首页|模拟睡眠对脓毒症患者生物钟基因Bmal1、Per2表达和免疫功能、短期临床转归的影响

模拟睡眠对脓毒症患者生物钟基因Bmal1、Per2表达和免疫功能、短期临床转归的影响

扫码查看
[目的]探讨模拟睡眠对脓毒症患者生物钟基因脑-骨骼肌ARNT样基因1(Bmal1)、周期基因2(Per2)表达和免疫功能、短期临床转归的影响.[方法]80例脓毒症患者,随机分为对照组(常规对症治疗)和观察组(常规对症治疗联合模拟睡眠干预),每组40例.比较两组患者治疗前及治疗7 d后炎症因子[白细胞介素-6(IL-6)、IL-8、肿瘤坏死因子-α(TNF-α)和C反应蛋白(CRP)]、Bmal1和Per2表达水平、免疫功能、序贯器官衰竭评估评分(SOFA)、急性生理学与慢性健康状况评分Ⅱ(APACHE Ⅱ)及机械通气时间、EICU住院时间和28 d病死率.[结果]两组治疗7 d后IL-6、IL-8、TNF-α、CRP均较治疗前降低(P<0.05),且观察组各指标低于对照组(P<0.05);两组Bmal1、Per2 mRNA表达较治疗前升高(P<0.05),且观察组上述指标高于对照组(P<0.05);两组CD4+、CD4+/CD8+较治疗前升高(P<0.05),CD8+较治疗前降低(P<0.05),且观察组CD4+、CD4+/CD8+高于对照组(P<0.05),CD8+低于对照组(P<0.05);两组SOFA评分和APACHE Ⅱ评分较治疗前降低(P<0.05),且观察组低于对照组(P<0.05).观察组机械通气时间、EICU住院时间短于对照组(P<0.05);观察组28 d病死率低于对照组,但差异无统计学意义(P>0.05).[结论]模拟睡眠能改善脓毒症患者生物钟基因Bmal1、Per2节律异常情况,增强免疫功能,减轻患者全身炎症反应,改善短期临床转归.
Effect of Simulated Sleep on the Expression of Circadian Clock Genes Bmal1,Per2,Immune Func-tion,and Short-term Clinical Outcomes in Patients with Sepsis
[Objective]To explore the effect of simulated sleep on the expression of circadian clock genes Brain and Muscle ARNT-Like 1(Bmal1)and Period 2(Per2),immune function,and short-term clinical outcomes in patients with sepsis.[Methods]Eighty sepsis patients were randomly divided into the control group(with stand-ard symptomatic treatment)and the observation group(with standard symptomatic treatment combined with sim-ulated sleep intervention),with 40 patients in each group.The study compared the levels of inflammatory factors[interleukin-6(IL-6),IL-8,tumor necrosis factor-alpha(TNF-α),and C-Reactive Protein(CRP)],Bmal1 and Per2 expression,immune function,Sequential Organ Failure Assessment(SOFA)score,Acute Physiology and Chronic Health Evaluation Ⅱ(APACHE Ⅱ)score,mechanical ventilation duration,ICU stay duration,and 28-day mortality rate between the two groups before treatment and 7 days after treatment.[Results]After 7 days of treatment,both groups showed reduced levels of IL-6,IL-8,TNF-α,and CRP compared to before treatment(P<0.05),with the observation group presenting even lower levels than the control group(P<0.05).Both groups exhibited increased expression of Bmal1 and Per2 mRNA(P<0.05)after 7 days of treatment compared to before treatment,with higher expression of Bmal1 and Per2 in the observation group than the control group(P<0.05).The levels of CD4+,CD4+/CD8+increased,while CD8+decreased in both groups compared to before treatment(P<0.05),and the observation group showed higher CD4+,CD4+/CD8+and lower CD8+than the control group(P<0.05).Both groups had reduced SOFA and APACHE Ⅱ scores compared to before treatment(P<0.05),with lower scores in the observation group(P<0.05).The observation group had shorter mechanical ven-tilation and ICU stay durations(P<0.05),but the difference in 28-day mortality rate was not statistically signifi-cant between the two groups(P>0.05).[Conclusion]Simulated sleep can improve the dysregulation of circadian clock genes Bmal1 and Per2 in sepsis patients,enhance immune function,reduce systemic inflammatory response,and improve short-term clinical outcomes.

SepsisBiological Clocks/GEGenesImmunologic Tests

李铮、居培红、华玮、张雯艳、黄侃、石斌

展开 >

上海杨浦区中心医院(同济大学附属杨浦医院)急诊医学科,上海 200090

脓毒症 生物钟/遗传学 基因 免疫学试验

上海市杨浦区中心医院院级立项项目(2020)

Se1202003

2024

医学临床研究
湖南省医学会

医学临床研究

影响因子:0.595
ISSN:1671-7171
年,卷(期):2024.41(5)