Abstract
Background: Despite having a work related deterioration in peak expiratory flow (PEF), many workers with occupational asthma show a low degree of within day diurnal variability atypical of non-occupational asthma. It was hypothesised that these workers would have a neutrophilic rather than an eosinophilic airway inflammatory response.
Methods: Thirty eight consecutive workers with occupational asthma induced by low molecular weight agents underwent sputum induction and assessment of airway physiology while still exposed at work.
Results: Only 14 (36.8%) of the 38 workers had sputum eosinophilia (>2.2%). Both eosinophilic and non-eosinophilic groups had sputum neutrophilia (mean (SD) 59.5 (19.6)% and 55.1 (18.8)%, respectively). The diurnal variation and magnitude of fall in PEF during work periods was not significantly different between workers with and without sputum eosinophilia. Those with eosinophilia had a lower forced expiratory volume in 1 second (FEV1; 61.4% v 83% predicted, mean difference 21.6, 95% confidence interval (CI) 9.2 to 34.1, p=0.001) and greater methacholine reactivity (geometric mean PD20 253 µg v 1401 µg, p=0.007). They also had greater bronchodilator reversibility (397 ml v 161 ml, mean difference 236, 95% CI of difference 84 to 389, p=0.003) which was unrelated to differences in baseline FEV1. The presence of sputum eosinophilia did not relate to the causative agent, duration of exposure, atopy, or lack of treatment.
Conclusions: Asthma caused by low molecular weight agents can be separated into eosinophilic and non-eosinophilic pathophysiological variants with the latter predominating. Both groups had evidence of sputum neutrophilia. Sputum eosinophilia was associated with more severe disease and greater bronchodilator reversibility but no difference in PEF response to work exposure.
Full Text
The Full Text of this article is available as a PDF (155.8 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Belda J., Leigh R., Parameswaran K., O'Byrne P. M., Sears M. R., Hargreave F. E. Induced sputum cell counts in healthy adults. Am J Respir Crit Care Med. 2000 Feb;161(2 Pt 1):475–478. doi: 10.1164/ajrccm.161.2.9903097. [DOI] [PubMed] [Google Scholar]
- Burge P. S., O'Brien I. M., Harries M. G. Peak flow rate records in the diagnosis of occupational asthma due to isocyanates. Thorax. 1979 Jun;34(3):317–323. doi: 10.1136/thx.34.3.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burge P. S., Pantin C. F., Newton D. T., Gannon P. F., Bright P., Belcher J., McCoach J., Baldwin D. R., Burge C. B. Development of an expert system for the interpretation of serial peak expiratory flow measurements in the diagnosis of occupational asthma. Midlands Thoracic Society Research Group. Occup Environ Med. 1999 Nov;56(11):758–764. doi: 10.1136/oem.56.11.758. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chan-Yeung M., Obata H., Dittrick M., Chan H., Abboud R. Airway inflammation, exhaled nitric oxide, and severity of asthma in patients with western red cedar asthma. Am J Respir Crit Care Med. 1999 May;159(5 Pt 1):1434–1438. doi: 10.1164/ajrccm.159.5.9807007. [DOI] [PubMed] [Google Scholar]
- Côté J., Kennedy S., Chan-Yeung M. Sensitivity and specificity of PC20 and peak expiratory flow rate in cedar asthma. J Allergy Clin Immunol. 1990 Mar;85(3):592–598. doi: 10.1016/0091-6749(90)90098-o. [DOI] [PubMed] [Google Scholar]
- Di Franco A., Vagaggini B., Bacci E., Bartoli M. L., Cianchetti S., Carnevali S., Dente F. L., Giannini D., Macchioni P., Ruocco L. Leukocyte counts in hypertonic saline-induced sputum in subjects with occupational asthma. Respir Med. 1998 Mar;92(3):550–557. doi: 10.1016/s0954-6111(98)90307-9. [DOI] [PubMed] [Google Scholar]
- Fahy J. V., Boushey H. A. Effect of low-dose beclomethasone dipropionate on asthma control and airway inflammation. Eur Respir J. 1998 Jun;11(6):1240–1247. doi: 10.1183/09031936.98.11061240. [DOI] [PubMed] [Google Scholar]
- Gibson P. G., Simpson J. L., Saltos N. Heterogeneity of airway inflammation in persistent asthma : evidence of neutrophilic inflammation and increased sputum interleukin-8. Chest. 2001 May;119(5):1329–1336. doi: 10.1378/chest.119.5.1329. [DOI] [PubMed] [Google Scholar]
- Jatakanon A., Uasuf C., Maziak W., Lim S., Chung K. F., Barnes P. J. Neutrophilic inflammation in severe persistent asthma. Am J Respir Crit Care Med. 1999 Nov;160(5 Pt 1):1532–1539. doi: 10.1164/ajrccm.160.5.9806170. [DOI] [PubMed] [Google Scholar]
- Jones P. W., Quirk F. H., Baveystock C. M., Littlejohns P. A self-complete measure of health status for chronic airflow limitation. The St. George's Respiratory Questionnaire. Am Rev Respir Dis. 1992 Jun;145(6):1321–1327. doi: 10.1164/ajrccm/145.6.1321. [DOI] [PubMed] [Google Scholar]
- Kharitonov S., Alving K., Barnes P. J. Exhaled and nasal nitric oxide measurements: recommendations. The European Respiratory Society Task Force. Eur Respir J. 1997 Jul;10(7):1683–1693. doi: 10.1183/09031936.97.10071683. [DOI] [PubMed] [Google Scholar]
- Lemière C., Pizzichini M. M., Balkissoon R., Clelland L., Efthimiadis A., O'Shaughnessy D., Dolovich J., Hargreave F. E. Diagnosing occupational asthma: use of induced sputum. Eur Respir J. 1999 Mar;13(3):482–488. doi: 10.1183/09031936.99.13348299. [DOI] [PubMed] [Google Scholar]
- Louis R., Lau L. C., Bron A. O., Roldaan A. C., Radermecker M., Djukanović R. The relationship between airways inflammation and asthma severity. Am J Respir Crit Care Med. 2000 Jan;161(1):9–16. doi: 10.1164/ajrccm.161.1.9802048. [DOI] [PubMed] [Google Scholar]
- Miller M. R., Dickinson S. A., Hitchings D. J. The accuracy of portable peak flow meters. Thorax. 1992 Nov;47(11):904–909. doi: 10.1136/thx.47.11.904. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Obata H., Dittrick M., Chan H., Chan-Yeung M. Sputum eosinophils and exhaled nitric oxide during late asthmatic reaction in patients with western red cedar asthma. Eur Respir J. 1999 Mar;13(3):489–495. doi: 10.1183/09031936.99.13348999. [DOI] [PubMed] [Google Scholar]
- Park H. S., Jung K. S., Hwang S. C., Nahm D. H., Yim H. E. Neutrophil infiltration and release of IL-8 in airway mucosa from subjects with grain dust-induced occupational asthma. Clin Exp Allergy. 1998 Jun;28(6):724–730. doi: 10.1046/j.1365-2222.1998.00299.x. [DOI] [PubMed] [Google Scholar]
- Pavord I. D., Pizzichini M. M., Pizzichini E., Hargreave F. E. The use of induced sputum to investigate airway inflammation. Thorax. 1997 Jun;52(6):498–501. doi: 10.1136/thx.52.6.498. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perrin B., Lagier F., L'Archevêque J., Cartier A., Boulet L. P., Côté J., Malo J. L. Occupational asthma: validity of monitoring of peak expiratory flow rates and non-allergic bronchial responsiveness as compared to specific inhalation challenge. Eur Respir J. 1992 Jan;5(1):40–48. [PubMed] [Google Scholar]
- Pizzichini E., Pizzichini M. M., Efthimiadis A., Dolovich J., Hargreave F. E. Measuring airway inflammation in asthma: eosinophils and eosinophilic cationic protein in induced sputum compared with peripheral blood. J Allergy Clin Immunol. 1997 Apr;99(4):539–544. doi: 10.1016/s0091-6749(97)70082-4. [DOI] [PubMed] [Google Scholar]
- Spanevello A., Confalonieri M., Sulotto F., Romano F., Balzano G., Migliori G. B., Bianchi A., Michetti G. Induced sputum cellularity. Reference values and distribution in normal volunteers. Am J Respir Crit Care Med. 2000 Sep;162(3 Pt 1):1172–1174. doi: 10.1164/ajrccm.162.3.9908057. [DOI] [PubMed] [Google Scholar]
- Vyas A., Pickering C. A., Oldham L. A., Francis H. C., Fletcher A. M., Merrett T., Niven R. M. Survey of symptoms, respiratory function, and immunology and their relation to glutaraldehyde and other occupational exposures among endoscopy nursing staff. Occup Environ Med. 2000 Nov;57(11):752–759. doi: 10.1136/oem.57.11.752. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wenzel S. E., Schwartz L. B., Langmack E. L., Halliday J. L., Trudeau J. B., Gibbs R. L., Chu H. W. Evidence that severe asthma can be divided pathologically into two inflammatory subtypes with distinct physiologic and clinical characteristics. Am J Respir Crit Care Med. 1999 Sep;160(3):1001–1008. doi: 10.1164/ajrccm.160.3.9812110. [DOI] [PubMed] [Google Scholar]
- Yan K., Salome C., Woolcock A. J. Rapid method for measurement of bronchial responsiveness. Thorax. 1983 Oct;38(10):760–765. doi: 10.1136/thx.38.10.760. [DOI] [PMC free article] [PubMed] [Google Scholar]
