Cardiometabolic & kidneyRandomised controlled trial

Mineralocorticoid Receptor Antagonism Prevents Aortic Plaque Progression and Reduces Left Ventricular Mass and Fibrosis in Patients With Type 2 Diabetes and Chronic Kidney Disease: The MAGMA Trial

CirculationPublished

  • Randomised controlled trial
  • double-blind
  • placebo-controlled

Authors' conclusion

Among patients with diabetes with moderate to severe chronic kidney disease at elevated cardiovascular risk, treatment with spironolactone prevented progression of aortic wall volume and resulted in regression of LV mass and favorable alterations in native T1, suggesting amelioration of left-ventricular fibrosis.

Study context

Population
High-risk T2DM with CKD (not receiving dialysis) on maximum tolerated renin-angiotensin system blockademodified ITT
Participants
79 participants
Comparison
Spironolactone vs placebo
  • Spironolactonen = 37
  • Placebon = 42reference
Primary endpoint
Change in thoracic aortic wall volume, absolute or percent (ΔTWV or ΔPWV), by 3T MRI
Follow-up
12 months

Primary result

As reported in the abstract

GroupValueΔTWV
Placeboaverage change in PWV 7.1 ± 10.7 %1.2±1.7 cm3
Spironolactoneaverage change in PWV 0.87 ± 10.0 %0.037±1.9 cm3
  • Spironolactone vs Placebo: P = 0.028 — PWV
  • Spironolactone vs Placebo: P = 0.022 — ΔTWV

Secondary outcomes

OutcomeSpironolactonePlaceboP value
Change in LV mass · 12 months−5.8 ± 8.4 g3.1 ± 8.4 gP = 0.001
Change in LV native T1 (fibrosis) · 12 months−10.1 ± 36.3 ms26.0 ± 41.9 msP = 6.33×10-4

Mediation analysis

Spironolactone effect on aortic wall volume and myocardial mass remained significant after adjustment for ambulatory and central BP

Plasma proteomics

Dominant effect of spironolactone on oxidative stress, inflammation and leukocyte activation pathways

Original publication

Mineralocorticoid Receptor Antagonism Prevents Aortic Plaque Progression and Reduces Left Ventricular Mass and Fibrosis in Patients With Type 2 Diabetes and Chronic Kidney Disease: The MAGMA Trial. Circulation. Published 12 August 2024. doi:10.1161/circulationaha.123.067620

Summarised from the published abstract; every number is checked against it