Cargando…

Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?

OBJECTIVE: To identify predictors of low hemoglobin A(1c) (HbA(1c)) (<5.0%) and to investigate the association of low HbA(1c) with cause-specific mortality and risk of liver disease hospitalization. RESEARCH DESIGN AND METHODS: Prospective cohort study of 13,288 participants in the Atherosclerosi...

Descripción completa

Detalles Bibliográficos
Autores principales: Aggarwal, Vikas, Schneider, Andrea L.C., Selvin, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447844/
https://www.ncbi.nlm.nih.gov/pubmed/22855733
http://dx.doi.org/10.2337/dc11-2531
_version_ 1782244175853387776
author Aggarwal, Vikas
Schneider, Andrea L.C.
Selvin, Elizabeth
author_facet Aggarwal, Vikas
Schneider, Andrea L.C.
Selvin, Elizabeth
author_sort Aggarwal, Vikas
collection PubMed
description OBJECTIVE: To identify predictors of low hemoglobin A(1c) (HbA(1c)) (<5.0%) and to investigate the association of low HbA(1c) with cause-specific mortality and risk of liver disease hospitalization. RESEARCH DESIGN AND METHODS: Prospective cohort study of 13,288 participants in the Atherosclerosis Risk in Communities Study. Logistic regression was used to identify cross-sectional correlates of low HbA(1c), and Cox proportional hazards models were used to estimate the association of low HbA(1c) with cause-specific mortality. RESULTS: Compared with participants with HbA(1c) in the normal range (5.0 to <5.7%), participants with low HbA(1c) were younger, less likely to smoke, had lower BMI, lower white cell count and fibrinogen levels, and lower prevalence of hypercholesterolemia and history of coronary heart disease. However, this group was more likely to have anemia and had a higher mean corpuscular volume. In adjusted Cox models with HbA(1c) of 5.0 to <5.7% as the reference group, HbA(1c) <5.0% was associated with a significantly increased risk of all-cause mortality (hazard ratio [HR]: 1.32, 95% CI: 1.13–1.55) and of cancer death (1.47, 95% CI: 1.16–1.84). We also noted nonsignificant trends toward increased risk of death from cardiovascular causes (1.27, 95% CI: 0.93–1.75) and respiratory causes (1.42, 95% CI: 0.78–2.56). There was a J-shaped association between HbA(1c) and risk of liver disease hospitalization. CONCLUSIONS: No single cause of death appeared to drive the association between low HbA(1c) and total mortality. These results add to evidence that low HbA(1c) values may be a generalized marker of mortality risk in the general population.
format Online
Article
Text
id pubmed-3447844
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher American Diabetes Association
record_format MEDLINE/PubMed
spelling pubmed-34478442013-10-01 Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state? Aggarwal, Vikas Schneider, Andrea L.C. Selvin, Elizabeth Diabetes Care Original Research OBJECTIVE: To identify predictors of low hemoglobin A(1c) (HbA(1c)) (<5.0%) and to investigate the association of low HbA(1c) with cause-specific mortality and risk of liver disease hospitalization. RESEARCH DESIGN AND METHODS: Prospective cohort study of 13,288 participants in the Atherosclerosis Risk in Communities Study. Logistic regression was used to identify cross-sectional correlates of low HbA(1c), and Cox proportional hazards models were used to estimate the association of low HbA(1c) with cause-specific mortality. RESULTS: Compared with participants with HbA(1c) in the normal range (5.0 to <5.7%), participants with low HbA(1c) were younger, less likely to smoke, had lower BMI, lower white cell count and fibrinogen levels, and lower prevalence of hypercholesterolemia and history of coronary heart disease. However, this group was more likely to have anemia and had a higher mean corpuscular volume. In adjusted Cox models with HbA(1c) of 5.0 to <5.7% as the reference group, HbA(1c) <5.0% was associated with a significantly increased risk of all-cause mortality (hazard ratio [HR]: 1.32, 95% CI: 1.13–1.55) and of cancer death (1.47, 95% CI: 1.16–1.84). We also noted nonsignificant trends toward increased risk of death from cardiovascular causes (1.27, 95% CI: 0.93–1.75) and respiratory causes (1.42, 95% CI: 0.78–2.56). There was a J-shaped association between HbA(1c) and risk of liver disease hospitalization. CONCLUSIONS: No single cause of death appeared to drive the association between low HbA(1c) and total mortality. These results add to evidence that low HbA(1c) values may be a generalized marker of mortality risk in the general population. American Diabetes Association 2012-10 2012-09-11 /pmc/articles/PMC3447844/ /pubmed/22855733 http://dx.doi.org/10.2337/dc11-2531 Text en © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Aggarwal, Vikas
Schneider, Andrea L.C.
Selvin, Elizabeth
Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?
title Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?
title_full Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?
title_fullStr Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?
title_full_unstemmed Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?
title_short Low Hemoglobin A(1c) in Nondiabetic Adults: An elevated risk state?
title_sort low hemoglobin a(1c) in nondiabetic adults: an elevated risk state?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447844/
https://www.ncbi.nlm.nih.gov/pubmed/22855733
http://dx.doi.org/10.2337/dc11-2531
work_keys_str_mv AT aggarwalvikas lowhemoglobina1cinnondiabeticadultsanelevatedriskstate
AT schneiderandrealc lowhemoglobina1cinnondiabeticadultsanelevatedriskstate
AT selvinelizabeth lowhemoglobina1cinnondiabeticadultsanelevatedriskstate