Association of matrix metalloproteinase 9 polymorphisms with adolescent idiopathic scoliosis in Chinese Han female.
- VernacularTitle:基质金属蛋白酶9基因多态性与汉族女性青少年特发性脊柱侧凸的关联分析
- Author:
Dong-sheng HUANG
1
;
Guo-yan LIANG
;
Pei-qiang SU
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Asian Continental Ancestry Group; genetics; Child; China; Female; Genetic Association Studies; Genetic Predisposition to Disease; genetics; Genotype; Humans; Matrix Metalloproteinase 9; genetics; Phenotype; Polymorphism, Single Nucleotide; genetics; Scoliosis; genetics
- From: Chinese Journal of Medical Genetics 2011;28(5):532-535
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo determine whether the matrix metalloproteinase 9 gene (MMP9) polymorphism is associated with the onset or progression of adolescent idiopathic scoliosis (AIS) in Chinese Han female.
METHODSThree single nucleotide polymorphisms (SNPs) (rs17576, rs2250889, rs1805088) were genotyped through TaqMan-based real-time PCR assay in 190 AIS patients and 190 controls, all of whom were females from Chinese Han population with matched age. Analyses performed included Hardy Weinberg equilibrium test, Pearson chi-square test, Logistic regression analysis, linkage disequilibrium analysis and haplotype analysis. The mean maximum Cobb angles with different genotypes in case-only dataset were also compared.
RESULTSAll 3 SNPs have reached Hardy-Weinberg equilibrium in the controls. Genotype and allele frequencies of all SNPs were found similar between cases and controls by Pearson chi-square test and Logistic regression. Genotype-phenotype analysis showed that patients with CC genotype in rs2250889 featured larger maximum Cobb angles.
CONCLUSIONMMP9 may not be a predisposition gene of AIS in Han female. However, homozygous mutation in rs2250889 can render scoliosis more severe, implying that MMP9 defect may result in deterioration of AIS.