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Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis

Low density lipoprotein receptor-related protein 1 (LRP1) C766T polymorphism (rs1799986) has been extensively investigated for Alzheimer’s disease (AD) susceptibility. However, results in different studies have been contradictory. Therefore, we conducted a meta-analysis containing 6455 AD cases and...

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Autores principales: Wang, Yun, Liu, Shengyuan, Wang, Jingjing, Zhang, Jie, Hua, Yaqiong, Li, Hua, Tan, Huibiao, Kuai, Bin, Wang, Biao, Sheng, Sitong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559589/
https://www.ncbi.nlm.nih.gov/pubmed/28814781
http://dx.doi.org/10.1038/s41598-017-08335-w
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author Wang, Yun
Liu, Shengyuan
Wang, Jingjing
Zhang, Jie
Hua, Yaqiong
Li, Hua
Tan, Huibiao
Kuai, Bin
Wang, Biao
Sheng, Sitong
author_facet Wang, Yun
Liu, Shengyuan
Wang, Jingjing
Zhang, Jie
Hua, Yaqiong
Li, Hua
Tan, Huibiao
Kuai, Bin
Wang, Biao
Sheng, Sitong
author_sort Wang, Yun
collection PubMed
description Low density lipoprotein receptor-related protein 1 (LRP1) C766T polymorphism (rs1799986) has been extensively investigated for Alzheimer’s disease (AD) susceptibility. However, results in different studies have been contradictory. Therefore, we conducted a meta-analysis containing 6455 AD cases and 6304 controls from 26 independent case–control studies to determine whether there was an association between the LRP1 C766T polymorphism and AD susceptibility. The combined analysis showed that there was no significant association between LRP1 C766T polymorphism and AD susceptibility (TT + CT versus CC: OR = 0.920, 95% CI = 0.817–1.037, P = 0.172). In subgroup analysis, significant decreased AD susceptibility was found among Asian population in allele model (T versus C: OR = 0.786, 95% CI = 0.635–0.974, P = 0.028) and dominant model (TT + CT versus CC: OR = 0.800, 95% CI = 0.647–0.990, P = 0.040). Moreover, T allele of LRP1 C766T was statistically associated with late onset of AD (LOAD) (T versus C: OR = 0.858, 95% CI = 0.748–0.985, P = 0.029; TT + CT versus CC: OR = 0.871, 95% CI = 0.763–0.994, P = 0.040). In conclusion, our meta-analysis suggested that LRP1 C766T polymorphism was associated with lower risk of AD in Asian, and could reduce LOAD risk especially. Considering some limitations of our meta-analysis, further large-scale studies should be done to reach a more comprehensive understanding.
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spelling pubmed-55595892017-08-18 Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis Wang, Yun Liu, Shengyuan Wang, Jingjing Zhang, Jie Hua, Yaqiong Li, Hua Tan, Huibiao Kuai, Bin Wang, Biao Sheng, Sitong Sci Rep Article Low density lipoprotein receptor-related protein 1 (LRP1) C766T polymorphism (rs1799986) has been extensively investigated for Alzheimer’s disease (AD) susceptibility. However, results in different studies have been contradictory. Therefore, we conducted a meta-analysis containing 6455 AD cases and 6304 controls from 26 independent case–control studies to determine whether there was an association between the LRP1 C766T polymorphism and AD susceptibility. The combined analysis showed that there was no significant association between LRP1 C766T polymorphism and AD susceptibility (TT + CT versus CC: OR = 0.920, 95% CI = 0.817–1.037, P = 0.172). In subgroup analysis, significant decreased AD susceptibility was found among Asian population in allele model (T versus C: OR = 0.786, 95% CI = 0.635–0.974, P = 0.028) and dominant model (TT + CT versus CC: OR = 0.800, 95% CI = 0.647–0.990, P = 0.040). Moreover, T allele of LRP1 C766T was statistically associated with late onset of AD (LOAD) (T versus C: OR = 0.858, 95% CI = 0.748–0.985, P = 0.029; TT + CT versus CC: OR = 0.871, 95% CI = 0.763–0.994, P = 0.040). In conclusion, our meta-analysis suggested that LRP1 C766T polymorphism was associated with lower risk of AD in Asian, and could reduce LOAD risk especially. Considering some limitations of our meta-analysis, further large-scale studies should be done to reach a more comprehensive understanding. Nature Publishing Group UK 2017-08-16 /pmc/articles/PMC5559589/ /pubmed/28814781 http://dx.doi.org/10.1038/s41598-017-08335-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Yun
Liu, Shengyuan
Wang, Jingjing
Zhang, Jie
Hua, Yaqiong
Li, Hua
Tan, Huibiao
Kuai, Bin
Wang, Biao
Sheng, Sitong
Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
title Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
title_full Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
title_fullStr Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
title_full_unstemmed Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
title_short Association between LRP1 C766T polymorphism and Alzheimer’s disease susceptibility: a meta-analysis
title_sort association between lrp1 c766t polymorphism and alzheimer’s disease susceptibility: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559589/
https://www.ncbi.nlm.nih.gov/pubmed/28814781
http://dx.doi.org/10.1038/s41598-017-08335-w
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