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液体超负荷和组织钠蓄积是透析患者发生蛋白质能量营养不良的主要驱动因素。

Fluid Overload and Tissue Sodium Accumulation as Main Drivers of Protein Energy Malnutrition in Dialysis Patients.

机构信息

School of Medicine, Montpellier University, 34000 Montpellier, France.

Global Medical Office, FMC-France, 94260 Fresnes, France.

出版信息

Nutrients. 2022 Oct 25;14(21):4489. doi: 10.3390/nu14214489.

DOI:10.3390/nu14214489
PMID:36364751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9658859/
Abstract

Protein energy malnutrition is recognized as a leading cause of morbidity and mortality in dialysis patients. Protein-energy-wasting process is observed in about 45% of the dialysis population using common biomarkers worldwide. Although several factors are implicated in protein energy wasting, inflammation and oxidative stress mechanisms play a central role in this pathogenic process. In this in-depth review, we analyzed the implication of sodium and water accumulation, as well as the role of fluid overload and fluid management, as major contributors to protein-energy-wasting process. Fluid overload and fluid depletion mimic a tide up and down phenomenon that contributes to inducing hypercatabolism and stimulates oxidation phosphorylation mechanisms at the cellular level in particular muscles. This endogenous metabolic water production may contribute to hyponatremia. In addition, salt tissue accumulation likely contributes to hypercatabolic state through locally inflammatory and immune-mediated mechanisms but also contributes to the perturbation of hormone receptors (i.e., insulin or growth hormone resistance). It is time to act more precisely on sodium and fluid imbalance to mitigate both nutritional and cardiovascular risks. Personalized management of sodium and fluid, using available tools including sodium management tool, has the potential to more adequately restore sodium and water homeostasis and to improve nutritional status and outcomes of dialysis patients.

摘要

蛋白质能量营养不良被认为是透析患者发病率和死亡率的主要原因。使用全球常见的生物标志物,约有 45%的透析人群存在蛋白质能量消耗过程。尽管有几种因素与蛋白质能量消耗有关,但炎症和氧化应激机制在这一发病过程中起着核心作用。在本次深入审查中,我们分析了钠和水蓄积的影响,以及液体超负荷和液体管理的作用,因为它们是导致蛋白质能量消耗过程的主要因素。液体超负荷和液体耗竭模拟了一种潮汐涨落现象,导致细胞水平的过度分解代谢,并刺激氧化磷酸化机制,特别是肌肉中的氧化磷酸化机制。这种内源性代谢水的产生可能导致低钠血症。此外,盐组织蓄积可能通过局部炎症和免疫介导的机制导致分解代谢亢进状态,也可能导致激素受体(如胰岛素或生长激素抵抗)紊乱。现在是时候更准确地处理钠和液体失衡问题,以减轻营养和心血管风险了。使用包括钠管理工具在内的现有工具对钠和液体进行个性化管理,有可能更充分地恢复钠和水的内稳态,并改善透析患者的营养状况和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/cde4026268df/nutrients-14-04489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/695424361863/nutrients-14-04489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/b0df9d40e9f1/nutrients-14-04489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/ee6b50130c36/nutrients-14-04489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/cde4026268df/nutrients-14-04489-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/695424361863/nutrients-14-04489-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/b0df9d40e9f1/nutrients-14-04489-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/ee6b50130c36/nutrients-14-04489-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bec8/9658859/cde4026268df/nutrients-14-04489-g004.jpg

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