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Aldehyde dehydrogenase 2 genetic variations may increase susceptibility to Parkinson's disease in Han Chinese population.
Zhang, Xiong; Ye, Yang-Lie; Wang, Ya-Nan; Liu, Fang-Fang; Liu, Xue-Xia; Hu, Bei-Lei; Zou, Ming; Zhu, Jian-Hong.
Afiliação
  • Zhang X; Department of Neurology, The Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China; Department of Preventive Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Ye YL; Department of Neurology, The Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Wang YN; Department of Preventive Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Liu FF; Department of Preventive Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Liu XX; Department of Preventive Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Hu BL; Department of Neurology, The Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Zou M; Department of Neurology, The Second Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Zhu JH; Department of Preventive Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China; Key Laboratory of Watershed Science and Health of Zhejiang Province, Wenzhou Medical University, Wenzhou, Zhejiang, China. Electronic address: jianhong.zhu@gmail.com.
Neurobiol Aging ; 36(9): 2660.e9-13, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26130061
ABSTRACT
Genetic variations of ALDH2, encoding aldehyde dehydrogenase-2 which regulates aldehyde oxidation in the brain, have been recently suggested to impact on the association of pesticide exposure with Parkinson's disease (PD). However, the link between ALDH2 polymorphism and PD remains elusive. In the present study, tag-single nucleotide polymorphisms of ALDH2, including rs4767944, rs441, and rs671, were extracted and analyzed in a Chinese cohort consisting of 584 PD patients and 582 controls. Results from genotyping analyses showed that rs4767944 (p = 0.002), but not rs441 and rs671, were associated with PD. The C allele of rs4767944 served a risk factor toward PD. Further analysis presented a significant association between haplotype frequencies and the risk for PD, primarily driven by the preponderance of the C-T-A (p = 0.03) or C-T-G (p = 0.003) haplotype of rs4767944, rs441, and rs671 in PD patients. In conclusion, these novel results suggest an association between PD susceptibility and ALDH2 genetic variations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Aldeído Desidrogenase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Aging Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Aldeído Desidrogenase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Aging Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China