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Associations Between Biomarkers of Exposure and Lung Cancer Risk Among Exclusive Cigarette Smokers in the Golestan Cohort Study Publisher Pubmed



Rostron BL1 ; Wang J1 ; Etemadi A2, 3 ; Thakur S1 ; Chang JT1 ; Bhandari D4 ; Botelho JC4 ; De Jesus VR4 ; Feng J4 ; Gail MH5 ; Inouechoi M2 ; Malekzadeh R3 ; Pourshams A3 ; Poustchi H6 Show All Authors
Authors
  1. Rostron BL1
  2. Wang J1
  3. Etemadi A2, 3
  4. Thakur S1
  5. Chang JT1
  6. Bhandari D4
  7. Botelho JC4
  8. De Jesus VR4
  9. Feng J4
  10. Gail MH5
  11. Inouechoi M2
  12. Malekzadeh R3
  13. Pourshams A3
  14. Poustchi H6
  15. Roshandel G7
  16. Shiels MS8
  17. Wang Q9
  18. Wang Y4
  19. Xia B4
  20. Boffetta P10, 11
  21. Brennan P12
  22. Abnet CC2
  23. Calafat AM4
  24. Wang L4
  25. Blount BC4
  26. Freedman ND2
  27. Chang CM1

Source: International Journal of Environmental Research and Public Health Published:2021


Abstract

Biomarkers of tobacco exposure are known to be associated with disease risk but previous studies are limited in number and restricted to certain regions. We conducted a nested case–control study examining baseline levels and subsequent lung cancer incidence among current male exclusive cigarette smokers in the Golestan Cohort Study in Iran. We calculated geometric mean biomarker concentrations for 28 matched cases and 52 controls for the correlation of biomarker levels among controls and for adjusted odds’ ratios (ORs) for lung cancer incidence by biomarker concentration, accounting for demographic characteristics, smoking quantity and duration, and opium use. Lung cancer cases had higher average levels of most biomarkers including total nicotine equivalents (TNE-2), 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), and 3-hydroxyfluorene (3-FLU). Many biomarkers correlated highly with one another including TNE-2 with NNAL and N-Acetyl-S-(2-cyanoethyl)-L-cysteine (2CYEMA), and N-Acetyl-S-(4-hydroxy-2-buten-1-yl)-L-cysteine (t4HBEMA) with N-Acetyl-S-(3-hydroxypropyl-1-methyl)-L-cysteine (3HMPMA) and N-Acetyl-S-(4-hydroxy-2-methyl-2-buten-1-yl)-L-cysteine (4HMBEMA). Lung cancer risk increased with concentration for several biomarkers, including TNE-2 (OR = 2.22, 95% CI = 1.03, 4.78) and NNN (OR = 2.44, 95% CI = 1.13, 5.27), and estimates were significant after further adjustment for demographic and smoking characteristics for 2CYEMA (OR = 2.17, 95% CI = 1.03, 4.55), N-Acetyl-S-(2-carbamoylethyl)-L-cysteine (2CAEMA) (OR = 2.14, 95% CI = 1.01, 4.55), and N-Acetyl-S-(2-hydroxypropyl)-L-cysteine (2HPMA) (OR = 2.85, 95% CI = 1.04, 7.81). Estimates were not significant with adjustment for opium use. Concentrations of many biomarkers were higher at the baseline for participants who subsequently developed lung cancer than among the matched controls. Odds of lung cancer were higher for several biomarkers including with adjustment for smoking exposure for some but not with adjustment for opium use. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
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