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HbA1c and brain health across the entire glycaemic spectrum

AIM: To understand the relationship between HbA1c and brain health across the entire glycaemic spectrum. MATERIALS AND METHODS: We used data from the UK Biobank cohort consisting of 500,000 individuals aged 40–69 years. HbA1c and diabetes diagnosis were used to define baseline glycaemic categories....

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Autores principales: Garfield, Victoria, Farmaki, Aliki‐Eleni, Eastwood, Sophie V., Mathur, Rohini, Rentsch, Christopher T., Bhaskaran, Krishnan, Smeeth, Liam, Chaturvedi, Nish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261644/
https://www.ncbi.nlm.nih.gov/pubmed/33464682
http://dx.doi.org/10.1111/dom.14321
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author Garfield, Victoria
Farmaki, Aliki‐Eleni
Eastwood, Sophie V.
Mathur, Rohini
Rentsch, Christopher T.
Bhaskaran, Krishnan
Smeeth, Liam
Chaturvedi, Nish
author_facet Garfield, Victoria
Farmaki, Aliki‐Eleni
Eastwood, Sophie V.
Mathur, Rohini
Rentsch, Christopher T.
Bhaskaran, Krishnan
Smeeth, Liam
Chaturvedi, Nish
author_sort Garfield, Victoria
collection PubMed
description AIM: To understand the relationship between HbA1c and brain health across the entire glycaemic spectrum. MATERIALS AND METHODS: We used data from the UK Biobank cohort consisting of 500,000 individuals aged 40–69 years. HbA1c and diabetes diagnosis were used to define baseline glycaemic categories. Our outcomes included incident all‐cause dementia, vascular dementia (VD), Alzheimer's dementia (AD), hippocampal volume (HV), white matter hyperintensity (WMH) volume, cognitive function and decline. The reference group was normoglycaemic individuals (HbA1c ≥35 & <42 mmol/mol). Our maximum analytical sample contained 449,973 individuals with complete data. RESULTS: Prediabetes and known diabetes increased incident VD (HR 1.54; 95% CI = 1.04, 2.28 and HR 2.97; 95% CI = 2.26, 3.90, respectively). Known diabetes increased all‐cause and AD risk (HR 1.91; 95% CI = 1.66, 2.21 and HR 1.84; 95% CI = 1.44, 2.36, respectively). Prediabetes and known diabetes elevated the risks of cognitive decline (OR 1.42; 1.48, 2.96 and OR 1.39; 1.04, 1.75, respectively). Prediabetes, undiagnosed and known diabetes conferred higher WMH volumes (3%, 22% and 7%, respectively) and lower HV (36, 80 and 82 mm(3), respectively), whereas low‐normal HbA1c had 1% lower WMH volume and 12 mm(3) greater HV. CONCLUSION: Both prediabetes and known diabetes are harmful in terms of VD, cognitive decline and AD risks, as well as lower HV. Associations appeared to be somewhat driven by antihypertensive medication, which implies that certain cardiovascular drugs may ameliorate some of the excess risk. Low‐normal HbA1c levels, however, are associated with more favourable brain health outcomes and warrant more in‐depth investigation.
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spelling pubmed-82616442021-07-12 HbA1c and brain health across the entire glycaemic spectrum Garfield, Victoria Farmaki, Aliki‐Eleni Eastwood, Sophie V. Mathur, Rohini Rentsch, Christopher T. Bhaskaran, Krishnan Smeeth, Liam Chaturvedi, Nish Diabetes Obes Metab Original Articles AIM: To understand the relationship between HbA1c and brain health across the entire glycaemic spectrum. MATERIALS AND METHODS: We used data from the UK Biobank cohort consisting of 500,000 individuals aged 40–69 years. HbA1c and diabetes diagnosis were used to define baseline glycaemic categories. Our outcomes included incident all‐cause dementia, vascular dementia (VD), Alzheimer's dementia (AD), hippocampal volume (HV), white matter hyperintensity (WMH) volume, cognitive function and decline. The reference group was normoglycaemic individuals (HbA1c ≥35 & <42 mmol/mol). Our maximum analytical sample contained 449,973 individuals with complete data. RESULTS: Prediabetes and known diabetes increased incident VD (HR 1.54; 95% CI = 1.04, 2.28 and HR 2.97; 95% CI = 2.26, 3.90, respectively). Known diabetes increased all‐cause and AD risk (HR 1.91; 95% CI = 1.66, 2.21 and HR 1.84; 95% CI = 1.44, 2.36, respectively). Prediabetes and known diabetes elevated the risks of cognitive decline (OR 1.42; 1.48, 2.96 and OR 1.39; 1.04, 1.75, respectively). Prediabetes, undiagnosed and known diabetes conferred higher WMH volumes (3%, 22% and 7%, respectively) and lower HV (36, 80 and 82 mm(3), respectively), whereas low‐normal HbA1c had 1% lower WMH volume and 12 mm(3) greater HV. CONCLUSION: Both prediabetes and known diabetes are harmful in terms of VD, cognitive decline and AD risks, as well as lower HV. Associations appeared to be somewhat driven by antihypertensive medication, which implies that certain cardiovascular drugs may ameliorate some of the excess risk. Low‐normal HbA1c levels, however, are associated with more favourable brain health outcomes and warrant more in‐depth investigation. Blackwell Publishing Ltd 2021-02-14 2021-05 /pmc/articles/PMC8261644/ /pubmed/33464682 http://dx.doi.org/10.1111/dom.14321 Text en © 2021 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Garfield, Victoria
Farmaki, Aliki‐Eleni
Eastwood, Sophie V.
Mathur, Rohini
Rentsch, Christopher T.
Bhaskaran, Krishnan
Smeeth, Liam
Chaturvedi, Nish
HbA1c and brain health across the entire glycaemic spectrum
title HbA1c and brain health across the entire glycaemic spectrum
title_full HbA1c and brain health across the entire glycaemic spectrum
title_fullStr HbA1c and brain health across the entire glycaemic spectrum
title_full_unstemmed HbA1c and brain health across the entire glycaemic spectrum
title_short HbA1c and brain health across the entire glycaemic spectrum
title_sort hba1c and brain health across the entire glycaemic spectrum
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8261644/
https://www.ncbi.nlm.nih.gov/pubmed/33464682
http://dx.doi.org/10.1111/dom.14321
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