Al-Janabi Fatma Luai Mahdi, Moussa Fatme, Taleb Sarah, Leutscher Peter Derek Christian, Søndergaard Marc Meller, Melgaard Dorte, Søgaard Peter, Torp-Pedersen Christian, Kragholm Kristian, Krogager Maria Lukács
Faculty of Medicine, Aalborg University, Aalborg, Denmark.
North Denmark Regional Hospital, Center for Clinical Research, Hjorring, Denmark.
Hypertens Res. 2025 Jan;48(1):378-387. doi: 10.1038/s41440-024-01894-2. Epub 2024 Oct 31.
The risk of hyperkalemia in relation to different combinations of antihypertensive therapy remains to be elucidated. In this Danish register-based study, we aimed to investigate the risk of developing hyperkalemia in relation to different combinations of antihypertensive therapy. Using incidence density matching, we matched a hyperkalemic patient to five normokalemic patients on eGFR groups, age, sex, and time between study entry and date of potassium measurement. Combination therapies were subdivided into eight groups: beta blockers (BB) + calcium channel blockers (CCB), BB + renin angiotensin system inhibitors (RASi), BB + RASi + mineralocorticoid receptor antagonists (MRA), CCB + RASi, CCB + RASi + thiazides, CCB + thiazides, RASi + thiazides, and other combinations. Multivariable conditional logistic regression was used to estimate the odds of hyperkalemia within 90 days for each of the eight antihypertensive combination therapies. A total of 793 patients with hyperkalemia were matched to 3598 normokalemic patients. In multivariable analysis, odds of developing hyperkalemia when being treated with BB + RASi + MRA was 1.95 (95% CI, 1.39-2.72) compared to RASi + thiazides (reference). CCB + thiazides (OR, 0.76 [95% CI, 0.45-1.28]) and CCB + RASi + Thiazid (OR 0.81 [95% CI, 0.51-1.28]) were among the others not significantly associated with hyperkalemia. Combinations of BB + RASi + MRA were significantly associated with an increased risk of developing hyperkalemia within 90 days of initiating treatment. Patients treated with BB + RASi + MRA within 90 days of treatment initiation, were associated with an increased hyperkalemia risk. When treating hypertensive patients with combination antihypertensive therapy, identifying and monitoring patients with a high risk of dyskalemias is a crucial goal to avoid serious adverse effects and detrimental outcomes related to dyskalemia.
与不同降压治疗组合相关的高钾血症风险仍有待阐明。在这项基于丹麦登记处的研究中,我们旨在调查与不同降压治疗组合相关的发生高钾血症的风险。使用发病密度匹配法,我们根据估算肾小球滤过率(eGFR)分组、年龄、性别以及研究入组至血钾测量日期之间的时间,将一名高钾血症患者与五名血钾正常的患者进行匹配。联合治疗被细分为八组:β受体阻滞剂(BB)+钙通道阻滞剂(CCB)、BB+肾素血管紧张素系统抑制剂(RASi)、BB+RASi+盐皮质激素受体拮抗剂(MRA)、CCB+RASi、CCB+RASi+噻嗪类利尿剂、CCB+噻嗪类利尿剂、RASi+噻嗪类利尿剂以及其他组合。采用多变量条件逻辑回归来估计八种降压联合治疗中每种治疗在90天内发生高钾血症的几率。共有793例高钾血症患者与3598例血钾正常的患者进行了匹配。在多变量分析中,与RASi+噻嗪类利尿剂(参照组)相比,接受BB+RASi+MRA治疗时发生高钾血症的几率为1.95(95%置信区间,1.39 - 2.72)。CCB+噻嗪类利尿剂(比值比,0.76 [95%置信区间,0.45 - 1.28])和CCB+RASi+噻嗪类利尿剂(比值比0.81 [95%置信区间,0.51 - 1.28])等其他组与高钾血症无显著关联。BB+RASi+MRA组合与开始治疗后90天内发生高钾血症风险增加显著相关。在开始治疗90天内接受BB+RASi+MRA治疗的患者,其高钾血症风险增加。在使用联合降压治疗高血压患者时,识别和监测有发生血钾异常高风险的患者是避免与血钾异常相关的严重不良反应和有害后果的关键目标。