.5 It is therefore not routinely used for pulmonary evaluation in systemic sclerosis. In contrast, induced sputum is a noninvasive tool that can be used to collect cellular and soluble materials from lung airways. It is well accepted by patients, requires inexpensive medical equipment, is safer than bronchoalveolar lavage, and can be repeated as frequently as needed.6,7 Induced sputum sampling has been validated as an approach to study bronchial inflammation in asthma8,9 and chronic obstructive lung disorders.10 Promising results have been reported in the evaluation of various interstitial lung disorders, including idiopathic type pulmonary fibrosis,11,12 sarcoidosis,13 hypersensitivity pneumonitis,14 and lung involvement in Crohn disease.15 Fireman et al16 observed a significantly higher percentage of neutrophils and a lower percentage of macrophages in the induced sputum of subjects with idiopathic pulmonary fibrosis.
Evidence of the potential use of induced sputum for the evaluation of inflammation associated with systemic sclerosis is very limited. The purpose of our current study was to explore the possible usefulness of induced sputum cellular analysis in the assessment of systemic sclerosis subjects and to investigate its possible relationship with disease manifestations.
QUICK LOOK
Current knowledge
Induced sputum sampling has been validated as an approach to study bronchial inflammation in asthma and chronic obstructive lung disorders. Promising results have been reported in the evaluation of various interstitial lung disorders, including idiopathic type pulmonary fibrosis. Evidence of the potential use of induced sputum for the evaluation of inflammation associated with systemic sclerosis is very limited.
What this paper contributes to our knowledge
The induced sputum samples of subjects with systemic sclerosis contained a higher neutrophil count and lower lymphocyte count compared with the healthy controls. Induced sputum analysis of systemic sclerosis subjects, including those with restrictive lung disease, showed changes in cellular pattern and correlation with several highly relevant clinical and pulmonary function testing parameters.
Methods
The study was approved by the medical ethics committee of Tel Aviv Sourasky Medical Center, and written informed consent was obtained from all participants.
Subjects
Twenty consecutive patients with systemic sclerosis (19 females and 1 male) who were being treated and followed up at the Department of Rheumatology of the Tel Aviv Sourasky Medical Center (Tel Aviv, Israel) and 16 apparently healthy volunteers participated in this study. Exclusion criteria were the presence of other chronic inflammatory lung disease and acute upper or lower lung disease within the 3 months before study entry.
Clinical Assessment
Clinical assessment was performed on the same day as induced sputum and PFT. Each subject gave a complete past medical history, including the current use of medications, and underwent a physical examination that included the modified Rodnan skin score, presence of digital ulcers, tender and swollen joint count, clinical symptoms (dyspnea, cough, dyspepsia, and dysphagia), and patient and physician disease activity evaluation by a visual activity score (10–100). Laboratory assessment included erythrocyte sedimentation rate and C-reactive protein level.
Pulmonary Function Tests
PFTs (spirometry, lung volumes, and diffusing capacity) were performed with a Masterlab spirometer (E. Jaeger, Wurzburg, Germany) using standard protocols according to the American Thoracic Society specifications.17
Induced Sputum Collection and Processing
Sputum was induced by inhalation of hypertonic saline generated by a Aerosonic Ultrasonic Nebulizer 5000D/5000I (DeVilbriss-Health Care Corporation, Somerset, Pennsylvania), a method shown to correlate well with bronchoalveolar lavage.18 Induced sputum was recovered after a 20-min inhalation of 3% saline with an ultrasonic nebulizer through a mouthpiece without a valve or nose clip. Ten minutes after the start of nebulization and every 5 min thereafter, the subjects were asked to rinse their nose and mouth with water to minimize contamination of the nasal secretions with saliva. They were encouraged to cough and expectorate sputum into a sterile plastic container. The sputum was always processed within 2 h. The cells in the sputum were dispersed by mechanical disruption in dithiothreitol, cytospins were prepared, and the supernatant was collected for the measurement of fluid phase constituents. CD4/CD8 subsets were identified by fluorescence-activated cell sorting.
Statistical Analysis
Demographic and clinical parameters of the studied population were summarized, by mean ± SD for continuous data and 95% CI for the mean. Categorical data were summarized by ratio. Despite the small number of subjects, since a normal distribution and P plot were found, differences between groups were evaluated for continuous data by the t test and for categorical data by the chi-square test. Pearson correlation was used to evaluate the association between sputum cytology, PFT tests, and continuous data related to systemic sclerosis. A p value of 0.05 was considered significant.
Results
Characteristics of the Subjects and Controls
The demographic data and baseline characteristics of the study population are provided in Table 1. Thirty-six participants were included in this study: 20 were systemic sclerosis subjects, of whom 13 (65%) had the diffuse type and 7 (35%) had limited type (CREST syndrome). Their results were compared with those of 16 healthy controls. The subject and control groups were similar in sex (mostly women) (see Table 1) and age (mean age 52.3 ± 17.1 y for systemic sclerosis and 57.9 ± 10.4 y for controls). The mean disease duration, calculated from the onset of the first non-Raynaud symptom, was 8.7 ± 9.2 y. Seven subjects had a restrictive pattern on PFT. None of the participants had pulmonary artery hypertension. At the time of evaluation, 9 subjects (45%) were receiving immunosuppressive therapy (3 mofetil mycophenolate, 5 methotrexate, and one rituximab).
Cigarette Smoking
There were 6 smokers in the control group and none in the systemic sclerosis group.
Pulmonary Function
The total lung capacity (TLC), FVC, and single-breath diffusion capacity of carbon monoxide for alveolar volume results of the systemic sclerosis group were significantly lower than those of the controls (P < .001, P < .001, and P = .003, respectively).
Subjects with diffuse type systemic sclerosis (n = 13) had lower TLC levels and significantly decreased FVC levels compared with the subjects with limited type systemic sclerosis (Table 2).
Induced Sputum
In all participants, the induction of sputum was well tolerated, and no adverse effects were observed. The induced sputum of the systemic sclerosis subjects contained a higher neutrophil count (P = .09) and a lower lymphocyte count (P = .045) compared with the control group (Table 3). There was no difference in induced sputum cytology between the various types of systemic sclerosis.
Correlation between induced sputum cellularity and clinical findings revealed a significant positive correlation among several clinical, PFT and induced sputum findings (modified Rodnan skin score and CD3 [P = .044], modified Rodnan skin score and CD4 [P = .04], and modified Rodnan skin score and percentage neutrophils [P = .059]). The neutrophil counts in the subjects' induced sputum were inversely associated with TLC and FVC (P = .02 and P = .002, respectively).
The induced sputum samples from the subgroup of systemic sclerosis subjects with PFT restrictive pattern contained a significantly lower percentage of lymphocytes (P = .004) and a lower CD4/CD8 ratio (P = .03) compared with controls (Table 4). The restrictive pattern also correlated positively with the induced sputum cytology count and several clinical, laboratory, and PFT parameters (disease duration and CD4/CD8 ratio [P = .033], TLC and CD3 [P = .053], TLC and FVC and percentage macrophages [P = .033 and P = .052, respectively]), DLCO/VA and percentage macrophages [P = .032], and C-reactive protein and percentage lymphocytes, percentage macrophages, and neutrophils [P = .02, P = .008, and P = .006, respectively]). There was a negative correlation between TLC and the neutrophil count (P = .043).
The induced sputum from subjects with interstitial lung disease contained a statistically significantly lower CD4/CD8 ratio then those without interstitial lung disease (2.81 ± 2.55 and 4.13 ± 1.37, respectively, P = .05). No significant differences were found in the other induced sputum parameters. The same trend for CD4/CD8 ratio was observed in the subgroup of systemic sclerosis subjects receiving immunosuppressive treatment compared with non-treated subjects (2.87 ± 1.15 and 4.44 ± 2.4, respectively). Finally, there was no difference in induced sputum cytology content between the subjects with an obstructive pattern and the controls.
Discussion
Lung involvement is one of the leading causes of morbidity and mortality in systemic sclerosis.19 Early diagnosis of pulmonary manifestations and additional tools for monitoring them in systemic sclerosis are unmet needs. The use of induced sputum, a noninvasive diagnostic procedure, is well established in detecting alveolitis secondary to several inflammatory lung diseases. The role of induced sputum analysis in the assessment of systemic sclerosis patients, however, is not well defined. We evaluated the cellular profile and the clinical utility of the induced sputum procedure in subjects with systemic sclerosis with and without pulmonary involvement and compared the results with those of healthy controls.
The induced sputum analyses revealed lower lymphocyte and higher neutrophil counts in the samples of the subjects with systemic sclerosis compared with the controls. Abnormal findings, including lower lymphocyte counts and reduced CD4/CD8 ratios, were also prominent in the subgroup of systemic sclerosis subjects with a restrictive PFT pattern compared with controls. We also demonstrated correlations between the induced sputum findings and several clinical parameters, including PFT. Taken together, our results showed that the relatively simple, noninvasive induced sputum methodology is capable of detecting subclinical respiratory airway inflammation in subjects with systemic sclerosis who have no symptoms of respiratory involvement.
Our findings support those of previous studies. Vatrella et al20 found that induced sputum samples from subjects with connective tissue disease contained a significantly higher percentage of neutrophils and a lower percentage of macrophages compared with healthy subjects. Damjanov et al21 reported a higher percentage of neutrophils, lymphocytes, and eosinophils in the induced sputum of subjects with systemic sclerosis compared with healthy controls.
Sánchez-Vidaurre et al22 evaluated induced sputum of 25 subjects with systemic sclerosis and found a high percentage of neutrophils in the sputum and significant negative correlation between sputum total cell count and single-breath diffusion capacity of carbon monoxide regardless of the presence of signs of pulmonary involvement.
Yilmaz et al23 also reported an increase in mean macrophage and lymphocyte counts in the induced sputum of 20 subjects with systemic sclerosis compared with the control group, but unlike in other studies, including ours, they demonstrated a decreased number of neutrophils in the induced sputum of subjects with systemic sclerosis in comparison with the control group. In addition, in our study, we also found correlations between clinical and lung functional parameters and induced sputum findings in the total patient population and in those with restrictive PFT pattern.
Conclusions
Noninvasive induced sputum analysis of subjects with systemic sclerosis reveals changes in cellular patterns and correlations with several selected clinical and PFT parameters. It can be useful as a complementary method for identifying airway inflammation in patients with systemic sclerosis. Future studies are needed with a larger number of subjects to validate the role of induced sputum analysis in the detection and evaluation of patients with systemic sclerosis.
Acknowledgments
We thank Esther Eshkol for editorial assistance.
Footnotes
- Correspondence: Irena Litinsky MD, Department of Rheumatology, Tel Aviv Medical Center, 6 Weizmann Street, Tel Aviv 64239, Israel. E-mail: litinskyira{at}yahoo.com.
The authors have disclosed no conflicts of interest.
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