Data have revealed increases in cardiovascular (CVD) and neurodegenerative diseases in First Responders (FR) who were present at the Ground Zero over the 9/11-13/01 period. While it has yet not been shown if WTC (World Trade Center) dusts were causative for these pathologies in FR, our study of SHR rats exposed to WTC dusts [in paradigms mimicking mouthbreathing FR] noted significantly changes in CV function and cardiac gap junction protein expression, and ultrastructural remodeling like that seen in heart failure. These rats also had persistent (up to 1 yr post-exposure) reductions in airway ciliated cells and dust clearance from the lung. It is thus likely exposures to WTC dusts resulted in exaggerated responses in situ compared to that by other urban air pollutants, including particulate matter (PM). We know long-term exposure to ambient PM caused a heart failure phenotype in mice (decreased cardiac function and impaired cell function) and neurologic as well as Alzheimer disease (AD)-like changes (increased levels of BACE protein, APP processing, and A? [amyloid-?]) in their brains. As both CVD and AD are age-related, share risk-factors, have overlapping bio-chemistries, and are characterized by aggregates of amyloid precursor protein (found in AD brains and CVD hearts), based on the ?heart-to-head? pathogenesis paradigm, we hypothesize here that inhalation of Ground Zero dust particles likely led - in a manner exaggerating that caused by PM - to alterations in cardiac and cognitive function, so as to impart severe chronic impacts on FR health. As models, SHR rats will be exposed to WTC dust (using paradigms as in current WTC project: 2 consecutive days, 2 hr/d, intratracheal inhalation, using dusts collected on-site 9/12-13/01). Both longitudinally and at fixed timepoints over a 1-yr post-exposure period, data will be obtained in support of two inter-related Aims.
Aim 1 will define effects of WTC dust exposures on CV function and A? aggregate accumulation in the heart.
Aim 2 will assess effects of the exposures on development of neurodegenerative disease. We are aware there is as-yet no documented link between AD and FR exposures at Ground Zero. However, as with the long-expected increased risk for lung cancer, one cannot outright preclude a possibility of this specific pathology developing simply due to absence of epidemiologic data to- date. Accordingly, in a Supplemental Aim, exposed rats will undergo additional cognitive studies and brain levels of Neuropeptide-Y and N-acetylaspartate will be examined to see if there were changes induced over time reflective of PTSD, an well-documented outcome among exposed FR. The studies will allow us, for the first time, to determine the time-course of any WTC dust-induced onset/progression of CV dysfunction and neurodegenerative disorders in exposed hosts. The studies address NIOSH goals (CVD Cross-Sector Program, Public Safety Program [Priority 1: Reduce chronic illnesses among firefighters] and FFFFIPP [Goal 1: Reduce CV deaths among firefighters]), keep with major r2p initiatives to reduce illness among firefighters/FR via NIOSH-generated knowledge, interventions, technologies, and fulfill the Zadroga Act research mandate.

Public Health Relevance

The proposed studies seek to gain a better understanding of the bases for the still-increasing incidence of cardiovascular (CV) and neurodegenerative anomalies reported in 9/11 First Responders (FR). These landmark studies will be performed in a rat model exposed to WTC dusts obtained in/unique to the critical first 72 hr after the buildings collapsed, using relevant exposure scenarios that mimic mouthbreathing exposures and dust levels faced by FR during that critical period. Results from these studies will allow us to: further clarify whether exposure to WTC dust exacerbates the CV and neurologic phenotype, i.e., effects that have led to changes in CV and brain health of exposed FR; ascertain if the dusts were themselves capable of inducing an Alzheimer Disease/PTSD phenotype in exposed hosts; obtain important biochemical/molecular clues to the etiologies for the increasingly evident CV/neurologic problems seen in these exposed FR.

Agency
National Institute of Health (NIH)
Institute
National Institute for Occupational Safety and Health (NIOSH)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01OH012056-01
Application #
10064225
Study Section
Special Emphasis Panel (ZOH1)
Program Officer
Yiin, James
Project Start
2020-07-01
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Ohio State University
Department
Type
Schools of Nursing
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210