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Acta Cardiologica Sinica logoLink to Acta Cardiologica Sinica
letter
. 2018 Jul;34(4):363. doi: 10.6515/ACS.201807_34(4).20180307A

Spironolactone Use to Treat Hypertension: in the Right Patient Groups at the Right Time

Yusuf Ziya Şener 1, Cem Çöteli 1, Metin Okşul 1
PMCID: PMC6066948  PMID: 30065576

To the Editor:

We read the article which was about firstline use of spironolactone as monotherapy in the treatment of stage 1 essential hypertension published by Attar et al. with great interest.1

Angiotensin converting enzyme inhibitors, angiotensin receptor blockers, calcium channel blockers and thiazide diuretics are suggested to be preferred as firstline treatment in patients with stage 1 essential hypertension. Spironolactone is recommended in patients with resistant hypertension which is defined as uncontrolled blood pressure despite three antihyperternsive drug combination including a diuretic.2

Spironolactone is a mineralocorticoid receptor antagonist and causes anti-androgenic side effects.3 These anti-andgrogenic effects can be miserable in males but spironolactone can be a good option for women with polycystic ovary syndrome (PCOS) in whom excess androgens leads menstrual abnormalities, hirsutism and infertility.4 There are conflicting datas about the effects of spironolactone on glucose metabolism. Spironolactone increases HbA1C levels and has negative effects on glucose metabolism in patients with heart failure and diabetes while it has positive effects on glucose metabolism in patients with hyperandrogenism.5 Mineralocorticoid receptors are expressed in osteoblasts and osteoclasts and they are supported to play role in glucocorticoid related osteoporosis.6

By the light of these datas, firstline use of spironolactone in stage 1 essential hypertension doesn’t seem rational due to having other efficient options with less and tolerable side effects. Spironolactone should be preferred in selected patient groups including patients with heart failure, osteoporosis and in patients who can benefit from antiandrogenic effects of the drug such as patients with PCOS or prostat carcinoma.

REFERENCES

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