A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians
Objective Genome‐wide association studies (GWAS) and their subsequent meta‐analyses have changed the landscape of genetics in rheumatoid arthritis (RA) by uncovering several novel genes. Such studies are heavily weighted by samples from Caucasian populations, but they explain only a small proportion...
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creator | Negi, Sapna Juyal, Garima Senapati, Sabyasachi Prasad, Pushplata Gupta, Aditi Singh, Shalini Kashyap, Sujit Kumar, Ashok Kumar, Uma Gupta, Rajiva Kaur, Satbir Agrawal, Suraksha Aggarwal, Amita Ott, Jurg Jain, Sanjay Juyal, Ramesh C. Thelma, B. K. |
description | Objective
Genome‐wide association studies (GWAS) and their subsequent meta‐analyses have changed the landscape of genetics in rheumatoid arthritis (RA) by uncovering several novel genes. Such studies are heavily weighted by samples from Caucasian populations, but they explain only a small proportion of total heritability. Our previous studies in genetically distinct North Indian RA cohorts have demonstrated apparent allelic/genetic heterogeneity between North Indian and Western populations, warranting GWAS in non‐European populations. We undertook this study to detect additional disease‐associated loci that may be collectively important in the presence or absence of genes with a major effect.
Methods
High‐quality genotypes for >600,000 single‐nucleotide polymorphisms (SNPs) in 706 RA patients and 761 controls from North India were generated in the discovery stage. Twelve SNPs showing suggestive association (P < 5 × 10−5) were then tested in an independent cohort of 927 RA patients and 1,148 controls. Additional disease‐associated loci were determined using support vector machine (SVM) analyses. Fine‐mapping of novel loci was performed by using imputation.
Results
In addition to the expected association of the HLA locus with RA, we identified association with a novel intronic SNP of ARL15 (rs255758) on chromosome 5 (Pcombined = 6.57 × 10−6; odds ratio 1.42). Genotype–phenotype correlation by assaying adiponectin levels demonstrated the functional significance of this novel gene in disease pathogenesis. SVM analysis confirmed this association along with that of a few more replication stage genes.
Conclusion
In this first GWAS of RA among North Indians, ARL15 emerged as a novel genetic risk factor in addition to the classic HLA locus, which suggests that population‐specific genetic loci as well as those shared between Asian and European populations contribute to RA etiology. Furthermore, our study reveals the potential of machine learning methods in unraveling gene–gene interactions using GWAS data. |
doi_str_mv | 10.1002/art.38110 |
format | Article |
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Genome‐wide association studies (GWAS) and their subsequent meta‐analyses have changed the landscape of genetics in rheumatoid arthritis (RA) by uncovering several novel genes. Such studies are heavily weighted by samples from Caucasian populations, but they explain only a small proportion of total heritability. Our previous studies in genetically distinct North Indian RA cohorts have demonstrated apparent allelic/genetic heterogeneity between North Indian and Western populations, warranting GWAS in non‐European populations. We undertook this study to detect additional disease‐associated loci that may be collectively important in the presence or absence of genes with a major effect.
Methods
High‐quality genotypes for >600,000 single‐nucleotide polymorphisms (SNPs) in 706 RA patients and 761 controls from North India were generated in the discovery stage. Twelve SNPs showing suggestive association (P < 5 × 10−5) were then tested in an independent cohort of 927 RA patients and 1,148 controls. Additional disease‐associated loci were determined using support vector machine (SVM) analyses. Fine‐mapping of novel loci was performed by using imputation.
Results
In addition to the expected association of the HLA locus with RA, we identified association with a novel intronic SNP of ARL15 (rs255758) on chromosome 5 (Pcombined = 6.57 × 10−6; odds ratio 1.42). Genotype–phenotype correlation by assaying adiponectin levels demonstrated the functional significance of this novel gene in disease pathogenesis. SVM analysis confirmed this association along with that of a few more replication stage genes.
Conclusion
In this first GWAS of RA among North Indians, ARL15 emerged as a novel genetic risk factor in addition to the classic HLA locus, which suggests that population‐specific genetic loci as well as those shared between Asian and European populations contribute to RA etiology. Furthermore, our study reveals the potential of machine learning methods in unraveling gene–gene interactions using GWAS data.</description><identifier>ISSN: 0004-3591</identifier><identifier>ISSN: 2326-5191</identifier><identifier>EISSN: 1529-0131</identifier><identifier>EISSN: 2326-5205</identifier><identifier>DOI: 10.1002/art.38110</identifier><identifier>PMID: 23918589</identifier><identifier>CODEN: ARHEAW</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>ADP-Ribosylation Factors - genetics ; Arthritis, Rheumatoid - genetics ; Asian Continental Ancestry Group - genetics ; European Continental Ancestry Group - genetics ; Female ; Gene Frequency ; Genetic Loci ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Genotype ; Humans ; Male ; Polymorphism, Single Nucleotide</subject><ispartof>Arthritis & rheumatology (Hoboken, N.J.), 2013-12, Vol.65 (12), p.3026-3035</ispartof><rights>Copyright © 2013 by the American College of Rheumatology</rights><rights>Copyright © 2013 by the American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3860-4a9a20e164f13a1b0a819aef27de8669a9b118f2f5c86773377d2d5b26de28ba3</citedby><cites>FETCH-LOGICAL-c3860-4a9a20e164f13a1b0a819aef27de8669a9b118f2f5c86773377d2d5b26de28ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fart.38110$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fart.38110$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23918589$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Negi, Sapna</creatorcontrib><creatorcontrib>Juyal, Garima</creatorcontrib><creatorcontrib>Senapati, Sabyasachi</creatorcontrib><creatorcontrib>Prasad, Pushplata</creatorcontrib><creatorcontrib>Gupta, Aditi</creatorcontrib><creatorcontrib>Singh, Shalini</creatorcontrib><creatorcontrib>Kashyap, Sujit</creatorcontrib><creatorcontrib>Kumar, Ashok</creatorcontrib><creatorcontrib>Kumar, Uma</creatorcontrib><creatorcontrib>Gupta, Rajiva</creatorcontrib><creatorcontrib>Kaur, Satbir</creatorcontrib><creatorcontrib>Agrawal, Suraksha</creatorcontrib><creatorcontrib>Aggarwal, Amita</creatorcontrib><creatorcontrib>Ott, Jurg</creatorcontrib><creatorcontrib>Jain, Sanjay</creatorcontrib><creatorcontrib>Juyal, Ramesh C.</creatorcontrib><creatorcontrib>Thelma, B. K.</creatorcontrib><title>A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians</title><title>Arthritis & rheumatology (Hoboken, N.J.)</title><addtitle>Arthritis Rheum</addtitle><description>Objective
Genome‐wide association studies (GWAS) and their subsequent meta‐analyses have changed the landscape of genetics in rheumatoid arthritis (RA) by uncovering several novel genes. Such studies are heavily weighted by samples from Caucasian populations, but they explain only a small proportion of total heritability. Our previous studies in genetically distinct North Indian RA cohorts have demonstrated apparent allelic/genetic heterogeneity between North Indian and Western populations, warranting GWAS in non‐European populations. We undertook this study to detect additional disease‐associated loci that may be collectively important in the presence or absence of genes with a major effect.
Methods
High‐quality genotypes for >600,000 single‐nucleotide polymorphisms (SNPs) in 706 RA patients and 761 controls from North India were generated in the discovery stage. Twelve SNPs showing suggestive association (P < 5 × 10−5) were then tested in an independent cohort of 927 RA patients and 1,148 controls. Additional disease‐associated loci were determined using support vector machine (SVM) analyses. Fine‐mapping of novel loci was performed by using imputation.
Results
In addition to the expected association of the HLA locus with RA, we identified association with a novel intronic SNP of ARL15 (rs255758) on chromosome 5 (Pcombined = 6.57 × 10−6; odds ratio 1.42). Genotype–phenotype correlation by assaying adiponectin levels demonstrated the functional significance of this novel gene in disease pathogenesis. SVM analysis confirmed this association along with that of a few more replication stage genes.
Conclusion
In this first GWAS of RA among North Indians, ARL15 emerged as a novel genetic risk factor in addition to the classic HLA locus, which suggests that population‐specific genetic loci as well as those shared between Asian and European populations contribute to RA etiology. Furthermore, our study reveals the potential of machine learning methods in unraveling gene–gene interactions using GWAS data.</description><subject>ADP-Ribosylation Factors - genetics</subject><subject>Arthritis, Rheumatoid - genetics</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Female</subject><subject>Gene Frequency</subject><subject>Genetic Loci</subject><subject>Genetic Predisposition to Disease</subject><subject>Genome-Wide Association Study</subject><subject>Genotype</subject><subject>Humans</subject><subject>Male</subject><subject>Polymorphism, Single Nucleotide</subject><issn>0004-3591</issn><issn>2326-5191</issn><issn>1529-0131</issn><issn>2326-5205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkdFqFTEQhoMo9li98AUk4E0Ft80ku9nkcinaFg4KpxUvl-xmlqbsbo5JtnLu-gg-o09i2lO9EEQIEwa--ZjhJ-Q1sGNgjJ-YkI6FAmBPyAoqrgsGAp6SFWOsLESl4YC8iPEmt1xU4jk54EKDqpRekbuGnuHsJ_x59-Ors0ibGH3vTHJ-ppdpsTu6wVs0Y6TNZg3Ve2roJ3-LY65znjlfN_RyiT1uk-vc6NLu3od08IFurnGZTPLO0iak6-CSi9TNeTJ39GK2zszxJXk2ZDu-evwPyZePH65Oz4v157OL02Zd9EJJVpRGG84QZDmAMNAxo0AbHHhtUUmpje4A1MCHqleyroWoa8tt1XFpkavOiENytPdug_-2YEzt5PLa42hm9EtsQQqtlZLA_o-WktcSylpm9O1f6I1fwpwPeaAY5Ccy9W5P9cHHGHBot8FNJuxaYO19gm1OsH1IMLNvHo1LN6H9Q_6OLAMne-C7G3H3b1PbbK72yl-I9qTa</recordid><startdate>201312</startdate><enddate>201312</enddate><creator>Negi, Sapna</creator><creator>Juyal, Garima</creator><creator>Senapati, Sabyasachi</creator><creator>Prasad, Pushplata</creator><creator>Gupta, Aditi</creator><creator>Singh, Shalini</creator><creator>Kashyap, Sujit</creator><creator>Kumar, Ashok</creator><creator>Kumar, Uma</creator><creator>Gupta, Rajiva</creator><creator>Kaur, Satbir</creator><creator>Agrawal, Suraksha</creator><creator>Aggarwal, Amita</creator><creator>Ott, Jurg</creator><creator>Jain, Sanjay</creator><creator>Juyal, Ramesh C.</creator><creator>Thelma, B. K.</creator><general>Wiley Subscription Services, Inc</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>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>201312</creationdate><title>A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians</title><author>Negi, Sapna ; Juyal, Garima ; Senapati, Sabyasachi ; Prasad, Pushplata ; Gupta, Aditi ; Singh, Shalini ; Kashyap, Sujit ; Kumar, Ashok ; Kumar, Uma ; Gupta, Rajiva ; Kaur, Satbir ; Agrawal, Suraksha ; Aggarwal, Amita ; Ott, Jurg ; Jain, Sanjay ; Juyal, Ramesh C. ; Thelma, B. K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3860-4a9a20e164f13a1b0a819aef27de8669a9b118f2f5c86773377d2d5b26de28ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>ADP-Ribosylation Factors - genetics</topic><topic>Arthritis, Rheumatoid - genetics</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>European Continental Ancestry Group - genetics</topic><topic>Female</topic><topic>Gene Frequency</topic><topic>Genetic Loci</topic><topic>Genetic Predisposition to Disease</topic><topic>Genome-Wide Association Study</topic><topic>Genotype</topic><topic>Humans</topic><topic>Male</topic><topic>Polymorphism, Single Nucleotide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Negi, Sapna</creatorcontrib><creatorcontrib>Juyal, Garima</creatorcontrib><creatorcontrib>Senapati, Sabyasachi</creatorcontrib><creatorcontrib>Prasad, Pushplata</creatorcontrib><creatorcontrib>Gupta, Aditi</creatorcontrib><creatorcontrib>Singh, Shalini</creatorcontrib><creatorcontrib>Kashyap, Sujit</creatorcontrib><creatorcontrib>Kumar, Ashok</creatorcontrib><creatorcontrib>Kumar, Uma</creatorcontrib><creatorcontrib>Gupta, Rajiva</creatorcontrib><creatorcontrib>Kaur, Satbir</creatorcontrib><creatorcontrib>Agrawal, Suraksha</creatorcontrib><creatorcontrib>Aggarwal, Amita</creatorcontrib><creatorcontrib>Ott, Jurg</creatorcontrib><creatorcontrib>Jain, Sanjay</creatorcontrib><creatorcontrib>Juyal, Ramesh C.</creatorcontrib><creatorcontrib>Thelma, B. 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K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians</atitle><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle><addtitle>Arthritis Rheum</addtitle><date>2013-12</date><risdate>2013</risdate><volume>65</volume><issue>12</issue><spage>3026</spage><epage>3035</epage><pages>3026-3035</pages><issn>0004-3591</issn><issn>2326-5191</issn><eissn>1529-0131</eissn><eissn>2326-5205</eissn><coden>ARHEAW</coden><abstract>Objective
Genome‐wide association studies (GWAS) and their subsequent meta‐analyses have changed the landscape of genetics in rheumatoid arthritis (RA) by uncovering several novel genes. Such studies are heavily weighted by samples from Caucasian populations, but they explain only a small proportion of total heritability. Our previous studies in genetically distinct North Indian RA cohorts have demonstrated apparent allelic/genetic heterogeneity between North Indian and Western populations, warranting GWAS in non‐European populations. We undertook this study to detect additional disease‐associated loci that may be collectively important in the presence or absence of genes with a major effect.
Methods
High‐quality genotypes for >600,000 single‐nucleotide polymorphisms (SNPs) in 706 RA patients and 761 controls from North India were generated in the discovery stage. Twelve SNPs showing suggestive association (P < 5 × 10−5) were then tested in an independent cohort of 927 RA patients and 1,148 controls. Additional disease‐associated loci were determined using support vector machine (SVM) analyses. Fine‐mapping of novel loci was performed by using imputation.
Results
In addition to the expected association of the HLA locus with RA, we identified association with a novel intronic SNP of ARL15 (rs255758) on chromosome 5 (Pcombined = 6.57 × 10−6; odds ratio 1.42). Genotype–phenotype correlation by assaying adiponectin levels demonstrated the functional significance of this novel gene in disease pathogenesis. SVM analysis confirmed this association along with that of a few more replication stage genes.
Conclusion
In this first GWAS of RA among North Indians, ARL15 emerged as a novel genetic risk factor in addition to the classic HLA locus, which suggests that population‐specific genetic loci as well as those shared between Asian and European populations contribute to RA etiology. Furthermore, our study reveals the potential of machine learning methods in unraveling gene–gene interactions using GWAS data.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>23918589</pmid><doi>10.1002/art.38110</doi><tpages>10</tpages></addata></record> |
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subjects | ADP-Ribosylation Factors - genetics Arthritis, Rheumatoid - genetics Asian Continental Ancestry Group - genetics European Continental Ancestry Group - genetics Female Gene Frequency Genetic Loci Genetic Predisposition to Disease Genome-Wide Association Study Genotype Humans Male Polymorphism, Single Nucleotide |
title | A Genome‐Wide Association Study Reveals ARL15, a Novel Non‐HLA Susceptibility Gene for Rheumatoid Arthritis in North Indians |
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