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慢性肝病晚期患者多因素干预(家庭运动、支链氨基酸和益生菌)的虚弱生物标志物。

Biomarkers of Frailty in Patients with Advanced Chronic Liver Disease Undergoing a Multifactorial Intervention Consisting of Home Exercise, Branched-Chain Amino Acids, and Probiotics.

机构信息

Department of Agricultural and Food Sciences, University of Bologna, 47521 Cesena, Italy.

Institut de Recerca Sant Pau (IR Sant Pau), 08041 Barcelona, Spain.

出版信息

Biomolecules. 2024 Nov 6;14(11):1410. doi: 10.3390/biom14111410.

DOI:10.3390/biom14111410
PMID:39595586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11592179/
Abstract

Frailty in cirrhosis or advanced chronic liver disease (ACLD) is a relevant prognostic factor. In the present study, we aimed to analyze potential biomarkers associated with frailty and its improvement in patients with ACLD. We analyzed the serum of outpatients with ACLD who participated in a previous study (Román, Hepatol Commun 2024) in which frailty was assessed using the liver frailty index (LFI), and patients who were frail or prefrail were randomized to a multifactorial intervention (home exercise, branched-chain amino acids, and probiotics) or control for 12 months. We determined a biomarker battery of inflammation, bacterial translocation, and liver damage in blood and urine and blood metabolomics by H-NMR. Thirty-seven patients were included. According to the LFI, 32 patients were frail or prefrail, and 5 were robust. At baseline, LFI correlated with LBP, sCD163, mtDNA, FGF-21, urinary NGAL, urinary claudin-3, and the metabolites mannose, ethanol, and isoleucine. During the study, patients in the intervention group showed an improvement in LFI and a decrease in CRP, LBP, sCD163, and ccK18 compared to the control group. Metabolomics showed a decrease in dimethyl sulfone and creatinine and an increase in malonate, ornithine, isoleucine, and valine in the intervention group. We conclude that frailty in patients with ACLD is associated with biomarkers of systemic inflammation, bacterial translocation, and liver damage, and alterations of amino acid and short-chain fatty acid metabolism.

摘要

肝硬化或晚期慢性肝病 (ACLD) 患者的虚弱是一个重要的预后因素。在本研究中,我们旨在分析与 ACLD 患者虚弱及其改善相关的潜在生物标志物。我们分析了先前一项研究(Román,Hepatol Commun 2024)中参与研究的 ACLD 门诊患者的血清,该研究使用肝脏虚弱指数 (LFI) 评估虚弱,将虚弱或虚弱前期的患者随机分为多因素干预(家庭运动、支链氨基酸和益生菌)或对照组,干预时间为 12 个月。我们通过 H-NMR 确定了血液和尿液中的炎症、细菌易位和肝损伤的生物标志物组和血液代谢组学。共纳入 37 例患者。根据 LFI,32 例患者为虚弱或虚弱前期,5 例患者为健壮。基线时,LFI 与 LBP、sCD163、mtDNA、FGF-21、尿 NGAL、尿 Claudin-3 以及甘露糖、乙醇和异亮氨酸等代谢物相关。在研究过程中,与对照组相比,干预组患者的 LFI 改善,CRP、LBP、sCD163 和 ccK18 降低。代谢组学显示干预组中二甲基砜和肌酐减少,丙二酸盐、鸟氨酸、异亮氨酸和缬氨酸增加。我们得出结论,ACLD 患者的虚弱与全身炎症、细菌易位和肝损伤的生物标志物以及氨基酸和短链脂肪酸代谢的改变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/d091ed1b71f8/biomolecules-14-01410-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/15878bf58cab/biomolecules-14-01410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/0d734b0ba998/biomolecules-14-01410-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/15fc56ef4d2b/biomolecules-14-01410-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/e9b0b7cd9fa4/biomolecules-14-01410-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/210d922f566e/biomolecules-14-01410-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/7c0eb713f8c8/biomolecules-14-01410-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/d091ed1b71f8/biomolecules-14-01410-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/15878bf58cab/biomolecules-14-01410-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/0d734b0ba998/biomolecules-14-01410-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/15fc56ef4d2b/biomolecules-14-01410-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/e9b0b7cd9fa4/biomolecules-14-01410-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/210d922f566e/biomolecules-14-01410-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/7c0eb713f8c8/biomolecules-14-01410-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/128b/11592179/d091ed1b71f8/biomolecules-14-01410-g007.jpg

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