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Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease
Cognitive decline in early-stage Alzheimer’s disease (AD) may depend on genetic variability. In the Swedish BioFINDER study, we used polygenic scores (PGS) (for AD, intelligence, and educational attainment) to predict longitudinal cognitive change (measured by mini-mental state examination (MMSE) [p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494841/ https://www.ncbi.nlm.nih.gov/pubmed/34615922 http://dx.doi.org/10.1038/s41598-021-99310-z |
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author | Kumar, Atul Shoai, Maryam Palmqvist, Sebastian Stomrud, Erik Hardy, John Mattsson-Carlgren, Niklas Hansson, Oskar |
author_facet | Kumar, Atul Shoai, Maryam Palmqvist, Sebastian Stomrud, Erik Hardy, John Mattsson-Carlgren, Niklas Hansson, Oskar |
author_sort | Kumar, Atul |
collection | PubMed |
description | Cognitive decline in early-stage Alzheimer’s disease (AD) may depend on genetic variability. In the Swedish BioFINDER study, we used polygenic scores (PGS) (for AD, intelligence, and educational attainment) to predict longitudinal cognitive change (measured by mini-mental state examination (MMSE) [primary outcome] and other cognitive tests) over a mean of 4.2 years. We included 260 β-amyloid (Aβ) negative cognitively unimpaired (CU) individuals, 121 Aβ-positive CU (preclinical AD), 50 Aβ-negative mild cognitive impairment (MCI) patients, and 127 Aβ-positive MCI patients (prodromal AD). Statistical significance was determined at Bonferroni corrected p value < 0.05. The PGS for intelligence (beta = 0.1, p = 2.9e−02) was protective against decline in MMSE in CU and MCI participants regardless of Aβ status. The polygenic risk score for AD (beta = − 0.12, p = 9.4e−03) was correlated with the rate of change in MMSE and was partially mediated by Aβ-pathology (mediation effect 20%). There was no effect of education PGS on cognitive measures. Genetic variants associated with intelligence mitigate cognitive decline independent of Aβ-pathology, while effects of genetic variants associated with AD are partly mediated by Aβ-pathology. |
format | Online Article Text |
id | pubmed-8494841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84948412021-10-08 Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease Kumar, Atul Shoai, Maryam Palmqvist, Sebastian Stomrud, Erik Hardy, John Mattsson-Carlgren, Niklas Hansson, Oskar Sci Rep Article Cognitive decline in early-stage Alzheimer’s disease (AD) may depend on genetic variability. In the Swedish BioFINDER study, we used polygenic scores (PGS) (for AD, intelligence, and educational attainment) to predict longitudinal cognitive change (measured by mini-mental state examination (MMSE) [primary outcome] and other cognitive tests) over a mean of 4.2 years. We included 260 β-amyloid (Aβ) negative cognitively unimpaired (CU) individuals, 121 Aβ-positive CU (preclinical AD), 50 Aβ-negative mild cognitive impairment (MCI) patients, and 127 Aβ-positive MCI patients (prodromal AD). Statistical significance was determined at Bonferroni corrected p value < 0.05. The PGS for intelligence (beta = 0.1, p = 2.9e−02) was protective against decline in MMSE in CU and MCI participants regardless of Aβ status. The polygenic risk score for AD (beta = − 0.12, p = 9.4e−03) was correlated with the rate of change in MMSE and was partially mediated by Aβ-pathology (mediation effect 20%). There was no effect of education PGS on cognitive measures. Genetic variants associated with intelligence mitigate cognitive decline independent of Aβ-pathology, while effects of genetic variants associated with AD are partly mediated by Aβ-pathology. Nature Publishing Group UK 2021-10-06 /pmc/articles/PMC8494841/ /pubmed/34615922 http://dx.doi.org/10.1038/s41598-021-99310-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kumar, Atul Shoai, Maryam Palmqvist, Sebastian Stomrud, Erik Hardy, John Mattsson-Carlgren, Niklas Hansson, Oskar Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease |
title | Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease |
title_full | Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease |
title_fullStr | Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease |
title_full_unstemmed | Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease |
title_short | Genetic effects on longitudinal cognitive decline during the early stages of Alzheimer’s disease |
title_sort | genetic effects on longitudinal cognitive decline during the early stages of alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494841/ https://www.ncbi.nlm.nih.gov/pubmed/34615922 http://dx.doi.org/10.1038/s41598-021-99310-z |
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