STAT4 rs7574865 G/T polymorphism is associated with rheumatoid arthritis and disease activity, but not with anti-CCP antibody levels in a Mexican population
Rheumatoid arthritis (RA) is a systemic autoimmune disease in whose etiology genetic factors are known to play an important role. Among the genes associated with RA, STAT4 could be an important factor in conducting helper T cells toward the pro-inflammatory Th1 and Th17 lineages. The aim of this stu...
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creator | Durán-Avelar, Ma. de Jesús Vibanco-Pérez, Norberto Hernández-Pacheco, Raquel Rocío Castro-Zambrano, América del Carmen Ortiz-Martínez, Liliana Zambrano-Zaragoza, José Francisco |
description | Rheumatoid arthritis (RA) is a systemic autoimmune disease in whose etiology genetic factors are known to play an important role. Among the genes associated with RA,
STAT4
could be an important factor in conducting helper T cells toward the pro-inflammatory Th1 and Th17 lineages. The aim of this study is to determine the association of the
STAT4
polymorphism rs7574865 with RA, disease activity, and anti-cyclic citrullinated peptide (CCP) antibody levels in a Mexican population. Genotyping was carried out using the Taqman® system from Applied Biosystems in 140 patients with RA and 150 healthy subjects. Disease activity was evaluated by a rheumatologist using the DAS28 and Spanish-HAQ-DI instruments. Anti-CCP levels were determined by ELISA. Associations of the genotypes of rs7574865 with DAS28, HAQ, and anti-CCP antibody levels with RA were determined. Findings showed that the GT and TT genotypes and the T allele from rs7574865 were all associated as risk factors for RA, independently of their anti-CCP status. An association with moderate-to-high disease activity (DAS28 ≥ 3.2) was also found. Additionally, patients with the GT or TT genotypes showed lower HAQ values than those who carried the GG genotype. No differences in anti-CCP antibody levels or DAS28 and genotypes were found. This work supports the association of the
STAT4
rs7574865 polymorphism with RA and disease activity, but not with anti-CCP antibody levels in a Mexican population. |
doi_str_mv | 10.1007/s10067-016-3320-z |
format | Article |
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STAT4
could be an important factor in conducting helper T cells toward the pro-inflammatory Th1 and Th17 lineages. The aim of this study is to determine the association of the
STAT4
polymorphism rs7574865 with RA, disease activity, and anti-cyclic citrullinated peptide (CCP) antibody levels in a Mexican population. Genotyping was carried out using the Taqman® system from Applied Biosystems in 140 patients with RA and 150 healthy subjects. Disease activity was evaluated by a rheumatologist using the DAS28 and Spanish-HAQ-DI instruments. Anti-CCP levels were determined by ELISA. Associations of the genotypes of rs7574865 with DAS28, HAQ, and anti-CCP antibody levels with RA were determined. Findings showed that the GT and TT genotypes and the T allele from rs7574865 were all associated as risk factors for RA, independently of their anti-CCP status. An association with moderate-to-high disease activity (DAS28 ≥ 3.2) was also found. Additionally, patients with the GT or TT genotypes showed lower HAQ values than those who carried the GG genotype. No differences in anti-CCP antibody levels or DAS28 and genotypes were found. This work supports the association of the
STAT4
rs7574865 polymorphism with RA and disease activity, but not with anti-CCP antibody levels in a Mexican population.</description><identifier>ISSN: 0770-3198</identifier><identifier>EISSN: 1434-9949</identifier><identifier>DOI: 10.1007/s10067-016-3320-z</identifier><identifier>PMID: 27234231</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>Adult ; Aged ; Alleles ; Antibodies - blood ; Arthritis, Rheumatoid - ethnology ; Arthritis, Rheumatoid - genetics ; Case-Control Studies ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Humans ; Immunoglobulin G - blood ; Male ; Medicine ; Medicine & Public Health ; Mexico ; Middle Aged ; Original Article ; Peptides, Cyclic - immunology ; Polymorphism, Single Nucleotide ; Rheumatology ; Risk Factors ; STAT4 Transcription Factor - genetics ; Th1 Cells - cytology ; Th17 Cells - cytology</subject><ispartof>Clinical rheumatology, 2016-12, Vol.35 (12), p.2909-2914</ispartof><rights>International League of Associations for Rheumatology (ILAR) 2016</rights><rights>Clinical Rheumatology is a copyright of Springer, 2016.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-535f05dfe10f7bf2e5c2e0e93b5e5a6884a7fc1589336654f8e1419872d91d513</citedby><cites>FETCH-LOGICAL-c405t-535f05dfe10f7bf2e5c2e0e93b5e5a6884a7fc1589336654f8e1419872d91d513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10067-016-3320-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10067-016-3320-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27234231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Durán-Avelar, Ma. de Jesús</creatorcontrib><creatorcontrib>Vibanco-Pérez, Norberto</creatorcontrib><creatorcontrib>Hernández-Pacheco, Raquel Rocío</creatorcontrib><creatorcontrib>Castro-Zambrano, América del Carmen</creatorcontrib><creatorcontrib>Ortiz-Martínez, Liliana</creatorcontrib><creatorcontrib>Zambrano-Zaragoza, José Francisco</creatorcontrib><title>STAT4 rs7574865 G/T polymorphism is associated with rheumatoid arthritis and disease activity, but not with anti-CCP antibody levels in a Mexican population</title><title>Clinical rheumatology</title><addtitle>Clin Rheumatol</addtitle><addtitle>Clin Rheumatol</addtitle><description>Rheumatoid arthritis (RA) is a systemic autoimmune disease in whose etiology genetic factors are known to play an important role. Among the genes associated with RA,
STAT4
could be an important factor in conducting helper T cells toward the pro-inflammatory Th1 and Th17 lineages. The aim of this study is to determine the association of the
STAT4
polymorphism rs7574865 with RA, disease activity, and anti-cyclic citrullinated peptide (CCP) antibody levels in a Mexican population. Genotyping was carried out using the Taqman® system from Applied Biosystems in 140 patients with RA and 150 healthy subjects. Disease activity was evaluated by a rheumatologist using the DAS28 and Spanish-HAQ-DI instruments. Anti-CCP levels were determined by ELISA. Associations of the genotypes of rs7574865 with DAS28, HAQ, and anti-CCP antibody levels with RA were determined. Findings showed that the GT and TT genotypes and the T allele from rs7574865 were all associated as risk factors for RA, independently of their anti-CCP status. An association with moderate-to-high disease activity (DAS28 ≥ 3.2) was also found. Additionally, patients with the GT or TT genotypes showed lower HAQ values than those who carried the GG genotype. No differences in anti-CCP antibody levels or DAS28 and genotypes were found. This work supports the association of the
STAT4
rs7574865 polymorphism with RA and disease activity, but not with anti-CCP antibody levels in a Mexican population.</description><subject>Adult</subject><subject>Aged</subject><subject>Alleles</subject><subject>Antibodies - blood</subject><subject>Arthritis, Rheumatoid - ethnology</subject><subject>Arthritis, Rheumatoid - genetics</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotype</subject><subject>Humans</subject><subject>Immunoglobulin G - blood</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mexico</subject><subject>Middle Aged</subject><subject>Original Article</subject><subject>Peptides, Cyclic - immunology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Rheumatology</subject><subject>Risk Factors</subject><subject>STAT4 Transcription Factor - genetics</subject><subject>Th1 Cells - cytology</subject><subject>Th17 Cells - cytology</subject><issn>0770-3198</issn><issn>1434-9949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkd2KFDEQhYMo7jj6AN5IwBsvbDf_P5fLoLvCioLjdZPurnaydHfGJL3r7LP4sGa2VxFB8KZSkO-couog9JySN5QQfZpKVboiVFWcM1LdPkArKriorBX2IVoRrUnFqTUn6ElKV4QQZix9jE6YZlwwTlfox-ft2VbgmLTUwiiJz0-3eB-GwxjifufTiH3CLqXQepehwzc-73DcwTy6HHyHXcy76PMRmjrc-QQuAXZt9tc-H17jZs54CnnRuSn7arP5dNc0oTvgAa5hSNhP2OEP8N23birT9_Pgsg_TU_Sod0OCZ_fvGn1593a7uaguP56_35xdVq0gMleSy57IrgdKet30DGTLgIDljQTplDHC6b6l0ljOlZKiN0BFuYpmnaWdpHyNXi2--xi-zZByPfrUwjC4CcKcamqEEowVp_9AmVLGmnLdNXr5F3oV5jiVRY6G1Cq9UHSh2hhSitDX--hHFw81JfUx5XpJuS4p18eU69uieXHvPDcjdL8Vv2ItAFuAVL6mrxD_GP1P15-98LH9</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Durán-Avelar, Ma. de Jesús</creator><creator>Vibanco-Pérez, Norberto</creator><creator>Hernández-Pacheco, Raquel Rocío</creator><creator>Castro-Zambrano, América del Carmen</creator><creator>Ortiz-Martínez, Liliana</creator><creator>Zambrano-Zaragoza, José Francisco</creator><general>Springer London</general><general>Springer Nature 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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20161201</creationdate><title>STAT4 rs7574865 G/T polymorphism is associated with rheumatoid arthritis and disease activity, but not with anti-CCP antibody levels in a Mexican population</title><author>Durán-Avelar, Ma. de Jesús ; Vibanco-Pérez, Norberto ; Hernández-Pacheco, Raquel Rocío ; Castro-Zambrano, América del Carmen ; Ortiz-Martínez, Liliana ; Zambrano-Zaragoza, José Francisco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-535f05dfe10f7bf2e5c2e0e93b5e5a6884a7fc1589336654f8e1419872d91d513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Alleles</topic><topic>Antibodies - blood</topic><topic>Arthritis, Rheumatoid - ethnology</topic><topic>Arthritis, Rheumatoid - genetics</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotype</topic><topic>Humans</topic><topic>Immunoglobulin G - blood</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mexico</topic><topic>Middle Aged</topic><topic>Original Article</topic><topic>Peptides, Cyclic - immunology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Rheumatology</topic><topic>Risk Factors</topic><topic>STAT4 Transcription Factor - genetics</topic><topic>Th1 Cells - cytology</topic><topic>Th17 Cells - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Durán-Avelar, Ma. de Jesús</creatorcontrib><creatorcontrib>Vibanco-Pérez, Norberto</creatorcontrib><creatorcontrib>Hernández-Pacheco, Raquel Rocío</creatorcontrib><creatorcontrib>Castro-Zambrano, América del Carmen</creatorcontrib><creatorcontrib>Ortiz-Martínez, Liliana</creatorcontrib><creatorcontrib>Zambrano-Zaragoza, José Francisco</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Durán-Avelar, Ma. de Jesús</au><au>Vibanco-Pérez, Norberto</au><au>Hernández-Pacheco, Raquel Rocío</au><au>Castro-Zambrano, América del Carmen</au><au>Ortiz-Martínez, Liliana</au><au>Zambrano-Zaragoza, José Francisco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>STAT4 rs7574865 G/T polymorphism is associated with rheumatoid arthritis and disease activity, but not with anti-CCP antibody levels in a Mexican population</atitle><jtitle>Clinical rheumatology</jtitle><stitle>Clin Rheumatol</stitle><addtitle>Clin Rheumatol</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>35</volume><issue>12</issue><spage>2909</spage><epage>2914</epage><pages>2909-2914</pages><issn>0770-3198</issn><eissn>1434-9949</eissn><abstract>Rheumatoid arthritis (RA) is a systemic autoimmune disease in whose etiology genetic factors are known to play an important role. Among the genes associated with RA,
STAT4
could be an important factor in conducting helper T cells toward the pro-inflammatory Th1 and Th17 lineages. The aim of this study is to determine the association of the
STAT4
polymorphism rs7574865 with RA, disease activity, and anti-cyclic citrullinated peptide (CCP) antibody levels in a Mexican population. Genotyping was carried out using the Taqman® system from Applied Biosystems in 140 patients with RA and 150 healthy subjects. Disease activity was evaluated by a rheumatologist using the DAS28 and Spanish-HAQ-DI instruments. Anti-CCP levels were determined by ELISA. Associations of the genotypes of rs7574865 with DAS28, HAQ, and anti-CCP antibody levels with RA were determined. Findings showed that the GT and TT genotypes and the T allele from rs7574865 were all associated as risk factors for RA, independently of their anti-CCP status. An association with moderate-to-high disease activity (DAS28 ≥ 3.2) was also found. Additionally, patients with the GT or TT genotypes showed lower HAQ values than those who carried the GG genotype. No differences in anti-CCP antibody levels or DAS28 and genotypes were found. This work supports the association of the
STAT4
rs7574865 polymorphism with RA and disease activity, but not with anti-CCP antibody levels in a Mexican population.</abstract><cop>London</cop><pub>Springer London</pub><pmid>27234231</pmid><doi>10.1007/s10067-016-3320-z</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Alleles Antibodies - blood Arthritis, Rheumatoid - ethnology Arthritis, Rheumatoid - genetics Case-Control Studies Female Gene Frequency Genetic Predisposition to Disease Genotype Humans Immunoglobulin G - blood Male Medicine Medicine & Public Health Mexico Middle Aged Original Article Peptides, Cyclic - immunology Polymorphism, Single Nucleotide Rheumatology Risk Factors STAT4 Transcription Factor - genetics Th1 Cells - cytology Th17 Cells - cytology |
title | STAT4 rs7574865 G/T polymorphism is associated with rheumatoid arthritis and disease activity, but not with anti-CCP antibody levels in a Mexican population |
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