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Association of SOD2 p.V16A polymorphism with Parkinson's disease: A meta-analysis in Han Chinese.
Wu, Yih-Ru; Chang, Kuo-Hsuan; Chao, Chih-Ying; Lin, Chih-Hsin; Chen, Yi-Chun; Liu, Tsai-Wei; Lee-Chen, Guey-Jen; Chen, Chiung-Mei.
Afiliação
  • Wu YR; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan; School of Medicine, Chang Gung University, Taoyuan City, Taiwan.
  • Chang KH; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan; School of Medicine, Chang Gung University, Taoyuan City, Taiwan.
  • Chao CY; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan.
  • Lin CH; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan.
  • Chen YC; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan; School of Medicine, Chang Gung University, Taoyuan City, Taiwan.
  • Liu TW; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan.
  • Lee-Chen GJ; Department of Life Science, National Taiwan Normal University, Taipei, Taiwan. Electronic address: t43019@ntnu.edu.tw.
  • Chen CM; Department of Neurology, Chang Gung Memorial Hospital Linkou Medical Center, Taoyuan City, Taiwan; School of Medicine, Chang Gung University, Taoyuan City, Taiwan. Electronic address: cmchen@cgmh.org.tw.
J Formos Med Assoc ; 120(1 Pt 2): 501-507, 2021 Jan.
Article em En | MEDLINE | ID: mdl-32620460
ABSTRACT

BACKGROUND:

Oxidative stress could participate in the pathogenesis of Parkinson's disease (PD). However, the role of genetic variation of superoxide dismutase 2 (SOD2), an important regulator against oxidative stress, in PD remains to be elucidated.

METHODS:

We screened SOD2 gene variation by sequencing cDNA from 72 patients with early onset PD. A cohort of PD (n = 609) and ethnically matched controls (n = 681) were further examined for the identified sequence variant by PCR and NaeI restriction analysis.

RESULTS:

Only a reported c.47T>C polymorphism (rs4880, SOD2 p.V16A) was found by cDNA sequencing. Case-control study of c.47T>C revealed that genotype and allele frequencies were in Hardy-Weinberg equilibrium in both patients and healthy controls. In a recessive model, those with CC genotype had a 2.61-fold increased risk of PD (95% CI 1.08-6.30, P = 0.03) compared to subjects with TT and TC genotypes. Significant association between CC genotype and PD in non-smokers was also observed after stratification according to the history of smoking (3.54-fold increased risk of PD, 95% CI 1.17-10.72, P = 0.02). Meta-analysis by combining studies of Chinese in China, Singapore, and Taiwan (total 2302 cases and 2029 controls) consistently showed CC genotype with increased risk of PD (OR = 1.77, 95% CI 1.15-2.71, P = 0.01).

CONCLUSION:

Our findings demonstrate that SOD2 p.V16A may play a role in the susceptibility of PD in Han Chinese.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Superóxido Dismutase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Formos Med Assoc Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Superóxido Dismutase Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans País/Região como assunto: Asia Idioma: En Revista: J Formos Med Assoc Ano de publicação: 2021 Tipo de documento: Article