Shift workers represent nearly 20 % of the US working population, and this occupational hazard conveys increased risk for myriad of pathologies. Our preclinical research provides insight into the basis of shift-work disease. In our previous work, we have revealed that dysregulated inflammation occurs in animal models of shift work, with broad suppression under basal conditions and hypersensitivity to inflammatory challenge. Since aberrant inflammatory responses would be expected to increase stroke, myocardial infarction, diabetes, and cancer, as is observed in shift work epidemiological studies, we hypothesize that chronic dysregulation of inflammation due to environmental disruption underlies the increased risk of disease in career shift workers. In this application, we will conduct a cross-sectional pilot study of human day workers and shift workers exposed to temporally changing occupational environments.
We aim to test the hypothesis that humans exposed to shift-work environments develop 1), decreased expression of immune markers, and 2), aberrant inflammatory responses upon ex-vivo endotoxin activation. Furthermore, we will measure individual light exposure parameters, activity/rest changes and expression of stress and metabolic hormones to link a comprehensive immune profile to specific shift-work exposure history. Our initial goal is to uncover aberrant inflammatory responses defined as those in which the critical balance between pro- and anti- inflammatory signaling processes is disrupted and then determine if the severity of disruption relates to increased shift-work exposure. Long term, our ultimately goal is to establish a preventive medicine research program that will investigate inflammatory responses in actual shift workers using a low-invasive, blood based ex-vivo assay. Follow-up longitudinal studies will develop this assay into a diagnostic tool to identify biological markers linked to the duration of shift-work exposure and to basal biological changes predictive of disease risk. Identification of biological markers of shift-work related environmental disruption may reveal a mechanistic link between shift-work exposure and disease risk, and may become a future tool for workplace intervention by preventive identification of aberrant inflammatory responses in specific shift scheduling systems. .

Public Health Relevance

Recently classified by the World Health Organization as a potential carcinogen, shift-work exposure and its health consequences has vast social and economic costs for both employees and employers in a society that works around the clock. Since minority groups are more likely to engage in shift work, quality research initiatives that seek to understand the disease risks associated with these hazardous occupational environments may significantly impact both health equity and overall public health. This project will seek to leverage a blood-based, low invasive approach to uncover potential biomarkers of disease risk in shift workers.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Pilot Research Project (SC2)
Project #
5SC2GM125493-02
Application #
9658530
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Krasnova, Irina N
Project Start
2018-03-01
Project End
2021-02-28
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Morehouse School of Medicine
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
102005451
City
Atlanta
State
GA
Country
United States
Zip Code
30310