Diabetes Mellitus-Related All-Cause and Cardiovascular Mortality in a National Cohort of Adults.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
19 02 2019
Historique:
entrez: 20 2 2019
pubmed: 20 2 2019
medline: 7 3 2020
Statut: ppublish

Résumé

Background Diabetes mellitus is a risk factor for cardiovascular disease ( CVD ) and has been associated with 2- to 4-fold higher mortality. Diabetes mellitus-related mortality has not been reassessed in individuals receiving routine care in the United States in the contemporary era of CVD risk reduction. Methods and Results We retrospectively studied 963 648 adults receiving care in the US Veterans Affairs Healthcare System from 2002 to 2014; mean follow-up was 8 years. We estimated associations of diabetes mellitus status and hemoglobin A1c (HbA1c) with all-cause and CVD mortality using covariate-adjusted incidence rates and multivariable Cox proportional hazards regression. Of participants, 34% had diabetes mellitus. Compared with nondiabetic individuals, patients with diabetes mellitus had 7.0 (95% CI , 6.7-7.4) and 3.5 (95% CI, 3.3-3.7) deaths/1000-person-years higher all-cause and CVD mortality, respectively. The age-, sex-, race-, and ethnicity-adjusted hazard ratio for diabetes mellitus-related mortality was 1.29 (95% CI, 1.28-1.31), and declined with adjustment for CVD risk factors (hazard ratio, 1.18 [95% CI, 1.16-1.19]) and glycemia (hazard ratio, 1.03 [95% CI, 1.02-1.05]). Among individuals with diabetes mellitus, CVD mortality increased as HbA1c exceeded 7% (hazard ratios, 1.11 [95% CI, 1.08-1.14], 1.25 [95% CI, 1.22-1.29], and 1.52 [95% CI, 1.48-1.56] for HbA1c 7%-7.9%, 8%-8.9%, and ≥9%, respectively, relative to HbA1c 6%-6.9%). HbA1c 6% to 6.9% was associated with the lowest mortality risk irrespective of CVD history or age. Conclusions Diabetes mellitus remains significantly associated with all-cause and CVD mortality, although diabetes mellitus-related excess mortality is lower in the contemporary era than previously. We observed a gradient of mortality risk with increasing HbA1c >6% to 6.9%, suggesting HbA1c remains an informative predictor of outcomes even if causality cannot be inferred.

Identifiants

pubmed: 30776949
doi: 10.1161/JAHA.118.011295
pmc: PMC6405678
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e011295

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK111024
Pays : United States
Organisme : NIDDK NIH HHS
ID : R21 DK099716
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK098246
Pays : United States
Organisme : CSRD VA
ID : I01 CX001025
Pays : United States
Organisme : FDA HHS
ID : R01 FD003527
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Sridharan Raghavan (S)

1 Department of Veterans Affairs Eastern Colorado Healthcare System Aurora CO.
2 Division of Hospital Medicine University of Colorado School of Medicine Aurora CO.
3 Colorado Cardiovascular Outcomes Research Consortium Aurora CO.

Jason L Vassy (JL)

4 Department of Veterans Affairs Boston Healthcare System Boston MA.
5 Department of Medicine Harvard Medical School Boston MA.

Yuk-Lam Ho (YL)

4 Department of Veterans Affairs Boston Healthcare System Boston MA.

Rebecca J Song (RJ)

4 Department of Veterans Affairs Boston Healthcare System Boston MA.

David R Gagnon (DR)

4 Department of Veterans Affairs Boston Healthcare System Boston MA.
6 Department of Biostatistics Boston University School of Public Health Boston MA.

Kelly Cho (K)

4 Department of Veterans Affairs Boston Healthcare System Boston MA.
5 Department of Medicine Harvard Medical School Boston MA.

Peter W F Wilson (PWF)

7 Department of Veterans Affairs Atlanta Medical Center Atlanta GA.
8 Division of Cardiology Emory University School of Medicine Atlanta GA.

Lawrence S Phillips (LS)

7 Department of Veterans Affairs Atlanta Medical Center Atlanta GA.
9 Division of Endocrinology Emory University School of Medicine Atlanta GA.

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Classifications MeSH