Mineralocorticoid receptor blockade improves coronary microvascular function in individuals with type 2 diabetes

Rajesh Garg, Ajay D. Rao, Maria Baimas-George, Shelley Hurwitz, Courtney Foster, Ravi V. Shah, Michael Jerosch-Herold, Raymond Y. Kwong, Marcelo F. Di Carli, Gail K. Adler

Research output: Contribution to journalArticlepeer-review

83 Scopus citations

Abstract

Reduced coronary flow reserve (CFR), an indicator of coronary microvascular dysfunction, is seen in type 2 diabetes mellitus (T2DM) and predicts cardiac mortality. Since aldosterone plays a key role in vascular injury, the aim of this study was to determine whether mineralocorticoid receptor (MR) blockade improves CFR in individuals with T2DM. Sixty-four men and women with well-controlled diabetes on chronic ACE inhibition (enalapril 20 mg/day) were randomized to add-on therapy of spironolactone 25 mg, hydrochlorothiazide (HCTZ) 12.5 mg, or placebo for 6 months. CFR was assessed by cardiac positron emission tomography at baseline and at the end of treatment. There were significant and similar decreases in systolic blood pressure with spironolactone and HCTZ but not with placebo. CFR improved with treatment in the spironolactone group as compared with the HCTZ group and with the combined HCTZ and placebo groups. The increase in CFR with spironolactone remained significant after controlling for baseline CFR, change in BMI, race, and statin use. Treatment with spironolactone improved coronary microvascular function, raising the possibility that MR blockade could have beneficial effects in preventing cardiovascular disease in patients with T2DM.

Original languageEnglish (US)
Pages (from-to)236-242
Number of pages7
JournalDiabetes
Volume64
Issue number1
DOIs
StatePublished - Jan 1 2015
Externally publishedYes

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism

Fingerprint

Dive into the research topics of 'Mineralocorticoid receptor blockade improves coronary microvascular function in individuals with type 2 diabetes'. Together they form a unique fingerprint.

Cite this