血清镁浓度需要修订,特别是在肾功能衰竭

M. Malaki
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引用次数: 0

摘要

亲爱的编辑,血浆镁浓度保持在很窄的范围内。在负镁平衡状态下,最初的损失来自细胞外空间,而与骨储存的平衡在几周后才开始。根据文献,正常血浆镁浓度为1.7-2.1 mg/dL (0.7-0.9 mmol,或1.4-1.8 mEq/L)全身镁的一半存在于软组织,另一半存在于骨骼,1%存在于血液中。目前还不可能评估总镁储量,血清镁水平评估不能显示总血清状态,镁离子测量已在选定的中心进行,但没有批准更有益的产量。口服补充后,镁具有较长的生物半衰期,在包括血清在内的大多数组织中平衡缓慢。研究表明,在1.94 mg/dL和2.19 mg/dL的临界值下,临床镁缺乏症发生率分别为10%和1%。结果表明,血清镁浓度(SMC)低于2.1 mg/dL会增加2型糖尿病的发病风险,而0.85 mmol/L或2.1 mg/dL可视为合理的SMC下限低镁血症新定义的重要性在特殊情况下更为突出,因为低镁血症通过机械通气需求增加、通气支持持续时间延长、不可逆肾功能障碍等机制增加了脓毒症和危重症患者的死亡率。在一项研究中,1.5毫克/分升的镁水平比2毫克/分升的镁水平增加了细菌感染的风险在终末期肾病患者中,镁水平低于1.94 mg/dL可使冠心病死亡风险增加33%,这使得作者对SMC在1.7-2.67 mg/dL作为临床事务中保密的临床有用参考的有效性存在争议;例如镁的作用在慢性肾脏疾病预防血管钙化是众所周知的和血清镁低于1.94 mg / dL已经批准,可以与死亡率增加有关专性临床医生改变低切断SMC低至0.8水平更易/ L (1.94 mg / dL)但它可能不够,因为在患者血液透析后3年随访结果表明,血清镁在2.77 mg / dL与更高的死亡率与2.77毫克/分升相比另一项研究更进一步,表明血清镁超过3mg /dL可以减少软组织钙化b[6],这可以解释为什么在维持血液透析的患者中,与高镁血症患者相比,正常血清镁水平与更高的心血管死亡率相关
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum magnesium concentration a need for revision especially in renal failure
Dear Editor, Plasma magnesium concentration is kept within narrow limits. In states of negative magnesium balance, initial losses come from the extracellular space while equilibrium with bone stores does not begin for several weeks. Normal plasma magnesium concentration based on literature is 1.7–2.1 mg/dL (0.7–0.9 mmol, or 1.4–1.8 mEq/L).[1] Half of the total body magnesium is present in soft tissue and another half in bone and 1% is present in the blood. Assessment of total magnesium store is impossible at now and serum magnesium level evaluation cannot show total serum status, magnesium ion measurement has been done in selected centers without approved more beneficial yields. Magnesium has a long biological half‐life after oral supplementation and equilibrates slowly in most tissue including serum. It has been shown that at cut‐off levels of 1.94 mg/dL and 2.19 mg/dL clinical magnesium deficiency occurred in 10% and 1%, respectively. It was shown that serum magnesium concentration (SMC) lower than 2.1 mg/dL increases the risk of Diabetes mellitus type 2 and levels of 0.85 mmol/L or 2.1 mg/dL can be considered as an reasonable lower limit of SMC.[2] Importance of new definition for hypomagnesemia has been more prominent in special conditions because of hypomagnesemia increase mortality in septic and critically ill patients by mechanisms such as increased need for mechanical ventilation and longer duration of ventilation support, irreversible renal dysfunction. in a study magnesium level of 1.5 mg/dL versus 2 mg/dL increases the risk of bacterial infection.[3] In end‐stage renal disease magnesium level below 1.94 mg/dL increase death risk of coronary heart disease up to 33% make that authors were debated about validity of SMC in an accepted reference of 1.7–2.67 mg/dL as a confidential clinical useful reference in clinical affairs; for example the role of magnesium as a protective against vascular calcification in chronic kidney disease is well known and serum magnesium lower than 1.94 mg/dL has been approved that can be associated with increased mortality that obligate clinician to change lower cut off level of SMC as low as 0.8 mmol/L (1.94 mg/dL) but it may not be enough because in patients under hemodialysis after 3 years followed up was shown that serum magnesium under 2.77 mg/dL was associated with higher mortality compared to higher 2.77 mg/dL.[4] Other study goes beyond and shows serum magnesium over 3 mg/dL can decrease soft tissue calcification[5] it can explain why in patients under maintenace hemodialysis normal serum magnesium levels was associated with higher cardiovascular mortality compared to patients with hypermagnesemia.[6]
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