Analysis of Toll-like Receptor 9 Gene Polymorphisms in Sepsis

To analyze the effect of TLR-9 (-1486 T>C) and TLR-9 (C>T) gene polymorphisms both at TLR-9 levels and together with their sepsis parameters. In this regard, the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used in order to detect TLR-9 gene polym...

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Veröffentlicht in:In vivo (Athens) 2016-09, Vol.30 (5), p.639-643
Hauptverfasser: Atalan, Nazan, Karagedik, Hande, Acar, Leyla, Isbir, Selim, Yilmaz, Seda Gulec, Ergen, Arzu, Isbir, Turgay
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container_end_page 643
container_issue 5
container_start_page 639
container_title In vivo (Athens)
container_volume 30
creator Atalan, Nazan
Karagedik, Hande
Acar, Leyla
Isbir, Selim
Yilmaz, Seda Gulec
Ergen, Arzu
Isbir, Turgay
description To analyze the effect of TLR-9 (-1486 T>C) and TLR-9 (C>T) gene polymorphisms both at TLR-9 levels and together with their sepsis parameters. In this regard, the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used in order to detect TLR-9 gene polymorphisms, whereas the ELISA technique was used to analyze TLR-9 serum levels in 80 sepsis patients and 100 healthy individuals. The study group consisted of 80 patients with a diagnosis of sepsis and 100 healthy individuals. TLR-9 C>T polymorphism was identified by PCR-RFLP. There was no substantial difference observed between sepsis and control groups in terms of TLR-9 (-1486 T>C) and TLR-9 (C>T) genotype and allele distribution. When serum TLR-9 levels were compared to TLR-9 (-1486 T>C) and TLR-9 (C>T) genotype and allele distribution, there was a statistically substantial decrease in TLR-9 serum levels of both TLR-9 (-1486 T>C) TT and TLR-9 (C>T) TT individuals in the sepsis group (p=0.011 and p=0.036, respectively). There is no relation between sepsis and both TLR-9 (C>T) and TLR-9(-1486 T>C) polymorphisms; however, there is a relation between sepsis and decreased serum TLR-9 levels of both TLR-9 (-1486 T>C) TT and TLR-9 (C>T) TT polymorphisms due to sepsis-associated immunosuppression.
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In this regard, the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used in order to detect TLR-9 gene polymorphisms, whereas the ELISA technique was used to analyze TLR-9 serum levels in 80 sepsis patients and 100 healthy individuals. The study group consisted of 80 patients with a diagnosis of sepsis and 100 healthy individuals. TLR-9 C&gt;T polymorphism was identified by PCR-RFLP. There was no substantial difference observed between sepsis and control groups in terms of TLR-9 (-1486 T&gt;C) and TLR-9 (C&gt;T) genotype and allele distribution. When serum TLR-9 levels were compared to TLR-9 (-1486 T&gt;C) and TLR-9 (C&gt;T) genotype and allele distribution, there was a statistically substantial decrease in TLR-9 serum levels of both TLR-9 (-1486 T&gt;C) TT and TLR-9 (C&gt;T) TT individuals in the sepsis group (p=0.011 and p=0.036, respectively). There is no relation between sepsis and both TLR-9 (C&gt;T) and TLR-9(-1486 T&gt;C) polymorphisms; however, there is a relation between sepsis and decreased serum TLR-9 levels of both TLR-9 (-1486 T&gt;C) TT and TLR-9 (C&gt;T) TT polymorphisms due to sepsis-associated immunosuppression.</description><identifier>EISSN: 1791-7549</identifier><identifier>PMID: 27566084</identifier><language>eng</language><publisher>Greece</publisher><subject>Adult ; Aged ; Alleles ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Risk Factors ; Sepsis - genetics ; Sepsis - pathology ; Toll-Like Receptor 9 - genetics</subject><ispartof>In vivo (Athens), 2016-09, Vol.30 (5), p.639-643</ispartof><rights>Copyright © 2016 International Institute of Anticancer Research (Dr. John G. 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In this regard, the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was used in order to detect TLR-9 gene polymorphisms, whereas the ELISA technique was used to analyze TLR-9 serum levels in 80 sepsis patients and 100 healthy individuals. The study group consisted of 80 patients with a diagnosis of sepsis and 100 healthy individuals. TLR-9 C&gt;T polymorphism was identified by PCR-RFLP. There was no substantial difference observed between sepsis and control groups in terms of TLR-9 (-1486 T&gt;C) and TLR-9 (C&gt;T) genotype and allele distribution. When serum TLR-9 levels were compared to TLR-9 (-1486 T&gt;C) and TLR-9 (C&gt;T) genotype and allele distribution, there was a statistically substantial decrease in TLR-9 serum levels of both TLR-9 (-1486 T&gt;C) TT and TLR-9 (C&gt;T) TT individuals in the sepsis group (p=0.011 and p=0.036, respectively). There is no relation between sepsis and both TLR-9 (C&gt;T) and TLR-9(-1486 T&gt;C) polymorphisms; however, there is a relation between sepsis and decreased serum TLR-9 levels of both TLR-9 (-1486 T&gt;C) TT and TLR-9 (C&gt;T) TT polymorphisms due to sepsis-associated immunosuppression.</description><subject>Adult</subject><subject>Aged</subject><subject>Alleles</subject><subject>Female</subject><subject>Genetic Association Studies</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Risk Factors</subject><subject>Sepsis - genetics</subject><subject>Sepsis - pathology</subject><subject>Toll-Like Receptor 9 - genetics</subject><issn>1791-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j09LwzAYh4Mgbk6_guTopZA_Td7k4GEMnYOB4nYvafsGo2lTm_awb6_iPD2X5_nB74IsOVhegCrtglzn_MGYBsbEFVkIUFozUy7Jw7p38ZRDpsnTY4qxiOET6Rs2OExppJZusUf6muKpS-PwHnKXaejpAYef6IZcehcz3p65Ioenx-Pmudi_bHeb9b4YBOdTAVLpshFKgIbWa-mcRFUz77VjGgUwqAGcaaUCXvrWWG4EsxpqpYQt5Yrc_60OY_qaMU9VF3KDMboe05wrbriSWmrzq96d1bnusK2GMXRuPFX_h-U3hPhOng</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Atalan, Nazan</creator><creator>Karagedik, Hande</creator><creator>Acar, Leyla</creator><creator>Isbir, Selim</creator><creator>Yilmaz, Seda Gulec</creator><creator>Ergen, Arzu</creator><creator>Isbir, Turgay</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20160901</creationdate><title>Analysis of Toll-like Receptor 9 Gene Polymorphisms in Sepsis</title><author>Atalan, Nazan ; Karagedik, Hande ; Acar, Leyla ; Isbir, Selim ; Yilmaz, Seda Gulec ; Ergen, Arzu ; Isbir, Turgay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-73564c252767df63aa3e5b0ff6a06e2707b77a8d35714fd891820967b552943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alleles</topic><topic>Female</topic><topic>Genetic Association Studies</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Risk Factors</topic><topic>Sepsis - genetics</topic><topic>Sepsis - pathology</topic><topic>Toll-Like Receptor 9 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atalan, Nazan</creatorcontrib><creatorcontrib>Karagedik, Hande</creatorcontrib><creatorcontrib>Acar, Leyla</creatorcontrib><creatorcontrib>Isbir, Selim</creatorcontrib><creatorcontrib>Yilmaz, Seda Gulec</creatorcontrib><creatorcontrib>Ergen, Arzu</creatorcontrib><creatorcontrib>Isbir, Turgay</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>In vivo (Athens)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atalan, Nazan</au><au>Karagedik, Hande</au><au>Acar, Leyla</au><au>Isbir, Selim</au><au>Yilmaz, Seda Gulec</au><au>Ergen, Arzu</au><au>Isbir, Turgay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Toll-like Receptor 9 Gene Polymorphisms in Sepsis</atitle><jtitle>In vivo (Athens)</jtitle><addtitle>In Vivo</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>30</volume><issue>5</issue><spage>639</spage><epage>643</epage><pages>639-643</pages><eissn>1791-7549</eissn><abstract>To analyze the effect of TLR-9 (-1486 T&gt;C) and TLR-9 (C&gt;T) gene polymorphisms both at TLR-9 levels and together with their sepsis parameters. 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There is no relation between sepsis and both TLR-9 (C&gt;T) and TLR-9(-1486 T&gt;C) polymorphisms; however, there is a relation between sepsis and decreased serum TLR-9 levels of both TLR-9 (-1486 T&gt;C) TT and TLR-9 (C&gt;T) TT polymorphisms due to sepsis-associated immunosuppression.</abstract><cop>Greece</cop><pmid>27566084</pmid><tpages>5</tpages></addata></record>
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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Adult
Aged
Alleles
Female
Genetic Association Studies
Genetic Predisposition to Disease
Genotype
Humans
Male
Middle Aged
Polymorphism, Single Nucleotide
Risk Factors
Sepsis - genetics
Sepsis - pathology
Toll-Like Receptor 9 - genetics
title Analysis of Toll-like Receptor 9 Gene Polymorphisms in Sepsis
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