Division of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA,
Chakri Naruebodindra Medical Institute, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Samut Prakan, Thailand,
Nephron. 2024;148(8):553-562. doi: 10.1159/000539674. Epub 2024 Jun 11.
The association between magnesium level and progression to acute kidney disease (AKD) in acute kidney injury (AKI) patients was not well studied. With AKI transition to AKD, the burden of the disease on mortality, morbidity, and healthcare costs increases. Serum magnesium disturbances are linked with a decline in renal function and increased risk of death in CKD and hemodialysis patients. This study aims to assess the significance of magnesium derangements as a risk factor for the progression of AKI to AKD in critically ill patients.
This study was conducted among patients with AKI admitted to the intensive care units at Mayo Clinic from 2007 to 2017. Serum magnesium at AKI onset was categorized into five groups of <1.7, 1.7-1.9, 1.9-2.1, 2.1-2.3, and ≥2.3 mg/dL, with 1.9-2.1 mg/dL as the reference group. AKD was defined as AKI that persisted >7 days following the AKI onset. Logistic regression was used to evaluate the association between magnesium and AKD.
Among 20,198 critically ill patients with AKI, the mean age was 66 ± 16 years, and 57% were male. The mean serum magnesium at AKI onset was 1.9 ± 0.4 mg/dL. The overall incidence of AKD was 31.4%. The association between serum magnesium and AKD followed a U-shaped pattern. In multivariable analysis, serum magnesium levels were associated with increased risk of AKD with the odds ratio of 1.17 (95% CI: 1.07-1.29), 1.13 (95% CI: 1.01-1.26), and 1.65 (95% CI: 1.48-1.84) when magnesium levels were <1.7, 2.1-2.3, and ≥2.3 mg/dL, respectively.
Among patients with AKI, magnesium level derangement was an independent risk for AKD in critically ill AKI patients. Monitoring serum magnesium and proper correction in critically ill patients with AKI should be considered an AKD preventive intervention in future trials.
镁水平与急性肾损伤(AKI)患者向急性肾疾病(AKD)进展之间的关系尚未得到充分研究。随着 AKI 向 AKD 的转变,疾病对死亡率、发病率和医疗保健成本的负担增加。血清镁紊乱与肾功能下降和慢性肾脏病及血液透析患者死亡风险增加有关。本研究旨在评估镁紊乱作为危重症 AKI 患者 AKI 进展的危险因素的意义。
本研究纳入 2007 年至 2017 年期间在梅奥诊所重症监护病房住院的 AKI 患者。AKI 发病时的血清镁分为 5 组:<1.7、1.7-1.9、1.9-2.1、2.1-2.3 和≥2.3mg/dL,以 1.9-2.1mg/dL 为参考组。AKD 定义为 AKI 发病后持续>7 天。使用逻辑回归评估镁与 AKD 之间的关系。
在 20198 例危重症 AKI 患者中,平均年龄为 66±16 岁,57%为男性。AKI 发病时的平均血清镁水平为 1.9±0.4mg/dL。AKD 的总发生率为 31.4%。血清镁与 AKD 之间的关系呈 U 形。多变量分析显示,血清镁水平与 AKD 的风险增加相关,比值比分别为 1.17(95%CI:1.07-1.29)、1.13(95%CI:1.01-1.26)和 1.65(95%CI:1.48-1.84),当镁水平分别为 <1.7、2.1-2.3 和≥2.3mg/dL 时。
在 AKI 患者中,镁水平紊乱是危重症 AKI 患者 AKD 的独立危险因素。在未来的试验中,应考虑监测危重症 AKI 患者的血清镁水平并进行适当纠正,以作为 AKD 的预防干预措施。