dc.contributor.author | Kuźma, E | |
dc.contributor.author | Hannon, E | |
dc.contributor.author | Zhou, A | |
dc.contributor.author | Lourida, I | |
dc.contributor.author | Bethel, A | |
dc.contributor.author | Levine, DA | |
dc.contributor.author | Lunnon, K | |
dc.contributor.author | Thompson-Coon, J | |
dc.contributor.author | Hyppönen, E | |
dc.contributor.author | Llewellyn, DJ | |
dc.date.accessioned | 2018-10-04T12:09:36Z | |
dc.date.issued | 2018-06-08 | |
dc.description.abstract | BACKGROUND: Numerous risk factors for dementia are well established, though the causal nature of these associations remains unclear. OBJECTIVE: To systematically review Mendelian randomization (MR) studies investigating causal relationships between risk factors and global cognitive function or dementia. METHODS: We searched five databases from inception to February 2017 and conducted citation searches including MR studies investigating the association between any risk factor and global cognitive function, all-cause dementia or dementia subtypes. Two reviewers independently assessed titles and abstracts, full-texts, and study quality. RESULTS: We included 18 MR studies investigating education, lifestyle factors, cardiovascular factors and related biomarkers, diabetes related and other endocrine factors, and telomere length. Studies were of predominantly good quality, however eight received low ratings for sample size and statistical power. The most convincing causal evidence was found for an association of shorter telomeres with increased risk of Alzheimer's disease (AD). Causal evidence was weaker for smoking quantity, vitamin D, homocysteine, systolic blood pressure, fasting glucose, insulin sensitivity, and high-density lipoprotein cholesterol. Well-replicated associations were not present for most exposures and we cannot fully discount survival and diagnostic bias, or the potential for pleiotropic effects. CONCLUSIONS: Genetic evidence supported a causal association between telomere length and AD, whereas limited evidence for other risk factors was largely inconclusive with tentative evidence for smoking quantity, vitamin D, homocysteine, and selected metabolic markers. The lack of stronger evidence for other risk factors may reflect insufficient statistical power. Larger well-designed MR studies would therefore help establish the causal status of these dementia risk factors. | en_GB |
dc.description.sponsorship | This work was supported by the Mary Kinross Charitable Trust (DJL and EK), Halpin Trust (DJL, EK and IL), the James Tudor Foundation (DJL and EK), National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care (CLAHRC) for the South West Peninsula (IL, JTC, AB and DJL) and the National Institute on Aging of the National Institutes of Health under Award Number RF1AG055654 (DJL). | en_GB |
dc.identifier.citation | Vol. 64 (1), pp. 181 - 193 | en_GB |
dc.identifier.doi | 10.3233/JAD-180013 | |
dc.identifier.uri | http://hdl.handle.net/10871/34193 | |
dc.language.iso | en | en_GB |
dc.publisher | IOS Press | en_GB |
dc.relation.url | https://www.ncbi.nlm.nih.gov/pubmed/29865062 | en_GB |
dc.rights | © 2018 – IOS Press and the authors. All rights reserved. This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC 4.0) | en_GB |
dc.subject | Alzheimer’s disease | en_GB |
dc.subject | Mendelian randomization | en_GB |
dc.subject | cognition | en_GB |
dc.subject | dementia | en_GB |
dc.subject | instrumental variable | en_GB |
dc.subject | risk factor | en_GB |
dc.title | Which Risk Factors Causally Influence Dementia? A Systematic Review of Mendelian Randomization Studies | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2018-10-04T12:09:36Z | |
exeter.place-of-publication | Netherlands | en_GB |
dc.description | This is the final version. Available from IOS Press via the DOI in this record. | en_GB |
dc.identifier.journal | Journal of Alzheimer's Disease | en_GB |