痴呆症患者的护理伙伴睡眠不佳与炎症基因表达:行为睡眠干预试点试验

Yeonsu Song, Jennifer L Martin, Susan M McCurry, M. Kelly, Edmond Teng, Cathy A. Alessi, Michael R Irwin, Steve Cole
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引用次数: 0

摘要

睡眠不足与炎症增加有关,从而增加了慢性疾病和死亡的风险。然而,行为睡眠干预对家庭护理伙伴(CP)上游炎症系统的影响尚不清楚。本研究探讨了行为睡眠干预计划对炎症基因表达的作用。 这是一项随机对照试验的一部分,该试验针对有睡眠问题的痴呆症患者护理伴侣进行睡眠干预。30对夫妇被随机分配到睡眠干预组或对照组。CP的睡眠结果通过一周的动图和睡眠日记以及匹兹堡睡眠质量指数(PSQI)进行评估。其他信息包括 CP 人口统计数据、体重指数 (BMI) 和护理任务强度。所有结果均在基线、治疗后和 3 个月随访时收集。 从基线到治疗后或 3 个月随访期间,两组的基因表达均未出现任何明显的差异变化。炎症基因表达的减少与更多的良好睡眠(即夜间入睡或保持睡眠)显著相关。在控制了组别(干预组/对照组)、时间点(基线、治疗后和 3 个月的随访)和 CP 特征(如年龄、种族)后,这一发现仍具有重要意义。 虽然改善睡眠与炎症基因表达的减少有关,但这项研究并未证明行为睡眠干预比对照组有任何益处,这很可能是由于样本较少。需要进行样本量更大的研究,以检验与痴呆症患者CP炎症生物学相关的睡眠紊乱的具体方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Poor Sleep and Inflammatory Gene Expression Among Care Partners of Persons Living with Dementia: A Pilot Trial of a Behavioral Sleep Intervention
Poor sleep is associated with increased inflammation, thereby increasing the risk of chronic diseases and mortality. However, the effects of behavioral sleep interventions on the upstream inflammatory system are unknown among family care partners (CP). The present study explored the role of a behavioral sleep intervention program on inflammatory gene expression. This was part of a randomized controlled trial of a sleep intervention for dementia care dyads with sleep problems. Thirty dyads were randomized to sleep intervention or control groups. Sleep outcomes for CP were assessed with one week of actigraphy and sleep diary, and the Pittsburgh Sleep Quality Index (PSQI). Other information included CP demographics, body mass index (BMI), and intensity of caregiving tasks. All outcomes were collected at baseline, post-treatment, and 3-month follow-up. Neither group showed any significant differential changes in gene expression from baseline to post-treatment or 3-month follow-up. A decrease in inflammatory gene expression was significantly associated with more nights of good sleep (i.e., nights without trouble falling or staying asleep at night). This finding remained significant after controlling for group (intervention/control), timepoint (baseline, post-treatment, and 3-month follow-up), and CP characteristics (e.g., age, ethnicity). Although better sleep was associated with decreased inflammatory gene expression, this study did not demonstrate any benefits of a behavioral sleep intervention over control, most likely due to a small sample. Studies with larger sample sizes are needed to test the specific aspects of disturbed sleep that relate to inflammatory biology among CP of persons living with dementia.
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