Literature DB >> 20478361

Lack of replication of a previously reported association between polymorphism in the 3'UTR of the alpha-synuclein gene and Parkinson's disease in Chinese subjects.

F-Y Hu1, W-B Hu, L Liu, L-H Yu, J Xi, X-H He, M-R Zhu, Z-L Liu, Y-M Xu.   

Abstract

Recent studies have implicated polymorphisms in the 3' untranslated region (3'UTR) of the alpha-synuclein (SNCA) gene in the development of Parkinson's disease (PD). Single nucleotide polymorphism (SNP) rs356165 is one of polymorphisms located in the 3'UTR and its association with PD has been reported but remains controversial. Herein, we conducted a case-control study to further evaluate the possible association between SNP rs356165 and PD in Chinese. All subjects (330 PD patients and 300 normal controls) were successfully genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. No statistically significant difference in genotype frequency between cases and controls was observed (P=0.863), suggesting no association of SNP rs356165 with PD in our population. Thus, it may be premature to conclude an association between the 3'UTR of the SNCA gene and PD, and this association should be further examined in different ethnic populations. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20478361     DOI: 10.1016/j.neulet.2010.05.022

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  8 in total

1.  Association between rs6812193 polymorphism and sporadic Parkinson's disease susceptibility.

Authors:  Qiang Huo; Tao Li; Peiqing Zhao; Lianqing Wang
Journal:  Neurol Sci       Date:  2015-03-29       Impact factor: 3.307

2.  Using polymorphisms in FKBP5 to define biologically distinct subtypes of posttraumatic stress disorder: evidence from endocrine and gene expression studies.

Authors:  Divya Mehta; Mariya Gonik; Torsten Klengel; Monika Rex-Haffner; Andreas Menke; Jennifer Rubel; Kristina B Mercer; Benno Pütz; Bekh Bradley; Florian Holsboer; Kerry J Ressler; Bertram Müller-Myhsok; Elisabeth B Binder
Journal:  Arch Gen Psychiatry       Date:  2011-05-02

Review 3.  Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A Review.

Authors:  Clarissa Loureiro das Chagas Campêlo; Regina Helena Silva
Journal:  Parkinsons Dis       Date:  2017-07-11

4.  Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTR.

Authors:  Elizabeth S Barrie; Sung-Ha Lee; John T Frater; Maria Kataki; Douglas W Scharre; Wolfgang Sadee
Journal:  Mol Genet Genomic Med       Date:  2018-05-06       Impact factor: 2.183

5.  A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.

Authors:  Yuan Zhang; Li Shu; Qiying Sun; Hongxu Pan; Jifeng Guo; Beisha Tang
Journal:  Front Mol Neurosci       Date:  2018-10-25       Impact factor: 5.639

6.  Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson's disease in Chinese Han population.

Authors:  Xin-xin Liao; Zi-xiong Zhan; Ying-ying Luo; Kai Li; Jun-ling Wang; Ji-feng Guo; Xin-xiang Yan; Kun Xia; Bei-sha Tang; Lu Shen
Journal:  BMC Neurol       Date:  2013-12-11       Impact factor: 2.474

7.  Variants in SNCA Gene Are Associated with Parkinson's Disease Risk and Cognitive Symptoms in a Brazilian Sample.

Authors:  Clarissa L C Campêlo; Fernanda C Cagni; Diego de Siqueira Figueredo; Luiz G Oliveira; Antônio B Silva-Neto; Priscila T Macêdo; José R Santos; Geison S Izídio; Alessandra M Ribeiro; Tiago G de Andrade; Clécio de Oliveira Godeiro; Regina H Silva
Journal:  Front Aging Neurosci       Date:  2017-06-20       Impact factor: 5.750

8.  SNCA 3' UTR Genetic Variants in Patients with Parkinson's Disease.

Authors:  Antonela Blažeković; Kristina Gotovac Jerčić; Fran Borovečki
Journal:  Biomolecules       Date:  2021-11-30
  8 in total

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