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id:"swepub:oai:DiVA.org:uu-319682"
 

Sökning: id:"swepub:oai:DiVA.org:uu-319682" > Second line initiat...

  • Nyström, ThomasKarolinska Institutet (författare)

Second line initiation of insulin compared with DPP-4 inhibitors after metformin monotherapy is associated with increased risk of all-cause mortality, cardiovascular events, and severe hypoglycemia

  • Artikel/kapitelEngelska2017

Förlag, utgivningsår, omfång ...

  • ELSEVIER IRELAND LTD,2017
  • electronicrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:uu-319682
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-319682URI
  • https://doi.org/10.1016/j.diabres.2016.12.004DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:135312736URI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:art swepub-publicationtype

Anmärkningar

  • Aims: The objective of this nationwide study was to compare the risk of all-cause mortality, fatal and nonfatal cardiovascular disease (CVD), and severe hypoglycemia in patients with type 2 diabetes (T2D) on metformin monotherapy treatment starting second-line treatment with either insulin or dipeptidyl peptidase-4 inhibitor (DPP-4i). Methods: All patients with T2D in Sweden who initiated second-line treatment with insulin or DPP-4i after metformin monotherapy during 2007-2014 identified in the Swedish Prescribed Drug Register were followed for outcome in the Cause of Death and National Patient Registers. Insulin and DPP-4i patients were matched 1: 1 using propensity-score matching. Comparisons between groups were performed using unadjusted Cox regression models. Additionally, multivariate adjusted survival models were used to test the results using the full population without matching. Results: Of 27,767 mono-metformin-treated patients, 55.7% started insulin and 44.3% a DPP-4i, and after matching both groups had 9278 patients each. Median follow-up (patients years) times were 3.84 (37,578) and 3.93 (37,983) for insulin and DPP-4i-groups, respectively. Insulin compared with DPP-4i was associated with higher risk of subsequent all-cause mortality, fatal and nonfatal CVD, and severe hypoglycemia; adjusted HR (95% CI): 1.69 (1.45-1.96); 1.39 (1.21-1.61); and 4.35 (2.26-8.35), respectively. When performing multivariate adjusted analyses on the full population similar results were found. Conclusions: Initiation of insulin, compared with DPP-4i treatment, was associated with an increased risk of subsequent all-cause mortality, fatal and nonfatal CVD, and severe hypoglycemia. Results from randomized trials will be important to elucidate causal relationships.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Bodegard, JohanAstraZeneca Nordic Baltic, Sodertalje, Sweden. (författare)
  • Nathanson, DavidKarolinska Institutet (författare)
  • Thuresson, MarcusStatisticon AB, Uppsala, Sweden. (författare)
  • Norhammard, AnnaKarolinska Inst, Dept Med, Cardiol Unit, Stockholm, Sweden.;Capio St Gorans Hosp, Stockholm, Sweden. (författare)
  • Eriksson, Jan W.Uppsala universitet,Klinisk diabetologi och metabolism(Swepub:uu)janer909 (författare)
  • Karolinska InstitutetAstraZeneca Nordic Baltic, Sodertalje, Sweden. (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Diabetes Research and Clinical Practice: ELSEVIER IRELAND LTD123, s. 199-2080168-82271872-8227

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