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Association of COL4A1 gene polymorphisms with cerebral palsy in a Chinese Han population.
Bi, D; Wang, H; Shang, Q; Xu, Y; Wang, F; Chen, M; Ma, C; Sun, Y; Zhao, X; Gao, C; Wang, L; Zhu, C; Xing, Q.
Afiliación
  • Bi D; Department of Pediatrics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Wang H; Children's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Shang Q; Department of Pediatrics, Zhengzhou Children's Hospital, Zhengzhou, China.
  • Xu Y; Department of Pediatrics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Wang F; Department of Neurosurgery, Tongji Hospital, Tongji University, Shanghai, China.
  • Chen M; Children's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Ma C; Department of Pediatrics, Zhengzhou Children's Hospital, Zhengzhou, China.
  • Sun Y; Department of Pediatrics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zhao X; Children's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Gao C; Department of Pediatrics, Zhengzhou Children's Hospital, Zhengzhou, China.
  • Wang L; Children's Hospital and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Zhu C; Department of Pediatrics, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Xing Q; Center for Brain Repair and Rehabilitation, University of Gothenburg, Gothenburg, Sweden.
Clin Genet ; 90(2): 149-55, 2016 08.
Article en En | MEDLINE | ID: mdl-26748532
ABSTRACT
The basement membrane (BM) is an extracellular matrix associated with overlying cells and is important for proper tissue development, stability, and physiology. COL4A1 is the most abundant component of type IV collagen in the BM, and COL4A1 variants can present with variable phenotypes that might be related to cerebral palsy (CP). We postulated, therefore, that variations in the COL4A1 gene might play an important role in the etiology of CP. In this study, six single nucleotide polymorphisms (SNPs) in the COL4A1 gene were genotyped among 351 CP patients and 220 healthy controls from the Chinese Han population. Significant association was found for an association between CP and rs1961495 (allele p = 0.008, odds ratio (OR) = 1.387, 95% confidence interval (CI) = 1.088-1.767) and rs1411040 (allele p = 0.009, OR = 1.746, 95% CI = 1.148-2.656) SNPs of the COL4A1 gene. Multifactor dimensionality reduction analysis suggested that these SNPs had interactive effects on the risk of CP. This study is the first attempt to investigate the contribution of polymorphisms in the COL4A1 gene to the susceptibility of CP in a Chinese Han population. This study shows an association of the COL4A1 gene with CP and suggests a potential role of COL4A1 in the pathogenesis of CP.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Parálisis Cerebral / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Colágeno Tipo IV Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Año: 2016 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Parálisis Cerebral / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Colágeno Tipo IV Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Clin Genet Año: 2016 Tipo del documento: Article País de afiliación: China