Department of Emergency Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Shock. 2019 May;51(5):580-584. doi: 10.1097/SHK.0000000000001208.
Mitochondrial dysfunction has been implicated as a key cellular event leading to organ dysfunction in sepsis. Our objective is to measure changes in mitochondrial bioenergetics in subjects with early presentation of sepsis to provide insight into the incompletely understood pathophysiology of the dysregulated host response in sepsis.
Prospective observational study.
Single site tertiary academic emergency department.
We enrolled a total of 48 subjects in the study, 10 with sepsis or septic shock, 10 with infection without sepsis, 14 older and 14 younger healthy controls.
Peripheral blood mononuclear cells were measured with high-resolution respirometry (OROBOROS O2K).
The median age in patients with sepsis, infection only, older control and younger controls were 63, 34, 61, and 29 years old, respectively. In the Sepsis group, the median 1st 24-h SOFA score was 8, and the initial median lactate was 4.2 mmol/dL, compared with 1.1 in the Infection Group. The 30-day mortality of the sepsis/septic shock group was 50%, with a median length of stay of 7-days. The Sepsis Group had significantly lower routine and Max respiration when compared with the other groups as well as uncoupled Complex I respiration. There was also a significant decrease in ATP-linked respiration along with the Spare Reserve Capacity in the Sepsis Group when compared with the other group. There were no age-related differences in respiration between the Older and Younger control group.
Bedside measurement of mitochondrial respiration can be minimally invasive and performed in a timely manner. Mitochondrial dysfunction, detected by decreased oxygen consumption utilized for energy production and depleted cellular bioenergetics reserve.
线粒体功能障碍被认为是导致脓毒症器官功能障碍的关键细胞事件。我们的目的是测量早期脓毒症患者中线粒体生物能的变化,以深入了解脓毒症中宿主反应失调的病理生理学尚不完全清楚的情况。
前瞻性观察性研究。
单一地点的三级学术急诊病房。
我们总共招募了 48 名受试者,其中 10 名患有脓毒症或感染性休克,10 名患有感染但无脓毒症,14 名年龄较大的健康对照者和 14 名年龄较小的健康对照者。
使用高分辨率呼吸仪(OROBOROS O2K)测量外周血单核细胞。
脓毒症患者、仅有感染患者、年龄较大的健康对照组和年龄较小的健康对照组的中位年龄分别为 63、34、61 和 29 岁。在脓毒症组中,第 1 个 24 小时 SOFA 评分中位数为 8,初始中位乳酸值为 4.2mmol/dL,而感染组为 1.1mmol/dL。脓毒症/感染性休克组的 30 天死亡率为 50%,中位住院时间为 7 天。与其他组相比,脓毒症组的常规和最大呼吸明显降低,以及解偶联的复合物 I 呼吸。与其他组相比,脓毒症组的 ATP 连接呼吸以及备用储备容量也明显减少。在年龄较大的健康对照组和年龄较小的健康对照组之间,呼吸没有与年龄相关的差异。
床边测量线粒体呼吸可以微创进行,并且可以及时进行。线粒体功能障碍可通过减少用于能量产生的耗氧量和耗尽细胞生物能储备来检测。