Literature DB >> 24630593

SMN1 duplications contribute to sporadic amyotrophic lateral sclerosis susceptibility: evidence from a meta-analysis.

Xue-Bin Wang1, Ning-Hua Cui2, Jia-Jia Gao1, Xue-Ping Qiu1, Fang Zheng3.   

Abstract

OBJECTIVE: To investigate the association between SMN1 and SMN2 copy number variations (CNVs) and sporadic amyotrophic lateral sclerosis (SALS) by a meta-analysis.
METHODS: Through searching PubMed and EMBASE database (or manual searching) up to November 2013 using the following keywords: "survival motor neuron gene", "SMN", and "amyotrophic lateral sclerosis", "ALS" or "motor neuron disease". Nine studies were identified as eligible for this meta-analysis. The association between SMN genes and the SALS risk was investigated based on SMN1 and SMN2 CNVs. The heterogeneity across the studies was tested, as was publication bias.
RESULTS: The analysis showed significant association for SMN1 duplications in SALS risk: the risk estimates were OR=1.76, 95%CI=1.33-2.32, p<0.0001 (still significant when the p value was Bonferroni adjusted to 0.01). However, there was no significant association between SMN1 deletions and SALS risk after Bonferroni correction (OR=1.78, 95%CI=1.02-3.11, p=0.04). In addition, SMN2 copy number statuses were not associated with SALS in our pooled study. No evidence of publication bias was observed.
CONCLUSION: Our meta-analysis suggested that SMN1 duplications are a genetic risk factor in SALS, while there was no modulator effect of the SMN2 gene. In addition, it was possible that SMN1 deletions in predisposition to SALS vary across different countries. More studies were required to warrant the findings of this study.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Copy number variants; Meta-analysis; SALS; SMN1 deletions; SMN1 duplications; SMN2 homozygous deletions; Susceptibility

Mesh:

Substances:

Year:  2014        PMID: 24630593     DOI: 10.1016/j.jns.2014.02.026

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  9 in total

1.  Single-Cell Analysis of SMN Reveals Its Broader Role in Neuromuscular Disease.

Authors:  Natalia Rodriguez-Muela; Nadia K Litterman; Erika M Norabuena; Jesse L Mull; Maria José Galazo; Chicheng Sun; Shi-Yan Ng; Nina R Makhortova; Andrew White; Maureen M Lynes; Wendy K Chung; Lance S Davidow; Jeffrey D Macklis; Lee L Rubin
Journal:  Cell Rep       Date:  2017-02-07       Impact factor: 9.423

Review 2.  Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.

Authors:  Giuseppe Marangi; Bryan J Traynor
Journal:  Brain Res       Date:  2014-10-12       Impact factor: 3.252

3.  Valproate Treatment in an ALS Patient Carrying a c.194G>A Spastin Mutation and SMN2 Homozygous Deletion.

Authors:  Lucio Tremolizzo; Gessica Sala; Elisa Conti; Virginia Rodriguez-Menendez; Antonella Fogli; Angela Michelucci; Paolo Simi; Silvana Penco; Christian Lunetta; Massimo Corbo; Carlo Ferrarese
Journal:  Case Rep Neurol Med       Date:  2014-07-17

Review 4.  Motor Neuron Gene Therapy: Lessons from Spinal Muscular Atrophy for Amyotrophic Lateral Sclerosis.

Authors:  Andrew P Tosolini; James N Sleigh
Journal:  Front Mol Neurosci       Date:  2017-12-07       Impact factor: 5.639

Review 5.  Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.

Authors:  Giovanna Morello; Maria Guarnaccia; Antonio Gianmaria Spampinato; Valentina La Cognata; Velia D'Agata; Sebastiano Cavallaro
Journal:  Mol Neurobiol       Date:  2017-01-24       Impact factor: 5.590

6.  The Effect of SMN Gene Dosage on ALS Risk and Disease Severity.

Authors:  Jan Veldink; Philip Van Damme; Matthieu Moisse; Ramona A J Zwamborn; Joke van Vugt; Rick van der Spek; Wouter van Rheenen; Brendan Kenna; Kristel Van Eijk; Kevin Kenna; Philippe Corcia; Philippe Couratier; Patrick Vourc'h; Orla Hardiman; Russell McLaughin; Marc Gotkine; Vivian Drory; Nicola Ticozzi; Vincenzo Silani; Mamede de Carvalho; Jesús S Mora Pardina; Monica Povedano; Peter M Andersen; Markus Weber; Nazli A Başak; Xiao Chen; Michael A Eberle; Ammar Al-Chalabi; Chris Shaw; Pamela J Shaw; Karen E Morrison; John E Landers; Jonathan D Glass; Wim Robberecht; Michael van Es; Leonard van den Berg
Journal:  Ann Neurol       Date:  2021-01-15       Impact factor: 10.422

7.  SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis.

Authors:  Jeroen W Bos; Ewout J N Groen; Renske I Wadman; Chantall A D Curial; Naomi N Molleman; Marinka Zegers; Paul W J van Vught; Reinier Snetselaar; Raymon Vijzelaar; W Ludo van der Pol; Leonard H van den Berg
Journal:  Neurol Genet       Date:  2021-06-22

Review 8.  Copy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative Diseases.

Authors:  Matthew E R Butchbach
Journal:  Front Mol Biosci       Date:  2016-03-10

Review 9.  A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15.

Authors:  Alessia Casamassa; Daniela Ferrari; Maurizio Gelati; Massimo Carella; Angelo Luigi Vescovi; Jessica Rosati
Journal:  Int J Mol Sci       Date:  2020-03-09       Impact factor: 5.923

  9 in total

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