接受包括家庭锻炼、支链氨基酸和益生菌在内的多因素干预的晚期慢性肝病患者的虚弱生物标志物

IF 4.8 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomolecules Pub Date : 2024-11-06 DOI:10.3390/biom14111410
Luca Laghi, Maria Àngels Ortiz, Giacomo Rossi, Eva Román, Carlo Mengucci, Elisabet Cantó, Lucia Biagini, Elisabet Sánchez, Maria Mulet, Álvaro García-Osuna, Eulàlia Urgell, Naujot Kaur, Maria Poca, Josep Padrós, Maria Josep Nadal, Berta Cuyàs, Edilmar Alvarado, Silvia Vidal, Elena Juanes, Andreu Ferrero-Gregori, Àngels Escorsell, German Soriano
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引用次数: 0

摘要

肝硬化或晚期慢性肝病(ACLD)患者的虚弱是一个相关的预后因素。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。我们分析了门诊 ACLD 患者的血清,这些患者参加了之前的一项研究(Román,Hepatol Commun 2024),该研究使用肝脏虚弱指数(LFI)评估患者的虚弱程度,并将虚弱或虚弱前期的患者随机分配到多因素干预(家庭锻炼、支链氨基酸和益生菌)或对照组,为期 12 个月。我们测定了血液和尿液中炎症、细菌转运和肝损伤的生物标记物,并通过 1H-NMR 测定了血液代谢组学。共纳入 37 名患者。根据 LFI,32 名患者属于虚弱或虚弱前期,5 名患者属于强健期。基线时,LFI 与 LBP、sCD163、mtDNA、FGF-21、尿 NGAL、尿 claudin-3 以及代谢物甘露糖、乙醇和异亮氨酸相关。在研究期间,与对照组相比,干预组患者的 LFI 有所改善,CRP、LBP、sCD163 和 ccK18 有所下降。代谢组学显示,干预组患者的二甲基砜和肌酐含量下降,丙二酸、鸟氨酸、异亮氨酸和缬氨酸含量上升。我们的结论是,ACLD 患者的虚弱与全身炎症、细菌转运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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomarkers of Frailty in Patients with Advanced Chronic Liver Disease Undergoing a Multifactorial Intervention Consisting of Home Exercise, Branched-Chain Amino Acids, and Probiotics.

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 1H-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.

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来源期刊
Biomolecules
Biomolecules Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
3.60%
发文量
1640
审稿时长
18.28 days
期刊介绍: Biomolecules (ISSN 2218-273X) is an international, peer-reviewed open access journal focusing on biogenic substances and their biological functions, structures, interactions with other molecules, and their microenvironment as well as biological systems. Biomolecules publishes reviews, regular research papers and short communications.  Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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