Myogenic Underactive Bladder and Heart Failure Resemblance: A Novel Role for SGLT2 Inhibition?

Eur Urol Focus. 2022 Nov;8(6):1783-1786. doi: 10.1016/j.euf.2022.04.016. Epub 2022 May 20.

Abstract

The heart and bladder share physiological biomechanical determinants of contraction. Heart failure (HF) and myogenic underactive bladder (mUAB) also share similarities in their pathophysiology. In both cases there is muscle injury that is directly linked to disease stage. In the final stage, both myocardium and detrusor show marked fibrosis and lower contractility. While HF has an established pharmacological treatment, there are still no effective drugs for mUAB. This mini-review explores the similarities between HF and mUAB and suggests that, as in HF, SGLT2 inhibitors may also have a beneficial role in mUAB. PATIENT SUMMARY: To date, there is no treatment for underactive bladder caused by problems with the bladder muscle (mUAB). We review similarities between this condition and heart failure and hypothesize that a recent drug class with striking results in heart failure might also have a beneficial role in mUAB.

Keywords: Bladder remodeling; Diabetic cystopathy; Heart failure; Inhibitor; SGLT2; Underactive bladder.

Publication types

  • Review

MeSH terms

  • Heart Failure* / drug therapy
  • Humans
  • Urinary Bladder, Underactive*