Peeters Laura E J, Tjong Leonardien K, Rietdijk Wim J R, van Gelder Teun, Koch Birgit C P, Versmissen Jorie
Department of Hospital Pharmacy, Erasmus MC, University Medical Centre Rotterdam, 3015CN Rotterdam, The Netherlands.
Department of Internal Medicine, Erasmus MC, University Medical Centre Rotterdam, 3015CN Rotterdam, The Netherlands.
Biomedicines. 2022 Jan 8;10(1):137. doi: 10.3390/biomedicines10010137.
We aim to investigate sex differences in blood concentrations of spironolactone and the active metabolite canrenone in resistant hypertension patients. Furthermore, sex differences in adherence for spironolactone and other antihypertensive drugs (AHDs) were studied. The patients in this post hoc study had all participated in a single-blind randomized controlled trial called RHYME-RCT (Dutch Trial Register, NL6736). Concentrations in blood of several AHDs were assessed in RHYME-RCT to investigate adherence to treatment. This allowed for a comparison of drug exposure to spironolactone and canrenone between males and females. In linear regression models, no statistically significant sex differences (N = 35) in spironolactone (B =-10.23, SE = 7.92, = 0.206) or canrenone (B = 1.24, SE = 10.96, = 0.911) concentrations after adjustment for dose and time between sampling and intake were found. Furthermore, no statistically significant differences in non-adherence to spironolactone were found between sexes (N = 54, male 15% vs. female 38%, = 0.100), but non-adherence to spironolactone was associated with non-adherence to other AHDs ( ≤ 0.001). Spironolactone and canrenone concentrations were not different between males and females with resistant hypertension. Although not statistically significant, females were twice as likely to be non-adherent to spironolactone compared to males, and thereby also more likely to be non-adherent to other AHDs.
我们旨在研究顽固性高血压患者中螺内酯及其活性代谢产物坎利酮血药浓度的性别差异。此外,还研究了螺内酯及其他抗高血压药物(AHDs)依从性的性别差异。这项事后研究中的患者均参与了一项名为RHYME-RCT的单盲随机对照试验(荷兰试验注册编号:NL6736)。在RHYME-RCT中评估了几种AHDs的血药浓度,以调查治疗依从性。这使得能够比较男性和女性之间螺内酯和坎利酮的药物暴露情况。在多元线性回归模型中,在校正剂量以及采样与服药之间的时间后,未发现螺内酯(B=-10.23,标准误=7.92,P=0.206)或坎利酮(B=1.24,标准误=10.96,P=0.911)浓度存在统计学显著的性别差异(N=35)。此外,未发现性别之间在螺内酯不依从性方面存在统计学显著差异(N=54,男性15% vs.女性38%,P=0.100),但螺内酯不依从性与其他AHDs的不依从性相关(P≤0.001)。顽固性高血压男性和女性之间的螺内酯和坎利酮浓度没有差异。尽管无统计学显著性,但女性不依从螺内酯的可能性是男性的两倍,因此也更有可能不依从其他AHDs。