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复原力干预改善青少年和年轻成人造血干细胞移植受者中与压力相关的基因表达。

Resilience Intervention Improves Stress-Related Gene Expression in Adolescent and Young Adult HCT Recipients.

作者信息

Taylor Mallory R, Cole Steve W, Bradford Miranda C, Zhou Chuan, Fladeboe Kaitlyn M, Knight Jennifer M, Baker K Scott, Yi-Frazier Joyce P, Rosenberg Abby R

机构信息

Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington; Ben Towne Center for Childhood Cancer Research, Seattle Children's Research Institute, Seattle, Washington.

Departments of Psychiatry & Biobehavioral Sciences and Medicine, UCLA School of Medicine, Los Angeles, California.

出版信息

Transplant Cell Ther. 2024 Dec;30(12):1209.e1-1209.e7. doi: 10.1016/j.jtct.2024.09.014. Epub 2024 Sep 19.

Abstract

Overactivation of the stress response can influence cancer outcomes through immune-related pathways. Adolescents and young adults (AYAs) undergoing hematopoietic cell transplantation (HCT) are at risk for poor outcomes, yet there are limited behavioral interventions and no psychosocial biomarker data for this population. The Conserved Transcriptional Response to Adversity (CTRA) is an inflammation-related pattern observed in conditions of heightened stress and is associated with HCT outcomes. The objective of the current study was to explore the CTRA gene regulatory impact of Promoting Resilience in Stress Management (PRISM) intervention among AYAs receiving HCT. We hypothesized that patients who received the intervention would have favorable gene expression signatures compared to those in the control arm. This was an ancillary study within a randomized trial testing the PRISM intervention on psychosocial outcomes among AYAs aged 12 to 24 years receiving HCT (NCT03640325). CTRA was quantified through genome-wide transcriptional profiles obtained from whole blood collected at baseline, 1-, and 3-month post-HCT. Group differences in CTRA gene expression were estimated using mixed-effect linear models. There were no baseline group differences in CTRA expression, but PRISM participants showed a greater decline in CTRA at 1 month compared to controls (β -0.301 ± SE 0.114, P = .016), even when controlling for demographic (Group × Time interaction: F(2, 18) = 7.41, P = .004; β -0.386 ± 0.127, P = .007) and clinical covariates (Group × Time interaction: F(2, 20) = 7.03, P = .005; β -0.480 ± 0.144, P = .003). These differences were not detectable at 3 months (β -0.147 ± SE 0.120, P = .235). There was a change in stress-related gene expression among AYAs randomized to a psychosocial intervention. The stress-inflammation axis may be a targetable pathway in the AYA HCT population.

摘要

应激反应的过度激活可通过免疫相关途径影响癌症预后。接受造血细胞移植(HCT)的青少年和青年(AYA)面临预后不良的风险,但针对该人群的行为干预有限,且尚无心理社会生物标志物数据。保守的逆境转录反应(CTRA)是在压力增强的情况下观察到的一种与炎症相关的模式,与HCT预后相关。本研究的目的是探讨促进压力管理复原力(PRISM)干预对接受HCT的AYA的CTRA基因调控的影响。我们假设接受干预的患者与对照组相比,将具有良好的基因表达特征。这是一项随机试验中的辅助研究,该试验测试了PRISM干预对12至24岁接受HCT的AYA心理社会结局的影响(NCT03640325)。通过从HCT基线、1个月和3个月时采集的全血中获得的全基因组转录谱对CTRA进行量化。使用混合效应线性模型估计CTRA基因表达的组间差异。CTRA表达在基线时无组间差异,但与对照组相比,PRISM参与者在1个月时CTRA下降幅度更大(β -0.301 ± 标准误0.114,P = 0.016),即使在控制了人口统计学因素(组×时间交互作用:F(2, 18) = 7.41,P = 0.004;β -0.386 ± 0.127,P = 0.007)和临床协变量后也是如此(组×时间交互作用:F(2, 20) = 7.03,P = 0.005;β -0.480 ± 0.144,P = 0.003)。这些差异在3个月时未被检测到(β -0.147 ± 标准误0.120,P = 0.235)。随机接受心理社会干预的AYA中,与压力相关的基因表达发生了变化。应激-炎症轴可能是AYA-HCT人群中一个可靶向的途径。

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