Impact of ischaemic heart disease severity and age on risk of cardiovascular outcome in diabetes patients in Sweden: a nationwide observational study.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
03 04 2019
Historique:
entrez: 6 4 2019
pubmed: 6 4 2019
medline: 10 5 2020
Statut: epublish

Résumé

To compare short-term cardiovascular (CV) outcome in type 2 diabetes (T2D) patients without ischaemic heart disease (IHD), with IHD but no prior myocardial infarction (MI), and those with prior MI; and assess the impact on risk of age when initiating first-time glucose-lowering drug (GLD). Cohort study linking morbidity, mortality and medication data from Swedish national registries. First-time users of GLD during 2007-2016. Predicted cumulative incidence for the CV outcome (MI, stroke and CV mortality) was estimated. A Cox model was developed where age at GLD start and CV risk was modelled. 260 070 first-time GLD users were included, 221 226 (85%) had no IHD, 16 294 (6%) had stable IHD-prior MI and 22 550 (9%) had IHD+MI. T2D patients without IHD had a lower risk of CV outcome compared with the IHD populations (±prior MI), (3-year incidence 4.78% vs 5.85% and 8.04%). The difference in CV outcome was primarily driven by a relative greater MI risk among the IHD patients. For T2D patients without IHD, an almost linear association between age at start of GLD and relative risk was observed, whereas in IHD patients, the younger (<60 years) patients had a relative greater risk compared with older patients. T2D patients without IHD had a lower risk of the CV outcome compared with the T2D populations with IHD, primarily driven by a greater risk of MI. For T2D patients without IHD, an almost linear association between age at start of GLD and relative risk was observed, whereas in IHD patients, the younger patients had a relative greater risk compared with older patients. Our findings suggest that intense risk prevention should be the key strategy in the management of T2D patients, especially for younger patients.

Identifiants

pubmed: 30948612
pii: bmjopen-2018-027199
doi: 10.1136/bmjopen-2018-027199
pmc: PMC6500345
doi:

Substances chimiques

Hypoglycemic Agents 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e027199

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: LPH, DL, JB and KSA are employed by AstraZeneca. MT is employed at Statisticon for which AstraZeneca is a client. TJ, BS, DE and MJ report no conflict of interest relevant to this article. At the time this research was performed, DL was employed by Uppsala University, but has since been employed by AstraZeneca.

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Auteurs

Tomas Jernberg (T)

Department of Clinical Sciences, Danderyd University Hospital, Karolinska Institute, Stockholm, Sweden.

Daniel Lindholm (D)

UCR-Uppsala Clinical Research center, Uppsala Clinical Research center, Uppsala, Sweden.

Lars Pål Hasvold (LP)

Medical Department, AstraZeneca Nordic, Oslo, Norway.

Bodil Svennblad (B)

UCR-Uppsala Clinical Research center, Uppsala Clinical Research center, Uppsala, Sweden.

Johan Bodegård (J)

Medical Department, AstraZeneca Nordic, Oslo, Norway.

Karolina Sundell Andersson (K)

Global Medical Affairs CardioVascular, Renal and Metabolic, AstraZeneca R&D, Gothenburg, Sweden.

Marcus Thuresson (M)

Statisticon, Stockholm, Sweden.

David Erlinge (D)

Clinical Science, Lunds Universitet, Lund, Sweden.

Magnus Janzon (M)

Cardiology, Linkopings Universitet, Linkoping, Sweden.

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Classifications MeSH