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Hum. Reprod. Advance Access published online on November 7, 2006

Human Reproduction, doi:10.1093/humrep/del428
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© The Author 2006. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Received July 14, 2006
Revised September 28, 2006
Accepted October 5, 2006

Article

DNA damage in human sperm is related to urinary levels of phthalate monoester and oxidative metabolites

R. Hauser 1 *, J.D. Meeker 2, N.P. Singh 3, M.J. Silva 4, L. Ryan 5, S. Duty 6, and A.M. Calafat 4

1 Department of Environmental Health, Harvard School of Public Health, Boston, MA, USA; Vincent Memorial Obstetrics & Gynecology Service, Andrology Laboratory and In Vitro Fertilization Unit, Massachusetts General Hospital, Boston, MA, USA
2 Department of Environmental Health Sciences, University of Michigan, Ann Arbor, MI, USA
3 Department of Bioengineering, University of Washington, Seattle, WA, USA
4 National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA, USA
5 Department of Biostatistics, Harvard School of Public Health, Boston, MA, USA
6 Department of Environmental Health, Harvard School of Public Health, Boston, MA, USA; Department of Nursing, School for Health Studies, Simmons College, Boston, MA, USA

* To whom correspondence should be addressed.
R. Hauser, E-mail: rhauser{at}hohp.harvard.edu


   Abstract

BACKGROUND: The ubiquitous use of phthalate esters in plastics, personal care products and food packaging materials results in widespread general population exposure. In this report, we extend our preliminary study on the relationship between urinary concentrations of phthalate metabolites and sperm DNA damage among a larger sample of men and include measurements of mono-(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP) and mono-(2-ethyl-5-oxohexyl) phthalate (MEOHP), two oxidative metabolites of di-(2-ethylhexyl) phthalate (DEHP). METHODS: Among 379 men from an infertility clinic, urinary concentrations of phthalate metabolites were measured using isotope-dilution high-performance liquid chromatography-tandem mass spectrometry. Sperm DNA damage measurements, assessed with the neutral comet assay, included comet extent (CE), percentage of DNA in tail (Tail%) and tail distributed moment (TDM). RESULTS: Monoethyl phthalate (MEP), a metabolite of diethyl phthalate, was associated with increased DNA damage, confirming our previous findings. Mono-(2-ethylhexyl) phthalate (MEHP), a metabolite of DEHP, was associated with DNA damage after adjustment for the oxidative DEHP metabolites. After adjustment for MEHHP, for an interquartile range increase in urinary MEHP, CE increased 17.3% [95% confidence interval (CI) = 8.7-25.7%], TDM increased 14.3% (95% CI = 6.8-21.7%) and Tail% increased 17.5% (95% CI = 3.5-31.5%). CONCLUSIONS: Sperm DNA damage was associated with MEP and with MEHP after adjusting for DEHP oxidative metabolites, which may serve as phenotypic markers of DEHP metabolism to ‘less toxic’ metabolites. The urinary levels of phthalate metabolites among these men were similar to those reported for the US general population, suggesting that exposure to some phthalates may affect the population distribution of sperm DNA damage.

Keywords: phthalates/urinary metabolites/DNA damage/comet assay/human sperm.
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