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Relationship of oxidative stress in hepatitis B infection activity with HBV DNA and fibrosis
The aim of this study was to evaluate oxidative stress in various clinical forms of hepatitis B infection and to investigate its role in the development of the chronic form of the disease. Ninety-three patients with inactive hepatitis B surface antigen (HbsAg) carrier state (IHBCS), 65 patients with...
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Published in: | Annals of laboratory medicine 2012, 32(2), , pp.113-118 |
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creator | Duygu, Fazilet Karsen, Hasan Aksoy, Nurten Taskin, Abdullah |
description | The aim of this study was to evaluate oxidative stress in various clinical forms of hepatitis B infection and to investigate its role in the development of the chronic form of the disease.
Ninety-three patients with inactive hepatitis B surface antigen (HbsAg) carrier state (IHBCS), 65 patients with chronic hepatitis B infection (CHB), and 42 healthy adults were included in the study. The following values were measured and compared in patient groups: total antioxidant status (TAS), total oxidative stress (TOS), oxidative stress index (OSI), sulfhydryl (SH), lipid peroxidation (LOOH), catalase (CAT), and ceruloplasmin. In patients with chronic hepatitis B, these values were compared with HBV DNA and fibrosis levels.
ALT, TOS, LOOH, and OSI levels were higher in the CHB group compared to the other groups (P |
doi_str_mv | 10.3343/alm.2012.32.2.113 |
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Ninety-three patients with inactive hepatitis B surface antigen (HbsAg) carrier state (IHBCS), 65 patients with chronic hepatitis B infection (CHB), and 42 healthy adults were included in the study. The following values were measured and compared in patient groups: total antioxidant status (TAS), total oxidative stress (TOS), oxidative stress index (OSI), sulfhydryl (SH), lipid peroxidation (LOOH), catalase (CAT), and ceruloplasmin. In patients with chronic hepatitis B, these values were compared with HBV DNA and fibrosis levels.
ALT, TOS, LOOH, and OSI levels were higher in the CHB group compared to the other groups (P<0.001). Catalase levels increased in the CHB and IHBCS groups compared to the control group (P<0.001). Total aminooxidant and ceruloplasmin levels were found to be lowest in the CHB group and highest in the control group (P<0.001). Sulfhyrdyl was higher in the control group compared to the other groups (P<0.001). In the CHB group, there was no correlation between the HBV DNA and OSI (P>0.05).
These finding suggested that oxidative stress is associated with hepatitis B activity.</description><identifier>ISSN: 2234-3806</identifier><identifier>EISSN: 2234-3814</identifier><identifier>DOI: 10.3343/alm.2012.32.2.113</identifier><identifier>PMID: 22389877</identifier><language>eng</language><publisher>Korea (South): The Korean Society for Laboratory Medicine</publisher><subject>Adolescent ; Adult ; Aged ; Alanine Transaminase - blood ; Antioxidants - metabolism ; Carrier State ; Catalase - blood ; DNA, Viral - analysis ; Female ; Fibrosis ; Hepatitis B - metabolism ; Hepatitis B - pathology ; Hepatitis B Surface Antigens - blood ; Hepatitis B virus - genetics ; Hepatitis B, Chronic - metabolism ; Hepatitis B, Chronic - pathology ; Humans ; Lipid Peroxidation ; Male ; Middle Aged ; Original ; Oxidative Stress ; Sulfhydryl Compounds - blood ; Young Adult ; 병리학</subject><ispartof>Annals of Laboratory Medicine, 2012, 32(2), , pp.113-118</ispartof><rights>The Korean Society for Laboratory Medicine. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-547869a2cd576913489006291ccba1ecf844cc7d828299d10910da002ff437de3</citedby><cites>FETCH-LOGICAL-c431t-547869a2cd576913489006291ccba1ecf844cc7d828299d10910da002ff437de3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289775/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289775/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22389877$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001639303$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Duygu, Fazilet</creatorcontrib><creatorcontrib>Karsen, Hasan</creatorcontrib><creatorcontrib>Aksoy, Nurten</creatorcontrib><creatorcontrib>Taskin, Abdullah</creatorcontrib><title>Relationship of oxidative stress in hepatitis B infection activity with HBV DNA and fibrosis</title><title>Annals of laboratory medicine</title><addtitle>Ann Lab Med</addtitle><description>The aim of this study was to evaluate oxidative stress in various clinical forms of hepatitis B infection and to investigate its role in the development of the chronic form of the disease.
Ninety-three patients with inactive hepatitis B surface antigen (HbsAg) carrier state (IHBCS), 65 patients with chronic hepatitis B infection (CHB), and 42 healthy adults were included in the study. The following values were measured and compared in patient groups: total antioxidant status (TAS), total oxidative stress (TOS), oxidative stress index (OSI), sulfhydryl (SH), lipid peroxidation (LOOH), catalase (CAT), and ceruloplasmin. In patients with chronic hepatitis B, these values were compared with HBV DNA and fibrosis levels.
ALT, TOS, LOOH, and OSI levels were higher in the CHB group compared to the other groups (P<0.001). Catalase levels increased in the CHB and IHBCS groups compared to the control group (P<0.001). Total aminooxidant and ceruloplasmin levels were found to be lowest in the CHB group and highest in the control group (P<0.001). Sulfhyrdyl was higher in the control group compared to the other groups (P<0.001). In the CHB group, there was no correlation between the HBV DNA and OSI (P>0.05).
These finding suggested that oxidative stress is associated with hepatitis B activity.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Alanine Transaminase - blood</subject><subject>Antioxidants - metabolism</subject><subject>Carrier State</subject><subject>Catalase - blood</subject><subject>DNA, Viral - analysis</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Hepatitis B - metabolism</subject><subject>Hepatitis B - pathology</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B, Chronic - metabolism</subject><subject>Hepatitis B, Chronic - pathology</subject><subject>Humans</subject><subject>Lipid Peroxidation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Oxidative Stress</subject><subject>Sulfhydryl Compounds - blood</subject><subject>Young Adult</subject><subject>병리학</subject><issn>2234-3806</issn><issn>2234-3814</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpVUcFOGzEQtapWBQEfwKXyrb1kscfeXftSKdACkaIiIeCEZDleu3HZ7AZ7k5a_Z0IgKr48z8x7zyM_Qo45K4SQ4sS2iwIYh0JAAQXn4gPZBxByJBSXH3d3Vu2Ro5z_MDwV0jX7TPZwprSq631yf-1bO8S-y_O4pH2g_b_YYGPtaR6Sz5nGjs79EltDzPQUy-DdRkAtwjoOT_RvHOb08vSO_vg1prZraIiz1OeYD8mnYNvsj17xgNye_7w5uxxNry4mZ-PpyEnBh1Epa1VpC64p60pzIZXGXUFz52aWexeUlM7VjQIFWjecac4ayxiEIEXdeHFAvm19uxTMg4umt_EFf_fmIZnx9c3EcAkSFFK_b6nL1WzhG-e7IdnWLFNc2PT0Inw_6eIcbdZGgNJ1XaLB11eD1D-ufB7MImbn29Z2vl9lo6EqmSwlIJNvmQ4_Iycfdq9wZjYRGozQbCJEcwMGI0TNl__X2yneAhPPa8yXqA</recordid><startdate>20120301</startdate><enddate>20120301</enddate><creator>Duygu, Fazilet</creator><creator>Karsen, Hasan</creator><creator>Aksoy, Nurten</creator><creator>Taskin, Abdullah</creator><general>The Korean Society for Laboratory Medicine</general><general>대한진단검사의학회</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>7X8</scope><scope>5PM</scope><scope>ACYCR</scope></search><sort><creationdate>20120301</creationdate><title>Relationship of oxidative stress in hepatitis B infection activity with HBV DNA and fibrosis</title><author>Duygu, Fazilet ; Karsen, Hasan ; Aksoy, Nurten ; Taskin, Abdullah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-547869a2cd576913489006291ccba1ecf844cc7d828299d10910da002ff437de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Alanine Transaminase - blood</topic><topic>Antioxidants - metabolism</topic><topic>Carrier State</topic><topic>Catalase - blood</topic><topic>DNA, Viral - analysis</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Hepatitis B - metabolism</topic><topic>Hepatitis B - pathology</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B virus - genetics</topic><topic>Hepatitis B, Chronic - metabolism</topic><topic>Hepatitis B, Chronic - pathology</topic><topic>Humans</topic><topic>Lipid Peroxidation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Oxidative Stress</topic><topic>Sulfhydryl Compounds - blood</topic><topic>Young Adult</topic><topic>병리학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duygu, Fazilet</creatorcontrib><creatorcontrib>Karsen, Hasan</creatorcontrib><creatorcontrib>Aksoy, Nurten</creatorcontrib><creatorcontrib>Taskin, Abdullah</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><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Annals of laboratory medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duygu, Fazilet</au><au>Karsen, Hasan</au><au>Aksoy, Nurten</au><au>Taskin, Abdullah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship of oxidative stress in hepatitis B infection activity with HBV DNA and fibrosis</atitle><jtitle>Annals of laboratory medicine</jtitle><addtitle>Ann Lab Med</addtitle><date>2012-03-01</date><risdate>2012</risdate><volume>32</volume><issue>2</issue><spage>113</spage><epage>118</epage><pages>113-118</pages><issn>2234-3806</issn><eissn>2234-3814</eissn><abstract>The aim of this study was to evaluate oxidative stress in various clinical forms of hepatitis B infection and to investigate its role in the development of the chronic form of the disease.
Ninety-three patients with inactive hepatitis B surface antigen (HbsAg) carrier state (IHBCS), 65 patients with chronic hepatitis B infection (CHB), and 42 healthy adults were included in the study. The following values were measured and compared in patient groups: total antioxidant status (TAS), total oxidative stress (TOS), oxidative stress index (OSI), sulfhydryl (SH), lipid peroxidation (LOOH), catalase (CAT), and ceruloplasmin. In patients with chronic hepatitis B, these values were compared with HBV DNA and fibrosis levels.
ALT, TOS, LOOH, and OSI levels were higher in the CHB group compared to the other groups (P<0.001). Catalase levels increased in the CHB and IHBCS groups compared to the control group (P<0.001). Total aminooxidant and ceruloplasmin levels were found to be lowest in the CHB group and highest in the control group (P<0.001). Sulfhyrdyl was higher in the control group compared to the other groups (P<0.001). In the CHB group, there was no correlation between the HBV DNA and OSI (P>0.05).
These finding suggested that oxidative stress is associated with hepatitis B activity.</abstract><cop>Korea (South)</cop><pub>The Korean Society for Laboratory Medicine</pub><pmid>22389877</pmid><doi>10.3343/alm.2012.32.2.113</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Alanine Transaminase - blood Antioxidants - metabolism Carrier State Catalase - blood DNA, Viral - analysis Female Fibrosis Hepatitis B - metabolism Hepatitis B - pathology Hepatitis B Surface Antigens - blood Hepatitis B virus - genetics Hepatitis B, Chronic - metabolism Hepatitis B, Chronic - pathology Humans Lipid Peroxidation Male Middle Aged Original Oxidative Stress Sulfhydryl Compounds - blood Young Adult 병리학 |
title | Relationship of oxidative stress in hepatitis B infection activity with HBV DNA and fibrosis |
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