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Pharmacology · Cardiovascular drugs: finerenone
Sample itemA man with type 2 diabetes and albuminuric chronic kidney disease remains albuminuric on a maximally tolerated ACE inhibitor, with serum potassium 4.4 mmol/L. A mineralocorticoid receptor antagonist without a steroid nucleus, with little gynaecomastia, is added. Which drug is it?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Finerenone
Finerenone is a non-steroidal, selective mineralocorticoid receptor antagonist that reduces progression of diabetic kidney disease and cardiovascular events. Because it is non-steroidal it causes little gynaecomastia or sexual dysfunction, though hyperkalaemia needs monitoring. Spironolactone and eplerenone are steroidal.
Option by option
A. Amiloride
Amiloride blocks the epithelial sodium channel and is not an aldosterone receptor antagonist.
B. Spironolactone
Spironolactone is steroidal and commonly causes gynaecomastia.
C. Finerenone (correct)
Correct. Finerenone is the non-steroidal mineralocorticoid receptor antagonist.
D. Eplerenone
Eplerenone is a steroidal MR antagonist with little anti-androgen effect, but it has a steroid nucleus.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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