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P2483Differential effects of novel antidiabetics on arterial stiffness in patients with type 2 diabetes mellitus

Authors :
A Thanopoulou
A Vryonidou
K Batzias
Evanthia Bletsa
Gerasimos Siasos
E Oikonomou
Panagiota K. Stampouloglou
Dimitrios Tousoulis
Alexis Antonopoulos
S A Paschou
Zoi Pallantza
N Tentolouris
E Kassi
Vicky Tsigkou
N. Gouliopoulos
Source :
European Heart Journal. 40
Publication Year :
2019
Publisher :
Oxford University Press (OUP), 2019.

Abstract

Background Arterial stiffness flags increased cardiovascular disease risk in type 2 diabetes mellitus (T2DM) patients. There is limited data on how novel anti-diabetic agents affect arterial stiffness. Purpose To investigate the effects of novel anti-diabetic agents on arterial stiffness in T2DM patients. Patients and methods We enrolled 64 consecutive patients under stable antidiabetic therapy who did not achieve therapeutic targets. Subjects were assessed to receive an additional antidiabetic agent to optimize glucose control; dipeptidyl peptidase-4 inhibitor (DPP4i, n=14), glucagon like peptide-1 receptor agonist (GLP1RA, n=21), sodium/glucose cotransporter-2 inhibitor (SGLT2i, n=21) or long-acting insulin (n=8). Glycosylated hemoglobin (HbA1c) as well as carotid-femoral pulse wave velocity (PWV) and augmentation index (Alx) were measured (as indices of arterial stiffness) were measured at baseline and 3 months after treatment intensification. Results There were no differences between the study groups in traditional risk factors, or baseline HbA1c, PWV and Alx levels (p=NS for all). All groups achieved better glycemic control in terms of HbA1c values between baseline and follow-up (for DPP4i: 7.4±0.2% vs 6.7±0.2%, for GLP1RA: 8.3±0.2% vs 6.9±0.1%, for SGLT2i: 7.5±0.1% vs 6.7±0.1% and for insulin 9.8±0.5% vs 7.7±0.4%, p Conclusions These preliminary data provide evidence that treatment intensification -particularly with GLP1RA, and SGLT2i- benefits vascular properties, a finding which could partly explain the positive findings of recent randomized clinical trails in this field. Acknowledgement/Funding None

Details

ISSN :
15229645 and 0195668X
Volume :
40
Database :
OpenAIRE
Journal :
European Heart Journal
Accession number :
edsair.doi...........6ecee8c7dab04548b66ef6926bee78cb
Full Text :
https://doi.org/10.1093/eurheartj/ehz748.0813