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Sökning: WFRF:(Rydén Lars) > (2020-2024) > SOdium-glucose CO-t...

SOdium-glucose CO-transporter inhibition in patients with newly detected Glucose Abnormalities and a recent Myocardial Infarction (SOCOGAMI)

Lundin, Magnus (författare)
Karolinska Institutet
Ferrannini, Giulia (författare)
Karolinska Institutet
Mellbin, Linda (författare)
Karolinska Inst, Dept Med Solna, Stockholm, Sweden.;Karolinska Univ Hosp, Dept Cardiol, Stockholm, Sweden.
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Johansson, Isabelle (författare)
Karolinska Institutet
Norhammar, Anna (författare)
Karolinska Institutet
Näsman, Per, Docent, 1954- (författare)
KTH,Centrum för transportstudier, CTS
Shahim, Bahira (författare)
Karolinska Institutet
Smetana, Stina (författare)
Karolinska Univ Hosp, Dept Cardiol, Stockholm, Sweden.
Venkateshvaran, Ashwin (författare)
Karolinska Institutet
Wang, Anne (författare)
Karolinska Inst, Dept Med Solna, Stockholm, Sweden.;Karolinska Univ Hosp, Dept Cardiol, Stockholm, Sweden.
Sorensson, Peder (författare)
Karolinska Institutet
Ryden, Lars (författare)
Karolinska Institutet
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Karolinska Institutet Karolinska Inst, Dept Med Solna, Stockholm, Sweden;Karolinska Univ Hosp, Dept Cardiol, Stockholm, Sweden. (creator_code:org_t)
Elsevier BV, 2022
2022
Engelska.
Ingår i: Diabetes Research and Clinical Practice. - : Elsevier BV. - 0168-8227 .- 1872-8227. ; 193, s. 110141-
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Aims/hypothesis: Established dysglycaemia (impaired glucose tolerance [IGT] or type 2 diabetes [T2DM]) is a risk factor for further cardiovascular events in patients with coronary artery disease. Sodium-glucose cotransporter 2 inhibitors reduce this risk. The aim of the present investigation was to test the hypothesis that empagliflozin exerts beneficial effects on myocardial function in patients with a recent acute coronary syndrome and newly detected dysglycaemia. Methods: Forty-two patients (mean age 67.5 years, 81 % male) with recent myocardial infarction (n = 36) or unstable angina (n = 6) and newly detected IGT (n = 27) or T2DM (n = 15) were randomised to 25 mg of empagliflozin daily (n = 20) or placebo (n = 22) on top of ongoing therapy. They were investigated with oral glucose tolerance tests, stress-perfusion cardiac magnetic resonance imaging (CMR) and echocardiography at three occasions: before randomisation, after seven months on study drug and three months following cessation of such drug. Primary outcome was a change in left ventricular (LV) end-diastolic volume (LVEDV) and secondary outcomes were a change in a) systolic and diastolic LV function; b) coronary flow reserve; c) myocardial extracellular volume (ECV) in non-infarcted myocardium; d) aortic pulse wave velocity. Results: Empagliflozin induced a significant decrease in fasting and post load glucose (p < 0.05) and body weight (p < 0.01). Empagliflozin did not influence LVEDV, LV systolic or mass indexes, coronary flow reserve, ECV or aortic pulse wave velocity. Echocardiographic indices of LV diastolic function (E/e' and mitral E/A ratio) were not influenced. No safety concerns were identified. Conclusions/interpretation: Empagliflozin had predicted effects on the dysglycaemia but did not influence vari-ables expressing LV function, coronary flow reserve and ECV. An explanation may be that the LV function of the patients was within the normal range.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

Dysglycaemia
Acute coronary syndrome
SGLT-2-inhibition
Empagliflozin
Cardiac magnetic resonance tomography
Echocardiography

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