4.4 Article

Updated Meta-Analysis of BIN1, CR1, MS4A6A, CLU, and ABCA7 Variants in Alzheimer's Disease

Journal

JOURNAL OF MOLECULAR NEUROSCIENCE
Volume 64, Issue 3, Pages 471-477

Publisher

SPRINGERNATURE
DOI: 10.1007/s12031-018-1045-y

Keywords

Meta-analysis; Alzheimer's disease; LOAD; GWAS SNPs

Funding

  1. Universidade Federal do Espirito Santo - UFES
  2. Fundo de Amparo e Pesquisa do Espirito Santo - FAPES
  3. Departamento de Ciencia e Tecnologia do Ministerio da Saude - Decit
  4. Secretaria de Ciencia, Tecnologia e Insumos Estrategicos do Ministerio da Saude - SCTIE/ MS
  5. Fundo de Apoio a Ciencia e Tecnologia do Municipio de Vitoria - FACITEC
  6. Ministerio da Ciencia, Tecnologia e Inovacao - MCTI
  7. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPQ
  8. Ministerio da Educacao - MEC
  9. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - CAPES

Ask authors/readers for more resources

Genome-wide association studies (GWAS) have associated several genetic variants with late-onset Alzheimer's disease (LOAD), a neurodegenerative disease. Among those, rs3764650 ABCA7, rs6656401 CR1, and rs744373 BIN1 were associated as risk factors for LOAD, while rs11136000 CLU and rs610932 MS4A6A were protective. Recently, several case-control studies have investigated the association of these polymorphisms with AD. However, not all meta-analyses analyzed these variants across different ethnic groups. Therefore, we performed an updated meta-analysis of rs3764650 ABCA7, rs6656401 CR1, rs744373 BIN1, rs11136000 CLU, and rs610932 MS4A6A variants associated with LOAD, considering different ethnic populations. We utilized samples from 38 articles, comprising a total of 24,771 patients and 35,324 controls obtained through the PubMed database. Odds ratios (ORs) with 95% confidence intervals (CI) for polymorphisms were calculated by allelic comparison as an additive genetic model. We validated the risk for LOAD with BIN1 (rs744373), CR1 (rs6656401), and ABCA7 (rs376465), as well as the protective association for MS4A6A (rs610932) and CLU (rs11136000) variants.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available