Inflammatory biomarkers predict airflow obstruction after exposure to World Trade Center dust
- PMID: 21998260
- PMCID: PMC3425337
- DOI: 10.1378/chest.11-1202
Inflammatory biomarkers predict airflow obstruction after exposure to World Trade Center dust
Abstract
Background: The World Trade Center (WTC) collapse on September 11, 2001, produced airflow obstruction in a majority of firefighters receiving subspecialty pulmonary evaluation (SPE) within 6.5 years post-September 11, 2001.
Methods: In a cohort of 801 never smokers with normal pre-September 11, 2001, FEV1, we correlated inflammatory biomarkers and CBC counts at monitoring entry within 6 months of September 11, 2001, with a median FEV(1) at SPE (34 months; interquartile range, 25-57). Cases of airflow obstruction had FEV(1) less than the lower limit of normal (LLN) (100 of 801; 70 of 100 had serum), whereas control subjects had FEV(1) greater than or equal to LLN (153 of 801; 124 of 153 had serum).
Results: From monitoring entry to SPE years later, FEV(1) declined 12% in cases and increased 3% in control subjects. Case subjects had elevated serum macrophage derived chemokine (MDC), granulocyte-macrophage colony-stimulating factor (GM-CSF), granulocyte colony-stimulating factor, and interferon inducible protein-10 levels. Elevated GM-CSF and MDC increased the risk for subsequent FEV(1) less than LLN by 2.5-fold (95% CI, 1.2-5.3) and 3.0-fold (95% CI, 1.4-6.1) in a logistic model adjusted for exposure, BMI, age on September 11, 2001, and polymorphonuclear neutrophils. The model had sensitivity of 38% (95% CI, 27-51) and specificity of 88% (95% CI, 80-93).
Conclusions: Inflammatory biomarkers can be risk factors for airflow obstruction following dust and smoke exposure. Elevated serum GM-CSF and MDC levels soon after WTC exposure were associated with increased risk of airflow obstruction in subsequent years. Biomarkers of inflammation may help identify pathways producing obstruction after irritant exposure.
Figures
Comment in
-
Can we predict who will develop chronic sequelae of acute inhalational injury?Chest. 2012 Aug;142(2):278-279. doi: 10.1378/chest.12-0126. Chest. 2012. PMID: 22871748 No abstract available.
Similar articles
-
Biomarkers of World Trade Center Particulate Matter Exposure: Physiology of Distal Airway and Blood Biomarkers that Predict FEV₁ Decline.Semin Respir Crit Care Med. 2015 Jun;36(3):323-33. doi: 10.1055/s-0035-1547349. Epub 2015 May 29. Semin Respir Crit Care Med. 2015. PMID: 26024341 Free PMC article. Review.
-
Metabolic syndrome biomarkers predict lung function impairment: a nested case-control study.Am J Respir Crit Care Med. 2012 Feb 15;185(4):392-9. doi: 10.1164/rccm.201109-1672OC. Epub 2011 Nov 17. Am J Respir Crit Care Med. 2012. PMID: 22095549 Free PMC article.
-
Cardiovascular biomarkers predict susceptibility to lung injury in World Trade Center dust-exposed firefighters.Eur Respir J. 2013 May;41(5):1023-30. doi: 10.1183/09031936.00077012. Epub 2012 Aug 16. Eur Respir J. 2013. PMID: 22903969 Free PMC article.
-
Blood Leukocyte Concentrations, FEV1 Decline, and Airflow Limitation. A 15-Year Longitudinal Study of World Trade Center-exposed Firefighters.Ann Am Thorac Soc. 2018 Feb;15(2):173-183. doi: 10.1513/AnnalsATS.201703-276OC. Ann Am Thorac Soc. 2018. PMID: 29099614 Free PMC article.
-
The evolving spectrum of pulmonary disease in responders to the World Trade Center tragedy.Am J Ind Med. 2011 Sep;54(9):649-60. doi: 10.1002/ajim.20987. Am J Ind Med. 2011. PMID: 23236631 Review.
Cited by
-
Biomarkers of World Trade Center Particulate Matter Exposure: Physiology of Distal Airway and Blood Biomarkers that Predict FEV₁ Decline.Semin Respir Crit Care Med. 2015 Jun;36(3):323-33. doi: 10.1055/s-0035-1547349. Epub 2015 May 29. Semin Respir Crit Care Med. 2015. PMID: 26024341 Free PMC article. Review.
-
Metabolic syndrome biomarkers predict lung function impairment: a nested case-control study.Am J Respir Crit Care Med. 2012 Feb 15;185(4):392-9. doi: 10.1164/rccm.201109-1672OC. Epub 2011 Nov 17. Am J Respir Crit Care Med. 2012. PMID: 22095549 Free PMC article.
-
Post-September 11, 2001, Incidence of Systemic Autoimmune Diseases in World Trade Center-Exposed Firefighters and Emergency Medical Service Workers.Mayo Clin Proc. 2016 Jan;91(1):23-32. doi: 10.1016/j.mayocp.2015.09.019. Epub 2015 Dec 9. Mayo Clin Proc. 2016. PMID: 26682920 Free PMC article.
-
Particulate matter inhalation and the exacerbation of cardiopulmonary toxicity due to metabolic disease.Exp Biol Med (Maywood). 2021 Apr;246(7):822-834. doi: 10.1177/1535370220983275. Epub 2021 Jan 19. Exp Biol Med (Maywood). 2021. PMID: 33467887 Free PMC article. Review.
-
Characterization of Persistent Uncontrolled Asthma Symptoms in Community Members Exposed to World Trade Center Dust and Fumes.Int J Environ Res Public Health. 2020 Sep 11;17(18):6645. doi: 10.3390/ijerph17186645. Int J Environ Res Public Health. 2020. PMID: 32933057 Free PMC article.
References
-
- Lioy PJ, Georgopoulos P. The anatomy of the exposures that occurred around the World Trade Center site: 9/11 and beyond Ann N Y Acad Sci. 2006;107654–79. - PubMed
-
- Prezant DJ, Weiden M, Banauch GI, et al. Cough and bronchial responsiveness in firefighters at the World Trade Center site N Engl J Med. 2002;34711806–815. - PubMed
-
- Banauch GI, Dhala A, Alleyne D, et al. Bronchial hyperreactivity and other inhalation lung injuries in rescue/recovery workers after the World Trade Center collapse Crit Care Med. 2005;33(supp 1):S102–S106. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- U01CA008617/CA/NCI NIH HHS/United States
- U10 OH008243/OH/NIOSH CDC HHS/United States
- T32 ES007267/ES/NIEHS NIH HHS/United States
- UL1 RR029893/RR/NCRR NIH HHS/United States
- 1UL1RR029893/RR/NCRR NIH HHS/United States
- K23HL084191/HL/NHLBI NIH HHS/United States
- U10-OH008242/OH/NIOSH CDC HHS/United States
- R01 HL090316/HL/NHLBI NIH HHS/United States
- T32-ES007267/ES/NIEHS NIH HHS/United States
- K24A1080298/PHS HHS/United States
- U10-OH008243/OH/NIOSH CDC HHS/United States
- K23 HL084191/HL/NHLBI NIH HHS/United States
- U10 OH008242/OH/NIOSH CDC HHS/United States
- R01HL090316/HL/NHLBI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical