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Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease

BACKGROUND: Studies have shown that low haemoglobin and anaemia are associated with poor cognition, and anaemia is known to be associated with Alzheimer’s disease (AD), but the mechanism of this risk is unknown. Here, we first seek to confirm the association between cognition and anaemia and secondl...

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Autores principales: Winchester, Laura M., Powell, John, Lovestone, Simon, Nevado-Holgado, Alejo J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022699/
https://www.ncbi.nlm.nih.gov/pubmed/29954452
http://dx.doi.org/10.1186/s13073-018-0556-z
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author Winchester, Laura M.
Powell, John
Lovestone, Simon
Nevado-Holgado, Alejo J.
author_facet Winchester, Laura M.
Powell, John
Lovestone, Simon
Nevado-Holgado, Alejo J.
author_sort Winchester, Laura M.
collection PubMed
description BACKGROUND: Studies have shown that low haemoglobin and anaemia are associated with poor cognition, and anaemia is known to be associated with Alzheimer’s disease (AD), but the mechanism of this risk is unknown. Here, we first seek to confirm the association between cognition and anaemia and secondly, in order to further understand the mechanism of this association, to estimate the direction of causation using Mendelian randomisation. METHODS: Two independent cohorts were used in this analysis: AddNeuroMed, a longitudinal study of 738 subjects including AD and age-matched controls with blood cell measures, cognitive assessments and gene expression data from blood; and UK Biobank, a study of 502,649 healthy participants, aged 40–69 years with cognitive test measures and blood cell indices at baseline. General linear models were calculated using cognitive function as the outcome with correction for age, sex and education. In UK Biobank, SNPs with known blood cell measure associations were analysed with Mendelian randomisation to estimate direction of causality. In AddNeuroMed, gene expression data was used in pathway enrichment analysis to identify associations reflecting biological function. RESULTS: Both sample sets evidence a reproducible association between cognitive performance and mean corpuscular haemoglobin (MCH), a measure of average mass of haemoglobin per red blood cell. Furthermore, in the AddNeuroMed cohort, where longitudinal samples were available, we showed a greater decline in red blood cell indices for AD patients when compared to controls (p values between 0.05 and 10(−6)). In the UK Biobank cohort, we found lower haemoglobin in participants with reduced cognitive function. There was a significant association for MCH and red blood cell distribution width (RDW, a measure of cell volume variability) compared to four cognitive function tests including reaction time and reasoning (p < 0.0001). Using Mendelian randomisation, we then showed a significant effect of MCH on the verbal–numeric and numeric traits, implying that anaemia has causative effect on cognitive performance. CONCLUSIONS: Lower haemoglobin levels in blood are associated to poor cognitive function and AD. We have used UK Biobank SNP data to determine the relationship between cognitive testing and haemoglobin measures and suggest that haemoglobin level and therefore anaemia does have a primary causal impact on cognitive performance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13073-018-0556-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-60226992018-07-09 Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease Winchester, Laura M. Powell, John Lovestone, Simon Nevado-Holgado, Alejo J. Genome Med Research BACKGROUND: Studies have shown that low haemoglobin and anaemia are associated with poor cognition, and anaemia is known to be associated with Alzheimer’s disease (AD), but the mechanism of this risk is unknown. Here, we first seek to confirm the association between cognition and anaemia and secondly, in order to further understand the mechanism of this association, to estimate the direction of causation using Mendelian randomisation. METHODS: Two independent cohorts were used in this analysis: AddNeuroMed, a longitudinal study of 738 subjects including AD and age-matched controls with blood cell measures, cognitive assessments and gene expression data from blood; and UK Biobank, a study of 502,649 healthy participants, aged 40–69 years with cognitive test measures and blood cell indices at baseline. General linear models were calculated using cognitive function as the outcome with correction for age, sex and education. In UK Biobank, SNPs with known blood cell measure associations were analysed with Mendelian randomisation to estimate direction of causality. In AddNeuroMed, gene expression data was used in pathway enrichment analysis to identify associations reflecting biological function. RESULTS: Both sample sets evidence a reproducible association between cognitive performance and mean corpuscular haemoglobin (MCH), a measure of average mass of haemoglobin per red blood cell. Furthermore, in the AddNeuroMed cohort, where longitudinal samples were available, we showed a greater decline in red blood cell indices for AD patients when compared to controls (p values between 0.05 and 10(−6)). In the UK Biobank cohort, we found lower haemoglobin in participants with reduced cognitive function. There was a significant association for MCH and red blood cell distribution width (RDW, a measure of cell volume variability) compared to four cognitive function tests including reaction time and reasoning (p < 0.0001). Using Mendelian randomisation, we then showed a significant effect of MCH on the verbal–numeric and numeric traits, implying that anaemia has causative effect on cognitive performance. CONCLUSIONS: Lower haemoglobin levels in blood are associated to poor cognitive function and AD. We have used UK Biobank SNP data to determine the relationship between cognitive testing and haemoglobin measures and suggest that haemoglobin level and therefore anaemia does have a primary causal impact on cognitive performance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13073-018-0556-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-28 /pmc/articles/PMC6022699/ /pubmed/29954452 http://dx.doi.org/10.1186/s13073-018-0556-z Text en © The Author(s). 2018 Open AccessThis 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
Winchester, Laura M.
Powell, John
Lovestone, Simon
Nevado-Holgado, Alejo J.
Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease
title Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease
title_full Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease
title_fullStr Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease
title_full_unstemmed Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease
title_short Red blood cell indices and anaemia as causative factors for cognitive function deficits and for Alzheimer’s disease
title_sort red blood cell indices and anaemia as causative factors for cognitive function deficits and for alzheimer’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022699/
https://www.ncbi.nlm.nih.gov/pubmed/29954452
http://dx.doi.org/10.1186/s13073-018-0556-z
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