Longitudinal stability in cigarette smokers of urinary biomarkers of exposure to the toxicants acrylonitrile and acrolein.

Ryan Vandrey, Stephen S Hecht, Dorothy Hatsukami, Eric C Donny, Jason D Robinson, Mustafa al'Absi, Andrew A Strasser, Paul M Cinciripini, Rachel Denlinger-Apte, Sharon S Allen, Menglan Chen, F Joseph McClernon, Neal L Benowitz, Sharon E Murphy, Chap T Le, Xianghua Luo, Joni Jensen, Chistopher Sipe, Steven G Carmella

Journal: PloS one 2019;14(1):e0210104

PMID: 30608961

Abstract

The urinary metabolites cyanoethyl mercapturic acid (CEMA) and 3-hydroxypropyl mercapturic acid (3-HPMA) have been widely used as biomarkers of exposure to acrylonitrile and acrolein, respectively, but there are no published data on their consistency over time in the urine of cigarette smokers. We provided, free of charge over a 20 week period, Spectrum NRC600/601 research cigarettes to cigarette smokers in the control arm of a randomized clinical trial of the reduced nicotine cigarette. Urine samples were collected at weeks 4, 8, 12, 16, and 20 and analyzed for CEMA and 3-HPMA, and total nicotine equivalents (TNE) using validated methods. Creatinine-corrected intra-class correlation coefficients for CEMA, 3-HPMA, and TNE were 0.67, 0.46, and 0.68, respectively, indicating good longitudinal consistency for CEMA, while that of 3-HPMA was fair. A strong correlation between CEMA and TNE values was observed. These data support the use of CEMA as a reliable biomarker of tobacco smoke exposure. This is the first report of the longitudinal stability of the biomarkers of acrylonitrile and acrolein exposure in smokers. The data indicate that CEMA, the biomarker of acrylonitrile exposure, is consistent over time in cigarette smokers, supporting its use. While 3-HPMA levels were less stable over time, this biomarker is nevertheless a useful monitor of human acrolein exposure because of its specificity to this toxicant.

Address: Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States of America.; Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, Minnesota, United States of America.; Department of Medicine, University of California, San Francisco, California, United States of America.; Department of Psychiatry and Behavioral Sciences, Duke University, Durham, North Carolina, United States of America.; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University, Baltimore, Maryland, United States of America.; Department of Family Medicine and Community Health, University of Minnesota Medical School, Minneapolis, Minnesota, United States of America.; Department of Behavioral and Social Sciences, Brown University, Providence, Rhode Island, United States of America.; Department of Behavioral Science, University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.; Department of Psychiatry, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.; Behavioral Medicine Laboratories, University of Minnesota Medical School, Duluth, Minnesota, United States of America.; Department of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America.
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