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A randomized controlled pilot study of inflammatory gene expression in response to a stress management intervention for stem cell transplant caregivers
被引:16
|作者:
Laudenslager, Mark L.
[1
]
Simoneau, Teresa L.
[1
,2
]
Philips, Sam
[1
]
Benitez, Patrick
[1
]
Natvig, Crystal
[1
]
Cole, Steve
[3
]
机构:
[1] Univ Colorado Denver, Dept Psychiat, Anschutz Med Campus,12700 E 17th Ave, Aurora, CO 80045 USA
[2] Presbyterian St Lukes Med Ctr, Denver, CO 80218 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
关键词:
Social genomics;
Allogeneic hematopoietic stem cell transplant;
Caregiver;
Stress;
Inflammatory pathways;
Peripheral blood lymphocytes;
BREAST-CANCER SURVIVORS;
NF-KAPPA-B;
PSYCHOSOCIAL INTERVENTION;
TRANSCRIPTOME DYNAMICS;
OLDER-ADULTS;
DISTRESS;
TRIAL;
CARE;
D O I:
10.1007/s10865-015-9709-3
中图分类号:
B849 [应用心理学];
学科分类号:
040203 ;
摘要:
Few studies have addressed whether stress-associated physiological changes in caregivers are reversible by psychological interventions mitigating distress. We report on pro-inflammatory, sympathetic, and oxidative stress gene expression in response to stress management for caregivers of allogeneic hematopoietic stem cell transplant (Allo-HSCT) patients. Following randomization by permuted block to either treatment as usual (TAU, n = 11) or a stress management intervention (PsychoEducation, Paced Respiration, and Relaxation, PEPRR, n = 13), twenty-four caregivers were selected at the conclusion of a larger trial of 149 caregivers. PEPRR was provided one-on-one beginning around transplant. Genome-wide transcriptional profiling was conducted on peripheral blood mononuclear cells collected prior to randomization and on completion of PEPRR 3 months post-transplant. Bioinformatics analysis of differentially expressed genes indicated reduced activity of transcription control pathways associated with inflammation (NF-kappa B), sympathetic nervous system (CREB), and oxidative stress (NRF2) in caregivers receiving PEPRR compared to TAU aligning with reductions in stress, depression, and anxiety. This suggests that PEPRR may alter transcriptomic effects reported for distressed individuals.
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页码:346 / 354
页数:9
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