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Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals

AIMS: In observational studies, type-2 diabetes is associated with increased risk of dementia; however, the causal nature of this association remains unanswered. In an unselected nationwide study of all Danes, we wanted to test whether type-2 diabetes is associated with dementia subtypes, and to tes...

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Autores principales: Thomassen, Jesper Qvist, Tolstrup, Janne Schurmann, Benn, Marianne, Frikke-Schmidt, Ruth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214711/
https://www.ncbi.nlm.nih.gov/pubmed/32326995
http://dx.doi.org/10.1017/S2045796020000347
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author Thomassen, Jesper Qvist
Tolstrup, Janne Schurmann
Benn, Marianne
Frikke-Schmidt, Ruth
author_facet Thomassen, Jesper Qvist
Tolstrup, Janne Schurmann
Benn, Marianne
Frikke-Schmidt, Ruth
author_sort Thomassen, Jesper Qvist
collection PubMed
description AIMS: In observational studies, type-2 diabetes is associated with increased risk of dementia; however, the causal nature of this association remains unanswered. In an unselected nationwide study of all Danes, we wanted to test whether type-2 diabetes is associated with dementia subtypes, and to test whether potential associations are of a causal nature. METHODS: In the current study of nationwide observational registry data in all Danes above the age of 65 years (n = 784 434) combined with genetic consortia data on 213 370 individuals, we investigated the associations between type-2 diabetes and Alzheimer's disease, vascular dementia, unspecified dementia and all-cause dementia, and whether observational associations were of a causal nature by applying a two-sample Mendelian randomisation strategy. We addressed key biases inherent in Mendelian randomisation approaches. RESULTS: Important confounders (age, ethnicity, size of community, region, civil status and education level) were captured on all 784 434 individuals and adjusted for in the models. Multifactorial adjusted hazard ratios were 1.13 (1.06–1.21) for Alzheimer's disease, 1.98 (1.83–2.14) for vascular dementia, 1.53 (1.48–1.59) for unspecified dementia and 1.48 (1.44–1.53) for all-cause dementia in persons with type-2 diabetes v. without. Results were similar for men and women. The two-sample Mendelian randomisation estimate for the association between the genetic instrument and Alzheimer's disease was 1.04 (0.98–1.10), consistent with sensitivity estimates, addressing pleiotropy, measurement bias and weak instrument bias. CONCLUSIONS: In a nationwide study of all Danes above the age of 65 years, we show that type-2 diabetes is associated with major subtypes of dementia – with particularly strong associations for vascular dementia and unspecified dementia – the two types of dementia with the most obvious vascular pathologies. Although the present two-sample Mendelian randomisation approach using genetic consortia data suggests that type-2 diabetes is not a direct cause of Alzheimer's disease, we were unable to test the causal nature of type-2 diabetes for vascular dementia and unspecified dementia, because no publicly available genetic consortia data yet exist for these dementia endpoints. The causal nature of type-2 diabetes for dementia with vascular pathologies is pivotal questions to solve for future public health recommendations and therapeutic advice.
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spelling pubmed-72147112020-05-18 Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals Thomassen, Jesper Qvist Tolstrup, Janne Schurmann Benn, Marianne Frikke-Schmidt, Ruth Epidemiol Psychiatr Sci Original Articles AIMS: In observational studies, type-2 diabetes is associated with increased risk of dementia; however, the causal nature of this association remains unanswered. In an unselected nationwide study of all Danes, we wanted to test whether type-2 diabetes is associated with dementia subtypes, and to test whether potential associations are of a causal nature. METHODS: In the current study of nationwide observational registry data in all Danes above the age of 65 years (n = 784 434) combined with genetic consortia data on 213 370 individuals, we investigated the associations between type-2 diabetes and Alzheimer's disease, vascular dementia, unspecified dementia and all-cause dementia, and whether observational associations were of a causal nature by applying a two-sample Mendelian randomisation strategy. We addressed key biases inherent in Mendelian randomisation approaches. RESULTS: Important confounders (age, ethnicity, size of community, region, civil status and education level) were captured on all 784 434 individuals and adjusted for in the models. Multifactorial adjusted hazard ratios were 1.13 (1.06–1.21) for Alzheimer's disease, 1.98 (1.83–2.14) for vascular dementia, 1.53 (1.48–1.59) for unspecified dementia and 1.48 (1.44–1.53) for all-cause dementia in persons with type-2 diabetes v. without. Results were similar for men and women. The two-sample Mendelian randomisation estimate for the association between the genetic instrument and Alzheimer's disease was 1.04 (0.98–1.10), consistent with sensitivity estimates, addressing pleiotropy, measurement bias and weak instrument bias. CONCLUSIONS: In a nationwide study of all Danes above the age of 65 years, we show that type-2 diabetes is associated with major subtypes of dementia – with particularly strong associations for vascular dementia and unspecified dementia – the two types of dementia with the most obvious vascular pathologies. Although the present two-sample Mendelian randomisation approach using genetic consortia data suggests that type-2 diabetes is not a direct cause of Alzheimer's disease, we were unable to test the causal nature of type-2 diabetes for vascular dementia and unspecified dementia, because no publicly available genetic consortia data yet exist for these dementia endpoints. The causal nature of type-2 diabetes for dementia with vascular pathologies is pivotal questions to solve for future public health recommendations and therapeutic advice. Cambridge University Press 2020-04-24 /pmc/articles/PMC7214711/ /pubmed/32326995 http://dx.doi.org/10.1017/S2045796020000347 Text en © The Author(s) 2020 http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Thomassen, Jesper Qvist
Tolstrup, Janne Schurmann
Benn, Marianne
Frikke-Schmidt, Ruth
Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals
title Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals
title_full Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals
title_fullStr Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals
title_full_unstemmed Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals
title_short Type-2 diabetes and risk of dementia: observational and Mendelian randomisation studies in 1 million individuals
title_sort type-2 diabetes and risk of dementia: observational and mendelian randomisation studies in 1 million individuals
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214711/
https://www.ncbi.nlm.nih.gov/pubmed/32326995
http://dx.doi.org/10.1017/S2045796020000347
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