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Influence of smoking on levels of urinary 8-iso Prostaglandin F2α

BACKGROUND: To evaluate the reduced-risk potential of alternative tobacco products, biomarkers that are involved in the biological pathways affected by cigarette smoking and smoking cessation are needed. Isoprostanes, a measure of oxidative stress, appear to be influenced by smoking and reversible u...

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Detalles Bibliográficos
Autores principales: van der Plas, Angela, Pouly, Sandrine, de La Bourdonnaye, Guillaume, Baker, Gizelle, Lüdicke, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260378/
https://www.ncbi.nlm.nih.gov/pubmed/30519530
http://dx.doi.org/10.1016/j.toxrep.2018.11.011
Descripción
Sumario:BACKGROUND: To evaluate the reduced-risk potential of alternative tobacco products, biomarkers that are involved in the biological pathways affected by cigarette smoking and smoking cessation are needed. Isoprostanes, a measure of oxidative stress, appear to be influenced by smoking and reversible upon smoking cessation and therefore could be a good biomarker. This review aims at quantifying the effect of smoking and smoking cessation on levels of urinary 8-iso prostaglandin F(2α) (8-epi-PGF(2α)), an isoprostane. METHODS: PubMed and Scopus databases were searched for publications that reported 8-epi-PGF(2α) levels in smokers and nonsmokers as well as articles reporting the effect of smoking cessation on 8-epi-PGF(2α) levels. RESULTS: Eighteen studies assessing 8-epi-PGF(2α) levels by smoking status were identified. Five of the papers reported the results as quantity excreted in 24-hour urine (μg/24 h), and 15 reported creatinine adjusted values. The meta-analyses show increased levels of 8-epi-PGF(2α) in current smokers compared with nonsmokers (mean difference = 0.16, 95% confidence interval [95%CI]: 0.14–0.19 μg/24 h with inconsistency statistic [I(2)] = 98%; mean difference = 172.38, 95%CI: 152.75–192.01 pg/mg creatinine with I(2) = 89%, respectively). There were too few publications to perform a meta-analysis assessing the effects of smoking cessation on 8-epi-PGF(2α) levels. CONCLUSIONS: Due to the high heterogeneity among the studies included in these meta-analyses, it is difficult to generalize the results; however, our study indicates increased levels of 8-epi-PGF(2α) and therefore increased oxidative stress in smokers compared with nonsmokers. More studies are still needed to assess if 8-epi-PGF(2α) levels are reversible after cessation.