Literature DB >> 26188085

RIT2 rs12456492 polymorphism and the risk of Parkinson's disease: A meta-analysis.

Xiaona Zhang1, Mengyue Niu1, Hong Li1, Anmu Xie2.   

Abstract

Many published case-control studies have investigated the association between rs12456492(A/G) variant in RIT2 gene and the risk of Parkinson's disease(PD); however, an ambiguous conclusion remains elusive. Our aim was to evaluate the association of RIT2 rs12456492(A/G) polymorphism with the risk of PD. We searched the Pubmed, Science Direct, EMBASE and EBSCO databases up to May 2015 for related studies. A total of 5 studies with 2541 PD cases and 2531 controls were included in the meta-analysis based on the strict inclusion and exclusion criteria. STATA 12.0 statistics software was used to calculate available data from each study. The pooled odds ratios (OR) and 95% confidence interval (CI) were calculated to assess the genetic association between RIT2 rs12456492 polymorphism and the risk of PD. There is a significant association between rs12456492 and PD (Gvs.A:OR=1.024, 95%CI:1.112-1.303, P=0.001; GGvs.AA:OR=1.486, 95%CI:1.259-1.755, P=0.001; GAvs.AA:OR=1.217, 95%CI:1.071-1.383, P=0.003; GG+GAvs.AA:OR=1.290, 95%CI:1.143-1.455, P=0.001; GGvs.GA+AA:OR=1.262, 95%CI:1.097-1.451, P=0.001). The data of our meta-analysis indicates that the G allele, GG and GA genotype of rs12456492(A/G) polymorphism may increase the risk of PD.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Gene polymorphism; Meta-analysis; Parkinson’s disease

Mesh:

Substances:

Year:  2015        PMID: 26188085     DOI: 10.1016/j.neulet.2015.07.004

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


  7 in total

1.  Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder.

Authors:  Shima Yazdandoost Hamedani; Jalal Gharesouran; Rezvan Noroozi; Arezou Sayad; Mir Davood Omrani; Atefeh Mir; Sarah Sadat Aghabozrg Afjeh; Mehdi Toghi; Saba Manoochehrabadi; Soudeh Ghafouri-Fard; Mohammad Taheri
Journal:  Metab Brain Dis       Date:  2017-02-11       Impact factor: 3.584

2.  The human RIT2 core promoter short tandem repeat predominant allele is species-specific in length: a selective advantage for human evolution?

Authors:  Babak Emamalizadeh; Abofazl Movafagh; Hossein Darvish; Somayeh Kazeminasab; Monavvar Andarva; Pegah Namdar-Aligoodarzi; Mina Ohadi
Journal:  Mol Genet Genomics       Date:  2017-02-18       Impact factor: 3.291

3.  Dopamine transporter trafficking and Rit2 GTPase: Mechanism of action and in vivo impact.

Authors:  Rita R Fagan; Patrick J Kearney; Carolyn G Sweeney; Dino Luethi; Florianne E Schoot Uiterkamp; Klaus Schicker; Brian S Alejandro; Lauren C O'Connor; Harald H Sitte; Haley E Melikian
Journal:  J Biol Chem       Date:  2020-03-04       Impact factor: 5.157

4.  Genetic association study between RIT2 and Parkinson's disease in a Han Chinese population.

Authors:  Jun-Ying Li; Jin-Hong Zhang; Nan-Nan Li; Ling Wang; Zhong-Jiao Lu; Lan Cheng; Xiao-Yi Sun; Rong Peng
Journal:  Neurol Sci       Date:  2016-11-26       Impact factor: 3.307

5.  RIT2 Polymorphisms: Is There a Differential Association?

Authors:  Babak Emamalizadeh; Javad Jamshidi; Abolfazl Movafagh; Mina Ohadi; Mahmoud Shekari Khaniani; Somayyeh Kazeminasab; Akbar Biglarian; Shaghayegh Taghavi; Marzieh Motallebi; Atena Fazeli; Azadeh Ahmadifard; Gholam-Ali Shahidi; Peyman Petramfar; Neda Shahmohammadibeni; Tahereh Dadkhah; Ehteram Khademi; Abbas Tafakhori; Ali Khaligh; Tannaz Safaralizadeh; Ali Kowsari; Arash Mirabzadeh; Amir Ehtesham Shafiei Zarneh; Mehdi Khorrami; Parasto Shokraeian; Mohammad Javad Soltani Banavandi; Behnam Safarpour Lima; Monavvar Andarva; Elham Alehabib; Minoo Atakhorrami; Hossein Darvish
Journal:  Mol Neurobiol       Date:  2016-03-03       Impact factor: 5.590

Review 6.  RIT2: responsible and susceptible gene for neurological and psychiatric disorders.

Authors:  Yousef Daneshmandpour; Hossein Darvish; Babak Emamalizadeh
Journal:  Mol Genet Genomics       Date:  2018-06-02       Impact factor: 3.291

7.  Annotating pathogenic non-coding variants in genic regions.

Authors:  Sahar Gelfman; Quanli Wang; K Melodi McSweeney; Zhong Ren; Francesca La Carpia; Matt Halvorsen; Kelly Schoch; Fanni Ratzon; Erin L Heinzen; Michael J Boland; Slavé Petrovski; David B Goldstein
Journal:  Nat Commun       Date:  2017-08-09       Impact factor: 14.919

  7 in total

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