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血液透析患者循环 N-酰基乙醇胺水平与临床和实验室终点的关系。

Impact of Circulating N-Acylethanolamine Levels with Clinical and Laboratory End Points in Hemodialysis Patients.

机构信息

Division of Nephrology, Hypertension and Kidney Transplantation, University of California Irvine School of Medicine, Irvine, California, USA.

Tibor Rubin VA Medical Center, Long Beach, California, USA.

出版信息

Am J Nephrol. 2021;52(1):59-68. doi: 10.1159/000513381. Epub 2021 Feb 18.

DOI:10.1159/000513381
PMID:33601382
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7987690/
Abstract

BACKGROUND

Patients with ESRD on maintenance hemodialysis (MHD) are particularly susceptible to dysregulation of energy metabolism, which may manifest as protein energy wasting and cachexia. In recent years, the endocannabinoid system has been shown to play an important role in energy metabolism with potential relevance in ESRD. N-acylethanolamines are a class of fatty acid amides which include the major endocannabinoid ligand, anandamide, and the endogenous peroxisome proliferator-activated receptor-α agonists, oleoylethanolamide (OEA) and palmitoylethanolamide (PEA).

METHODS

Serum concentrations of OEA and PEA were measured in MHD patients and their correlations with various clinical/laboratory indices were examined. Secondarily, we evaluated the association of circulating PEA and OEA levels with 12-month all-cause mortality.

RESULTS

Both serum OEA and PEA levels positively correlated with high-density lipoprotein-cholesterol levels and negatively correlated with body fat and body anthropometric measures. Serum OEA levels correlated positively with serum interleukin-6 (IL-6) (rho = 0.19; p = 0.004). Serum PEA and IL-6 showed a similar but nonsignificant trend (rho = 0.12; p = 0.07). Restricted cubic spline analyses showed that increasing serum OEA and PEA both trended toward higher mortality risk, and these associations were statistically significant for PEA (PEA ≥4.7 pmol/mL; reference: PEA <4.7 pmol/mL) after adjustments in a Cox model (hazard ratio 2.99; 95% confidence interval 1.04, 8.64).

CONCLUSIONS

In MHD patients, OEA and PEA are significantly correlated with variables related to lipid metabolism and body mass. Additionally, higher serum levels of PEA are associated with mortality risk. Future studies are needed to examine the potential mechanisms responsible for these findings and their clinical implications.

摘要

背景

接受维持性血液透析(MHD)的终末期肾病(ESRD)患者特别容易出现能量代谢失调,可能表现为蛋白质能量消耗和恶病质。近年来,内源性大麻素系统在能量代谢中发挥着重要作用,其与 ESRD 可能具有相关性。酰基乙醇胺是一类脂肪酸酰胺,包括主要的内源性大麻素配体,即花生四烯酸乙醇胺(anandamide)和内源性过氧化物酶体增殖物激活受体-α激动剂,如油酰乙醇胺(OEA)和棕榈酰乙醇胺(PEA)。

方法

测量 MHD 患者的血清 OEA 和 PEA 浓度,并检查其与各种临床/实验室指标的相关性。其次,我们评估了循环 PEA 和 OEA 水平与 12 个月全因死亡率的关系。

结果

血清 OEA 和 PEA 水平均与高密度脂蛋白胆固醇水平呈正相关,与体脂和身体人体测量指标呈负相关。血清 OEA 水平与血清白细胞介素-6(IL-6)呈正相关(rho = 0.19;p = 0.004)。血清 PEA 和 IL-6 呈相似但无统计学意义的趋势(rho = 0.12;p = 0.07)。受限立方样条分析表明,血清 OEA 和 PEA 水平的升高均与更高的死亡风险相关,且在 Cox 模型校正后,PEA 具有统计学意义(PEA≥4.7 pmol/mL;参考:PEA<4.7 pmol/mL)(危险比 2.99;95%置信区间 1.04,8.64)。

结论

在 MHD 患者中,OEA 和 PEA 与与脂质代谢和体重相关的变量显著相关。此外,较高的血清 PEA 水平与死亡风险相关。需要进一步研究来探讨这些发现的潜在机制及其临床意义。

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Impact of circadian rhythmicity and sleep restriction on circulating endocannabinoid (eCB) N-arachidonoylethanolamine (anandamide).昼夜节律和睡眠限制对循环内源性大麻素(eCB)N-花生四烯酰乙醇胺(花生四烯酸酰胺)的影响。
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