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Clinical Biomarkers of World Trade Center Airway Hyperreactivity: A 16-Year Longitudinal Study



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  • Personal Author:
  • Description:
    RATIONALE: Development of airway hyperreactivity (AHR) related to environmental exposure is a significant global health risk. Similarly, Metabolic Syndrome (MetSyn) is also positively associated with the development of AHR and is a significant contributor to adverse health globally. OBJECTIVES: We propose to investigate if clinical biomarkers including those defining MetSyn are predictors of World Trade Center (WTC)-AHR in the longitudinally followed Fire Department of New York (FDNY) World Trade Center (WTC} exposed cohort. METHODS: A baseline cohort of male firefighters with FEV1 ≥LLN prior to 9/11 that had serum drawn prior to site closure on July 24, 2002(N=7,486) was assessed. Cases of WTC-AHR (N=539) were identified if they had either a positive BO response (FEV 1 increased by ≥12% and ≥200 ml) (N= 236) or had a positive methacholine challenge, defined as a PC20<16mg/mL (N=355). N:52 had both tests positive, WTC-AHR cases were compared to N=6947 subjects that did not develop WTC-AHR. We modeled the ability of MetSyn at the first post-9/11 exam to predict WTCAHR with Cox-proportional hazards regression and adjusted for age and smoking status. We additionally examined leukocyte subsets at the first exam as a comparison of a commonly associated marker of airway hyperreactivity. RESULTS: WTC-AHR cases compared to controls were significantly more likely to be older (40 vs 39), have slightly higher BMI (29 vs 28 kg/m2), have high intensity exposure (23% vs 16%), and have MetSyn compared to controls (20% vs 2%). There was a significant exposure dose response seen in the Cox regression models; the most highly exposed individuals present in the morning of 9/11 had 2.24-fold increased risk of developing WTC-AHR, and 75.9% increased risk if the individual arrived in the afternoon of 9/11 (p<0.001). Having 3 or more criteria of MetSyn increased risk of WTC-AHR by 65.4% (p<0.001). Having at least 5% eosinophilia on first post-9/11 differential independently increased the risk of WTC-AHR by 83.8%(p<0.001). Smoking history was not a significant risk factor in development of WTC·AHR. CONCLUSIONS: We assessed the utility of the clinical biomarkers to predict future AHR development in a population of WTC exposed individuals. These biomarkers are associated with dyslipidemia, insulin resistance, and cardiovascular disease, and suggest that systemic inflammation can contribute to future airway hyperreactivity. [Description provided by NIOSH]
  • Subjects:
  • Keywords:
  • ISSN:
    1073-449X
  • Document Type:
  • Funding:
  • Genre:
  • Place as Subject:
  • CIO:
  • Topic:
  • Location:
  • Volume:
    199
  • NIOSHTIC Number:
    nn:20066276
  • Citation:
    Am J Respir Crit Care Med 2019 May; 199(Abstract Issue):A2492
  • Email:
    kwons04@nyumc.org
  • Federal Fiscal Year:
    2019
  • Performing Organization:
    New York University School of Medicine
  • Peer Reviewed:
    False
  • Start Date:
    20170701
  • Source Full Name:
    American Journal of Respiratory and Critical Care Medicine
  • Supplement:
    Abstract Issue
  • End Date:
    20260630
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:b5e57179c24762751b1eb815cd1fe63396214731c736e9e6e2bb90e746224f3c39121fbb4e753b6dc728a9bef613e2fca5fbb4e0d624969bcff101098be66bb4
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  • File Type:
    Filetype[PDF - 360.41 KB ]
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