Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Endocrinology, Metabolism and Diabetes, Karolinska University Hospital, Stockholm, Sweden.
J Clin Endocrinol Metab. 2020 Oct 1;105(10):e3696-705. doi: 10.1210/clinem/dgaa194.
Calcium channel blockers (CCBs), beta-receptor blockers (BBs), angiotensin-converting enzyme inhibitors (ACEIs), and angiotensin II receptor blockers (ARBs) have occasionally been reported to cause severe hyponatremia. The aim was to explore the association between CCBs, BBs, ACEIs, and ARBs and hospitalization due to hyponatremia.
Patients hospitalized with a principal diagnosis of hyponatremia (n = 11 213) were compared with matched controls (n = 44 801). Linkage of national population-based registers was used to acquire data. Multivariable logistic regression adjusting for co-medications, diseases, previous hospitalizations, and socioeconomic factors was used to explore the association between hospitalization for severe hyponatremia and the use of different CCBs, BBs, ACEIs, and ARBs. Furthermore, newly initiated (≤90 days) and ongoing use were examined separately.
Adjusted odds ratios (aORs) (95% confidence interval) for the investigated 4 drug classes ranged from 0.86 (0.81-0.92) for CCBs to 1.15 (1.07-1.23) for ARBs. For newly initiated drugs, aORs spanned from 1.64 (1.35-1.98) for CCBs to 2.24 (1.87-2.68) for ACEIs. In contrast, the corresponding associations for ongoing therapy were not elevated, ranging from 0.81 (0.75-0.86) for CCBs to 1.08 (1.00-1.16) for ARBs. In the CCBs subgroups, aOR for newly initiated vascular CCBs was 1.95 (1.62-2.34) whereas aOR for ongoing treatment was 0.82 (0.77-0.88).
For newly initiated CCBs, BBs, ACEIs, and ARBs, the risk of hospitalization due to hyponatremia was moderately elevated. In contrast, there was no evidence that ongoing treatment with investigated antihypertensive drugs increased the risk for hospitalization due to hyponatremia.
钙通道阻滞剂(CCBs)、β受体阻滞剂(BBs)、血管紧张素转换酶抑制剂(ACEIs)和血管紧张素 II 受体阻滞剂(ARBs)偶尔会导致严重的低钠血症。本研究旨在探讨 CCBs、BBs、ACEIs 和 ARBs 与低钠血症住院之间的关联。
将因低钠血症(n = 11 213)住院的患者与匹配的对照组(n = 44 801)进行比较。使用国家基于人群的登记处进行链接获取数据。使用多变量逻辑回归调整合并用药、疾病、既往住院和社会经济因素,以探讨严重低钠血症住院与不同 CCBs、BBs、ACEIs 和 ARBs 使用之间的关联。此外,还分别检查了新开始(≤90 天)和持续使用的情况。
所研究的 4 种药物类别的调整后比值比(aOR)(95%置信区间)范围为 CCBs 的 0.86(0.81-0.92)至 ARBs 的 1.15(1.07-1.23)。对于新开始的药物,aOR 范围为 CCBs 的 1.64(1.35-1.98)至 ACEIs 的 2.24(1.87-2.68)。相比之下,正在进行的治疗的相应关联没有升高,范围为 CCBs 的 0.81(0.75-0.86)至 ARBs 的 1.08(1.00-1.16)。在 CCBs 亚组中,新开始的血管 CCBs 的 aOR 为 1.95(1.62-2.34),而正在进行的治疗的 aOR 为 0.82(0.77-0.88)。
对于新开始的 CCBs、BBs、ACEIs 和 ARBs,低钠血症住院的风险适度升高。相比之下,没有证据表明正在使用的研究降压药物会增加因低钠血症住院的风险。