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Smoke Exposure Associated With Higher Urinary Benzene Biomarker Muconic Acid (Muca) in Golestan Cohort Study Participants Publisher Pubmed



Bhandari D1 ; Zhu Y1 ; Zhang C1 ; Zhu W1 ; Alexandridis A2 ; Etemadi A3, 4 ; Freedman ND3 ; Chang C2 ; Abnet CC3 ; Dawsey SM3 ; Inouechoi M3 ; Poustchi H4 ; Pourshams A4 ; Boffetta P5, 6 Show All Authors
Authors
  1. Bhandari D1
  2. Zhu Y1
  3. Zhang C1
  4. Zhu W1
  5. Alexandridis A2
  6. Etemadi A3, 4
  7. Freedman ND3
  8. Chang C2
  9. Abnet CC3
  10. Dawsey SM3
  11. Inouechoi M3
  12. Poustchi H4
  13. Pourshams A4
  14. Boffetta P5, 6
  15. Malekzadeh R4
  16. Blount B1
Show Affiliations
Authors Affiliations
  1. 1. Tobacco and Volatiles Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, United States
  2. 2. Center for Tobacco Products, Food and Drug Administration, Silver Spring, MD, United States
  3. 3. Metabolic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States
  4. 4. Digestive Oncology Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY, United States
  6. 6. Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy

Source: Biomarkers Published:2023


Abstract

Background. Benzene is a known human carcinogen. Human exposure to benzene can be assessed by measuring trans, trans-muconic acid (MUCA) in urine. Golestan Province in northeastern Iran has been reported to have high incidence of esophageal cancer linked to the use of tobacco products. This manuscript evaluates the urinary MUCA concentrations among the participants of the Golestan Cohort Study (GCS). Methods. We analyzed MUCA concentration in 177 GCS participants’ urine samples and performed nonparametric pairwise multiple comparisons to determine statistically significant difference among six different product use groups. Mixed effects model was fitted on 22 participants who exclusively smoked cigarette and 51 participants who were classified as nonusers. The urinary MUCA data were collected at the baseline and approximately five years later, and intraclass correlation coefficient (ICC) was calculated from the model. Results. Compared with nonusers, tobacco smoking was associated with higher urinary MUCA concentrations. Based on the nonparametric test of pairwise multiple comparisons, MUCA concentrations among participants who smoked combusted tobacco products were statistically significantly higher compared to nonusers. Urinary MUCA collected five years apart from the same individuals showed moderate reliability (ICC = 0.41), which was expected given the relatively short half-life (∼6 h) of MUCA. Conclusion. Our study revealed that tobacco smoke was positively associated with increased levels of urinary MUCA concentration, indicating that it is a significant source of benzene exposure among GCS participants. © This work was authored as part of the Contributor’s official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
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