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INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis
Inositol polyphosphate-5-phosphatase (INPP5D) was reported to be associated with Alzheimer's disease (AD) through modulating the inflammatory process and immune response. A recent genome-wide association study discovered a new locus single nucleotide polymorphism (SNP, rs35349669) of INPP5D whi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342472/ https://www.ncbi.nlm.nih.gov/pubmed/27750211 http://dx.doi.org/10.18632/oncotarget.12648 |
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author | Jing, Hua Zhu, Jun-Xia Wang, Hui-Fu Zhang, Wei Zheng, Zhan-Jie Kong, Ling-Li Tan, Chen-Chen Wang, Zi-Xuan Tan, Lin Tan, Lan |
author_facet | Jing, Hua Zhu, Jun-Xia Wang, Hui-Fu Zhang, Wei Zheng, Zhan-Jie Kong, Ling-Li Tan, Chen-Chen Wang, Zi-Xuan Tan, Lin Tan, Lan |
author_sort | Jing, Hua |
collection | PubMed |
description | Inositol polyphosphate-5-phosphatase (INPP5D) was reported to be associated with Alzheimer's disease (AD) through modulating the inflammatory process and immune response. A recent genome-wide association study discovered a new locus single nucleotide polymorphism (SNP, rs35349669) of INPP5D which was significantly associated with susceptibility to late-onset Alzheimer's disease (LOAD) in Caucasians. In this study, we investigated the relations between the INPP5D polymorphism rs35349669 and LOAD in Han Chinese population comprising 984 LOAD cases and 1352 healthy controls being matched for age and gender. Our results showed no obvious differences in the genotypic or allelic distributions of rs35349669 polymorphism between LOAD cases and healthy controls (genotype: p = 0.167; allele: p = 0.094). Additionally, when these data were stratified by APOEε4 status, there are still no evident differences in the genotypic or allelic distributions in APOEε4 carriers (p > 0.05). Furthermore, meta-analysis of 81964 individuals confirmed that rs35349669 was significantly associated with the risk for LOAD (OR=1.08, 95%CI=1.06-1.11), but the results remained negative in Chinese subgroup (OR=0.77, 95%CI=0.53-1.13). Overall, the current evidence did not indicate that INPP5D rs35349669 polymorphism play a role in the genetic predisposition to LOAD in Chinese population. |
format | Online Article Text |
id | pubmed-5342472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53424722017-03-24 INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis Jing, Hua Zhu, Jun-Xia Wang, Hui-Fu Zhang, Wei Zheng, Zhan-Jie Kong, Ling-Li Tan, Chen-Chen Wang, Zi-Xuan Tan, Lin Tan, Lan Oncotarget Research Paper: Gerotarget (Focus on Aging) Inositol polyphosphate-5-phosphatase (INPP5D) was reported to be associated with Alzheimer's disease (AD) through modulating the inflammatory process and immune response. A recent genome-wide association study discovered a new locus single nucleotide polymorphism (SNP, rs35349669) of INPP5D which was significantly associated with susceptibility to late-onset Alzheimer's disease (LOAD) in Caucasians. In this study, we investigated the relations between the INPP5D polymorphism rs35349669 and LOAD in Han Chinese population comprising 984 LOAD cases and 1352 healthy controls being matched for age and gender. Our results showed no obvious differences in the genotypic or allelic distributions of rs35349669 polymorphism between LOAD cases and healthy controls (genotype: p = 0.167; allele: p = 0.094). Additionally, when these data were stratified by APOEε4 status, there are still no evident differences in the genotypic or allelic distributions in APOEε4 carriers (p > 0.05). Furthermore, meta-analysis of 81964 individuals confirmed that rs35349669 was significantly associated with the risk for LOAD (OR=1.08, 95%CI=1.06-1.11), but the results remained negative in Chinese subgroup (OR=0.77, 95%CI=0.53-1.13). Overall, the current evidence did not indicate that INPP5D rs35349669 polymorphism play a role in the genetic predisposition to LOAD in Chinese population. Impact Journals LLC 2016-10-13 /pmc/articles/PMC5342472/ /pubmed/27750211 http://dx.doi.org/10.18632/oncotarget.12648 Text en Copyright: © 2016 Jing et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Gerotarget (Focus on Aging) Jing, Hua Zhu, Jun-Xia Wang, Hui-Fu Zhang, Wei Zheng, Zhan-Jie Kong, Ling-Li Tan, Chen-Chen Wang, Zi-Xuan Tan, Lin Tan, Lan INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis |
title | INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis |
title_full | INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis |
title_fullStr | INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis |
title_full_unstemmed | INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis |
title_short | INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis |
title_sort | inpp5d rs35349669 polymorphism with late-onset alzheimer's disease: a replication study and meta-analysis |
topic | Research Paper: Gerotarget (Focus on Aging) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342472/ https://www.ncbi.nlm.nih.gov/pubmed/27750211 http://dx.doi.org/10.18632/oncotarget.12648 |
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