Back to Search Start Over

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.

Authors :
Nyström, Thomas
Bodegard, Johan
Nathanson, David
Thuresson, Marcus
Norhammar, Anna
Eriksson, Jan W.
Source :
Diabetes Research & Clinical Practice. Jan2017, Vol. 123, p199-208. 10p.
Publication Year :
2017

Abstract

<bold>Aims: </bold>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).<bold>Methods: </bold>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.<bold>Results: </bold>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.<bold>Conclusions: </bold>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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01688227
Volume :
123
Database :
Academic Search Index
Journal :
Diabetes Research & Clinical Practice
Publication Type :
Academic Journal
Accession number :
120754780
Full Text :
https://doi.org/10.1016/j.diabres.2016.12.004