Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 6 de 6
Filtrer
1.
Environ Int ; 152: 106485, 2021 07.
Article de Anglais | MEDLINE | ID: mdl-33689906

RÉSUMÉ

BACKGROUND: Exposure to polycyclic aromatic hydrocarbons (PAHs) is a risk factor for esophageal squamous cell carcinoma (ESCC) in high-incidence areas of China, Iran and Brazil, but PAH assessments have not been conducted in East Africa, another ESCC hot spot. OBJECTIVE: To evaluate demographic or lifestyle factors associated with the PAH biomarker concentrations in the study population, and whether PAH metabolite concentrations showed any associations with esophageal precancerous lesions. METHODS: We recruited a community-based sample of 289 asymptomatic adults from a rural area of Kenya and performed Lugol's chromoendoscopy to detect esophageal squamous dysplasia (ESD); participants completed a questionnaire and provided a spot urine specimen. We analyzed urine for seven hydroxylated metabolites of naphthalene, fluorene, phenanthrene, and pyrene at the U.S. National Center for Environmental Health, and compared creatinine-corrected PAH metabolite concentrations with questionnaire data and the presence of ESD. RESULTS: PAH metabolite concentrations among never tobacco users in these rural Kenya residents were 2.4-28.1 times higher than those reported from never tobacco users in Iran, Brazil and the USA. Female sex, cooking indoors, having no post-primary education, and age <50, but not tobacco use, were positively and significantly associated with PAH metabolite concentrations. Almost all participants used wood as cooking fuel. Nine participants had advanced ESD. Adjusted logistic regression showed a significant association between 2-hydroxynaphthalene (OR = 4.19, 95%CI: 1.01-17.47) and advanced ESD. All other PAH metabolites had positive but non-significant associations with advanced ESD. CONCLUSIONS: Urinary PAH metabolite concentrations among never tobacco users are markedly higher in this group from Kenya than in other populations and are associated with indoor cooking with wood on open, unvented stoves. These metabolite concentrations were also associated with the presence of advanced esophageal dysplasia. Our findings underline the importance of assessing alternative cooking conditions to reduce PAH exposure in this population.


Sujet(s)
Tumeurs de l'oesophage , Carcinome épidermoïde de l'oesophage , Hydrocarbures aromatiques polycycliques , Adulte , Brésil , Cancérogènes , Chine , Tumeurs de l'oesophage/épidémiologie , Tumeurs de l'oesophage/étiologie , Femelle , Humains , Iran , Kenya/épidémiologie , Hydrocarbures aromatiques polycycliques/analyse , Bois/composition chimique
2.
Cancer Epidemiol Biomarkers Prev ; 27(3): 331-337, 2018 03.
Article de Anglais | MEDLINE | ID: mdl-29263183

RÉSUMÉ

Background: Consumption of maté, an infusion of the herb Ilex paraguariensis (yerba maté), is associated with increased risk of esophageal squamous cell carcinoma (ESCC), but the carcinogenic mechanism is unclear. Commercial brands of yerba maté contain high levels of carcinogenic polycyclic aromatic hydrocarbons (PAHs), which are acquired during the traditional drying process. The purpose of this study was to characterize exposure to PAHs in maté drinkers over a wide range of maté consumption.Methods: We recruited 244 adults who answered a questionnaire and collected a fasting spot urine specimen. We quantified urinary concentrations of seven PAH metabolites and assessed associations between self-reported recent maté consumption and urinary PAH metabolites by multivariate regression.Results: Recent maté consumption showed a significant dose-response association with 6 of 7 PAH metabolites in unadjusted models (Ptrend < 0.05). After adjustment for creatinine and potential confounders, concentrations of 2-naphthol, 1-hydroxyphenanthrene, and the sum of 2- and 3-hydroxyphenanthrene remained significantly associated with recent maté intake. The sum of the urinary concentrations of the phenanthrene metabolites was similar or higher among maté drinkers who did not smoke than among smokers who did not drink matéConclusions: Urinary concentrations of PAH metabolites were significantly associated with self-reported amounts of recent maté intake, and drinking maté increased urinary concentrations of some PAH metabolites as much as smoking cigarettes.Impact: Drinking maté is a source of exposure to potentially carcinogenic PAHs, consistent with the hypothesis that the PAH content of maté may contribute to the increased risk of ESCC in maté drinkers. Cancer Epidemiol Biomarkers Prev; 27(3); 331-7. ©2017 AACR.


Sujet(s)
Boissons/statistiques et données numériques , Tumeurs de l'oesophage/prévention et contrôle , Carcinome épidermoïde de l'oesophage/prévention et contrôle , Ilex paraguariensis/toxicité , Hydrocarbures aromatiques polycycliques/urine , Adulte , Boissons/effets indésirables , Brésil , Études transversales , Tumeurs de l'oesophage/étiologie , Carcinome épidermoïde de l'oesophage/étiologie , Femelle , Humains , Ilex paraguariensis/composition chimique , Mâle , Adulte d'âge moyen , Hydrocarbures aromatiques polycycliques/métabolisme , Hydrocarbures aromatiques polycycliques/toxicité , Autorapport/statistiques et données numériques , Fumer/effets indésirables , Fumer/urine
3.
Cancer Epidemiol Biomarkers Prev ; 23(1): 107-16, 2014 Jan.
Article de Anglais | MEDLINE | ID: mdl-24130226

RÉSUMÉ

BACKGROUND: Maté tea is a nonalcoholic infusion widely consumed in southern South America, and may increase risk of esophageal squamous cell carcinoma (ESCC) and other cancers due to polycyclic aromatic hydrocarbons (PAH) and/or thermal injury. METHODS: We pooled two case-control studies: a 1988 to 2005 Uruguay study and a 1986 to 1992 multinational study in Argentina, Brazil, Paraguay, and Uruguay, including 1,400 cases and 3,229 controls. We computed ORs and fitted a linear excess OR (EOR) model for cumulative maté consumption in liters/day-year (LPDY). RESULTS: The adjusted OR for ESCC with 95% confidence interval (CI) by ever compared with never use of maté was 1.60 (1.2-2.2). ORs increased linearly with LPDY (test of nonlinearity; P = 0.69). The estimate of slope (EOR/LPDY) was 0.009 (0.005-0.014) and did not vary with daily intake, indicating maté intensity did not influence the strength of association. EOR/LPDY estimates for consumption at warm, hot, and very hot beverage temperatures were 0.004 (-0.002-0.013), 0.007 (0.003-0.013), and 0.016 (0.009-0.027), respectively, and differed significantly (P < 0.01). EOR/LPDY estimates were increased in younger (<65) individuals and never alcohol drinkers, but these evaluations were post hoc, and were homogeneous by sex. CONCLUSIONS: ORs for ESCC increased linearly with cumulative maté consumption and were unrelated to intensity, so greater daily consumption for shorter duration or lesser daily consumption for longer duration resulted in comparable ORs. The strength of association increased with higher maté temperatures. IMPACT: Increased understanding of cancer risks with maté consumption enhances the understanding of the public health consequences given its purported health benefits.


Sujet(s)
Boissons/statistiques et données numériques , Carcinome épidermoïde/épidémiologie , Tumeurs de l'oesophage/épidémiologie , Ilex paraguariensis/composition chimique , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Boissons/effets indésirables , Boissons/analyse , Carcinome épidermoïde/étiologie , Études cas-témoins , Tumeurs de l'oesophage/étiologie , Carcinome épidermoïde de l'oesophage , Femelle , Humains , Mâle , Adulte d'âge moyen , Extraits de plantes/administration et posologie , Extraits de plantes/effets indésirables , Feuilles de plante/composition chimique , Amérique du Sud , Uruguay
4.
Environ Sci Technol ; 46(24): 13488-93, 2012 Dec 18.
Article de Anglais | MEDLINE | ID: mdl-23101992

RÉSUMÉ

Drinking maté, common in southern South America, may increase the risk of esophageal squamous cell carcinoma (ESCC). In 2006, we found high but variable polycyclic aromatic hydrocarbon (PAH) content in commercial yerba maté samples from eight Brazilian brands. The PAH content of new samples from the same brands, purchased in 2008, and four brands from a single manufacturer processed in different ways, obtained in 2010, were quantified to determine whether PAH concentration was still high, whether PAH content variation was brand specific, and whether processing method affects PAH content of commercial yerba maté. Concentrations of individual PAHs were quantified using gas chromatography/mass spectrometry with deuterated PAHs as internal standards. Median total PAH concentration was 1500 ng/g (range: 625-3710 ng/g) and 1090 ng/g (621-1990 ng/g) in 2008 and 2010 samples, respectively. Comparing 2006 and 2008 samples, some brands had high PAH concentrations in both years, while PAH concentration changed considerably in others. Benzo[a]pyrene concentrations ranged from 11.9 to 99.3 ng/g and 5.11 to 21.0 ng/g in 2008 and 2010 samples, respectively. The 2010 sample processed without touching smoke had the lowest benzo[a]pyrene content. These results support previous findings of very high total and carcinogenic PAH concentrations in yerba maté, perhaps contributing to the high incidence of ESCC in southern South America. The large PAH content variation by brand, batch, and processing method suggests it may be possible to reduce the content of carcinogenic PAHs in commercial yerba maté, making it a healthier beverage.


Sujet(s)
Benzo[a]pyrène/analyse , Cancérogènes/analyse , Manipulation des aliments , Ilex paraguariensis/composition chimique , Hydrocarbures aromatiques polycycliques/analyse , Brésil , Feuilles de plante/composition chimique
5.
Carcinogenesis ; 28(1): 112-7, 2007 Jan.
Article de Anglais | MEDLINE | ID: mdl-16864595

RÉSUMÉ

Polymorphisms in genes encoding polycyclic aromatic hydrocarbon (PAH) metabolizing enzymes may alter metabolism of these carcinogens and contribute to inter-individual difference in urine concentrations. We investigated the influence of genetic polymorphism on PAH metabolism in urine from 199 healthy subjects from Southern Brazil. We measured urine 1-hydroxypyrene glucuronide (1-OHPG) concentrations using immunoaffinity chromatography and synchronous fluorescence spectroscopy and genotyped subjects using standard methods. Genetic variants in CYP1B1 (rs1056827, rs1800440, rs10012) were strongly associated with urine 1-OHPG with P-values < 0.010. Variants in aryl hydrocarbon receptor (Ahr) (rs4986826), CYP1A1 (rs1799814) and CYP1A2 (rs2069514) were also, although less strongly, associated with changes in urine 1-OHPG concentrations. These variants had P-values of 0.074, 0.040 and 0.025, respectively. The median urine 1-OHPG concentrations (pmol/ml) in the homozygous wild-type and homozygous variants for CYP1B1 (rs10012) and the Ahr, CYP1A1 and CYP1A2 variants listed above were 2.16 and 0.10, 2.16 and 0.41, 2.03 and 0.46, 2.19 and 2.79, respectively. We found no effect of deletions in GST M1 or GST T1, or different alleles of UGT1A1*28. Adjusting for age, sex, place of residence, tobacco smoke exposure, maté drinking, cachaça and barbeque preparation had only a minor impact on the associations. A model containing just exposure variables had an r2 of 0.21; a model with single genotypes for Ahr, CYP1A1, CYP1A2 and CYP1B1 had an r2 of 0.10; and a model combining both exposure and genotype information had a total r2 of 0.33. Our results suggest that CYP1B1 genotypes are strongly associated with urine 1-OHPG concentrations in this population.


Sujet(s)
Aryl hydrocarbon hydroxylases/génétique , Cytochrome P-450 CYP1A1/génétique , Cytochrome P-450 CYP1A2/génétique , Glucuronates/urine , Glucuronosyltransferase/génétique , Glutathione transferase/génétique , Polymorphisme génétique , Récepteurs à hydrocarbure aromatique/génétique , Brésil/épidémiologie , Chromatographie d'affinité , Cytochrome P-450 CYP1B1 , Femelle , Humains , Mâle , Adulte d'âge moyen , Pyrènes
6.
BMC Cancer ; 6: 139, 2006 May 26.
Article de Anglais | MEDLINE | ID: mdl-16729889

RÉSUMÉ

BACKGROUND: The highest rates of esophageal squamous cell carcinoma (ESCC) in Brazil occur in Rio Grande do Sul, the most southern state, which has incidence rates of 20.4/100,000/year for men and 6.5/100,000/year for women. Exposure to carcinogenic polycyclic aromatic hydrocarbons (PAHs) through tobacco smoke and other sources may increase the risk of ESCC. The aims of the current study were to investigate the degree and sources of PAH exposure of the inhabitants of this region of southern Brazil. METHODS: Two hundred healthy adults (half smokers, half non smokers, half male and half female) were recruited, given a standardized questionnaire, and asked to provide a urine sample for measurement of 1-hydroxypyrene glucuronide (1-OHPG), a PAH metabolite). Urine 1-OHPG concentrations were measured using immunoaffinity chromatography and synchronous fluorescence spectroscopy and urine cotinine was measured using a dipstick test. We examined factors associated with 1-OHPG concentration using Wilcoxon tests and multiple linear regression. RESULTS: Urine 1-hydroxypyrene glucuronide (1-OHPG) was successfully measured on 199 subjects. The median (interquartile range) of urine 1-OHPG in the 199 participants was 2.09 pmol/mL (0.51, 5.84). Tobacco smoke exposure and maté drinking were statistically significantly associated with higher urine 1-OHPG concentrations in the multivariate linear regression model. CONCLUSION: Tobacco smoke and maté both contribute to high levels of benzo[a]pyrene exposure in the people of southern Brazil. This high PAH exposure may contribute to the high rates of ESCC observed in this population. The increased urine 1-OHPG concentrations associated with maté suggest that contaminants, not just thermal injury, may help explain the increased risk of ESCC previously reported for maté consumption.


Sujet(s)
Benzo[a]pyrène/pharmacocinétique , Boissons/effets indésirables , Cancérogènes environnementaux/pharmacocinétique , Cuisine (activité)/statistiques et données numériques , Glucuronates/urine , Ilex paraguariensis/effets indésirables , Hydrocarbures aromatiques polycycliques/pharmacocinétique , Fumée/effets indésirables , Fumer/effets indésirables , Pollution par la fumée de tabac/effets indésirables , Consommation d'alcool/épidémiologie , Benzo[a]pyrène/effets indésirables , Marqueurs biologiques , Biotransformation , Brésil/épidémiologie , Cancérogènes environnementaux/effets indésirables , Cocancérogenèse , Cuisine (activité)/méthodes , Cotinine/urine , Exposition environnementale , Tumeurs de l'oesophage/épidémiologie , Température élevée/effets indésirables , Incidence , Viande , Hydrocarbures aromatiques polycycliques/effets indésirables , Pyrènes , Enquêtes et questionnaires
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE