Cargando…

An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study

BACKGROUND: Diabetes is common in the older population and is increasing. Glycated hemoglobin (HbA(1c)) is an indicator of average blood glucose concentration over the past three months. The HbA(1c )test is currently one of clinical methods used to check diabetes control. Recent studies have suggest...

Descripción completa

Detalles Bibliográficos
Autores principales: Gao, Lu, Matthews, Fiona E, Sargeant, Lincoln A, Brayne, Carol, CFAS, MRC
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275259/
https://www.ncbi.nlm.nih.gov/pubmed/18267013
http://dx.doi.org/10.1186/1471-2458-8-54
_version_ 1782151844031627264
author Gao, Lu
Matthews, Fiona E
Sargeant, Lincoln A
Brayne, Carol
CFAS, MRC
author_facet Gao, Lu
Matthews, Fiona E
Sargeant, Lincoln A
Brayne, Carol
CFAS, MRC
author_sort Gao, Lu
collection PubMed
description BACKGROUND: Diabetes is common in the older population and is increasing. Glycated hemoglobin (HbA(1c)) is an indicator of average blood glucose concentration over the past three months. The HbA(1c )test is currently one of clinical methods used to check diabetes control. Recent studies have suggested diabetes is a risk factor for dementia, cognitive dysfunction and physical disability. In addition, there have reported the relationship between HbA(1c )and mortality on all cause, cardiovascular disease and cognitive function, but few studies have investigated the relationship concentrating on the older population. The aim of this study is to investigate the association between the level of HbA(1c )and mortality from all causes, incident cardiovascular disease, cognitive decline and physical disability in people aged 65 and over in England and Wales. METHODS: 1139 men and women aged 69 years and over who were participants in a ten year population based ageing multi-centre, longitudinal study who had HbA(1c )measurements after 5–6 years of follow up. All participants were flagged for death notification including causes at the Office of National Statistics. Information on health including vascular conditions, cognitive status, physical function and dementia were available from the study both before and after the HbA(1c )measurement. Survival analyses and logistic regression were conducted. RESULTS: Mortality from all causes, cardiovascular and ischaemic heart disease increased with increasing HbA(1c). Participants with diagnosed diabetes or who had HbA(1c)≥ 7% but no self-reported diabetes had increased mortality risk from all causes and cardiovascular diseases. The respondents in the group HbA(1c )≥7% who had not been diagnosed with diabetes had a significantly higher risk (odds ratio = 4.8 95% CI: 1.1 to 21.6) of developing dementia. Individuals who had self-reported diabetes but a HbA(1c )level <7% had mortality and dementia incidence comparable to individuals without diabetes and HbA(1c )<7%. CONCLUSION: The findings support previous reports that bio-markers of glucose metabolism are associated with long term outcomes, such as mortality and dementia.
format Text
id pubmed-2275259
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-22752592008-03-26 An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study Gao, Lu Matthews, Fiona E Sargeant, Lincoln A Brayne, Carol CFAS, MRC BMC Public Health Research Article BACKGROUND: Diabetes is common in the older population and is increasing. Glycated hemoglobin (HbA(1c)) is an indicator of average blood glucose concentration over the past three months. The HbA(1c )test is currently one of clinical methods used to check diabetes control. Recent studies have suggested diabetes is a risk factor for dementia, cognitive dysfunction and physical disability. In addition, there have reported the relationship between HbA(1c )and mortality on all cause, cardiovascular disease and cognitive function, but few studies have investigated the relationship concentrating on the older population. The aim of this study is to investigate the association between the level of HbA(1c )and mortality from all causes, incident cardiovascular disease, cognitive decline and physical disability in people aged 65 and over in England and Wales. METHODS: 1139 men and women aged 69 years and over who were participants in a ten year population based ageing multi-centre, longitudinal study who had HbA(1c )measurements after 5–6 years of follow up. All participants were flagged for death notification including causes at the Office of National Statistics. Information on health including vascular conditions, cognitive status, physical function and dementia were available from the study both before and after the HbA(1c )measurement. Survival analyses and logistic regression were conducted. RESULTS: Mortality from all causes, cardiovascular and ischaemic heart disease increased with increasing HbA(1c). Participants with diagnosed diabetes or who had HbA(1c)≥ 7% but no self-reported diabetes had increased mortality risk from all causes and cardiovascular diseases. The respondents in the group HbA(1c )≥7% who had not been diagnosed with diabetes had a significantly higher risk (odds ratio = 4.8 95% CI: 1.1 to 21.6) of developing dementia. Individuals who had self-reported diabetes but a HbA(1c )level <7% had mortality and dementia incidence comparable to individuals without diabetes and HbA(1c )<7%. CONCLUSION: The findings support previous reports that bio-markers of glucose metabolism are associated with long term outcomes, such as mortality and dementia. BioMed Central 2008-02-11 /pmc/articles/PMC2275259/ /pubmed/18267013 http://dx.doi.org/10.1186/1471-2458-8-54 Text en Copyright © 2008 Gao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gao, Lu
Matthews, Fiona E
Sargeant, Lincoln A
Brayne, Carol
CFAS, MRC
An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study
title An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study
title_full An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study
title_fullStr An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study
title_full_unstemmed An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study
title_short An investigation of the population impact of variation in HbA(1c )levels in older people in England and Wales: From a population based multi-centre longitudinal study
title_sort investigation of the population impact of variation in hba(1c )levels in older people in england and wales: from a population based multi-centre longitudinal study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275259/
https://www.ncbi.nlm.nih.gov/pubmed/18267013
http://dx.doi.org/10.1186/1471-2458-8-54
work_keys_str_mv AT gaolu aninvestigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT matthewsfionae aninvestigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT sargeantlincolna aninvestigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT braynecarol aninvestigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT cfasmrc aninvestigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT gaolu investigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT matthewsfionae investigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT sargeantlincolna investigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT braynecarol investigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy
AT cfasmrc investigationofthepopulationimpactofvariationinhba1clevelsinolderpeopleinenglandandwalesfromapopulationbasedmulticentrelongitudinalstudy