Associations between maternal plasma measurements of inflammatory markers and urinary levels of phenols and parabens during pregnancy: A repeated measures study

Maternal immune system regulation is critical for maintenance of a healthy pregnancy and fetal development. Exposure to phenols and parabens is widespread, and may be linked to systemic inflammation and alteration of circulating immunological biomarkers. We sought to characterize associations betwee...

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Veröffentlicht in:The Science of the total environment 2019-02, Vol.650 (Pt 1), p.1131-1140
Hauptverfasser: Aung, Max T., Ferguson, Kelly K., Cantonwine, David E., Bakulski, Kelly M., Mukherjee, Bhramar, Loch-Caruso, Rita, McElrath, Thomas F., Meeker, John D.
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container_end_page 1140
container_issue Pt 1
container_start_page 1131
container_title The Science of the total environment
container_volume 650
creator Aung, Max T.
Ferguson, Kelly K.
Cantonwine, David E.
Bakulski, Kelly M.
Mukherjee, Bhramar
Loch-Caruso, Rita
McElrath, Thomas F.
Meeker, John D.
description Maternal immune system regulation is critical for maintenance of a healthy pregnancy and fetal development. Exposure to phenols and parabens is widespread, and may be linked to systemic inflammation and alteration of circulating immunological biomarkers. We sought to characterize associations between repeated measures of individual urinary phenols, parabens and plasma inflammatory markers across pregnancy. In the LIFECODES prospective birth cohort, we conducted a nested preterm birth case-control study, including 130 cases and 352 controls. In urine samples collected from each participant at up to four study visits during pregnancy, we measured concentrations of six phenols and four parabens, as well as five plasma inflammatory markers. We used multivariable linear mixed models to analyze repeated measures of exposures on inflammatory markers. We created and applied inverse probability weights to account for the sampling approach. We observed bidirectional associations between select phenols and parabens and inflammatory markers. An interquartile range increase in triclosan (55.2 ng/mL) was associated with a 12.5% (95% CI: 3.67, 22.0) increase in C-reactive protein, a 7.95% (95% CI: 1.95, 14.3) increase in interleukin 10, and a 7.93% (95% CI: 3.82, 12,2) increase in tumor necrosis factor-α. Additionally, an interquartile range increase in 2,5-dichlorophenol (11.0 ng/mL) was associated with a 10% increase in C-reactive protein (95% CI: 1.92, 18.7). Conversely, an interquartile range increase in ethyl paraben (10.4 ng/mL) was associated with a 7.7% decrease in interleukin‑1β (95% CI: −14.1, −0.86). Our findings can be organized into two thematic frameworks, one where concentrations of urinary phenols and parabens during pregnancy reflected a pro-inflammatory relationship with immunological biomarkers, and the other contrary theme – an anti-inflammatory relationship. These findings have implications for fetal development and reproductive outcomes, and emphasize the need for further research on immunological mechanisms of phenol and paraben action during pregnancy. [Display omitted] •Phenol exposure during pregnancy was associated with systemic plasma immune biomarkers.•2,5-Dichlorophenol and triclosan were positively associated with C-reactive protein.•Triclosan was positively associated with tumor necrosis factor-α and interleukin-10.
doi_str_mv 10.1016/j.scitotenv.2018.08.356
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Exposure to phenols and parabens is widespread, and may be linked to systemic inflammation and alteration of circulating immunological biomarkers. We sought to characterize associations between repeated measures of individual urinary phenols, parabens and plasma inflammatory markers across pregnancy. In the LIFECODES prospective birth cohort, we conducted a nested preterm birth case-control study, including 130 cases and 352 controls. In urine samples collected from each participant at up to four study visits during pregnancy, we measured concentrations of six phenols and four parabens, as well as five plasma inflammatory markers. We used multivariable linear mixed models to analyze repeated measures of exposures on inflammatory markers. We created and applied inverse probability weights to account for the sampling approach. We observed bidirectional associations between select phenols and parabens and inflammatory markers. An interquartile range increase in triclosan (55.2 ng/mL) was associated with a 12.5% (95% CI: 3.67, 22.0) increase in C-reactive protein, a 7.95% (95% CI: 1.95, 14.3) increase in interleukin 10, and a 7.93% (95% CI: 3.82, 12,2) increase in tumor necrosis factor-α. Additionally, an interquartile range increase in 2,5-dichlorophenol (11.0 ng/mL) was associated with a 10% increase in C-reactive protein (95% CI: 1.92, 18.7). Conversely, an interquartile range increase in ethyl paraben (10.4 ng/mL) was associated with a 7.7% decrease in interleukin‑1β (95% CI: −14.1, −0.86). Our findings can be organized into two thematic frameworks, one where concentrations of urinary phenols and parabens during pregnancy reflected a pro-inflammatory relationship with immunological biomarkers, and the other contrary theme – an anti-inflammatory relationship. These findings have implications for fetal development and reproductive outcomes, and emphasize the need for further research on immunological mechanisms of phenol and paraben action during pregnancy. 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Exposure to phenols and parabens is widespread, and may be linked to systemic inflammation and alteration of circulating immunological biomarkers. We sought to characterize associations between repeated measures of individual urinary phenols, parabens and plasma inflammatory markers across pregnancy. In the LIFECODES prospective birth cohort, we conducted a nested preterm birth case-control study, including 130 cases and 352 controls. In urine samples collected from each participant at up to four study visits during pregnancy, we measured concentrations of six phenols and four parabens, as well as five plasma inflammatory markers. We used multivariable linear mixed models to analyze repeated measures of exposures on inflammatory markers. We created and applied inverse probability weights to account for the sampling approach. We observed bidirectional associations between select phenols and parabens and inflammatory markers. An interquartile range increase in triclosan (55.2 ng/mL) was associated with a 12.5% (95% CI: 3.67, 22.0) increase in C-reactive protein, a 7.95% (95% CI: 1.95, 14.3) increase in interleukin 10, and a 7.93% (95% CI: 3.82, 12,2) increase in tumor necrosis factor-α. Additionally, an interquartile range increase in 2,5-dichlorophenol (11.0 ng/mL) was associated with a 10% increase in C-reactive protein (95% CI: 1.92, 18.7). Conversely, an interquartile range increase in ethyl paraben (10.4 ng/mL) was associated with a 7.7% decrease in interleukin‑1β (95% CI: −14.1, −0.86). Our findings can be organized into two thematic frameworks, one where concentrations of urinary phenols and parabens during pregnancy reflected a pro-inflammatory relationship with immunological biomarkers, and the other contrary theme – an anti-inflammatory relationship. These findings have implications for fetal development and reproductive outcomes, and emphasize the need for further research on immunological mechanisms of phenol and paraben action during pregnancy. [Display omitted] •Phenol exposure during pregnancy was associated with systemic plasma immune biomarkers.•2,5-Dichlorophenol and triclosan were positively associated with C-reactive protein.•Triclosan was positively associated with tumor necrosis factor-α and interleukin-10.</description><subject>biomarkers</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - urine</subject><subject>C-reactive protein</subject><subject>case-control studies</subject><subject>Chlorinated phenols</subject><subject>Cytokines</subject><subject>Environmental Monitoring</subject><subject>Environmental Pollutants - blood</subject><subject>Environmental Pollutants - urine</subject><subject>Female</subject><subject>fetal development</subject><subject>Humans</subject><subject>immune system</subject><subject>inflammation</subject><subject>interleukin-10</subject><subject>interleukin-1beta</subject><subject>Male</subject><subject>Maternal Exposure - statistics &amp; numerical data</subject><subject>Parabens - metabolism</subject><subject>phenol</subject><subject>Phenols - blood</subject><subject>Phenols - urine</subject><subject>Pregnancy</subject><subject>premature birth</subject><subject>probability</subject><subject>Reproductive immunology</subject><subject>triclosan</subject><subject>tumor necrosis factor-alpha</subject><subject>urine</subject><issn>0048-9697</issn><issn>1879-1026</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2OFCEUhYnROO3oKyhLN1VC0UWBC5POxL9kEje6JjTc6qGloASqTb-Njyptz3R0JRsS7nfPuZeD0CtKWkoof7Nvs3ElFgiHtiNUtES0rOeP0IqKQTaUdPwxWhGyFo3kcrhCz3Lek3oGQZ-iK0YYEYLQFfq1yTkap4uLIeMtlJ8AAU-6QAra49nrPGk8gc5LgglCyTiO2IXR66lSMR0rnL5DylgHi5fkgq5vHg7g_6DzHYToz9VZJ72F6mNP3A7PCXZBB3N8izc4wQzV1j6YZZzLYo_P0ZNR-wwv7u9r9O3D-683n5rbLx8_32xuG9MTURrNudSGMyk4H8Zh3K6Z6a20dj1uwVJdl-WSryXRYhilIbzjnFrac0oH20lg1-jdWXdethNYU1dN2qs5ubrfUUXt1L-V4O7ULh4U71i1FFXg9b1Aij8WyEVNLhvwXgeIS1YdFbJnjPW0osMZNSnmnGC82FCiTvmqvbrkq075KiJUzbd2vvx7ykvfQ6AV2JyB-v1wcJBOQhAMWJfAFGWj-6_Jb48CwaA</recordid><startdate>20190210</startdate><enddate>20190210</enddate><creator>Aung, Max T.</creator><creator>Ferguson, Kelly K.</creator><creator>Cantonwine, David E.</creator><creator>Bakulski, Kelly M.</creator><creator>Mukherjee, Bhramar</creator><creator>Loch-Caruso, Rita</creator><creator>McElrath, Thomas F.</creator><creator>Meeker, John D.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5993-2799</orcidid></search><sort><creationdate>20190210</creationdate><title>Associations between maternal plasma measurements of inflammatory markers and urinary levels of phenols and parabens during pregnancy: A repeated measures study</title><author>Aung, Max T. ; 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numerical data</topic><topic>Parabens - metabolism</topic><topic>phenol</topic><topic>Phenols - blood</topic><topic>Phenols - urine</topic><topic>Pregnancy</topic><topic>premature birth</topic><topic>probability</topic><topic>Reproductive immunology</topic><topic>triclosan</topic><topic>tumor necrosis factor-alpha</topic><topic>urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aung, Max T.</creatorcontrib><creatorcontrib>Ferguson, Kelly K.</creatorcontrib><creatorcontrib>Cantonwine, David E.</creatorcontrib><creatorcontrib>Bakulski, Kelly M.</creatorcontrib><creatorcontrib>Mukherjee, Bhramar</creatorcontrib><creatorcontrib>Loch-Caruso, Rita</creatorcontrib><creatorcontrib>McElrath, Thomas F.</creatorcontrib><creatorcontrib>Meeker, John D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Science of the total environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aung, Max T.</au><au>Ferguson, Kelly K.</au><au>Cantonwine, David E.</au><au>Bakulski, Kelly M.</au><au>Mukherjee, Bhramar</au><au>Loch-Caruso, Rita</au><au>McElrath, Thomas F.</au><au>Meeker, John D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Associations between maternal plasma measurements of inflammatory markers and urinary levels of phenols and parabens during pregnancy: A repeated measures study</atitle><jtitle>The Science of the total environment</jtitle><addtitle>Sci Total Environ</addtitle><date>2019-02-10</date><risdate>2019</risdate><volume>650</volume><issue>Pt 1</issue><spage>1131</spage><epage>1140</epage><pages>1131-1140</pages><issn>0048-9697</issn><eissn>1879-1026</eissn><abstract>Maternal immune system regulation is critical for maintenance of a healthy pregnancy and fetal development. Exposure to phenols and parabens is widespread, and may be linked to systemic inflammation and alteration of circulating immunological biomarkers. We sought to characterize associations between repeated measures of individual urinary phenols, parabens and plasma inflammatory markers across pregnancy. In the LIFECODES prospective birth cohort, we conducted a nested preterm birth case-control study, including 130 cases and 352 controls. In urine samples collected from each participant at up to four study visits during pregnancy, we measured concentrations of six phenols and four parabens, as well as five plasma inflammatory markers. We used multivariable linear mixed models to analyze repeated measures of exposures on inflammatory markers. We created and applied inverse probability weights to account for the sampling approach. We observed bidirectional associations between select phenols and parabens and inflammatory markers. An interquartile range increase in triclosan (55.2 ng/mL) was associated with a 12.5% (95% CI: 3.67, 22.0) increase in C-reactive protein, a 7.95% (95% CI: 1.95, 14.3) increase in interleukin 10, and a 7.93% (95% CI: 3.82, 12,2) increase in tumor necrosis factor-α. Additionally, an interquartile range increase in 2,5-dichlorophenol (11.0 ng/mL) was associated with a 10% increase in C-reactive protein (95% CI: 1.92, 18.7). Conversely, an interquartile range increase in ethyl paraben (10.4 ng/mL) was associated with a 7.7% decrease in interleukin‑1β (95% CI: −14.1, −0.86). Our findings can be organized into two thematic frameworks, one where concentrations of urinary phenols and parabens during pregnancy reflected a pro-inflammatory relationship with immunological biomarkers, and the other contrary theme – an anti-inflammatory relationship. These findings have implications for fetal development and reproductive outcomes, and emphasize the need for further research on immunological mechanisms of phenol and paraben action during pregnancy. [Display omitted] •Phenol exposure during pregnancy was associated with systemic plasma immune biomarkers.•2,5-Dichlorophenol and triclosan were positively associated with C-reactive protein.•Triclosan was positively associated with tumor necrosis factor-α and interleukin-10.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30308801</pmid><doi>10.1016/j.scitotenv.2018.08.356</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5993-2799</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects biomarkers
Biomarkers - blood
Biomarkers - urine
C-reactive protein
case-control studies
Chlorinated phenols
Cytokines
Environmental Monitoring
Environmental Pollutants - blood
Environmental Pollutants - urine
Female
fetal development
Humans
immune system
inflammation
interleukin-10
interleukin-1beta
Male
Maternal Exposure - statistics & numerical data
Parabens - metabolism
phenol
Phenols - blood
Phenols - urine
Pregnancy
premature birth
probability
Reproductive immunology
triclosan
tumor necrosis factor-alpha
urine
title Associations between maternal plasma measurements of inflammatory markers and urinary levels of phenols and parabens during pregnancy: A repeated measures study
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