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Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population

GPR126 has been identified to be associated with AIS (Adolescent Idiopathic Scoliosis) in different populations, but data on the northern Chinese population are unavailable. Additionally, it is important to know the exact clinical phenotypes associated with specific genetic polymorphisms. Fourteen S...

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Autores principales: Liu, Gang, Liu, Sen, Lin, Mao, Li, Xiaoxin, Chen, Weisheng, Zuo, Yuzhi, Liu, Jiaqi, Niu, Yuchen, Zhao, Sen, Long, Bo, Wu, Zhihong, Wu, Nan, Qiu, Guixing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824397/
https://www.ncbi.nlm.nih.gov/pubmed/29363878
http://dx.doi.org/10.1111/jcmm.13486
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author Liu, Gang
Liu, Sen
Lin, Mao
Li, Xiaoxin
Chen, Weisheng
Zuo, Yuzhi
Liu, Jiaqi
Niu, Yuchen
Zhao, Sen
Long, Bo
Wu, Zhihong
Wu, Nan
Qiu, Guixing
author_facet Liu, Gang
Liu, Sen
Lin, Mao
Li, Xiaoxin
Chen, Weisheng
Zuo, Yuzhi
Liu, Jiaqi
Niu, Yuchen
Zhao, Sen
Long, Bo
Wu, Zhihong
Wu, Nan
Qiu, Guixing
author_sort Liu, Gang
collection PubMed
description GPR126 has been identified to be associated with AIS (Adolescent Idiopathic Scoliosis) in different populations, but data on the northern Chinese population are unavailable. Additionally, it is important to know the exact clinical phenotypes associated with specific genetic polymorphisms. Fourteen SNP (single nucleotide polymorphism) loci in GPR126 were genotyped in 480 northern Chinese Han AIS patients and 841 controls. These patients were classified into three types based on the PUMC classification system. Luciferase assays were used to investigate their regulation of GPR126 transcription activity. Combined and stratified genotype–phenotype association analyses were conducted. The alleles rs225694, rs7774095 and rs2294773 were significantly associated with AIS (P = 0.021, 0.048 and 0.023, respectively). rs225694 and rs7774095 potentially have regulatory functions for the GRP126 gene. Correlation analysis revealed that allele A of rs225694 was a risk allele only for PUMC type II AIS (P = 0.036) and allele G of rs2294773 was a risk allele only for PUMC type I AIS (P = 0.018). In summary, rs225694, rs7774095 and rs2294773 are significantly associated with disease in northern Chinese Han AIS patients. The SNPs rs225694 and rs2294773 are associated with different AIS PUMC classifications.
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spelling pubmed-58243972018-03-01 Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population Liu, Gang Liu, Sen Lin, Mao Li, Xiaoxin Chen, Weisheng Zuo, Yuzhi Liu, Jiaqi Niu, Yuchen Zhao, Sen Long, Bo Wu, Zhihong Wu, Nan Qiu, Guixing J Cell Mol Med Original Articles GPR126 has been identified to be associated with AIS (Adolescent Idiopathic Scoliosis) in different populations, but data on the northern Chinese population are unavailable. Additionally, it is important to know the exact clinical phenotypes associated with specific genetic polymorphisms. Fourteen SNP (single nucleotide polymorphism) loci in GPR126 were genotyped in 480 northern Chinese Han AIS patients and 841 controls. These patients were classified into three types based on the PUMC classification system. Luciferase assays were used to investigate their regulation of GPR126 transcription activity. Combined and stratified genotype–phenotype association analyses were conducted. The alleles rs225694, rs7774095 and rs2294773 were significantly associated with AIS (P = 0.021, 0.048 and 0.023, respectively). rs225694 and rs7774095 potentially have regulatory functions for the GRP126 gene. Correlation analysis revealed that allele A of rs225694 was a risk allele only for PUMC type II AIS (P = 0.036) and allele G of rs2294773 was a risk allele only for PUMC type I AIS (P = 0.018). In summary, rs225694, rs7774095 and rs2294773 are significantly associated with disease in northern Chinese Han AIS patients. The SNPs rs225694 and rs2294773 are associated with different AIS PUMC classifications. John Wiley and Sons Inc. 2018-01-24 2018-03 /pmc/articles/PMC5824397/ /pubmed/29363878 http://dx.doi.org/10.1111/jcmm.13486 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Liu, Gang
Liu, Sen
Lin, Mao
Li, Xiaoxin
Chen, Weisheng
Zuo, Yuzhi
Liu, Jiaqi
Niu, Yuchen
Zhao, Sen
Long, Bo
Wu, Zhihong
Wu, Nan
Qiu, Guixing
Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population
title Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population
title_full Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population
title_fullStr Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population
title_full_unstemmed Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population
title_short Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population
title_sort genetic polymorphisms of gpr126 are functionally associated with pumc classifications of adolescent idiopathic scoliosis in a northern han population
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824397/
https://www.ncbi.nlm.nih.gov/pubmed/29363878
http://dx.doi.org/10.1111/jcmm.13486
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