Literature DB >> 27367159

Effect of spironolactone on patients with resistant hypertension and obstructive sleep apnea.

Lirui Yang1, Huimin Zhang1, Menggengtuya Cai2, Yubao Zou1, Xiongjing Jiang1, Lei Song1, Erpeng Liang1, Jin Bian1, Haiying Wu1, Rutai Hui1.   

Abstract

OBJECTIVE: To examine whether spironolactone could reduce the severity of obstructive sleep apnea (OSA) and lower blood pressure in patients with resistant hypertension.
METHODS: This was a blank-controlled, single-center study. Patients with resistant hypertension and moderate-to-severe OSA (apnea-hypopnea index >15 events/h) were enrolled and randomly assigned to the therapy or control group. Patients in the therapy group were administered spironolactone 20 mg once daily (up to 40 mg once daily for 4 weeks, if required) in addition to original antihypertensive medication. Follow-up was 12 weeks.
RESULTS: Thirty patients were enrolled (n = 15 per group). After 12 weeks of follow-up, apnea-hypopnea index (21.8 ± 15.7 vs. 1.8 ± 12.8, p < 0.05), hypopnea index (9.8 ± 11.1 vs. -2.7 ± 16.8, p < 0.05), oxygen desaturation index (20.8 ± 15.0 vs. 0.3 ± 16.1, p < 0.05), clinical blood pressure, ambulatory blood pressure, and plasma aldosterone level (9.8 ± 6.3 vs. 2.9 ± 6.7, p < 0.05) were reduced significantly in the therapy group compared with the control group. No side effects were reported.
CONCLUSIONS: Spironolactone reduced the severity of OSA and reduced blood pressure in resistant hypertension patients with moderate-to-severe OSA. These findings may assist in the treatment of OSA in patients with resistant hypertension.

Entities:  

Keywords:  Aldosterone; apnea–hypopnea index; obstructive sleep apnea; resistant hypertension; spironolactone

Mesh:

Substances:

Year:  2016        PMID: 27367159     DOI: 10.3109/10641963.2015.1131290

Source DB:  PubMed          Journal:  Clin Exp Hypertens        ISSN: 1064-1963            Impact factor:   1.749


  16 in total

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10.  Signal Enhancement in the HPLC-ESI-MS/MS analysis of spironolactone and its metabolites using HFIP and NH4F as eluent additives.

Authors:  Kalev Takkis; Rudolf Aro; Lenne-Triin Kõrgvee; Heili Varendi; Jana Lass; Koit Herodes; Karin Kipper
Journal:  Anal Bioanal Chem       Date:  2017-02-21       Impact factor: 4.142

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