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Uric acid correlates to oxidation and inflammation in opposite directions in women

Identifieur interne : 000905 ( Pmc/Curation ); précédent : 000904; suivant : 000906

Uric acid correlates to oxidation and inflammation in opposite directions in women

Auteurs : Sheng Hui Wu [États-Unis] ; Xiao Ou Shu [États-Unis] ; Ginger Milne [États-Unis] ; Yong-Bing Xiang [République populaire de Chine] ; Xianglan Zhang [États-Unis] ; Qiuyin Cai [États-Unis] ; Sergio Fazio [États-Unis] ; Macrae F. Linton [États-Unis] ; Honglei Chen [États-Unis] ; Mark Purdue [Canada] ; Nathaniel Rothman [États-Unis] ; Yu-Tang Gao [République populaire de Chine] ; Wei Zheng [États-Unis] ; Gong Yang [États-Unis]

Source :

RBID : PMC:4989504

Abstract

Objective

To evaluate the association of uric acid (UA) levels with a panel of markers of oxidative stress and inflammation.

Methods

Plasma UA levels, along with a panel of oxidative stress and inflammatory markers, were measured in 755 Chinese women.

Results

Plasma UA levels were inversely associated with urinary levels of the oxidative stress marker F2-isoprostanes and positively correlated to levels of inflammatory markers such as C-reactive protein and some proinflammatory cytokines (tumor necrosis factor-α and interleukin-6) in blood as well as prostaglandin E2 metabolites in urine.

Conclusions

Plasma UA levels correlate to oxidation and inflammation biomarkers in opposite directions in women.


Url:
DOI: 10.3109/1354750X.2015.1068852
PubMed: 26301880
PubMed Central: 4989504

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PMC:4989504

Le document en format XML

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<title>Objective</title>
<p id="P1">To evaluate the association of uric acid (UA) levels with a panel of markers of oxidative stress and inflammation.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Plasma UA levels, along with a panel of oxidative stress and inflammatory markers, were measured in 755 Chinese women.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Plasma UA levels were inversely associated with urinary levels of the oxidative stress marker F
<sub>2</sub>
-isoprostanes and positively correlated to levels of inflammatory markers such as C-reactive protein and some proinflammatory cytokines (tumor necrosis factor-α and interleukin-6) in blood as well as prostaglandin E
<sub>2</sub>
metabolites in urine.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">Plasma UA levels correlate to oxidation and inflammation biomarkers in opposite directions in women.</p>
</sec>
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<contrib contrib-type="author">
<name>
<surname>Wu</surname>
<given-names>Sheng Hui</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A2">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Shu</surname>
<given-names>Xiao Ou</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
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<name>
<surname>Milne</surname>
<given-names>Ginger</given-names>
</name>
<xref ref-type="aff" rid="A3">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Xiang</surname>
<given-names>Yong-Bing</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Xianglan</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="aff" rid="A9">9</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cai</surname>
<given-names>Qiuyin</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
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<contrib contrib-type="author">
<name>
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<given-names>Sergio</given-names>
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<contrib contrib-type="author">
<name>
<surname>Linton</surname>
<given-names>MacRae F</given-names>
</name>
<xref ref-type="aff" rid="A5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Chen</surname>
<given-names>Honglei</given-names>
</name>
<xref ref-type="aff" rid="A6">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Purdue</surname>
<given-names>Mark</given-names>
</name>
<xref ref-type="aff" rid="A7">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rothman</surname>
<given-names>Nathaniel</given-names>
</name>
<xref ref-type="aff" rid="A8">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gao</surname>
<given-names>Yu-Tang</given-names>
</name>
<xref ref-type="aff" rid="A4">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Zheng</surname>
<given-names>Wei</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Yang</surname>
<given-names>Gong</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref ref-type="corresp" rid="cor1">*</xref>
</contrib>
</contrib-group>
<aff id="A1">
<label>1</label>
Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN</aff>
<aff id="A2">
<label>2</label>
The University of Texas Health Science Center at San Antonio-Laredo Campus, Department of Epidemiology & Biostatistics, Laredo, TX</aff>
<aff id="A3">
<label>3</label>
Division of Clinical Pharmacology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN</aff>
<aff id="A4">
<label>4</label>
Shanghai Cancer Institute, Shanghai, China</aff>
<aff id="A5">
<label>5</label>
Division of Cardiology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN</aff>
<aff id="A6">
<label>6</label>
Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC</aff>
<aff id="A7">
<label>7</label>
Ontario Institute for Cancer Research, Toronto, Canada</aff>
<aff id="A8">
<label>8</label>
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Bethesda, MD</aff>
<aff id="A9">
<label>9</label>
Division of Policy, Planning and Assessment, TN Department of Health, Nashville, TN</aff>
<author-notes>
<corresp id="cor1">
<label>*</label>
Correspondence to: Gong Yang, Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, 2525 West End Avenue, Suite 600 (IMPH), Nashville, TN 37203-1738, Phone: 615-936-0748, Fax: 615-936-8291,
<email>Gong.Yang@Vanderbilt.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted">
<day>3</day>
<month>8</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="ppub">
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>18</day>
<month>8</month>
<year>2016</year>
</pub-date>
<volume>20</volume>
<issue>4</issue>
<fpage>225</fpage>
<lpage>231</lpage>
<pmc-comment>elocation-id from pubmed: 10.3109/1354750X.2015.1068852</pmc-comment>
<abstract>
<sec id="S1">
<title>Objective</title>
<p id="P1">To evaluate the association of uric acid (UA) levels with a panel of markers of oxidative stress and inflammation.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Plasma UA levels, along with a panel of oxidative stress and inflammatory markers, were measured in 755 Chinese women.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">Plasma UA levels were inversely associated with urinary levels of the oxidative stress marker F
<sub>2</sub>
-isoprostanes and positively correlated to levels of inflammatory markers such as C-reactive protein and some proinflammatory cytokines (tumor necrosis factor-α and interleukin-6) in blood as well as prostaglandin E
<sub>2</sub>
metabolites in urine.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">Plasma UA levels correlate to oxidation and inflammation biomarkers in opposite directions in women.</p>
</sec>
</abstract>
<kwd-group>
<kwd>uric acid</kwd>
<kwd>inflammation</kwd>
<kwd>oxidative stress</kwd>
<kwd>biomarker</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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