Risk of first-time major cardiovascular event among individuals with newly diagnosed type 2 diabetes: data from Danish registers

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

  • Fulltext

    Forlagets udgivne version, 1,54 MB, PDF-dokument

Aims/hypothesis: We aimed to examine whether individuals with initial omission of glucose-lowering drug treatment (GLDT), including those achieving initial remission of type 2 diabetes, may experience a higher risk of major adverse cardiovascular events (MACE) compared with well-controlled individuals on GLDT after a new type 2 diabetes diagnosis in real-world clinical practice. Furthermore, we examined whether a higher risk could be related to lower initiation of statins and renin–angiotensin system inhibitors (RASi). Methods: In this cohort study, we used Danish registers to identify individuals with a first measured HbA1c between 48 and 57 mmol/mol (6.5–7.4%) from 2014 to 2020. Six months later, we divided participants into four groups according to GLDT and achieved HbA1c (<48 vs ≥48 mmol/mol [6.5%]): well-controlled and poorly controlled on GLDT; remission and persistent type 2 diabetes not on GLDT. We reported how much the standardised 5 year risk of MACE could be reduced for each group if initiation of statins and RASi was the same as in the well-controlled group on GLDT. Results: We included 14,221 individuals. Compared with well-controlled participants on GLDT, the 5 year standardised risk of MACE was higher in the three other exposure groups: by 3.3% (95% CI 1.6, 5.1) in the persistent type 2 diabetes group not on GLDT; 2.0% (95% CI 0.4, 3.7) in the remission group not on GLDT; and 3.5% (95% CI 1.3, 5.7) in the poorly controlled group on GLDT. Fewer individuals not on GLDT initiated statins and RASi compared with individuals on GLDT. If initiation of statins and RASi had been the same as in the well-controlled group on GLDT, participants not on GLDT could have reduced their risk of MACE by 2.1% (95% CI 1.2, 2.9) in the persistent type 2 diabetes group and by 1.1% (95% CI 0.4, 1.9) in the remission group. Conclusions/interpretation: Compared with well-controlled individuals on GLDT, individuals not on initial GLDT had a higher 5 year risk of MACE, even among those achieving remission of type 2 diabetes. This may be related to lower use of statins and RASi. Graphical Abstract: [Figure not available: see fulltext.].

OriginalsprogEngelsk
TidsskriftDiabetologia
Vol/bind66
Sider (fra-til)2017–2029
Antal sider13
ISSN0012-186X
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
FKK has served on scientific advisory panels and/or been part of speaker’s bureaus for, or served as a consultant to and/or received research support from 89bio, AstraZeneca, Bayer, Boehringer Ingelheim, Dawn Health, Eli Lilly, Gubra, Novo Nordisk, Pharmacosmos, Sanofi, Structure Therapeutics, Zealand Pharma and Zucara not related to the current study; and is a minority shareholder in Antag Therapeutics ApS and co-owner of Medicinsk Vægttab ApS. LK reports speaker’s fees from AstraZeneca, Bayer, Boehringer Ingelheim, Novartis and Novo Nordisk not related to the current study. CT-P has received grants for studies from Bayer and Novo Nordisk not related to the current study. MS reports speaker’s fees from Novo Nordisk, AstraZeneca, Novartis and Boehringer Ingelheim unrelated to the current work. NEB has received investigator-initiated grants from the Novo Nordisk Foundation, the Augustinus Foundation, the Kaj Hansen Foundation and Health Insurance Denmark unrelated to the current work. A-CR reports speaker’s fees from Novartis, AstraZeneca and BMS unrelated to the current study. The authors declare that there are no other relationships or activities that might bias, or be perceived to bias, their work.

Funding Information:
Open access funding provided by Zealand Region. The lead investigator ACF has received funding by an unrestricted Research Grant from Steno Diabetes Center Sjaelland for the conduct of the current study. The funder had no role in the study design, data analyses, data interpretation or drafting of the manuscript.

Publisher Copyright:
© 2023, The Author(s).

ID: 362319194