Associations between residential volatile organic compound exposures and liver injury markers: The role of biological sex and race

• Published in: Environmental research Vol. 221; p. 115228
• Main Authors: Wahlang, Banrida, Gao, Hong, Rai, Shesh N., Keith, Rachel J., McClain, Craig J., Srivastava, Sanjay, Cave, Mathew C., Bhatnagar, Aruni
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 15.03.2023
• Subjects: acrolein; Acrylamides; air; Air Pollutants - analysis; alkaline phosphatase; ALP; aspartate transaminase; benzene; bilirubin; biomarkers; Biomarkers - urine; death; dose response; Female; females; Humans; lifestyle; liver; Liver - chemistry; Liver injury; liver neoplasms; Male; metabolites; Race; Residential; Sex differences; styrene; Styrenes; VOCs; volatile organic compounds; Volatile Organic Compounds - analysis; 2MHA; Residential; ALP; ALT; HEAL; DHBMA; AMCC; CYMA; 3MHA+4MHA; Race; BMA; N-Acetyl-S-(4-hydroxy-2-buten-1-yl)-L-cysteine; BMI; VOCs; AST; Mandelic acid; PHEMA; Sex differences; CEMA; AAMA; PGA; limit of detection; 2HPMA; Liver injury; CVD; environment and action in Louisville; cytokeratin 18; GGT; UPLC-MS/MS; N-Acetyl-S-(3-hydroxypropyl-1-methyl)-L-cysteine; trans; 3HPMA
• ISSN: 0013-9351; 1096-0953; 1096-0953
• DOI: 10.1016/j.envres.2023.115228

While occupational exposures to volatile organic compounds (VOCs) have been linked to steatohepatitis and liver cancer in industrial workers, recent findings have also positively correlated low-dose, residential VOC exposures with liver injury markers. VOC sources are numerous; factors including biological make up (sex), socio-cultural constructs (gender, race) and lifestyle (smoking) can influence both VOC exposure levels and disease outcomes. Therefore, the current study's objective is to investigate how sex and race influence associations between residential VOC exposures and liver injury markers particularly in smokers vs. nonsmokers. Subjects (n = 663) were recruited from residential neighborhoods; informed consent was obtained. Exposure biomarkers included 16 urinary VOC metabolites. Serological disease biomarkers included liver enzymes, direct bilirubin, and hepatocyte death markers (cytokeratin K18). Pearson correlations and generalized linear models were conducted. Models were adjusted for common liver-related confounders and interaction terms. The study population constituted approximately 60% females (n = 401) and 40% males (n = 262), and a higher percent of males were smokers and/or frequent drinkers. Both sexes had a higher percent of White (75% females, 82% males) vs. Black individuals. Positive associations were identified for metabolites of acrolein, acrylamide, acrylonitrile, butadiene, crotonaldehyde, and styrene with alkaline phosphatase (ALP), a biomarker for cholestatic injury; and for the benzene metabolite with bilirubin; only in females. These associations were retained in female smokers. Similar associations were also observed between these metabolites and ALP only in White individuals (n = 514). In Black individuals (n = 114), the styrene metabolite was positively associated with aspartate transaminase. Interaction models indicated that positive associations for acrylamide/crotonaldehyde metabolites with ALP in females were dose-dependent. Most VOC associations with K18 markers were negative in this residential population. Overall, the findings demonstrated that biological sex, race, and smoking status influence VOC effects on liver injury and underscored the role of biological-social-lifestyle factor(s) interactions when addressing air pollution-related health disparities. [Display omitted] •16 urinary volatile organic compound (VOC) metabolites were measured in community residents.•Serum liver injury markers including alkaline phosphatase (ALP) were also measured.•Metabolites for VOCs such as acrolein and benzene were positively associated with ALP or bilirubin.•Associations between VOC metabolites and ALP were predominant in female smokers and White individuals.•In females, crotanaldehyde and acrylamide metabolite associations with ALP were dose-dependent.