Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.

Adolescent idiopathic scoliosis (AIS) is the most common spinal deformity, affecting around 2% of adolescents worldwide. Genetic factors play an important role in its etiology. Using a genome-wide association study (GWAS), we recently identified novel AIS susceptibility loci on chromosomes 10q24.31...

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Autores principales: Atsushi Miyake, Ikuyo Kou, Yohei Takahashi, Todd A Johnson, Yoji Ogura, Jin Dai, Xusheng Qiu, Atsushi Takahashi, Hua Jiang, Huang Yan, Katsuki Kono, Noriaki Kawakami, Koki Uno, Manabu Ito, Shohei Minami, Haruhisa Yanagida, Hiroshi Taneichi, Naoya Hosono, Taichi Tsuji, Teppei Suzuki, Hideki Sudo, Toshiaki Kotani, Ikuho Yonezawa, Michiaki Kubo, Tatsuhiko Tsunoda, Kota Watanabe, Kazuhiro Chiba, Yoshiaki Toyama, Yong Qiu, Morio Matsumoto, Shiro Ikegawa
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:38a6cba115224fc7bb584124dcaf5d2c2021-11-18T08:57:00ZIdentification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.1932-620310.1371/journal.pone.0072802https://doaj.org/article/38a6cba115224fc7bb584124dcaf5d2c2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24023777/?tool=EBIhttps://doaj.org/toc/1932-6203Adolescent idiopathic scoliosis (AIS) is the most common spinal deformity, affecting around 2% of adolescents worldwide. Genetic factors play an important role in its etiology. Using a genome-wide association study (GWAS), we recently identified novel AIS susceptibility loci on chromosomes 10q24.31 and 6q24.1. To identify more AIS susceptibility loci relating to its severity and progression, we performed GWAS by limiting the case subjects to those with severe AIS. Through a two-stage association study using a total of ∼12,000 Japanese subjects, we identified a common variant, rs12946942 that showed a significant association with severe AIS in the recessive model (P=4.00 × 10(-8), odds ratio [OR]=2.05). Its association was replicated in a Chinese population (combined P=6.43 × 10(-12), OR = 2.21). rs12946942 is on chromosome 17q24.3 near the genes SOX9 and KCNJ2, which when mutated cause scoliosis phenotypes. Our findings will offer new insight into the etiology and progression of AIS.Atsushi MiyakeIkuyo KouYohei TakahashiTodd A JohnsonYoji OguraJin DaiXusheng QiuAtsushi TakahashiHua JiangHuang YanKatsuki KonoNoriaki KawakamiKoki UnoManabu ItoShohei MinamiHaruhisa YanagidaHiroshi TaneichiNaoya HosonoTaichi TsujiTeppei SuzukiHideki SudoToshiaki KotaniIkuho YonezawaMichiaki KuboTatsuhiko TsunodaKota WatanabeKazuhiro ChibaYoshiaki ToyamaYong QiuMorio MatsumotoShiro IkegawaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 9, p e72802 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Atsushi Miyake
Ikuyo Kou
Yohei Takahashi
Todd A Johnson
Yoji Ogura
Jin Dai
Xusheng Qiu
Atsushi Takahashi
Hua Jiang
Huang Yan
Katsuki Kono
Noriaki Kawakami
Koki Uno
Manabu Ito
Shohei Minami
Haruhisa Yanagida
Hiroshi Taneichi
Naoya Hosono
Taichi Tsuji
Teppei Suzuki
Hideki Sudo
Toshiaki Kotani
Ikuho Yonezawa
Michiaki Kubo
Tatsuhiko Tsunoda
Kota Watanabe
Kazuhiro Chiba
Yoshiaki Toyama
Yong Qiu
Morio Matsumoto
Shiro Ikegawa
Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
description Adolescent idiopathic scoliosis (AIS) is the most common spinal deformity, affecting around 2% of adolescents worldwide. Genetic factors play an important role in its etiology. Using a genome-wide association study (GWAS), we recently identified novel AIS susceptibility loci on chromosomes 10q24.31 and 6q24.1. To identify more AIS susceptibility loci relating to its severity and progression, we performed GWAS by limiting the case subjects to those with severe AIS. Through a two-stage association study using a total of ∼12,000 Japanese subjects, we identified a common variant, rs12946942 that showed a significant association with severe AIS in the recessive model (P=4.00 × 10(-8), odds ratio [OR]=2.05). Its association was replicated in a Chinese population (combined P=6.43 × 10(-12), OR = 2.21). rs12946942 is on chromosome 17q24.3 near the genes SOX9 and KCNJ2, which when mutated cause scoliosis phenotypes. Our findings will offer new insight into the etiology and progression of AIS.
format article
author Atsushi Miyake
Ikuyo Kou
Yohei Takahashi
Todd A Johnson
Yoji Ogura
Jin Dai
Xusheng Qiu
Atsushi Takahashi
Hua Jiang
Huang Yan
Katsuki Kono
Noriaki Kawakami
Koki Uno
Manabu Ito
Shohei Minami
Haruhisa Yanagida
Hiroshi Taneichi
Naoya Hosono
Taichi Tsuji
Teppei Suzuki
Hideki Sudo
Toshiaki Kotani
Ikuho Yonezawa
Michiaki Kubo
Tatsuhiko Tsunoda
Kota Watanabe
Kazuhiro Chiba
Yoshiaki Toyama
Yong Qiu
Morio Matsumoto
Shiro Ikegawa
author_facet Atsushi Miyake
Ikuyo Kou
Yohei Takahashi
Todd A Johnson
Yoji Ogura
Jin Dai
Xusheng Qiu
Atsushi Takahashi
Hua Jiang
Huang Yan
Katsuki Kono
Noriaki Kawakami
Koki Uno
Manabu Ito
Shohei Minami
Haruhisa Yanagida
Hiroshi Taneichi
Naoya Hosono
Taichi Tsuji
Teppei Suzuki
Hideki Sudo
Toshiaki Kotani
Ikuho Yonezawa
Michiaki Kubo
Tatsuhiko Tsunoda
Kota Watanabe
Kazuhiro Chiba
Yoshiaki Toyama
Yong Qiu
Morio Matsumoto
Shiro Ikegawa
author_sort Atsushi Miyake
title Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
title_short Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
title_full Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
title_fullStr Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
title_full_unstemmed Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
title_sort identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/38a6cba115224fc7bb584124dcaf5d2c
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