治疗后尿液代谢物作为慢性疼痛的指标:一项实用临床试验的二级数据分析。

Dahee Wi, Diane M Flynn, Nathan Tintle, Jeffrey C Ransom, Honor M McQuinn, Tyler J Snow, Sotaro Shimada, Nicholas Ieronimakis, Ardith Z Doorenbos
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引用次数: 0

摘要

生物标志物可以通过客观地了解慢性疼痛的多维性来补充患者报告的结果。尿代谢物疼痛指标(UMPI)是四种尿液代谢物的组合,先前已证明与疼痛相关症状具有横断面相关性;然而,目前尚不清楚这些关联是否随时间而持续。本研究评估了干预后UMPI及其个体代谢物是否仍与慢性疼痛结局相关,这将支持其作为监测生物标志物的潜力。对一项实用临床试验的二次分析,148名患有慢性疼痛的现役军人提供了尿液样本,并在基线和6周随访后完成了11项自我报告的结果测量,无论是补充和综合健康还是标准康复护理疼痛干预。使用线性回归和混合模型检验相关性。干预后UMPI仍与身体功能和整体疼痛影响显著相关。乙基丙二酸与疲劳、愤怒和身体机能有关。值得注意的是,甲基丙二酸盐虽然在基线时不显著,但与干预后疼痛的相关性最强,包括与身体功能和疼痛影响的显著相关性。犬尿酸与睡眠相关障碍有关。焦谷氨酸调节后无显著相关性。代谢物和症状相关性在时间点之间没有统计学上的显著差异,表明这些相关性在短期内保持一致。UMPI可以作为一种可靠的、无创的生物标志物,用于跟踪慢性疼痛负担,特别是身体结果。研究结果支持将UMPI纳入生物学知情的慢性疼痛评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-Treatment Urine Metabolites as Indicators of Chronic Pain: A Secondary Data Analysis of a Pragmatic Clinical Trial.

Biomarkers may complement patient-reported outcomes by providing objective insight into the multidimensional nature of chronic pain. The urine metabolite pain indicator (UMPI), a composite of four urine metabolites, has previously demonstrated cross-sectional associations with pain-related symptoms; however, it is unclear whether these associations are consistent over time. This study evaluated whether the UMPI and its individual metabolites remain associated with chronic pain outcomes following intervention, which would support its potential as a monitoring biomarker. A secondary analysis of a pragmatic clinical trial, where 148 active-duty service members with chronic pain provided urine samples and completed 11 self-reported outcome measures at baseline and 6-week follow-up after either a complementary and integrative health or a standard rehabilitative care pain intervention. Associations were examined using linear regression and mixed models. The UMPI remained significantly associated with physical function and overall pain impact post-intervention. Ethylmalonic acid showed associations with fatigue, anger, and physical function. Notably, methylmalonate, while not significant at baseline, had the most robust association with pain post-intervention, including significant correlations with both physical function and pain impact. Kynurenic acid was associated with sleep-related impairment. Pyroglutamic acid showed no significant adjusted associations. No statistically significant differences in metabolite and symptom correlations were found between time points, suggesting that these associations remained consistent over the short term. The UMPI may serve as a reliable, noninvasive index biomarker for tracking chronic pain burden, particularly physical outcomes. Findings support integrating the UMPI into biologically informed chronic pain assessment.

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