代谢组学与癌症儿童疲劳和身体功能的关联:一项初步研究。

Janice S Withycombe, Jinbing Bai, Canhua Xiao, Ronald C Eldridge
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引用次数: 0

摘要

背景:疲劳是接受癌症治疗的儿童常见的症状。先前的研究表明疲劳和体力活动之间呈反比关系。人们对疲劳与身体机能的关系或疲劳的潜在生物学机制知之甚少。本研究探讨了疲劳、身体机能和相关代谢物之间的关系。方法:儿童(7-18岁)在癌症治疗期间的两个时间点使用儿童患者报告的结果测量信息系统(PROMIS)调查提供血清样本和自我报告的疲劳和下肢身体功能(活动能力)。PROMIS评分根据每个已建立的切割点分为高/低(高疲劳T = 47.5;高物理功能T >51.5)。高分辨率液相色谱-质谱法提取了29种与疲劳或身体功能相关的代谢物。描述性统计总结了PROMIS评分,线性混合效应模型估计了代谢物与年龄、性别和类固醇使用的关系。结果:40名儿童参与,其中女性占53%;7-12岁,38%;13-18岁62%;霍奇金淋巴瘤,33%;急性淋巴母细胞/淋巴细胞白血病,40%;骨肉瘤,10%;其他17%)。身体功能与疲劳呈负相关:T1 (r = -0.64;p .001)和T2 (r = -0.63;p措施)。一种代谢物(吲哚-3-乳酸)区分了低疲劳和高疲劳。5种代谢物(4-羟基苯甲酸、间香豆酸、肌醇、色氨酸和酪氨酸)在生理功能高低之间有显著差异。结论:这些发现证实了先前的研究,表明代谢物,特别是氨基酸,与疲劳和身体功能显著相关。所有重要的代谢物都与肠道微生物群有关。身体机能与疲劳呈负相关,为疲劳管理提供了另一种潜在的干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolomic Associations With Fatigue and Physical Function in Children With Cancer: A Pilot Study.

Background: Fatigue is a frequently reported symptom in children undergoing cancer treatment. Prior research shows an inverse relationship between fatigue and physical activity. Less is known about fatigue's relationship with physical function or the underlying biological mechanisms of fatigue. This study explored associations among fatigue, physical function, and associated metabolites. Methods: Children (7-18 years) provided serum samples and self-reports of fatigue and lower extremity physical function (mobility) using Pediatric Patient-Reported Outcomes Measurement Information System (PROMIS) surveys at two timepoints during cancer therapy. PROMIS scores were categorized as high/low per established cut points (high fatigue T >47.5; high physical function T >51.5). High-resolution liquid chromatography-mass spectrometry extracted 29 metabolites hypothesized a priori to be associated with fatigue or physical function. Descriptive statistics summarized PROMIS scores, and linear mixed effect models estimated metabolite associations adjusting for age, gender and steroid use. Results: Forty children participated (female, 53%; 7-12 years, 38%; 13-18 years 62%; Hodgkins Lymphoma, 33%; Acute Lymphoblastic/Lymphocytic Leukemia, 40%; Osteosarcoma, 10%; Other, 17%). Physical function and fatigue were inversely related: T1 (r = -0.64; p < .001) and T2 (r = -0.63; p < .001). One metabolite (indole-3-latic acid) differentiated between low and high fatigue. Five metabolites differentiated significantly between low and high physical function (4-Hydroxybenzoic acid, m-Coumaric acid, myoinositol, tryptophan, and tyrosine). Conclusions:These findings substantiate prior studies showing metabolites, particularly amino acids, significantly associated with fatigue and physical function. All significant metabolites were associated with the gut microbiome. Physical function was inversely corelated with fatigue providing another potential intervention for fatigue management.

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