Sadeghpour Majid, Bejani Ali, Kupaei Maryam Hosseini, Majd Seyed Jafar Amini, Najafi Afshin, Fakhari Shiva, Abdolizadeh Ali, Mohammadi Keivan
Department of General Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Student Research Committee, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Biol Trace Elem Res. 2024 Sep 10. doi: 10.1007/s12011-024-04368-1.
Chronic kidney disease (CKD) is a major cause of death and disability worldwide. It is usually diagnosed at early levels because of its slow progression. Treatment should consider CKD complications (such as electrolyte level imbalance, vascular calcification, and bone mineral disorders), as well as the development of CKD itself. Large-scale studies have shown that current treatment guidelines are nearly ineffective and fail to achieve treatment goals. Guidelines have not paid as much attention to magnesium (Mg) as the other electrolytes, while Mg has a significant role in the treatment goals of CKD. Hypomagnesemia is the only electrolyte imbalance that is equally prevalent in all stages of CKD. A lower plasma Mg level in each stage of CKD is associated with a higher risk of CKD progression and cardiac events. Magnesium exerts its effects both directly and via other ions. Mg supplementation increases insulin sensitivity while reducing proteinuria and inflammation. It lowers blood pressure and inhibits vascular calcification primarily because of its effects on calcium and phosphate, respectively. Vitamin D supplementation for low-active vitamin D in CKD patients increases vascular calcification and cardiac events, but magnesium supplementation enhances vitamin D levels and activity without increasing the risk of cardiac events. However, careful attention is required due to the potential threats of hypermagnesemia, particularly in advanced CKD stages. Starting magnesium supplementation early in patients' treatment plans will result in fewer side effects and more advantages. More original research is needed to determine its optimal dose and serum levels.
慢性肾脏病(CKD)是全球范围内死亡和残疾的主要原因。由于其进展缓慢,通常在早期阶段被诊断出来。治疗应考虑CKD并发症(如电解质水平失衡、血管钙化和骨矿物质紊乱)以及CKD本身的发展。大规模研究表明,当前的治疗指南几乎无效,无法实现治疗目标。指南对镁(Mg)的关注不如对其他电解质的关注多,而镁在CKD的治疗目标中具有重要作用。低镁血症是CKD各阶段中同样普遍存在的唯一电解质失衡。CKD各阶段较低的血浆镁水平与CKD进展和心脏事件的较高风险相关。镁通过直接作用和通过其他离子发挥作用。补充镁可提高胰岛素敏感性,同时减少蛋白尿和炎症。它降低血压并抑制血管钙化,主要分别是因为其对钙和磷的作用。对CKD患者补充低活性维生素D会增加血管钙化和心脏事件,但补充镁可提高维生素D水平和活性,而不会增加心脏事件的风险。然而,由于高镁血症的潜在威胁,需要谨慎关注,尤其是在CKD晚期阶段。在患者的治疗计划中尽早开始补充镁将导致更少的副作用和更多的益处。需要更多的原创研究来确定其最佳剂量和血清水平。