Impact of diabetes duration on left ventricular mass regression with empagliflozin

Author:

Moroney Michael12,Verma Raj12,Hibino Makoto3,Mazer C. David4567,Connelly Kim A.5789,Yan Andrew T.89,Quan Adrian15,Teoh Hwee1510,Verma Subodh151112,Puar Pankaj11213

Affiliation:

1. Division of Cardiac Surgery St. Michael's Hospital of Unity Health Toronto Toronto Ontario Canada

2. School of Medicine Royal College of Surgeons in Ireland Dublin Ireland

3. Division of Cardiothoracic Surgery Emory University School of Medicine Atlanta Georgia USA

4. Department of Anesthesia St. Michael's Hospital of Unity Health Toronto Toronto Ontario Canada

5. Li Ka Shing Knowledge Institute of St. Michael's Hospital Toronto Ontario Canada

6. Department of Anesthesiology and Pain Medicine University of Toronto Toronto Ontario Canada

7. Department of Physiology University of Toronto Toronto Ontario Canada

8. Department of Medicine University of Toronto Toronto Ontario Canada

9. Division of Cardiology St. Michael's Hospital of Unity Health Toronto Toronto Ontario Canada

10. Division of Endocrinology and Metabolism St. Michael's Hospital of Unity Health Toronto Toronto Ontario Canada

11. Department of Surgery University of Toronto Toronto Ontario Canada

12. Department of Pharmacology and Toxicology University of Toronto Toronto Ontario Canada

13. Faculty of Medicine University of British Columbia Vancouver British Columbia Canada

Abstract

AbstractAimsThe duration of type 2 diabetes mellitus (T2DM) is an important determinant of diabetes severity. The EMPA‐HEART CardioLink‐6 trial reported significant left ventricular (LV) mass indexed to body surface area (LVMi) regression in patients treated with the sodium‐glucose cotransporter 2 inhibitor (SGLT2i) empagliflozin for 6 months. This exploratory sub‐analysis of the same trial investigated the association between T2DM duration and LVMi regression.Methods and resultsA total of 97 individuals with T2DM and coronary artery disease (CAD) were randomly assigned to receive empagliflozin 10 mg daily or placebo. LVMi was measured at the baseline and 6 month visit using cardiac magnetic resonance imaging. The study population was divided into those with a baseline T2DM duration <10 years (n = 40) or ≥10 years (n = 57). A linear model adjusting for baseline values in each of the subgroups (ANCOVA) was used to assess the treatment effect of 6 month change in LVMi, LV end systolic volume indexed to body surface area, LV end diastolic volume indexed to body surface area and LV ejection fraction. Patients in the T2DM duration <10 years group (38 males [95.0%], median age 63 [IQR: 55 years to 70 years]) had a median T2DM duration of 4 years (IQR: 2.0 years to 7.0 years). Those in the T2DM duration ≥10 years group (52 males [91.2%], median age 65 [IQR: 57 years to 71 years]) had a median duration of 15 years (IQR: 12 years to 20 years). There was no significant difference in baseline LVMi according to T2DM duration (median 62 g/m2 [IQR: 53.1 g/m2 to 70.0 g/m2] for T2DM duration <10 years; median 57.5 g/m2 [IQR: 52.1 g/m2 to 66.2 g/m2] for T2DM duration ≥10 years; P = 0.11). Empagliflozin was associated with reductions in LVMi irrespective of duration of T2DM above and below 10 years (T2DM duration <10 years group, mean adjusted difference −2.90 g/m2 [95% CI: −6.64 g/m2 to 0.84 g/m2]; T2DM duration ≥10 years group, mean adjusted difference −3.69 g/m2 [95% CI: −0.14 g/m2 to −7.24 g/m2]; Pinteraction = 0.07).ConclusionsIn the EMPA‐HEART CardioLink‐6 trial, empagliflozin treatment was associated with reductions in LVMi in people with T2DM and CAD irrespective of the duration of diabetes assessed categorically above and below 10 years.

Funder

Boehringer Ingelheim

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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