Anti-B[aPDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons

[Anti-B[a]PDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons] We are currently evaluating anti-benzo[a]pyrenediolepoxide-(B[a]PDE)-DNA adduct levels in lymphomonocytes of humans exposed to polycyclic aromatic hydrocarbons (PAHs) to validate thi...

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Veröffentlicht in:Giornale italiano di medicina del lavoro ed ergonomia 2005-07, Vol.27 (3), p.312
Hauptverfasser: Pavanello, S, Pulliero, A, Lai, A, Gaiardo, A, Mastrangelo, G, Clonfero, E
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container_title Giornale italiano di medicina del lavoro ed ergonomia
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creator Pavanello, S
Pulliero, A
Lai, A
Gaiardo, A
Mastrangelo, G
Clonfero, E
description [Anti-B[a]PDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons] We are currently evaluating anti-benzo[a]pyrenediolepoxide-(B[a]PDE)-DNA adduct levels in lymphomonocytes of humans exposed to polycyclic aromatic hydrocarbons (PAHs) to validate this indicator of biologically effective dose in a surrogate tissue. The study protocol (October 2002-June 2005) implies: (a) a signed informed consent by each participant; (b) recruitment of 600 Padua municipal workers during visits at our outpatient clinic; (c) administration of a questionnaire regarding non occupational sources of PAH (B[a]P) exposure; (d) collection of blood (15 ml) and urine (200 ml) samples. Anti-B[a]PDE-DNA adduct levels in lymphomonocytes are detected by HPLC-fluorescence analysis. To date, 438 subjects have been examined (age range 20-62 years; 52% males). We found that: (i) anti-B[a]PDE-DNA adduct levels are significantly lower than those we previously found in coke-oven workers (N=95) occupationally exposed to high levels of PAHs (1.51 +/- 2.68 versus 4.07 +/- 3.78 anti-B[a]PDE-adduct/10(8) nucleotides, p < 0.001; 37% versus 97% positive subjects with > or =1 adduct/10(8) nucleotides; p < 0.001); (ii) smokers (23%) have significantly higher adduct levels than non smokers (p < 0.001); iii) non smokers who consume PAH-rich meals > or =52 times/year (142 subjects, 42%) have significantly increased adduct levels than those
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The study protocol (October 2002-June 2005) implies: (a) a signed informed consent by each participant; (b) recruitment of 600 Padua municipal workers during visits at our outpatient clinic; (c) administration of a questionnaire regarding non occupational sources of PAH (B[a]P) exposure; (d) collection of blood (15 ml) and urine (200 ml) samples. Anti-B[a]PDE-DNA adduct levels in lymphomonocytes are detected by HPLC-fluorescence analysis. To date, 438 subjects have been examined (age range 20-62 years; 52% males). We found that: (i) anti-B[a]PDE-DNA adduct levels are significantly lower than those we previously found in coke-oven workers (N=95) occupationally exposed to high levels of PAHs (1.51 +/- 2.68 versus 4.07 +/- 3.78 anti-B[a]PDE-adduct/10(8) nucleotides, p &lt; 0.001; 37% versus 97% positive subjects with &gt; or =1 adduct/10(8) nucleotides; p &lt; 0.001); (ii) smokers (23%) have significantly higher adduct levels than non smokers (p &lt; 0.001); iii) non smokers who consume PAH-rich meals &gt; or =52 times/year (142 subjects, 42%) have significantly increased adduct levels than those &lt;52 times/year (p &lt; 0.01). Dietary and smoking habits did not influence the occupationally-induced adduct levels in coke-oven workers. 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The study protocol (October 2002-June 2005) implies: (a) a signed informed consent by each participant; (b) recruitment of 600 Padua municipal workers during visits at our outpatient clinic; (c) administration of a questionnaire regarding non occupational sources of PAH (B[a]P) exposure; (d) collection of blood (15 ml) and urine (200 ml) samples. Anti-B[a]PDE-DNA adduct levels in lymphomonocytes are detected by HPLC-fluorescence analysis. To date, 438 subjects have been examined (age range 20-62 years; 52% males). We found that: (i) anti-B[a]PDE-DNA adduct levels are significantly lower than those we previously found in coke-oven workers (N=95) occupationally exposed to high levels of PAHs (1.51 +/- 2.68 versus 4.07 +/- 3.78 anti-B[a]PDE-adduct/10(8) nucleotides, p &lt; 0.001; 37% versus 97% positive subjects with &gt; or =1 adduct/10(8) nucleotides; p &lt; 0.001); (ii) smokers (23%) have significantly higher adduct levels than non smokers (p &lt; 0.001); iii) non smokers who consume PAH-rich meals &gt; or =52 times/year (142 subjects, 42%) have significantly increased adduct levels than those &lt;52 times/year (p &lt; 0.01). Dietary and smoking habits did not influence the occupationally-induced adduct levels in coke-oven workers. This is the first study that examines anti-B[a]PDE-DNA adduct levels in a large cohort showing that anti-B[a]PDE-DNA adducts can be detected in humans environmentally exposed to low doses of PAH (B[a]P and are modulated by smoke and dietary habits.</description><subject>7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide - analysis</subject><subject>Adult</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Diet</subject><subject>DNA Adducts - blood</subject><subject>DNA Adducts - drug effects</subject><subject>Environmental Monitoring</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Humans</subject><subject>Informed Consent</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Occupational Exposure</subject><subject>Polycyclic Aromatic Hydrocarbons - adverse effects</subject><subject>Polymerase Chain Reaction</subject><subject>Smoking</subject><subject>Surveys and Questionnaires</subject><subject>Tobacco Smoke Pollution</subject><issn>1592-7830</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j91KwzAYQHOhuDH3CpIXKOSvbXo5t_kDQwW982J8TVJaafKVpBPz9irOc3PuDpwLsuRlI4paS7Yg65Q-2A8VExWvr8iCV0KxUosliZswD8XtO7zs9sXuaUM7jB7mAQMdAh2zn3r0GNDk2SWKHe1PHkKiLnwOEYN3YYZxzNR9TZicpTPSCcdsshkHQyHib8zQPtuIBmKLIV2Tyw7G5NZnr8jr3f5t-1Acnu8ft5tDMZVKFFIBlxocM7WEVjnZccuZhlZz0FDpRukWQAlQpbPGNabTFbeMqcY0wK1ckZu_6nRqvbPHKQ4eYj7-r8tvmsNYBg</recordid><startdate>200507</startdate><enddate>200507</enddate><creator>Pavanello, S</creator><creator>Pulliero, A</creator><creator>Lai, A</creator><creator>Gaiardo, A</creator><creator>Mastrangelo, G</creator><creator>Clonfero, E</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200507</creationdate><title>Anti-B[aPDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons</title><author>Pavanello, S ; Pulliero, A ; Lai, A ; Gaiardo, A ; Mastrangelo, G ; Clonfero, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p542-34a138ae0c73ab4e3f1d108ab81a8a68948baa42a45edce9cf861d0049c9a1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>ita</language><creationdate>2005</creationdate><topic>7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide - analysis</topic><topic>Adult</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Diet</topic><topic>DNA Adducts - blood</topic><topic>DNA Adducts - drug effects</topic><topic>Environmental Monitoring</topic><topic>Female</topic><topic>Fluorescence</topic><topic>Humans</topic><topic>Informed Consent</topic><topic>Leukocytes, Mononuclear - drug effects</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Occupational Exposure</topic><topic>Polycyclic Aromatic Hydrocarbons - adverse effects</topic><topic>Polymerase Chain Reaction</topic><topic>Smoking</topic><topic>Surveys and Questionnaires</topic><topic>Tobacco Smoke Pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pavanello, S</creatorcontrib><creatorcontrib>Pulliero, A</creatorcontrib><creatorcontrib>Lai, A</creatorcontrib><creatorcontrib>Gaiardo, A</creatorcontrib><creatorcontrib>Mastrangelo, G</creatorcontrib><creatorcontrib>Clonfero, E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Giornale italiano di medicina del lavoro ed ergonomia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pavanello, S</au><au>Pulliero, A</au><au>Lai, A</au><au>Gaiardo, A</au><au>Mastrangelo, G</au><au>Clonfero, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-B[aPDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons</atitle><jtitle>Giornale italiano di medicina del lavoro ed ergonomia</jtitle><addtitle>G Ital Med Lav Ergon</addtitle><date>2005-07</date><risdate>2005</risdate><volume>27</volume><issue>3</issue><spage>312</spage><pages>312-</pages><issn>1592-7830</issn><abstract>[Anti-B[a]PDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons] We are currently evaluating anti-benzo[a]pyrenediolepoxide-(B[a]PDE)-DNA adduct levels in lymphomonocytes of humans exposed to polycyclic aromatic hydrocarbons (PAHs) to validate this indicator of biologically effective dose in a surrogate tissue. The study protocol (October 2002-June 2005) implies: (a) a signed informed consent by each participant; (b) recruitment of 600 Padua municipal workers during visits at our outpatient clinic; (c) administration of a questionnaire regarding non occupational sources of PAH (B[a]P) exposure; (d) collection of blood (15 ml) and urine (200 ml) samples. Anti-B[a]PDE-DNA adduct levels in lymphomonocytes are detected by HPLC-fluorescence analysis. To date, 438 subjects have been examined (age range 20-62 years; 52% males). We found that: (i) anti-B[a]PDE-DNA adduct levels are significantly lower than those we previously found in coke-oven workers (N=95) occupationally exposed to high levels of PAHs (1.51 +/- 2.68 versus 4.07 +/- 3.78 anti-B[a]PDE-adduct/10(8) nucleotides, p &lt; 0.001; 37% versus 97% positive subjects with &gt; or =1 adduct/10(8) nucleotides; p &lt; 0.001); (ii) smokers (23%) have significantly higher adduct levels than non smokers (p &lt; 0.001); iii) non smokers who consume PAH-rich meals &gt; or =52 times/year (142 subjects, 42%) have significantly increased adduct levels than those &lt;52 times/year (p &lt; 0.01). Dietary and smoking habits did not influence the occupationally-induced adduct levels in coke-oven workers. This is the first study that examines anti-B[a]PDE-DNA adduct levels in a large cohort showing that anti-B[a]PDE-DNA adducts can be detected in humans environmentally exposed to low doses of PAH (B[a]P and are modulated by smoke and dietary habits.</abstract><cop>Italy</cop><pmid>16240582</pmid></addata></record>
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subjects 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide - analysis
Adult
Chromatography, High Pressure Liquid
Diet
DNA Adducts - blood
DNA Adducts - drug effects
Environmental Monitoring
Female
Fluorescence
Humans
Informed Consent
Leukocytes, Mononuclear - drug effects
Male
Middle Aged
Occupational Exposure
Polycyclic Aromatic Hydrocarbons - adverse effects
Polymerase Chain Reaction
Smoking
Surveys and Questionnaires
Tobacco Smoke Pollution
title Anti-B[aPDE-DNA formation in lymphomonocytes of humans environmentally exposed to polycyclic aromatic hydrocarbons
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