Javascript must be enabled to continue!
Association study of IL-17RC, CHL1, DSCAM and CNTNAP2 genes polymorphisms with adolescent idiopathic scoliosis susceptibility in a Chinese Han population
View through CrossRef
Recently, several genome wide association studies suggested IL-17RC, CHL1, DSCAM and CNTNAP2 genes polymorphisms were associated with AIS. To confirm these associations, we performed this case-control study using data from 648 AIS patients and 573 healthy adolescent of Chinese Han population. A polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis was performed to detect the genotypes of polymorphic loci: rs708567 rs279545 in IL-17RC gene, and rs2055314, rs331894, rs2272524, rs2272522 in CHL1 gene, and rs2222973 in DSCAM gene, and rs2710102, rs11770843 in CNTNAP2 gene. Statistical analysis of genotype frequencies between AIS patients and controls were performed by χ2 test. Our results show that both the genotype frequency and allele frequency of loci rs708567 were significantly different between AIS patients and controls (P = 0.023, 0.028, respectively). As for polymorphic loci rs279545, rs2222973, rs279545, rs2055314, rs331894, rs2272524, rs2272522, no significant difference was found between AIS patients and controls either genotype or allele frequencies (p>0.05). Overall, our study found a significant association of IL-17RC gene polymorphisms with AIS in a Chinese Han population, indicating IL-17RC gene may be as a susceptibility gene for AIS; While CHL1, CNTNAP2 and DSCAM genes were not associated with AIS, suggesting that those genes may not be involved in the etiopathogenesis of AIS. However, association study of these genes with AIS in other races is needed to clarify the role of these genes in the etiology of AIS.
Title: Association study of IL-17RC, CHL1, DSCAM and CNTNAP2 genes polymorphisms with adolescent idiopathic scoliosis susceptibility in a Chinese Han population
Description:
Recently, several genome wide association studies suggested IL-17RC, CHL1, DSCAM and CNTNAP2 genes polymorphisms were associated with AIS.
To confirm these associations, we performed this case-control study using data from 648 AIS patients and 573 healthy adolescent of Chinese Han population.
A polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis was performed to detect the genotypes of polymorphic loci: rs708567 rs279545 in IL-17RC gene, and rs2055314, rs331894, rs2272524, rs2272522 in CHL1 gene, and rs2222973 in DSCAM gene, and rs2710102, rs11770843 in CNTNAP2 gene.
Statistical analysis of genotype frequencies between AIS patients and controls were performed by χ2 test.
Our results show that both the genotype frequency and allele frequency of loci rs708567 were significantly different between AIS patients and controls (P = 0.
023, 0.
028, respectively).
As for polymorphic loci rs279545, rs2222973, rs279545, rs2055314, rs331894, rs2272524, rs2272522, no significant difference was found between AIS patients and controls either genotype or allele frequencies (p>0.
05).
Overall, our study found a significant association of IL-17RC gene polymorphisms with AIS in a Chinese Han population, indicating IL-17RC gene may be as a susceptibility gene for AIS; While CHL1, CNTNAP2 and DSCAM genes were not associated with AIS, suggesting that those genes may not be involved in the etiopathogenesis of AIS.
However, association study of these genes with AIS in other races is needed to clarify the role of these genes in the etiology of AIS.
Related Results
Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model
Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by three core symptoms, specifically impaired social behavior, stereotypic/repetitive behaviors, and s...
CNTNAP2 Associated Neurodevelopmental Disorders: Intellectual Disability and Epilepsy comorbidity in Pakistani population.
CNTNAP2 Associated Neurodevelopmental Disorders: Intellectual Disability and Epilepsy comorbidity in Pakistani population.
Abstract
· Background:
The genetics of neurodevelopmental disorders is partially investigated due to the multiple additive risk factors found to be involved. Emergence of i...
Aberrant neuronal connectivity in CHL1‐deficient mice is associated with altered information processing‐related immediate early gene expression
Aberrant neuronal connectivity in CHL1‐deficient mice is associated with altered information processing‐related immediate early gene expression
AbstractIn humans, loss or alteration of the CHL1/CALL gene may contribute to mental impairment associated with the 3p‐syndrome, caused by distal deletions of the short (p) arm of ...
Idiopathic scoliosis
Idiopathic scoliosis
Introduction. Idiopathic scoliosis is a structural and lateral curvature of
the spine for which a currently recognizable cause has not been found and
there is no basic eviden...
Anesthesia Considerations in Scoliosis Surgery - A Clinical Communication
Anesthesia Considerations in Scoliosis Surgery - A Clinical Communication
Scoliosis is a condition of abnormal lateral curvature of the spinal column greater than 10 degrees as measured by Cobb’s angle. The two main groups of scoliosis are idiopathic sco...
Analisis Terapi Hydrotherapy untuk Skoliosis dari Sudut dari Sudut Pandang Penderita
Analisis Terapi Hydrotherapy untuk Skoliosis dari Sudut dari Sudut Pandang Penderita
Scoliosis is deformity spine which has deviation to lateral or abnormalities that spine is curved to right or left. The cause of scoliosis still unknown but it can be caused by gen...
The Impact of IL28B Gene Polymorphisms on Drug Responses
The Impact of IL28B Gene Polymorphisms on Drug Responses
To achieve high therapeutic efficacy in the patient, information on pharmacokinetics, pharmacodynamics, and pharmacogenetics is required. With the development of science and techno...
Automated Cobb Angle Measurement at Scale: Identifying Undiagnosed Scoliosis in the UK Biobank
Automated Cobb Angle Measurement at Scale: Identifying Undiagnosed Scoliosis in the UK Biobank
AbstractBackground contextAdult degenerative scoliosis develops after skeletal maturity in a previously normal spine, often as a result of age-related spinal degeneration, with its...

