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PADI4 and HLA-DRB1 are genetic risks for radiographic progression in RA patients, independent of ACPA status: results from the IORRA cohort study
Rheumatoid arthritis (RA) is a systemic, chronic inflammatory disease influenced by both genetic and environmental factors, leading to joint destruction and functional impairment. Recently, a large-scaled GWAS meta-analysis using more than 37,000 Japanese samples were conducted and 13 RA susceptibil...
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Published in: | PloS one 2013-04, Vol.8 (4), p.e61045-e61045 |
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description | Rheumatoid arthritis (RA) is a systemic, chronic inflammatory disease influenced by both genetic and environmental factors, leading to joint destruction and functional impairment. Recently, a large-scaled GWAS meta-analysis using more than 37,000 Japanese samples were conducted and 13 RA susceptibility loci were identified. However, it is not clear whether these loci have significant impact on joint destruction or not. This is the first study focused on the 13 loci to investigate independent genetic risk factors for radiographic progression in the first five years from onset of RA.
Sharp/van der Heijde score of hands at 5-year disease duration, which represents joint damage, were measured retrospectively and used as an outcome variable in 865 Japanese RA patients. Genetic factors regarded as putative risk factors were RA-susceptible polymorphisms identified by the Japanese GWAS meta-analysis, including HLA-DRB1 (shared epitope, SE), rs2240340 (PADI4), rs2230926 (TNFAIP3), rs3093024 (CCR6), rs11900673 (B3GNT2), rs2867461 (ANXA3), rs657075 (CSF2), rs12529514 (CD83), rs2233434 (NFKBIE), rs10821944 (ARID5B), rs3781913 (PDE2A-ARAP1), rs2841277 (PLD4) and rs2847297 (PTPN2). These putative genetic risk factors were assessed by a stepwise multiple regression analysis adjusted for possible non-genetic risk factors: autoantibody positivity (anti-citrullinated peptide antibody [ACPA] and rheumatoid factor), history of smoking, gender and age at disease onset.
The number of SE alleles (P = 0.002) and risk alleles of peptidyl arginine deiminase type IV gene (PADI4, P = 0.04) had significant impact on progressive joint destruction, as well as following non-genetic factors: ACPA positive (P = 0.0006), female sex (P = 0.006) and younger age of onset (P = 0.02).
In the present study, we found that PADI4 risk allele and HLA-DRB1 shared epitope are independent genetic risks for radiographic progression in Japanese rheumatoid arthritis patients. The results of this study give important knowledge of the risks on progressive joint damage in RA patients. |
doi_str_mv | 10.1371/journal.pone.0061045 |
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Sharp/van der Heijde score of hands at 5-year disease duration, which represents joint damage, were measured retrospectively and used as an outcome variable in 865 Japanese RA patients. Genetic factors regarded as putative risk factors were RA-susceptible polymorphisms identified by the Japanese GWAS meta-analysis, including HLA-DRB1 (shared epitope, SE), rs2240340 (PADI4), rs2230926 (TNFAIP3), rs3093024 (CCR6), rs11900673 (B3GNT2), rs2867461 (ANXA3), rs657075 (CSF2), rs12529514 (CD83), rs2233434 (NFKBIE), rs10821944 (ARID5B), rs3781913 (PDE2A-ARAP1), rs2841277 (PLD4) and rs2847297 (PTPN2). These putative genetic risk factors were assessed by a stepwise multiple regression analysis adjusted for possible non-genetic risk factors: autoantibody positivity (anti-citrullinated peptide antibody [ACPA] and rheumatoid factor), history of smoking, gender and age at disease onset.
The number of SE alleles (P = 0.002) and risk alleles of peptidyl arginine deiminase type IV gene (PADI4, P = 0.04) had significant impact on progressive joint destruction, as well as following non-genetic factors: ACPA positive (P = 0.0006), female sex (P = 0.006) and younger age of onset (P = 0.02).
In the present study, we found that PADI4 risk allele and HLA-DRB1 shared epitope are independent genetic risks for radiographic progression in Japanese rheumatoid arthritis patients. The results of this study give important knowledge of the risks on progressive joint damage in RA patients.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0061045</identifier><identifier>PMID: 23577190</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Age ; Alleles ; Antibodies - immunology ; Antigenic determinants ; Arginine ; Arginine deiminase ; Arthritis ; Arthritis, Rheumatoid - diagnostic imaging ; Arthritis, Rheumatoid - genetics ; Arthritis, Rheumatoid - pathology ; Arthrography ; Autoantibodies ; Autoimmunity ; Biology ; CCR6 protein ; CD83 antigen ; Citrulline ; Cohort analysis ; Cohort Studies ; Deoxyribonucleic acid ; Destruction ; Development and progression ; Disease Progression ; Disease susceptibility ; DNA ; Drb1 protein ; Environmental factors ; Epitopes ; Female ; Gender ; Genes ; Genetic factors ; Genetic Loci - genetics ; Genetic polymorphisms ; Genetic Predisposition to Disease - genetics ; Genetic testing ; Genomes ; Haplotypes ; Histocompatibility antigen HLA ; HLA antigens ; HLA-DRB1 Chains - genetics ; Humans ; Hydrolases - genetics ; Loci ; Male ; Medical records ; Medicine ; Meta-analysis ; Middle Aged ; Multiple regression analysis ; Patients ; Peptides, Cyclic - immunology ; Polymorphism, Single Nucleotide ; Population ; Protein-arginine deiminase ; Protein-Arginine Deiminases ; PTPN2 protein ; Regression analysis ; Rheumatoid arthritis ; Rheumatoid factor ; Rheumatology ; Risk analysis ; Risk factors ; Smoking</subject><ispartof>PloS one, 2013-04, Vol.8 (4), p.e61045-e61045</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Suzuki et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Suzuki et al 2013 Suzuki et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-dffc457575e3e71cf0936cc60a2c2564ee26bd83365f7ee531866e06e6cc21283</citedby><cites>FETCH-LOGICAL-c758t-dffc457575e3e71cf0936cc60a2c2564ee26bd83365f7ee531866e06e6cc21283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1330893543/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1330893543?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23577190$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ahuja, Sunil K.</contributor><creatorcontrib>Suzuki, Taku</creatorcontrib><creatorcontrib>Ikari, Katsunori</creatorcontrib><creatorcontrib>Yano, Koichiro</creatorcontrib><creatorcontrib>Inoue, Eisuke</creatorcontrib><creatorcontrib>Toyama, Yoshiaki</creatorcontrib><creatorcontrib>Taniguchi, Atsuo</creatorcontrib><creatorcontrib>Yamanaka, Hisashi</creatorcontrib><creatorcontrib>Momohara, Shigeki</creatorcontrib><title>PADI4 and HLA-DRB1 are genetic risks for radiographic progression in RA patients, independent of ACPA status: results from the IORRA cohort study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Rheumatoid arthritis (RA) is a systemic, chronic inflammatory disease influenced by both genetic and environmental factors, leading to joint destruction and functional impairment. Recently, a large-scaled GWAS meta-analysis using more than 37,000 Japanese samples were conducted and 13 RA susceptibility loci were identified. However, it is not clear whether these loci have significant impact on joint destruction or not. This is the first study focused on the 13 loci to investigate independent genetic risk factors for radiographic progression in the first five years from onset of RA.
Sharp/van der Heijde score of hands at 5-year disease duration, which represents joint damage, were measured retrospectively and used as an outcome variable in 865 Japanese RA patients. Genetic factors regarded as putative risk factors were RA-susceptible polymorphisms identified by the Japanese GWAS meta-analysis, including HLA-DRB1 (shared epitope, SE), rs2240340 (PADI4), rs2230926 (TNFAIP3), rs3093024 (CCR6), rs11900673 (B3GNT2), rs2867461 (ANXA3), rs657075 (CSF2), rs12529514 (CD83), rs2233434 (NFKBIE), rs10821944 (ARID5B), rs3781913 (PDE2A-ARAP1), rs2841277 (PLD4) and rs2847297 (PTPN2). These putative genetic risk factors were assessed by a stepwise multiple regression analysis adjusted for possible non-genetic risk factors: autoantibody positivity (anti-citrullinated peptide antibody [ACPA] and rheumatoid factor), history of smoking, gender and age at disease onset.
The number of SE alleles (P = 0.002) and risk alleles of peptidyl arginine deiminase type IV gene (PADI4, P = 0.04) had significant impact on progressive joint destruction, as well as following non-genetic factors: ACPA positive (P = 0.0006), female sex (P = 0.006) and younger age of onset (P = 0.02).
In the present study, we found that PADI4 risk allele and HLA-DRB1 shared epitope are independent genetic risks for radiographic progression in Japanese rheumatoid arthritis patients. The results of this study give important knowledge of the risks on progressive joint damage in RA patients.</description><subject>Age</subject><subject>Alleles</subject><subject>Antibodies - immunology</subject><subject>Antigenic determinants</subject><subject>Arginine</subject><subject>Arginine deiminase</subject><subject>Arthritis</subject><subject>Arthritis, Rheumatoid - diagnostic imaging</subject><subject>Arthritis, Rheumatoid - genetics</subject><subject>Arthritis, Rheumatoid - pathology</subject><subject>Arthrography</subject><subject>Autoantibodies</subject><subject>Autoimmunity</subject><subject>Biology</subject><subject>CCR6 protein</subject><subject>CD83 antigen</subject><subject>Citrulline</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Deoxyribonucleic acid</subject><subject>Destruction</subject><subject>Development and progression</subject><subject>Disease Progression</subject><subject>Disease susceptibility</subject><subject>DNA</subject><subject>Drb1 protein</subject><subject>Environmental factors</subject><subject>Epitopes</subject><subject>Female</subject><subject>Gender</subject><subject>Genes</subject><subject>Genetic factors</subject><subject>Genetic Loci - genetics</subject><subject>Genetic polymorphisms</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genetic testing</subject><subject>Genomes</subject><subject>Haplotypes</subject><subject>Histocompatibility antigen HLA</subject><subject>HLA antigens</subject><subject>HLA-DRB1 Chains - genetics</subject><subject>Humans</subject><subject>Hydrolases - genetics</subject><subject>Loci</subject><subject>Male</subject><subject>Medical records</subject><subject>Medicine</subject><subject>Meta-analysis</subject><subject>Middle Aged</subject><subject>Multiple regression analysis</subject><subject>Patients</subject><subject>Peptides, Cyclic - immunology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population</subject><subject>Protein-arginine deiminase</subject><subject>Protein-Arginine Deiminases</subject><subject>PTPN2 protein</subject><subject>Regression analysis</subject><subject>Rheumatoid arthritis</subject><subject>Rheumatoid factor</subject><subject>Rheumatology</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Smoking</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk11v0zAUhiMEYmPwDxBYQkIg0eKPxEm4QAodsEqVOpWPW8tzTlpvaRxsB7GfwT_mlHZTi3aBLCW287yvc47PSZKnjI6ZyNnbSzf4Trfj3nUwplQymmb3kmNWCj6SnIr7e_Oj5FEIl5RmopDyYXLERZbnrKTHye_z6nSaEt3V5GxWjU4XHxjRHsgSOojWEG_DVSCN88Tr2rql1_0Kt3uPUwjBuo7Yjiwq0utooYvhDa5r6AEfXSSuIdXkvCIh6jiEdwQ1QxvR0Ls1iSsg0_kCxcatnI9IDfX14-RBo9sAT3bvk-Tbp49fJ2ej2fzzdFLNRibPijiqm8akWY4DBOTMNLQU0hhJNTc8kykAlxd1IYTMmhwgEwxDByoBIc54IU6S51vfvnVB7bIZFBOCFqXIUoHEdEvUTl-q3tu19tfKaav-bji_VNpjklpAVWk4l0UNgqdpYS5SvCNZ5kVBmSyzGr3e704bLtZQG0yO1-2B6eGXzq7U0v1UAu-PZjkavNoZePdjgBDV2gYDbas7cMPmv7nMeVayTWQv_kHvjm5HLTUGYLvG4blmY6qqNC9EkWOxIDW-g8JRw9oaLL3G4v6B4PWBAJkIv-JSDyGo6ZfF_7Pz74fsyz12BbqNq-DaIWIJhkMw3YLGuxA8NLdJZlRtOucmG2rTOWrXOSh7tn9Bt6KbVhF_AEGNEUQ</recordid><startdate>20130408</startdate><enddate>20130408</enddate><creator>Suzuki, Taku</creator><creator>Ikari, Katsunori</creator><creator>Yano, Koichiro</creator><creator>Inoue, Eisuke</creator><creator>Toyama, Yoshiaki</creator><creator>Taniguchi, Atsuo</creator><creator>Yamanaka, Hisashi</creator><creator>Momohara, Shigeki</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130408</creationdate><title>PADI4 and HLA-DRB1 are genetic risks for radiographic progression in RA patients, independent of ACPA status: results from the IORRA cohort study</title><author>Suzuki, Taku ; Ikari, Katsunori ; Yano, Koichiro ; Inoue, Eisuke ; Toyama, Yoshiaki ; Taniguchi, Atsuo ; Yamanaka, Hisashi ; Momohara, Shigeki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-dffc457575e3e71cf0936cc60a2c2564ee26bd83365f7ee531866e06e6cc21283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Age</topic><topic>Alleles</topic><topic>Antibodies - immunology</topic><topic>Antigenic determinants</topic><topic>Arginine</topic><topic>Arginine deiminase</topic><topic>Arthritis</topic><topic>Arthritis, Rheumatoid - diagnostic imaging</topic><topic>Arthritis, Rheumatoid - genetics</topic><topic>Arthritis, Rheumatoid - pathology</topic><topic>Arthrography</topic><topic>Autoantibodies</topic><topic>Autoimmunity</topic><topic>Biology</topic><topic>CCR6 protein</topic><topic>CD83 antigen</topic><topic>Citrulline</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Deoxyribonucleic acid</topic><topic>Destruction</topic><topic>Development and progression</topic><topic>Disease Progression</topic><topic>Disease susceptibility</topic><topic>DNA</topic><topic>Drb1 protein</topic><topic>Environmental factors</topic><topic>Epitopes</topic><topic>Female</topic><topic>Gender</topic><topic>Genes</topic><topic>Genetic factors</topic><topic>Genetic Loci - genetics</topic><topic>Genetic polymorphisms</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Genetic testing</topic><topic>Genomes</topic><topic>Haplotypes</topic><topic>Histocompatibility antigen HLA</topic><topic>HLA antigens</topic><topic>HLA-DRB1 Chains - genetics</topic><topic>Humans</topic><topic>Hydrolases - genetics</topic><topic>Loci</topic><topic>Male</topic><topic>Medical records</topic><topic>Medicine</topic><topic>Meta-analysis</topic><topic>Middle Aged</topic><topic>Multiple regression analysis</topic><topic>Patients</topic><topic>Peptides, Cyclic - immunology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Population</topic><topic>Protein-arginine deiminase</topic><topic>Protein-Arginine Deiminases</topic><topic>PTPN2 protein</topic><topic>Regression analysis</topic><topic>Rheumatoid arthritis</topic><topic>Rheumatoid factor</topic><topic>Rheumatology</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Smoking</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suzuki, Taku</creatorcontrib><creatorcontrib>Ikari, Katsunori</creatorcontrib><creatorcontrib>Yano, Koichiro</creatorcontrib><creatorcontrib>Inoue, Eisuke</creatorcontrib><creatorcontrib>Toyama, Yoshiaki</creatorcontrib><creatorcontrib>Taniguchi, Atsuo</creatorcontrib><creatorcontrib>Yamanaka, Hisashi</creatorcontrib><creatorcontrib>Momohara, Shigeki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Taku</au><au>Ikari, Katsunori</au><au>Yano, Koichiro</au><au>Inoue, Eisuke</au><au>Toyama, Yoshiaki</au><au>Taniguchi, Atsuo</au><au>Yamanaka, Hisashi</au><au>Momohara, Shigeki</au><au>Ahuja, Sunil K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PADI4 and HLA-DRB1 are genetic risks for radiographic progression in RA patients, independent of ACPA status: results from the IORRA cohort study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-04-08</date><risdate>2013</risdate><volume>8</volume><issue>4</issue><spage>e61045</spage><epage>e61045</epage><pages>e61045-e61045</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Rheumatoid arthritis (RA) is a systemic, chronic inflammatory disease influenced by both genetic and environmental factors, leading to joint destruction and functional impairment. Recently, a large-scaled GWAS meta-analysis using more than 37,000 Japanese samples were conducted and 13 RA susceptibility loci were identified. However, it is not clear whether these loci have significant impact on joint destruction or not. This is the first study focused on the 13 loci to investigate independent genetic risk factors for radiographic progression in the first five years from onset of RA.
Sharp/van der Heijde score of hands at 5-year disease duration, which represents joint damage, were measured retrospectively and used as an outcome variable in 865 Japanese RA patients. Genetic factors regarded as putative risk factors were RA-susceptible polymorphisms identified by the Japanese GWAS meta-analysis, including HLA-DRB1 (shared epitope, SE), rs2240340 (PADI4), rs2230926 (TNFAIP3), rs3093024 (CCR6), rs11900673 (B3GNT2), rs2867461 (ANXA3), rs657075 (CSF2), rs12529514 (CD83), rs2233434 (NFKBIE), rs10821944 (ARID5B), rs3781913 (PDE2A-ARAP1), rs2841277 (PLD4) and rs2847297 (PTPN2). These putative genetic risk factors were assessed by a stepwise multiple regression analysis adjusted for possible non-genetic risk factors: autoantibody positivity (anti-citrullinated peptide antibody [ACPA] and rheumatoid factor), history of smoking, gender and age at disease onset.
The number of SE alleles (P = 0.002) and risk alleles of peptidyl arginine deiminase type IV gene (PADI4, P = 0.04) had significant impact on progressive joint destruction, as well as following non-genetic factors: ACPA positive (P = 0.0006), female sex (P = 0.006) and younger age of onset (P = 0.02).
In the present study, we found that PADI4 risk allele and HLA-DRB1 shared epitope are independent genetic risks for radiographic progression in Japanese rheumatoid arthritis patients. The results of this study give important knowledge of the risks on progressive joint damage in RA patients.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23577190</pmid><doi>10.1371/journal.pone.0061045</doi><tpages>e61045</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-04, Vol.8 (4), p.e61045-e61045 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1330893543 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Age Alleles Antibodies - immunology Antigenic determinants Arginine Arginine deiminase Arthritis Arthritis, Rheumatoid - diagnostic imaging Arthritis, Rheumatoid - genetics Arthritis, Rheumatoid - pathology Arthrography Autoantibodies Autoimmunity Biology CCR6 protein CD83 antigen Citrulline Cohort analysis Cohort Studies Deoxyribonucleic acid Destruction Development and progression Disease Progression Disease susceptibility DNA Drb1 protein Environmental factors Epitopes Female Gender Genes Genetic factors Genetic Loci - genetics Genetic polymorphisms Genetic Predisposition to Disease - genetics Genetic testing Genomes Haplotypes Histocompatibility antigen HLA HLA antigens HLA-DRB1 Chains - genetics Humans Hydrolases - genetics Loci Male Medical records Medicine Meta-analysis Middle Aged Multiple regression analysis Patients Peptides, Cyclic - immunology Polymorphism, Single Nucleotide Population Protein-arginine deiminase Protein-Arginine Deiminases PTPN2 protein Regression analysis Rheumatoid arthritis Rheumatoid factor Rheumatology Risk analysis Risk factors Smoking |
title | PADI4 and HLA-DRB1 are genetic risks for radiographic progression in RA patients, independent of ACPA status: results from the IORRA cohort study |
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