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Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study
BACKGROUND: Alzheimer’s disease (AD) and Parkinson’s disease (PD) are the top two common neurodegenerative diseases in elderly. Recent studies found the α-synuclein have a key role in AD. Although many clinical and pathological features between AD and PD are shared, the genetic association between t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311900/ https://www.ncbi.nlm.nih.gov/pubmed/30598082 http://dx.doi.org/10.1186/s12881-018-0721-7 |
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author | Han, Zhifa Tian, Rui Ren, Peng Zhou, Wenyang Wang, Pingping Luo, Meng Jin, Shuilin Jiang, Qinghua |
author_facet | Han, Zhifa Tian, Rui Ren, Peng Zhou, Wenyang Wang, Pingping Luo, Meng Jin, Shuilin Jiang, Qinghua |
author_sort | Han, Zhifa |
collection | PubMed |
description | BACKGROUND: Alzheimer’s disease (AD) and Parkinson’s disease (PD) are the top two common neurodegenerative diseases in elderly. Recent studies found the α-synuclein have a key role in AD. Although many clinical and pathological features between AD and PD are shared, the genetic association between them remains unclear, especially whether α-synuclein in PD genetically alters AD risk. RESULTS: We did not obtain any significant result (OR = 0.918, 95% CI: 0.782–1.076, P = 0.291) in MR analysis between PD and AD risk. In MR between α-synuclein in PD with AD risk, we only extracted rs356182 as the IV through a strict screening process. The result indicated a significant association based on IVW method (OR = 0.638, 95% CI: 0.485–0.838, P = 1.20E-03). In order to examine the robustness of the IVW method, we used other three complementary analytical methods and also obtained consistent results. CONCLUSION: The overall PD genetic risk factors did not predict AD risk, but the α-synuclein susceptibility genetic variants in PD reduce the AD risk. We believe that our findings may help to understand the association between them, which may be useful for future genetic studies for both diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0721-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6311900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63119002019-01-07 Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study Han, Zhifa Tian, Rui Ren, Peng Zhou, Wenyang Wang, Pingping Luo, Meng Jin, Shuilin Jiang, Qinghua BMC Med Genet Research BACKGROUND: Alzheimer’s disease (AD) and Parkinson’s disease (PD) are the top two common neurodegenerative diseases in elderly. Recent studies found the α-synuclein have a key role in AD. Although many clinical and pathological features between AD and PD are shared, the genetic association between them remains unclear, especially whether α-synuclein in PD genetically alters AD risk. RESULTS: We did not obtain any significant result (OR = 0.918, 95% CI: 0.782–1.076, P = 0.291) in MR analysis between PD and AD risk. In MR between α-synuclein in PD with AD risk, we only extracted rs356182 as the IV through a strict screening process. The result indicated a significant association based on IVW method (OR = 0.638, 95% CI: 0.485–0.838, P = 1.20E-03). In order to examine the robustness of the IVW method, we used other three complementary analytical methods and also obtained consistent results. CONCLUSION: The overall PD genetic risk factors did not predict AD risk, but the α-synuclein susceptibility genetic variants in PD reduce the AD risk. We believe that our findings may help to understand the association between them, which may be useful for future genetic studies for both diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0721-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-31 /pmc/articles/PMC6311900/ /pubmed/30598082 http://dx.doi.org/10.1186/s12881-018-0721-7 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Han, Zhifa Tian, Rui Ren, Peng Zhou, Wenyang Wang, Pingping Luo, Meng Jin, Shuilin Jiang, Qinghua Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study |
title | Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study |
title_full | Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study |
title_fullStr | Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study |
title_full_unstemmed | Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study |
title_short | Parkinson’s disease and Alzheimer’s disease: a Mendelian randomization study |
title_sort | parkinson’s disease and alzheimer’s disease: a mendelian randomization study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311900/ https://www.ncbi.nlm.nih.gov/pubmed/30598082 http://dx.doi.org/10.1186/s12881-018-0721-7 |
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