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Serum markers of oxidative stress and endometriosis
To assess the changes secondary to chronic inflammation in women with and without pelvic endometriosis by the determination of serum thiols and carbonyls. Sixty-seven women with endometriosis consecutively submitted to laparoscopy and 41 women without endometriosis consecutively submitted to tubal l...
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Published in: | Clinical and experimental obstetrics & gynecology 2014-01, Vol.41 (4), p.371-374 |
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container_title | Clinical and experimental obstetrics & gynecology |
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creator | Rosa e Silva, J C do Amara, V Ferreira Mendonça, J L Rosa e Silva, A C Japur de Sá Nakao, L S Poli Neto, O B Ferriani, R A |
description | To assess the changes secondary to chronic inflammation in women with and without pelvic endometriosis by the determination of serum thiols and carbonyls.
Sixty-seven women with endometriosis consecutively submitted to laparoscopy and 41 women without endometriosis consecutively submitted to tubal ligation (control group) were selected. Serum levels of total thiols and carbonyls were determined in both groups.
Patients with endometriosis had significantly lower thiol levels than controls (342.37 +/- 142.09 microM vs 559.60 +/- 294.05 microM) (p < 0.001), as well as significantly lower carbonyl levels (8.97 +/- 3.76 microM vs 16.40 +/- 9.26 microM) (p < 0.001). Other clinical characteristics were not associated with changes in marker levels. The cutoff point established by the ROC curve was 396.44 microM for the thiols, with 73.1% sensitivity and 80.5% specificity, and 14.9 microM for the carbonyls, with 94% sensitivity and 51.2% specificity.
The serum thiol levels revealed an increase in oxidative stress related to the development of pelvic endometriosis. |
doi_str_mv | 10.12891/ceog16992014 |
format | article |
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Sixty-seven women with endometriosis consecutively submitted to laparoscopy and 41 women without endometriosis consecutively submitted to tubal ligation (control group) were selected. Serum levels of total thiols and carbonyls were determined in both groups.
Patients with endometriosis had significantly lower thiol levels than controls (342.37 +/- 142.09 microM vs 559.60 +/- 294.05 microM) (p < 0.001), as well as significantly lower carbonyl levels (8.97 +/- 3.76 microM vs 16.40 +/- 9.26 microM) (p < 0.001). Other clinical characteristics were not associated with changes in marker levels. The cutoff point established by the ROC curve was 396.44 microM for the thiols, with 73.1% sensitivity and 80.5% specificity, and 14.9 microM for the carbonyls, with 94% sensitivity and 51.2% specificity.
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Sixty-seven women with endometriosis consecutively submitted to laparoscopy and 41 women without endometriosis consecutively submitted to tubal ligation (control group) were selected. Serum levels of total thiols and carbonyls were determined in both groups.
Patients with endometriosis had significantly lower thiol levels than controls (342.37 +/- 142.09 microM vs 559.60 +/- 294.05 microM) (p < 0.001), as well as significantly lower carbonyl levels (8.97 +/- 3.76 microM vs 16.40 +/- 9.26 microM) (p < 0.001). Other clinical characteristics were not associated with changes in marker levels. The cutoff point established by the ROC curve was 396.44 microM for the thiols, with 73.1% sensitivity and 80.5% specificity, and 14.9 microM for the carbonyls, with 94% sensitivity and 51.2% specificity.
The serum thiol levels revealed an increase in oxidative stress related to the development of pelvic endometriosis.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Endometriosis - blood</subject><subject>Endometriosis - physiopathology</subject><subject>Endometriosis - surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Laparoscopy</subject><subject>Lipid Peroxidation - physiology</subject><subject>Oxidative Stress - physiology</subject><subject>Sensitivity and Specificity</subject><subject>Sulfhydryl Compounds - blood</subject><issn>0390-6663</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpNkD1PwzAURT2AaCmMrCgjS8DPz7HrEVV8SZUYgDmynRcUaOrilyD491RQENNdjo50jxAnIM9BzR1cRErPYJxTEvSemEp0sjTG4EQcMr9IqbU1cCAmqgLUys6nAh8oj33R-_xKmYvUFumja_zQvVPBQybmwq-bgtZN6mnIXeKOj8R-61dMx7udiafrq8fFbbm8v7lbXC7LiKiGUkUfrXUmoNHRK4eArUTVVBZIVsbYEJqAvkEE8E63MZD2Hp0PiL61Gmfi7Me7yeltJB7qvuNIq5VfUxq5hqrSTiuwaouWP2jMiTlTW29ytz31WYOsv9vU_9ts-dOdegw9NX_0bxj8AlUBYW0</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Rosa e Silva, J C</creator><creator>do Amara, V Ferreira</creator><creator>Mendonça, J L</creator><creator>Rosa e Silva, A C Japur de Sá</creator><creator>Nakao, L S</creator><creator>Poli Neto, O B</creator><creator>Ferriani, R A</creator><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>7X8</scope></search><sort><creationdate>20140101</creationdate><title>Serum markers of oxidative stress and endometriosis</title><author>Rosa e Silva, J C ; do Amara, V Ferreira ; Mendonça, J L ; Rosa e Silva, A C Japur de Sá ; Nakao, L S ; Poli Neto, O B ; Ferriani, R A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-2cac7796b364ca29313f032d571e05667bbdb3ad3311a94fcbe4aa39ab33af743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Endometriosis - blood</topic><topic>Endometriosis - physiopathology</topic><topic>Endometriosis - surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Laparoscopy</topic><topic>Lipid Peroxidation - physiology</topic><topic>Oxidative Stress - physiology</topic><topic>Sensitivity and Specificity</topic><topic>Sulfhydryl Compounds - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosa e Silva, J C</creatorcontrib><creatorcontrib>do Amara, V Ferreira</creatorcontrib><creatorcontrib>Mendonça, J L</creatorcontrib><creatorcontrib>Rosa e Silva, A C Japur de Sá</creatorcontrib><creatorcontrib>Nakao, L S</creatorcontrib><creatorcontrib>Poli Neto, O B</creatorcontrib><creatorcontrib>Ferriani, R A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental obstetrics & gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosa e Silva, J C</au><au>do Amara, V Ferreira</au><au>Mendonça, J L</au><au>Rosa e Silva, A C Japur de Sá</au><au>Nakao, L S</au><au>Poli Neto, O B</au><au>Ferriani, R A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum markers of oxidative stress and endometriosis</atitle><jtitle>Clinical and experimental obstetrics & gynecology</jtitle><addtitle>Clin Exp Obstet Gynecol</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>41</volume><issue>4</issue><spage>371</spage><epage>374</epage><pages>371-374</pages><issn>0390-6663</issn><abstract>To assess the changes secondary to chronic inflammation in women with and without pelvic endometriosis by the determination of serum thiols and carbonyls.
Sixty-seven women with endometriosis consecutively submitted to laparoscopy and 41 women without endometriosis consecutively submitted to tubal ligation (control group) were selected. Serum levels of total thiols and carbonyls were determined in both groups.
Patients with endometriosis had significantly lower thiol levels than controls (342.37 +/- 142.09 microM vs 559.60 +/- 294.05 microM) (p < 0.001), as well as significantly lower carbonyl levels (8.97 +/- 3.76 microM vs 16.40 +/- 9.26 microM) (p < 0.001). Other clinical characteristics were not associated with changes in marker levels. The cutoff point established by the ROC curve was 396.44 microM for the thiols, with 73.1% sensitivity and 80.5% specificity, and 14.9 microM for the carbonyls, with 94% sensitivity and 51.2% specificity.
The serum thiol levels revealed an increase in oxidative stress related to the development of pelvic endometriosis.</abstract><cop>Canada</cop><pmid>25134278</pmid><doi>10.12891/ceog16992014</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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source | EZB Electronic Journals Library |
subjects | Adult Biomarkers - blood Endometriosis - blood Endometriosis - physiopathology Endometriosis - surgery Female Humans Laparoscopy Lipid Peroxidation - physiology Oxidative Stress - physiology Sensitivity and Specificity Sulfhydryl Compounds - blood |
title | Serum markers of oxidative stress and endometriosis |
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