Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/3643
DC FieldValueLanguage
dc.contributor.authorAndra, Syam S.-
dc.contributor.authorAndrianou, Xanthi-
dc.contributor.authorMakris, Konstantinos C.-
dc.contributor.authorChristophi, Costas A.-
dc.contributor.authorCharisiadis, Pantelis-
dc.contributor.authorKalyvas, Harris-
dc.date.accessioned2015-03-23T12:35:29Z-
dc.date.accessioned2015-12-08T11:09:28Z-
dc.date.available2015-03-23T12:35:29Z-
dc.date.available2015-12-08T11:09:28Z-
dc.date.issued2015-01-16-
dc.identifier.citationJournal of Environmental Science and Health, Part A: Toxic/Hazardous Substances and Environmental Engineering, 2015, vol. 50, no. 3, pp. 243-259.en_US
dc.identifier.issn15324117-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/3643-
dc.description.abstractEvidence for the association of bisphenol A (BPA) with type II diabetes mellitus (T2DM) has been inconsistent in human studies. In-vitro and animal studies indicate that chlorinated BPA derivatives aggravate BPA health effects via higher estrogenic activity and alteration of membrane-initiating signaling pathways. We evaluated the association between urinary monochlorinated BPA (mono-ClBPA) concentrations and the incidence of T2DM. In our cross-sectional study, we identified 20 adult participants (≥18 yr) who reported having T2DM (doctor-diagnosed) and 131 adults with normal health. First morning void urine samples were analyzed for total BPA and mono-ClBPA. Detection limits of the analytical method were 95 ng L−1 for BPA and 32 ng L−1 for mono-ClBPA. Multivariable logistic regression analyses and additive Bayesian network modeling were performed. After adjusting for age, gender, BMI, urinary total BPA and other confounders, the odds of having T2DM was 3.29 times higher (95% confidence interval, CI: 1.10, 11.4; P < 0.05) per unit increase in log-transformed and creatinine-adjusted urinary mono-ClBPA levels (n = 151); this relation did not hold for total BPA. The globally optimum Bayesian model corroborated the results of the logistic regression by expressing mono-ClBPA in the pathway of T2DM, and not for total BPA. An age-matched sensitivity analysis confirmed the increase in OR of T2DM by 3.04 times (95% CI: 1.10, 11.0; P < 0.05) per unit increase in log-transformed and creatinine-adjusted urinary mono-ClBPA concentration (n = 68). The urinary monochlorinated BPA derivative was significantly associated with T2DM, whereas the parent compound (total BPA) was not. Caution should be applied in interpreting these findings, as this is the first study to report this association and the sample size of participants with T2DM is small. Additional research with a larger sample size coupled with relevant toxicological studies is warranted.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Environmental Science and Health, Part A: Toxic/Hazardous Substances and Environmental Engineeringen_US
dc.rights© Taylor & Francisen_US
dc.subjectBisphenol Aen_US
dc.subjectExposure biomarkersen_US
dc.subjectMonochlorinated bisphenol Aen_US
dc.subjectType 2 diabetesen_US
dc.subjectTrihalomethanesen_US
dc.titlePreliminary evidence of the association between monochlorinated bisphenol A exposure and type II diabetes mellitus: a pilot studyen_US
dc.typeArticleen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationHarvard Universityen_US
dc.subject.categoryBasic Medicineen_US
dc.journalsSubscriptionen_US
dc.reviewPeer Revieweden
dc.countryCyprusen_US
dc.countryUnited Statesen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1080/10934529.2015.981111en_US
dc.dept.handle123456789/108en
dc.relation.issue3en_US
dc.relation.volume50en_US
cut.common.academicyear2015-2016en_US
dc.identifier.spage243en_US
dc.identifier.epage259en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.author.deptCyprus International Institute for Environmental and Public Health-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.deptCyprus International Institute for Environmental and Public Health-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0002-2906-5743-
crisitem.author.orcid0000-0001-5251-8619-
crisitem.author.orcid0000-0003-0503-1538-
crisitem.author.orcid0000-0001-7260-192X-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.author.parentorgFaculty of Health Sciences-
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