Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population
Adolescent idiopathic scoliosis (AIS) is a spinal deformity most commonly arising in apparently healthy girls around puberty. AIS has a strong genetic predisposition. Several genetic associations between AIS and single nucleotide polymorphisms (SNPs) have been reported; common SNPs in the genes for...
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| creator | Takahashi, Yohei Matsumoto, Morio Karasugi, Tatsuki Watanabe, Kota Chiba, Kazuhiro Kawakami, Noriaki Tsuji, Taichi Uno, Koki Suzuki, Teppei Ito, Manabu Sudo, Hideki Minami, Shohei Kotani, Toshiaki Kono, Katsuki Yanagida, Haruhisa Taneichi, Hiroshi Takahashi, Atsushi Toyama, Yoshiaki Ikegawa, Shiro |
| description | Adolescent idiopathic scoliosis (AIS) is a spinal deformity most commonly arising in apparently healthy girls around puberty. AIS has a strong genetic predisposition. Several genetic associations between AIS and single nucleotide polymorphisms (SNPs) have been reported; common SNPs in the genes for matrilin 1 (MATN1), melatonin receptor 1B (MTNR1B), tryptophan hydroxylase 1 (TPH1), and insulin‐like growth factor 1 (IGF1) are reported to be associated with AIS in Chinese. However, these associations have not been replicated so far. To confirm the associations, we compared these SNPs with AIS predisposition and curve severity in a population of Japanese females consisting of 798 AIS patients and 1,239 controls. All the subjects were genotyped using the PCR‐based Invader assay. We found no association of any of the SNPs with AIS predisposition or curve severity. Considering the statistical power and sample size of the present study, we concluded that these SNPs are not associated with either AIS predisposition or curve severity in Japanese. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 29: 1055–1058, 2011 |
| doi_str_mv | 10.1002/jor.21347 |
| format | Article |
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AIS has a strong genetic predisposition. Several genetic associations between AIS and single nucleotide polymorphisms (SNPs) have been reported; common SNPs in the genes for matrilin 1 (MATN1), melatonin receptor 1B (MTNR1B), tryptophan hydroxylase 1 (TPH1), and insulin‐like growth factor 1 (IGF1) are reported to be associated with AIS in Chinese. However, these associations have not been replicated so far. To confirm the associations, we compared these SNPs with AIS predisposition and curve severity in a population of Japanese females consisting of 798 AIS patients and 1,239 controls. All the subjects were genotyped using the PCR‐based Invader assay. We found no association of any of the SNPs with AIS predisposition or curve severity. Considering the statistical power and sample size of the present study, we concluded that these SNPs are not associated with either AIS predisposition or curve severity in Japanese. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 29: 1055–1058, 2011</description><identifier>ISSN: 0736-0266</identifier><identifier>EISSN: 1554-527X</identifier><identifier>DOI: 10.1002/jor.21347</identifier><identifier>PMID: 21308753</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; adolescent idiopathic scoliosis ; Aged ; Animals ; Asian Continental Ancestry Group - genetics ; Asian Continental Ancestry Group - statistics & numerical data ; association ; Cartilage Oligomeric Matrix Protein ; Child ; curve severity ; Extracellular Matrix Proteins - genetics ; Female ; Genetic Predisposition to Disease - ethnology ; Genotype ; Glycoproteins - genetics ; Humans ; Insulin-Like Growth Factor I - genetics ; Japan - epidemiology ; Matrilin Proteins ; Middle Aged ; Polymorphism, Single Nucleotide ; predisposition ; Receptor, Melatonin, MT2 - genetics ; Scoliosis - ethnology ; Scoliosis - genetics ; Tryptophan Hydroxylase - genetics ; Young Adult</subject><ispartof>Journal of orthopaedic research, 2011-07, Vol.29 (7), p.1055-1058</ispartof><rights>Copyright © 2011 Orthopaedic Research Society</rights><rights>Copyright © 2011 Orthopaedic Research Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4637-48aab2eba17c101b81f064d269f4df494eb46256bc97152812d134bdaa7959f03</citedby><cites>FETCH-LOGICAL-c4637-48aab2eba17c101b81f064d269f4df494eb46256bc97152812d134bdaa7959f03</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%2Fjor.21347$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjor.21347$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21308753$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takahashi, Yohei</creatorcontrib><creatorcontrib>Matsumoto, Morio</creatorcontrib><creatorcontrib>Karasugi, Tatsuki</creatorcontrib><creatorcontrib>Watanabe, Kota</creatorcontrib><creatorcontrib>Chiba, Kazuhiro</creatorcontrib><creatorcontrib>Kawakami, Noriaki</creatorcontrib><creatorcontrib>Tsuji, Taichi</creatorcontrib><creatorcontrib>Uno, Koki</creatorcontrib><creatorcontrib>Suzuki, Teppei</creatorcontrib><creatorcontrib>Ito, Manabu</creatorcontrib><creatorcontrib>Sudo, Hideki</creatorcontrib><creatorcontrib>Minami, Shohei</creatorcontrib><creatorcontrib>Kotani, Toshiaki</creatorcontrib><creatorcontrib>Kono, Katsuki</creatorcontrib><creatorcontrib>Yanagida, Haruhisa</creatorcontrib><creatorcontrib>Taneichi, Hiroshi</creatorcontrib><creatorcontrib>Takahashi, Atsushi</creatorcontrib><creatorcontrib>Toyama, Yoshiaki</creatorcontrib><creatorcontrib>Ikegawa, Shiro</creatorcontrib><title>Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population</title><title>Journal of orthopaedic research</title><addtitle>J. Orthop. Res</addtitle><description>Adolescent idiopathic scoliosis (AIS) is a spinal deformity most commonly arising in apparently healthy girls around puberty. AIS has a strong genetic predisposition. Several genetic associations between AIS and single nucleotide polymorphisms (SNPs) have been reported; common SNPs in the genes for matrilin 1 (MATN1), melatonin receptor 1B (MTNR1B), tryptophan hydroxylase 1 (TPH1), and insulin‐like growth factor 1 (IGF1) are reported to be associated with AIS in Chinese. However, these associations have not been replicated so far. To confirm the associations, we compared these SNPs with AIS predisposition and curve severity in a population of Japanese females consisting of 798 AIS patients and 1,239 controls. All the subjects were genotyped using the PCR‐based Invader assay. We found no association of any of the SNPs with AIS predisposition or curve severity. Considering the statistical power and sample size of the present study, we concluded that these SNPs are not associated with either AIS predisposition or curve severity in Japanese. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 29: 1055–1058, 2011</description><subject>Adolescent</subject><subject>adolescent idiopathic scoliosis</subject><subject>Aged</subject><subject>Animals</subject><subject>Asian Continental Ancestry Group - genetics</subject><subject>Asian Continental Ancestry Group - statistics & numerical data</subject><subject>association</subject><subject>Cartilage Oligomeric Matrix Protein</subject><subject>Child</subject><subject>curve severity</subject><subject>Extracellular Matrix Proteins - genetics</subject><subject>Female</subject><subject>Genetic Predisposition to Disease - ethnology</subject><subject>Genotype</subject><subject>Glycoproteins - genetics</subject><subject>Humans</subject><subject>Insulin-Like Growth Factor I - genetics</subject><subject>Japan - epidemiology</subject><subject>Matrilin Proteins</subject><subject>Middle Aged</subject><subject>Polymorphism, Single Nucleotide</subject><subject>predisposition</subject><subject>Receptor, Melatonin, MT2 - genetics</subject><subject>Scoliosis - ethnology</subject><subject>Scoliosis - genetics</subject><subject>Tryptophan Hydroxylase - genetics</subject><subject>Young Adult</subject><issn>0736-0266</issn><issn>1554-527X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1OGzEURq2qVUlpF32ByruqEgO2xz8zS0BNAIVQRanKzvLYnmJwxlN7BshD9R3rEGDXlXWl8x1d3w-AzxgdYoTI0W2IhwSXVLwBE8wYLRgR12_BBImSF4hwvgc-pHSLEBKYVO_BXoZRJVg5AX_nSt_B0EKVUtBODS50sLHDg7UdVCZ4m7TtBuiMC70abpyGSQfvQnIJqs7APtp7F8bkNzDaPsTBGphc99tb2I3a2zA4Y2Ef_GYdYn_j0jpB18HL49UCH8DL1WKJTw7g6sdZnra-89kUbwEFL1SvOpu24X70T5t9BO9a5ZP99Pzug5_T76vTs2J-NTs_PZ4XmvJSFLRSqiG2UVhojHBT4RZxagivW2paWlPbUE4Yb3QtMCMVJiZfrzFKiZrVLSr3wdedt4_hz2jTINcu38H7vFD-q6w4ZyUnNc3ktx2pY0gp2lb20a1V3EiM5LYcmcuRT-Vk9suzdWzW1rySL21k4GgHPDhvN_83yYur5Yuy2CVcGuzja0LFO8lFKZj8tZjJ6TWbTZeolKz8B4ujqXk</recordid><startdate>201107</startdate><enddate>201107</enddate><creator>Takahashi, Yohei</creator><creator>Matsumoto, Morio</creator><creator>Karasugi, Tatsuki</creator><creator>Watanabe, Kota</creator><creator>Chiba, Kazuhiro</creator><creator>Kawakami, Noriaki</creator><creator>Tsuji, Taichi</creator><creator>Uno, Koki</creator><creator>Suzuki, Teppei</creator><creator>Ito, Manabu</creator><creator>Sudo, Hideki</creator><creator>Minami, Shohei</creator><creator>Kotani, Toshiaki</creator><creator>Kono, Katsuki</creator><creator>Yanagida, Haruhisa</creator><creator>Taneichi, Hiroshi</creator><creator>Takahashi, Atsushi</creator><creator>Toyama, Yoshiaki</creator><creator>Ikegawa, Shiro</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>201107</creationdate><title>Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population</title><author>Takahashi, Yohei ; Matsumoto, Morio ; Karasugi, Tatsuki ; Watanabe, Kota ; Chiba, Kazuhiro ; Kawakami, Noriaki ; Tsuji, Taichi ; Uno, Koki ; Suzuki, Teppei ; Ito, Manabu ; Sudo, Hideki ; Minami, Shohei ; Kotani, Toshiaki ; Kono, Katsuki ; Yanagida, Haruhisa ; Taneichi, Hiroshi ; Takahashi, Atsushi ; Toyama, Yoshiaki ; Ikegawa, Shiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4637-48aab2eba17c101b81f064d269f4df494eb46256bc97152812d134bdaa7959f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>adolescent idiopathic scoliosis</topic><topic>Aged</topic><topic>Animals</topic><topic>Asian Continental Ancestry Group - genetics</topic><topic>Asian Continental Ancestry Group - statistics & numerical data</topic><topic>association</topic><topic>Cartilage Oligomeric Matrix Protein</topic><topic>Child</topic><topic>curve severity</topic><topic>Extracellular Matrix Proteins - genetics</topic><topic>Female</topic><topic>Genetic Predisposition to Disease - ethnology</topic><topic>Genotype</topic><topic>Glycoproteins - genetics</topic><topic>Humans</topic><topic>Insulin-Like Growth Factor I - genetics</topic><topic>Japan - epidemiology</topic><topic>Matrilin Proteins</topic><topic>Middle Aged</topic><topic>Polymorphism, Single Nucleotide</topic><topic>predisposition</topic><topic>Receptor, Melatonin, MT2 - genetics</topic><topic>Scoliosis - ethnology</topic><topic>Scoliosis - genetics</topic><topic>Tryptophan Hydroxylase - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takahashi, Yohei</creatorcontrib><creatorcontrib>Matsumoto, Morio</creatorcontrib><creatorcontrib>Karasugi, Tatsuki</creatorcontrib><creatorcontrib>Watanabe, Kota</creatorcontrib><creatorcontrib>Chiba, Kazuhiro</creatorcontrib><creatorcontrib>Kawakami, Noriaki</creatorcontrib><creatorcontrib>Tsuji, Taichi</creatorcontrib><creatorcontrib>Uno, Koki</creatorcontrib><creatorcontrib>Suzuki, Teppei</creatorcontrib><creatorcontrib>Ito, Manabu</creatorcontrib><creatorcontrib>Sudo, Hideki</creatorcontrib><creatorcontrib>Minami, Shohei</creatorcontrib><creatorcontrib>Kotani, Toshiaki</creatorcontrib><creatorcontrib>Kono, Katsuki</creatorcontrib><creatorcontrib>Yanagida, Haruhisa</creatorcontrib><creatorcontrib>Taneichi, Hiroshi</creatorcontrib><creatorcontrib>Takahashi, Atsushi</creatorcontrib><creatorcontrib>Toyama, Yoshiaki</creatorcontrib><creatorcontrib>Ikegawa, Shiro</creatorcontrib><collection>Istex</collection><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>Journal of orthopaedic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takahashi, Yohei</au><au>Matsumoto, Morio</au><au>Karasugi, Tatsuki</au><au>Watanabe, Kota</au><au>Chiba, Kazuhiro</au><au>Kawakami, Noriaki</au><au>Tsuji, Taichi</au><au>Uno, Koki</au><au>Suzuki, Teppei</au><au>Ito, Manabu</au><au>Sudo, Hideki</au><au>Minami, Shohei</au><au>Kotani, Toshiaki</au><au>Kono, Katsuki</au><au>Yanagida, Haruhisa</au><au>Taneichi, Hiroshi</au><au>Takahashi, Atsushi</au><au>Toyama, Yoshiaki</au><au>Ikegawa, Shiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population</atitle><jtitle>Journal of orthopaedic research</jtitle><addtitle>J. Orthop. Res</addtitle><date>2011-07</date><risdate>2011</risdate><volume>29</volume><issue>7</issue><spage>1055</spage><epage>1058</epage><pages>1055-1058</pages><issn>0736-0266</issn><eissn>1554-527X</eissn><abstract>Adolescent idiopathic scoliosis (AIS) is a spinal deformity most commonly arising in apparently healthy girls around puberty. AIS has a strong genetic predisposition. Several genetic associations between AIS and single nucleotide polymorphisms (SNPs) have been reported; common SNPs in the genes for matrilin 1 (MATN1), melatonin receptor 1B (MTNR1B), tryptophan hydroxylase 1 (TPH1), and insulin‐like growth factor 1 (IGF1) are reported to be associated with AIS in Chinese. However, these associations have not been replicated so far. To confirm the associations, we compared these SNPs with AIS predisposition and curve severity in a population of Japanese females consisting of 798 AIS patients and 1,239 controls. All the subjects were genotyped using the PCR‐based Invader assay. We found no association of any of the SNPs with AIS predisposition or curve severity. Considering the statistical power and sample size of the present study, we concluded that these SNPs are not associated with either AIS predisposition or curve severity in Japanese. © 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 29: 1055–1058, 2011</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21308753</pmid><doi>10.1002/jor.21347</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Adolescent adolescent idiopathic scoliosis Aged Animals Asian Continental Ancestry Group - genetics Asian Continental Ancestry Group - statistics & numerical data association Cartilage Oligomeric Matrix Protein Child curve severity Extracellular Matrix Proteins - genetics Female Genetic Predisposition to Disease - ethnology Genotype Glycoproteins - genetics Humans Insulin-Like Growth Factor I - genetics Japan - epidemiology Matrilin Proteins Middle Aged Polymorphism, Single Nucleotide predisposition Receptor, Melatonin, MT2 - genetics Scoliosis - ethnology Scoliosis - genetics Tryptophan Hydroxylase - genetics Young Adult |
| title | Lack of association between adolescent idiopathic scoliosis and previously reported single nucleotide polymorphisms in MATN1, MTNR1B, TPH1, and IGF1 in a Japanese population |
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