Literature DB >> 16222163

Polycyclic aromatic hydrocarbons and fatal ischemic heart disease.

Igor Burstyn1, Hans Kromhout, Timo Partanen, Ole Svane, Sverre Langård, Wolfgang Ahrens, Timo Kauppinen, Isabelle Stücker, Judith Shaham, Dick Heederik, Gilles Ferro, Pirjo Heikkilä, Mariëtte Hooiveld, Christoffer Johansen, Britt G Randem, Paolo Boffetta.   

Abstract

BACKGROUND: Several toxicologic and epidemiologic studies have produced evidence that occupational exposure to polycyclic aromatic hydrocarbons (PAH) is a risk factor for ischemic heart disease (IHD). However, a clear exposure-response relation has not been demonstrated.
METHODS: We studied a relation between exposure to PAH and mortality from IHD (418 cases) in a cohort of 12,367 male asphalt workers from Denmark, Finland, France, Germany, Israel, The Netherlands and Norway. The earliest follow up (country-specific) started in 1953 and the latest ended in 2000, averaging 17 years. Exposures to benzo(a)pyrene were assessed quantitatively using measurement-driven exposure models. Exposure to coal tar was assessed in a semiquantitative manner on the basis of information supplied by company representatives. We carried out sensitivity analyses to assess potential confounding by tobacco smoking.
RESULTS: Both cumulative and average exposure indices for benzo(a)pyrene were positively associated with mortality from IHD. The highest relative risk for fatal IHD was observed for average benzo(a)pyrene exposures of 273 ng/m or higher, for which the relative risk was 1.64 (95% confidence interval=1.13-2.38). Similar results were obtained for coal tar exposure. Sensitivity analysis indicated that even in a realistic scenario of confounding by smoking, we would observe approximately 20% to 40% excess risk in IHD in the highest PAH-exposure categories.
CONCLUSIONS: Our results lend support to the hypothesis that occupational PAH exposure causes fatal IHD and demonstrate a consistent exposure-response relation for this association.

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Year:  2005        PMID: 16222163     DOI: 10.1097/01.ede.0000181310.65043.2f

Source DB:  PubMed          Journal:  Epidemiology        ISSN: 1044-3983            Impact factor:   4.822


  55 in total

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Review 2.  An Overview of Occupational Risks From Climate Change.

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4.  Mechanistic Evaluation of Benzo[a]pyrene's Developmental Toxicities Mediated by Reduced Cyp19a1b Activity.

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5.  Structurally distinct polycyclic aromatic hydrocarbons induce differential transcriptional responses in developing zebrafish.

Authors:  Britton C Goodale; Susan C Tilton; Margaret M Corvi; Glenn R Wilson; Derek B Janszen; Kim A Anderson; Katrina M Waters; Robert L Tanguay
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6.  Metabolomic analysis to define and compare the effects of PAHs and oxygenated PAHs in developing zebrafish.

Authors:  Marc R Elie; Jaewoo Choi; Yasmeen M Nkrumah-Elie; Gregory D Gonnerman; Jan F Stevens; Robert L Tanguay
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7.  In utero exposure to benzo(a)pyrene predisposes offspring to cardiovascular dysfunction in later-life.

Authors:  G E Jules; S Pratap; A Ramesh; D B Hood
Journal:  Toxicology       Date:  2012-02-21       Impact factor: 4.221

8.  Benzo[a]pyrene induces intercellular adhesion molecule-1 through a caveolae and aryl hydrocarbon receptor mediated pathway.

Authors:  Elizabeth Oesterling; Michal Toborek; Bernhard Hennig
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Review 9.  A systematic review of occupational exposure to particulate matter and cardiovascular disease.

Authors:  Shona C Fang; Adrian Cassidy; David C Christiani
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10.  3-methylcholanthrene and benzo(a)pyrene modulate cardiac cytochrome P450 gene expression and arachidonic acid metabolism in male Sprague Dawley rats.

Authors:  Mona E Aboutabl; Beshay N M Zordoky; Ayman O S El-Kadi
Journal:  Br J Pharmacol       Date:  2009-12       Impact factor: 8.739

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