Evaluation of exenatide versus insulin glargine for the impact on endothelial functions and cardiovascular risk markers

2014 ◽  
Vol 106 (3) ◽  
pp. 567-575 ◽  
Author(s):  
Eren Gurkan ◽  
Ilhan Tarkun ◽  
Tayfun Sahin ◽  
Berrin Cetinarslan ◽  
Zeynep Canturk
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Pavle Vrebalov Cindro ◽  
Mladen Krnić ◽  
Darko Modun ◽  
Božo Smajić ◽  
Jonatan Vuković

Abstract Background and aims Diabetes mellitus type two is one of the major cardiovascular risk factors. Treatment of diabetes can reduce this risk, but the treatment options differ a lot in their risk-reducing capabilities. We compared the impact of insulin degludec (IDeg-100) and insulin glargine U300 (IGlar-300) on cardiovascular risk parameters - glycaemic variability (GV), arterial stiffness and lipid parameters - in insulin naive patients with DMT2. Methods To 23 individuals who previously had uncontrolled DMT2 on two or more oral antidiabetic drugs, IGlar-300 and IDeg-100 were applied for 12 weeks and then switched in a cross over design manner. Prior and after of each insulin phase, we analysed biochemical parameters,7-point SMBG profile over three days and arterial stiffness which was assessed indirectly by measuring the augmentation index (AIx) on the principles of applanation tonometry. Results There were no significant differences between IGlar-300 and IDeg-100 regarding reduction of mean glucose values and coefficient of variation (CV). Both insulins insignificantly reduced AIx for standardised pulse of 75 beats/min and without differences between them. IGlar-300 and IDeg-100 reduced triglycerides and increased HDL with no significant difference between the two insulins. IGlar-300 increased the total cholesterol level and IDeg-100 decreased total cholesterol, but without statistically significant difference. IGlar-300 increased LDL level by 0.508 mmol/L and IDeg-100 decreased LDL by 0.217 mmol/L, with statistically significant difference (p = 0.0215). Conclusions This study did not show significant difference between IGlar-300 and IDeg-100 regarding glycaemic parameters and augmentation index using the same dose of 0.2 IU/kg for both insulins, but it has revealed possible differences in impact on lipid profile. Trial Registration Clinicaltrials.gov, NCT04692415. Retrospectively registered on December 31th 2020.


2010 ◽  
Vol 6 (2) ◽  
pp. 10 ◽  
Author(s):  
Michael Hecht Olsen ◽  

In relatively young patients (men <55 and women >65 years of age), first-time hospitalisation for cardiovascular disease (CVD) strikes without warning since the traditional cardiovascular risk factors are often normal or only slightly elevated. Therefore, we need non-traditional cardiovascular risk markers more closely related to CVD that can reliably predict future CVD in individuals, making better targeted prevention and more individualised treatment possible. However, it has been difficult to find non-traditional cardiovascular risk markers suitable for risk assessment, underlining the importance of future research into the complex mechanisms that lead to CVD. Better understanding of these complex mechanisms might enable us to find better risk markers and improve future cardiovascular risk assessment and treatment.


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