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Increase of urinary malondialdehyde level by bisphenol A exposure: a longitudinal panel study

DC Field Value Language
dc.contributor.authorKim, Jin Hee-
dc.contributor.authorHong, Yun-Chul-
dc.date.accessioned2017-03-30T07:37:38Z-
dc.date.available2017-03-30T16:42:35Z-
dc.date.issued2017-02-15-
dc.identifier.citationEnvironmental Health, 16(1):8ko_KR
dc.identifier.urihttp://dx.doi.org/10.1186/s12940-017-0221-9-
dc.identifier.urihttps://hdl.handle.net/10371/110128-
dc.description.abstractBackground
To verify oxidative stress as a possible mechanism that establishes a relationship between exposure to bisphenol A (BPA) and adverse health outcomes in the elderly Korean population, we evaluated the relation between visit-to-visit variations in urinary BPA and oxidative stress biomarker.

Methods
To assess the relation between BPA and urinary malondialdehyde (MDA) as an oxidative stress biomarker, we used a mixed effect model after controlling for age, sex, BMI, drinking status, exercise, urinary cotinine level, PM10 on lag day 2, and mean temperature and dew point on the day. The relation between exposure to BPA and MDA level by sex of participants and polymorphisms of oxidative stress-related genes (COX2, EPHX1, HSP70-hom, PON1, eNOS, CAT, DRD2, SOD2, and MPO) was also evaluated.

Results
A significant association was found for BPA with MDA in both male and female elderly participants (male, β = 0.19 and p = 0.0003; female, β = 0.18 and p < .0001; and total, β = 0.18 and p < .0001). Furthermore, the association of BPA with MDA was found regardless of any genotype of the nine oxidative stress-related genes.

Conclusions
The results of our study suggest a strong association of BPA with oxidative stress, not related with sex and oxidative stress-related gene polymorphisms.
ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.subjectElderlyko_KR
dc.subjectBisphenol Ako_KR
dc.subjectOxidative stressko_KR
dc.subjectMalondialdehydeko_KR
dc.titleIncrease of urinary malondialdehyde level by bisphenol A exposure: a longitudinal panel studyko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김진희-
dc.contributor.AlternativeAuthor홍윤철-
dc.language.rfc3066en-
dc.rights.holderThe Author(s).-
dc.date.updated2017-03-27T07:24:35Z-
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