Literature DB >> 12826738

Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease.

Onofre Combarros1, Lucía Rodero, Jon Infante, Enrique Palacio, Javier Llorca, Carlos Fernández-Viadero, Nicolás Peña, José Berciano.   

Abstract

A vigorous controversy exists over whether tau tangles or amyloid-beta plaques are the primary cause of neurodegeneration in Alzheimer's disease (AD), and it is not well established whether genetic variation in tau is associated with AD. A recently identified novel protein, named Saitohin (STH), shares tissue expression pattern with tau, and preliminary evidence in a North American population indicates that a polymorphism at codon 7 (Q7R) of the STH gene is a predisposing factor for sporadic AD. A case-control study utilizing a clinically well-defined group of 315 sporadic AD patients and 307 control subjects was performed to test this association. The current study reveals that increased risk of AD associated with the STH RR genotype (OR 2.17, p = 0.04) is limited to late-onset (after the age of 72 years) AD cases. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 12826738     DOI: 10.1159/000071000

Source DB:  PubMed          Journal:  Dement Geriatr Cogn Disord        ISSN: 1420-8008            Impact factor:   2.959


  9 in total

1.  Association study of polymorphisms in LRP1, tau and 5-HTT genes and Alzheimer's disease in a sample of Colombian patients.

Authors:  D A Forero; G Arboleda; J J Yunis; R Pardo; H Arboleda
Journal:  J Neural Transm (Vienna)       Date:  2005-12-14       Impact factor: 3.575

2.  Serotonin transporter and saitohin genes in risk of Alzheimer's disease and frontotemporal lobar dementia: preliminary findings.

Authors:  Cristina Lorenzi; Alessandra Marcone; Adele Pirovano; Elena Marino; Francesco Cordici; Chiara Cerami; Dario Delmonte; Stefano F Cappa; Placido Bramanti; Enrico Smeraldi
Journal:  Neurol Sci       Date:  2010-09-18       Impact factor: 3.307

3.  The Q7R polymorphism in the saitohin gene is rare in a southern Chinese population.

Authors:  Kangguang Lin; Muni Tang; Yangbo Guo; Haiying Han; Yuhua Lin; Cui Ma
Journal:  Neurol Sci       Date:  2008-10-10       Impact factor: 3.307

Review 4.  Neurodegenerative aspects in vulnerability to schizophrenia spectrum disorders.

Authors:  Trevor Archer; Serafino Ricci; Danilo Garcia; Max Rapp Ricciardi
Journal:  Neurotox Res       Date:  2014-05-08       Impact factor: 3.911

5.  Association of rs62063857 variant of the saitohin gene with Parkinson's disease.

Authors:  Ezgi Sonmez; Mavi Deniz Ozel; Eylul Ece Islek; Ali Sazci; Halil Atilla Idrisoglu
Journal:  Cell Mol Neurobiol       Date:  2014-08-29       Impact factor: 5.046

Review 6.  Vascular endothelial growth factor gene promoter polymorphisms and Alzheimer's disease risk: a meta-analysis.

Authors:  Sheng-Yuan Liu; Fang-Fang Zeng; Zhong-Wei Chen; Chang-Yi Wang; Bin Zhao; Ke-Shen Li
Journal:  CNS Neurosci Ther       Date:  2013-04-10       Impact factor: 5.243

7.  Variation at APOE and STH loci and Alzheimer's disease.

Authors:  Lingjun Zuo; Christopher H van Dyck; Xingguang Luo; Henry R Kranzler; Bao-zhu Yang; Joel Gelernter
Journal:  Behav Brain Funct       Date:  2006-04-07       Impact factor: 3.759

8.  Saitohin Q7R polymorphism is associated with late-onset Alzheimer's disease susceptibility among caucasian populations: a meta-analysis.

Authors:  Rong Huang; Sai Tian; Rongrong Cai; Jie Sun; Wenqing Xia; Xue Dong; Yanjue Shen; Shaohua Wang
Journal:  J Cell Mol Med       Date:  2017-02-17       Impact factor: 5.310

Review 9.  Meta-analysis of the association between variants in MAPT and neurodegenerative diseases.

Authors:  Cheng-Cheng Zhang; Jun-Xia Zhu; Yu Wan; Lin Tan; Hui-Fu Wang; Jin-Tai Yu; Lan Tan
Journal:  Oncotarget       Date:  2017-07-04
  9 in total

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