Associations Between Residential Exposure to Volatile Organic Compounds and Liver Injury Markers

Author:

Wahlang Banrida123,Gripshover Tyler C14,Gao Hong156,Krivokhizhina Tatiana156,Keith Rachel J156,Sithu Israel D156,Rai Shesh N13578,Bhatnagar Aruni13456,McClain Craig J12345,Srivastava Sanjay14569,Cave Mathew C12345

Affiliation:

1. Superfund Research Center, the University of Louisville, Louisville, Kentucky 40202, USA

2. Division of Gastroenterology, Hepatology & Nutrition, Department of Medicine, the University of Louisville School of Medicine, Louisville, Kentucky 40202, USA

3. The Center for Integrative Environmental Health Sciences, University of Louisville, Louisville, Kentucky 40202, USA

4. Department of Pharmacology & Toxicology, the University of Louisville School of Medicine, Louisville, Kentucky 40202, USA

5. Envirome Institute, University of Louisville, Louisville, Kentucky 40202, USA

6. Division of Environmental Medicine, Department of Medicine, University of Louisville, Louisville, Kentucky 40202, USA

7. Department of Bioinformatics and Biostatistics, the School of Public Health and Information Sciences, the University of Louisville, Louisville, Kentucky 40202, USA

8. Biostatistics and Bioinformatics Facility, James Graham Brown Cancer Center, Louisville, Kentucky 40202, USA

9. Department of Biochemistry and Molecular Genetics, the University of Louisville School of Medicine, Louisville, Kentucky 40202, USA

Abstract

Abstract Occupational exposures to volatile organic compounds (VOCs) have been associated with numerous health complications including steatohepatitis and liver cancer. However, the potential impact of environmental/residential VOC exposures on liver health and function is largely unknown. To address this knowledge gap, the objective of this cross-sectional study is to investigate associations between VOCs and liver injury biomarkers in community residents. Subjects were recruited from six Louisville neighborhoods, and informed consent was obtained. Exposure biomarkers included 16 creatinine-adjusted urinary metabolites corresponding to 12 parent VOCs. Serological disease biomarkers measured included cytokertain-18 (K18 M65 and M30), liver enzymes, and direct bilirubin. Associations between exposure and disease biomarkers were assessed using generalized linear models. Smoking status was confirmed through urinary cotinine levels. The population comprised of approximately 60% females and 40% males; White persons accounted 78% of the population; with more nonsmokers (n = 413) than smokers (n = 250). When compared with nonsmokers, males (45%) and Black persons (26%) were more likely to be smokers. In the overall population, metabolites of acrolein, acrylonitrile, acrylamide, 1,3-butadiene, crotonaldehyde, styrene, and xylene were positively associated with alkaline phosphatase. These associations persisted in smokers, with the exception of crotonaldehyde, and addition of N,N-dimethylformamide and propylene oxide metabolites. Although no positive associations were observed for K18 M30, the benzene metabolite was positively associated with bilirubin, irrespective of smoking status. Taken together, the results demonstrated that selected VOCs were positively associated with liver injury biomarkers. These findings will enable better risk assessment and identification of populations vulnerable to liver disease.

Funder

The National Institute of Environmental Health Sciences

National Heart Blood and Lung Institute

National Institute of General Medical Sciences

National Institute on Alcohol Abuse and Alcoholism

Publisher

Oxford University Press (OUP)

Subject

Toxicology

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