Department of Anesthesiology and Critical Care Medicine, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA.
Proteomics Core, The Children's Hospital of Philadelphia, Philadelphia, PA.
Crit Care Med. 2021 Jul 1;49(7):1149-1158. doi: 10.1097/CCM.0000000000004923.
Circulating nucleosomes and their component histones have been implicated as pathogenic in sepsis and acute respiratory distress syndrome in adults. However, their role in pediatric acute respiratory distress syndrome is unknown.
We performed a prospective cohort study in children with acute respiratory distress syndrome, with plasma collection within 24 hours of acute respiratory distress syndrome onset. We associated nucleosome levels with severity of acute respiratory distress syndrome and with nonpulmonary organ failures and tested for association of nucleosomes with PICU mortality and ventilator-free days at 28 days in univariate and multivariable analyses. We also performed proteomics of DNA-bound plasma proteins in a matched case-control study of septic children with and without acute respiratory distress syndrome in order to identify specific histone proteins elevated in acute respiratory distress syndrome.
Large academic tertiary-care PICU.
Intubated children meeting Berlin criteria for acute respiratory distress syndrome.
None.
We enrolled 333 children with acute respiratory distress syndrome, with 69 nonsurvivors (21%). Plasma nucleosomes were correlated with acute respiratory distress syndrome severity and with the number of nonpulmonary organ failures at acute respiratory distress syndrome onset. Nucleosomes were higher (p < 0.001) in nonsurvivors (0.40 [interquartile range, 0.20-0.71] arbitrary units) relative to survivors (0.10 [interquartile range, 0.04-0.25] arbitrary units). Nucleosomes were associated with PICU mortality in multivariable analysis (adjusted odds ratio 1.84 per 1 sd increase; 95% CI, 1.38-2.45; p < 0.001). Nucleosomes were also associated with a lower probability of being extubated alive by day 28 after multivariable adjustment (adjusted subdistribution hazard ratio, 0.74; 95% CI, 0.63-0.88; p = 0.001). Proteomic analysis demonstrated higher levels of the core nucleosome histones H2A, H2B, H3, and H4 in septic children with acute respiratory distress syndrome, relative to septic children without acute respiratory distress syndrome.
Plasma nucleosomes are associated with acute respiratory distress syndrome severity, nonpulmonary organ failures, and worse outcomes in pediatric acute respiratory distress syndrome.
循环核小体及其组成组蛋白已被认为在成人脓毒症和急性呼吸窘迫综合征中具有致病性。然而,它们在儿科急性呼吸窘迫综合征中的作用尚不清楚。
我们对急性呼吸窘迫综合征患儿进行了前瞻性队列研究,在急性呼吸窘迫综合征发病后 24 小时内采集血浆。我们将核小体水平与急性呼吸窘迫综合征的严重程度以及非肺部器官衰竭相关联,并在单变量和多变量分析中检验核小体与儿科重症监护病房死亡率和 28 天无呼吸机天数的相关性。我们还对患有脓毒症和无急性呼吸窘迫综合征的儿童进行了配对病例对照研究,以进行 DNA 结合血浆蛋白的蛋白质组学分析,以鉴定在急性呼吸窘迫综合征中升高的特定组蛋白。
大型学术性三级儿科重症监护病房。
符合柏林急性呼吸窘迫综合征标准的气管插管患儿。
无。
我们纳入了 333 例急性呼吸窘迫综合征患儿,其中 69 例死亡(21%)。血浆核小体与急性呼吸窘迫综合征的严重程度以及急性呼吸窘迫综合征发病时非肺部器官衰竭的数量相关。与存活者(0.10 [四分位距,0.04-0.25] 任意单位)相比,死亡者(0.40 [四分位距,0.20-0.71] 任意单位)的核小体水平更高(p < 0.001)。在多变量分析中,核小体与儿科重症监护病房死亡率相关(调整后的优势比为每增加 1 个标准差 1.84;95%置信区间,1.38-2.45;p < 0.001)。在多变量调整后,核小体也与第 28 天活着拔管的可能性较低相关(调整后的亚分布风险比,0.74;95%置信区间,0.63-0.88;p = 0.001)。蛋白质组学分析表明,与无急性呼吸窘迫综合征的脓毒症患儿相比,患有急性呼吸窘迫综合征的脓毒症患儿的核心核小体组蛋白 H2A、H2B、H3 和 H4 水平更高。
血浆核小体与儿科急性呼吸窘迫综合征的严重程度、非肺部器官衰竭和预后较差相关。