CMPK1 and RBP3 are associated with corneal curvature in Asian populations
Corneal curvature (CC) measures the steepness of the cornea and is an important parameter for clinically diseases such as astigmatism and myopia. Despite the high heritability of CC, only two associated genes have been discovered to date. We performed a three-stage genome-wide association study meta...
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Veröffentlicht in: | Human molecular genetics 2014-11, Vol.23 (22), p.6129-6136 |
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creator | Chen, Peng Miyake, Masahiro Fan, Qiao Liao, Jiemin Yamashiro, Kenji Ikram, Mohammad K Chew, Merywn Vithana, Eranga N Khor, Chiea-Chuen Aung, Tin Tai, E-Shyong Wong, Tien-Yin Teo, Yik-Ying Yoshimura, Nagahisa Saw, Seang-Mei Cheng, Ching-Yu |
description | Corneal curvature (CC) measures the steepness of the cornea and is an important parameter for clinically diseases such as astigmatism and myopia. Despite the high heritability of CC, only two associated genes have been discovered to date. We performed a three-stage genome-wide association study meta-analysis in 12 660 Asian individuals. Our Stage 1 was done in multiethnic cohorts comprising 7440 individuals, followed by a Stage 2 replication in 2473 Chinese and Stage 3 in 2747 Japanese. The SNP array genotype data were imputed up to the 1000 Genomes Project Phase 1 cosmopolitan panel. The SNP association with the radii of CC was investigated in the linear regression model with the adjustment of age, gender and principal components. In addition to the known genes, MTOR (also known as FRAP1) and PDGFRA, we discovered two novel genes associated with CC: CMPK1 (rs17103186, P = 3.3 × 10(-12)) and RBP3 (rs11204213 [Val884Met], P = 1.1 × 10(-13)). The missense RBP3 SNP, rs11204213, was also associated with axial length (AL) (P = 4.2 × 10(-6)) and had larger effects on both CC and AL compared with other SNPs. The index SNPs at the four indicated loci explained 1.9% of CC variance across the Stages 1 and 2 cohorts, while 33.8% of CC variance was explained by the genome-wide imputation data. We identified two novel genes influencing CC, which are related to either corneal shape or eye size. This study provides additional insights into genetic architecture of corneal shape. |
doi_str_mv | 10.1093/hmg/ddu322 |
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Despite the high heritability of CC, only two associated genes have been discovered to date. We performed a three-stage genome-wide association study meta-analysis in 12 660 Asian individuals. Our Stage 1 was done in multiethnic cohorts comprising 7440 individuals, followed by a Stage 2 replication in 2473 Chinese and Stage 3 in 2747 Japanese. The SNP array genotype data were imputed up to the 1000 Genomes Project Phase 1 cosmopolitan panel. The SNP association with the radii of CC was investigated in the linear regression model with the adjustment of age, gender and principal components. In addition to the known genes, MTOR (also known as FRAP1) and PDGFRA, we discovered two novel genes associated with CC: CMPK1 (rs17103186, P = 3.3 × 10(-12)) and RBP3 (rs11204213 [Val884Met], P = 1.1 × 10(-13)). The missense RBP3 SNP, rs11204213, was also associated with axial length (AL) (P = 4.2 × 10(-6)) and had larger effects on both CC and AL compared with other SNPs. The index SNPs at the four indicated loci explained 1.9% of CC variance across the Stages 1 and 2 cohorts, while 33.8% of CC variance was explained by the genome-wide imputation data. We identified two novel genes influencing CC, which are related to either corneal shape or eye size. This study provides additional insights into genetic architecture of corneal shape.</description><identifier>ISSN: 0964-6906</identifier><identifier>EISSN: 1460-2083</identifier><identifier>DOI: 10.1093/hmg/ddu322</identifier><identifier>PMID: 24963161</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Aged ; Asian Continental Ancestry Group - genetics ; Child ; China ; Cohort Studies ; Cornea - chemistry ; Cornea - enzymology ; Cornea - metabolism ; Eye Diseases - enzymology ; Eye Diseases - genetics ; Eye Proteins - genetics ; Female ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Japan ; Male ; Middle Aged ; Nucleoside-Phosphate Kinase ; Polymorphism, Single Nucleotide ; Retinol-Binding Proteins - genetics</subject><ispartof>Human molecular genetics, 2014-11, Vol.23 (22), p.6129-6136</ispartof><rights>The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-b7b2f0e35f9afa889428a68520facd019d3d4a350bdb356d48a8e75e01447ae73</citedby><cites>FETCH-LOGICAL-c323t-b7b2f0e35f9afa889428a68520facd019d3d4a350bdb356d48a8e75e01447ae73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24963161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Peng</creatorcontrib><creatorcontrib>Miyake, Masahiro</creatorcontrib><creatorcontrib>Fan, Qiao</creatorcontrib><creatorcontrib>Liao, Jiemin</creatorcontrib><creatorcontrib>Yamashiro, Kenji</creatorcontrib><creatorcontrib>Ikram, Mohammad K</creatorcontrib><creatorcontrib>Chew, Merywn</creatorcontrib><creatorcontrib>Vithana, Eranga N</creatorcontrib><creatorcontrib>Khor, Chiea-Chuen</creatorcontrib><creatorcontrib>Aung, Tin</creatorcontrib><creatorcontrib>Tai, E-Shyong</creatorcontrib><creatorcontrib>Wong, Tien-Yin</creatorcontrib><creatorcontrib>Teo, Yik-Ying</creatorcontrib><creatorcontrib>Yoshimura, Nagahisa</creatorcontrib><creatorcontrib>Saw, Seang-Mei</creatorcontrib><creatorcontrib>Cheng, Ching-Yu</creatorcontrib><title>CMPK1 and RBP3 are associated with corneal curvature in Asian populations</title><title>Human molecular genetics</title><addtitle>Hum Mol Genet</addtitle><description>Corneal curvature (CC) measures the steepness of the cornea and is an important parameter for clinically diseases such as astigmatism and myopia. Despite the high heritability of CC, only two associated genes have been discovered to date. We performed a three-stage genome-wide association study meta-analysis in 12 660 Asian individuals. Our Stage 1 was done in multiethnic cohorts comprising 7440 individuals, followed by a Stage 2 replication in 2473 Chinese and Stage 3 in 2747 Japanese. The SNP array genotype data were imputed up to the 1000 Genomes Project Phase 1 cosmopolitan panel. The SNP association with the radii of CC was investigated in the linear regression model with the adjustment of age, gender and principal components. In addition to the known genes, MTOR (also known as FRAP1) and PDGFRA, we discovered two novel genes associated with CC: CMPK1 (rs17103186, P = 3.3 × 10(-12)) and RBP3 (rs11204213 [Val884Met], P = 1.1 × 10(-13)). The missense RBP3 SNP, rs11204213, was also associated with axial length (AL) (P = 4.2 × 10(-6)) and had larger effects on both CC and AL compared with other SNPs. The index SNPs at the four indicated loci explained 1.9% of CC variance across the Stages 1 and 2 cohorts, while 33.8% of CC variance was explained by the genome-wide imputation data. We identified two novel genes influencing CC, which are related to either corneal shape or eye size. This study provides additional insights into genetic architecture of corneal shape.</description><subject>Adult</subject><subject>Aged</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>Child</subject><subject>China</subject><subject>Cohort Studies</subject><subject>Cornea - chemistry</subject><subject>Cornea - enzymology</subject><subject>Cornea - metabolism</subject><subject>Eye Diseases - enzymology</subject><subject>Eye Diseases - genetics</subject><subject>Eye Proteins - genetics</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Genome-Wide Association Study</subject><subject>Humans</subject><subject>Japan</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nucleoside-Phosphate Kinase</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Retinol-Binding Proteins - genetics</subject><issn>0964-6906</issn><issn>1460-2083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90EtLAzEUhuEgiq3VjT9AshRhbG6TySxr8YYVi-g6nEkyNjI3kxnFf-9Iq6uzefjgvAidUnJJSc7nm_ptbu3AGdtDUyokSRhRfB9NSS5FInMiJ-goxndCqBQ8O0QTJnLJqaRTdL98XD9QDI3Fz1drjiE4DDG2xkPvLP7y_QabNjQOKmyG8An9MArf4EX00OCu7YYKet828RgdlFBFd7K7M_R6c_2yvEtWT7f3y8UqMZzxPimygpXE8bTMoQSlcsEUSJUyUoKxhOaWWwE8JYUteCqtUKBcljpChcjAZXyGzre7XWg_Bhd7XftoXFVB49oh6vGtNBNMUDXSiy01oY0xuFJ3wdcQvjUl-jedHtPpbboRn-12h6J29p_-teI_Hm1pgg</recordid><startdate>20141115</startdate><enddate>20141115</enddate><creator>Chen, Peng</creator><creator>Miyake, Masahiro</creator><creator>Fan, Qiao</creator><creator>Liao, Jiemin</creator><creator>Yamashiro, Kenji</creator><creator>Ikram, Mohammad K</creator><creator>Chew, Merywn</creator><creator>Vithana, Eranga N</creator><creator>Khor, Chiea-Chuen</creator><creator>Aung, Tin</creator><creator>Tai, E-Shyong</creator><creator>Wong, Tien-Yin</creator><creator>Teo, Yik-Ying</creator><creator>Yoshimura, Nagahisa</creator><creator>Saw, Seang-Mei</creator><creator>Cheng, Ching-Yu</creator><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></search><sort><creationdate>20141115</creationdate><title>CMPK1 and RBP3 are associated with corneal curvature in Asian populations</title><author>Chen, Peng ; Miyake, Masahiro ; Fan, Qiao ; Liao, Jiemin ; Yamashiro, Kenji ; Ikram, Mohammad K ; Chew, Merywn ; Vithana, Eranga N ; Khor, Chiea-Chuen ; Aung, Tin ; Tai, E-Shyong ; Wong, Tien-Yin ; Teo, Yik-Ying ; Yoshimura, Nagahisa ; Saw, Seang-Mei ; Cheng, Ching-Yu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-b7b2f0e35f9afa889428a68520facd019d3d4a350bdb356d48a8e75e01447ae73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>Child</topic><topic>China</topic><topic>Cohort Studies</topic><topic>Cornea - chemistry</topic><topic>Cornea - enzymology</topic><topic>Cornea - metabolism</topic><topic>Eye Diseases - enzymology</topic><topic>Eye Diseases - genetics</topic><topic>Eye Proteins - genetics</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Genome-Wide Association Study</topic><topic>Humans</topic><topic>Japan</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nucleoside-Phosphate Kinase</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Retinol-Binding Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Peng</creatorcontrib><creatorcontrib>Miyake, Masahiro</creatorcontrib><creatorcontrib>Fan, Qiao</creatorcontrib><creatorcontrib>Liao, Jiemin</creatorcontrib><creatorcontrib>Yamashiro, Kenji</creatorcontrib><creatorcontrib>Ikram, Mohammad K</creatorcontrib><creatorcontrib>Chew, Merywn</creatorcontrib><creatorcontrib>Vithana, Eranga N</creatorcontrib><creatorcontrib>Khor, Chiea-Chuen</creatorcontrib><creatorcontrib>Aung, Tin</creatorcontrib><creatorcontrib>Tai, E-Shyong</creatorcontrib><creatorcontrib>Wong, Tien-Yin</creatorcontrib><creatorcontrib>Teo, Yik-Ying</creatorcontrib><creatorcontrib>Yoshimura, Nagahisa</creatorcontrib><creatorcontrib>Saw, Seang-Mei</creatorcontrib><creatorcontrib>Cheng, Ching-Yu</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><jtitle>Human molecular genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Peng</au><au>Miyake, Masahiro</au><au>Fan, Qiao</au><au>Liao, Jiemin</au><au>Yamashiro, Kenji</au><au>Ikram, Mohammad K</au><au>Chew, Merywn</au><au>Vithana, Eranga N</au><au>Khor, Chiea-Chuen</au><au>Aung, Tin</au><au>Tai, E-Shyong</au><au>Wong, Tien-Yin</au><au>Teo, Yik-Ying</au><au>Yoshimura, Nagahisa</au><au>Saw, Seang-Mei</au><au>Cheng, Ching-Yu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CMPK1 and RBP3 are associated with corneal curvature in Asian populations</atitle><jtitle>Human molecular genetics</jtitle><addtitle>Hum Mol Genet</addtitle><date>2014-11-15</date><risdate>2014</risdate><volume>23</volume><issue>22</issue><spage>6129</spage><epage>6136</epage><pages>6129-6136</pages><issn>0964-6906</issn><eissn>1460-2083</eissn><abstract>Corneal curvature (CC) measures the steepness of the cornea and is an important parameter for clinically diseases such as astigmatism and myopia. Despite the high heritability of CC, only two associated genes have been discovered to date. We performed a three-stage genome-wide association study meta-analysis in 12 660 Asian individuals. Our Stage 1 was done in multiethnic cohorts comprising 7440 individuals, followed by a Stage 2 replication in 2473 Chinese and Stage 3 in 2747 Japanese. The SNP array genotype data were imputed up to the 1000 Genomes Project Phase 1 cosmopolitan panel. The SNP association with the radii of CC was investigated in the linear regression model with the adjustment of age, gender and principal components. In addition to the known genes, MTOR (also known as FRAP1) and PDGFRA, we discovered two novel genes associated with CC: CMPK1 (rs17103186, P = 3.3 × 10(-12)) and RBP3 (rs11204213 [Val884Met], P = 1.1 × 10(-13)). The missense RBP3 SNP, rs11204213, was also associated with axial length (AL) (P = 4.2 × 10(-6)) and had larger effects on both CC and AL compared with other SNPs. The index SNPs at the four indicated loci explained 1.9% of CC variance across the Stages 1 and 2 cohorts, while 33.8% of CC variance was explained by the genome-wide imputation data. We identified two novel genes influencing CC, which are related to either corneal shape or eye size. This study provides additional insights into genetic architecture of corneal shape.</abstract><cop>England</cop><pmid>24963161</pmid><doi>10.1093/hmg/ddu322</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Asian Continental Ancestry Group - genetics Child China Cohort Studies Cornea - chemistry Cornea - enzymology Cornea - metabolism Eye Diseases - enzymology Eye Diseases - genetics Eye Proteins - genetics Female Genetic Predisposition to Disease Genome-Wide Association Study Humans Japan Male Middle Aged Nucleoside-Phosphate Kinase Polymorphism, Single Nucleotide Retinol-Binding Proteins - genetics |
title | CMPK1 and RBP3 are associated with corneal curvature in Asian populations |
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