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Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis
BACKGROUND: Although many studies have estimated the association between the butyrylcholinesterase (BCHE) K variant and Alzheimer’s disease (AD) risk, the results are still controversial. We thus conducted this meta-analysis. MATERIAL/METHODS: We searched NCBI, Medline, Web of Science, and Embase da...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444173/ https://www.ncbi.nlm.nih.gov/pubmed/25978873 http://dx.doi.org/10.12659/MSM.892982 |
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author | Wang, Zongcheng Jiang, Yuren Wang, Xi Du, Yangsen Xiao, Dandan Deng, Youchao Wang, Jinlian |
author_facet | Wang, Zongcheng Jiang, Yuren Wang, Xi Du, Yangsen Xiao, Dandan Deng, Youchao Wang, Jinlian |
author_sort | Wang, Zongcheng |
collection | PubMed |
description | BACKGROUND: Although many studies have estimated the association between the butyrylcholinesterase (BCHE) K variant and Alzheimer’s disease (AD) risk, the results are still controversial. We thus conducted this meta-analysis. MATERIAL/METHODS: We searched NCBI, Medline, Web of Science, and Embase databases to find all eligible studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the association. RESULTS: We found a significant association between BCHE K variant and AD risk (OR=1.20; 95% CI 1.03–1.39; P=0.02). In the stratified analysis by ethnicity, we observed a significant association between BCHE K variant and AD risk in Asians (OR=1.32; 95% CI 1.02–1.72; P=0.04). However, no significant association between BCHE K variant and AD risk in Caucasians was found (OR=1.14; 95% CI 0.95–1.37; P=0.16). When stratified by the age of AD onset, we found that late-onset AD (LOAD) was significantly associated with BCHE K variant (OR=1.44; 95% CI 1.05–1.97; P=0.02). No significant association between BCHE K variant and early-onset AD (EOAD) risk was observed (OR=1.16; 95% CI 0.89–1.51; P=0.27). Compared with non-APOE ɛ4 and non-BCHE K carriers, no significant association between BCHE K variant and AD risk was found (OR=1.11; 95% CI 0.91–1.35; P=0.30). However, APOE ɛ4 carriers showed increased AD risk in both non-BCHE K carriers (OR=2.81; 95% CI 1.75–4.51; P=0.0001) and BCHE K carriers (OR=3.31; 95% CI 1.82–6.02; P=0.0001). CONCLUSIONS: The results of this meta-analysis indicate that BCHE K variant might be associated with AD risk. |
format | Online Article Text |
id | pubmed-4444173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44441732015-06-09 Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis Wang, Zongcheng Jiang, Yuren Wang, Xi Du, Yangsen Xiao, Dandan Deng, Youchao Wang, Jinlian Med Sci Monit Meta-Analysis BACKGROUND: Although many studies have estimated the association between the butyrylcholinesterase (BCHE) K variant and Alzheimer’s disease (AD) risk, the results are still controversial. We thus conducted this meta-analysis. MATERIAL/METHODS: We searched NCBI, Medline, Web of Science, and Embase databases to find all eligible studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the association. RESULTS: We found a significant association between BCHE K variant and AD risk (OR=1.20; 95% CI 1.03–1.39; P=0.02). In the stratified analysis by ethnicity, we observed a significant association between BCHE K variant and AD risk in Asians (OR=1.32; 95% CI 1.02–1.72; P=0.04). However, no significant association between BCHE K variant and AD risk in Caucasians was found (OR=1.14; 95% CI 0.95–1.37; P=0.16). When stratified by the age of AD onset, we found that late-onset AD (LOAD) was significantly associated with BCHE K variant (OR=1.44; 95% CI 1.05–1.97; P=0.02). No significant association between BCHE K variant and early-onset AD (EOAD) risk was observed (OR=1.16; 95% CI 0.89–1.51; P=0.27). Compared with non-APOE ɛ4 and non-BCHE K carriers, no significant association between BCHE K variant and AD risk was found (OR=1.11; 95% CI 0.91–1.35; P=0.30). However, APOE ɛ4 carriers showed increased AD risk in both non-BCHE K carriers (OR=2.81; 95% CI 1.75–4.51; P=0.0001) and BCHE K carriers (OR=3.31; 95% CI 1.82–6.02; P=0.0001). CONCLUSIONS: The results of this meta-analysis indicate that BCHE K variant might be associated with AD risk. International Scientific Literature, Inc. 2015-05-16 /pmc/articles/PMC4444173/ /pubmed/25978873 http://dx.doi.org/10.12659/MSM.892982 Text en © Med Sci Monit, 2015 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Meta-Analysis Wang, Zongcheng Jiang, Yuren Wang, Xi Du, Yangsen Xiao, Dandan Deng, Youchao Wang, Jinlian Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis |
title | Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis |
title_full | Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis |
title_fullStr | Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis |
title_full_unstemmed | Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis |
title_short | Butyrylcholinesterase K Variant and Alzheimer’s Disease Risk: A Meta-Analysis |
title_sort | butyrylcholinesterase k variant and alzheimer’s disease risk: a meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444173/ https://www.ncbi.nlm.nih.gov/pubmed/25978873 http://dx.doi.org/10.12659/MSM.892982 |
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