Metformin is associated with improved left ventricular diastolic function measured by tissue Doppler imaging in patients with diabetes
ObjectiveTo examine the association between selected glucose-lowering medications and left ventricular (LV) diastolic function in patients with diabetes.DesignRetrospective cohort study (years 2005–2008).MethodsEchocardiograms of 242 patients with diabetes undergoing coronary angiography were analyz...
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Veröffentlicht in: | European journal of endocrinology 2010-10, Vol.163 (4), p.593-599 |
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Sprache: | eng |
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Zusammenfassung: | ObjectiveTo examine the association between selected glucose-lowering medications and left ventricular (LV) diastolic function in patients with diabetes.DesignRetrospective cohort study (years 2005–2008).MethodsEchocardiograms of 242 patients with diabetes undergoing coronary angiography were analyzed. All patients had an LV ejection fraction (LVEF) ≥20% and were without atrial fibrillation, bundle branch block, valvular disease, or cardiac pacemaker. Patients were grouped according to the use of metformin (n=56), sulfonylureas (n=43), insulin (n=61), and combination treatment (n=82).ResultsMean age (66±10 years) and mean LVEF (45±11%) were similar across the groups. Mean isovolumic relaxation time (IVRT) was 66±31, 79±42, 69±23, and 66±29 ms in metformin, sulfonylureas, insulin, and combination treatment groups respectively (P=0.4). Mean early diastolic longitudinal tissue velocity (e′) was 5.3±1.6, 4.6±1.6, 5.3±1.8, and 5.4±1.7 cm/s in metformin, sulfonylureas, insulin, and combination treatment groups (P=0.04). In adjusted linear regression models, the use of metformin was associated with a shorter IVRT (parameter estimate −9.9 ms, P=0.049) and higher e′ (parameter estimate +0.52 cm/s, P=0.03), compared with no use of metformin. The effects of metformin were not altered by concomitant use of sulfonylureas or insulin (P for interactions >0.4).ConclusionsThe use of metformin is associated with improved LV relaxation, as compared with no use of metformin. |
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ISSN: | 0804-4643 1479-683X |
DOI: | 10.1530/EJE-10-0624 |