Tzira Despoina, Prezerakou Anargyroula, Papadatos Ioannis, Vintila Artemis, Bartzeliotou Anastasia, Apostolakou Filia, Papassotiriou Ioannis, Papaevangelou Vassiliki
Pediatric Intensive Care Unit, "P. & A. Kyriakou" Children's Hospital, Athens, Greece.
Department of Pediatrics, Thriasio General Hospital, Athens, Greece.
SAGE Open Med. 2018 Sep 25;6:2050312118802452. doi: 10.1177/2050312118802452. eCollection 2018.
Measurement of salivary biomarkers can provide important information regarding hypothalamic-pituitary-adrenal axis activity both under normal conditions as well as in response to psychological or physical stress. Our aim was to correlate salivary stress markers, such as cortisol, α-amylase and immunoglobulin A, with the Pediatric Risk Index Score of Mortality, underlying disease (pathologic, trauma and postoperative), need for mechanical ventilation/sedation and time lag between onset of illness and admission in children admitted in the pediatric intensive care unit.
We enrolled 79 pediatric intensive care unit patients (2-14 years) over a 2-year period, which satisfy the including criteria, but finally salivary biomarkers were evaluated in 65 patients. Saliva samples were collected within 24 h of admission at 8 a.m., 2 p.m. and 8 p.m. to examine potential disruption of circadian rhythm.
Overall, the salivary biomarkers were increased; specifically, median values were (a) cortisol at 8 a.m.: 50.04 nmol/L, 2 p.m.: 30.69 nmol/L and 8 p.m.: 247.12 nmol/L; (b) α-amylase: at 8 a.m.: 22.567 U/L; 2 p.m.: 22.702 U/L and 8 p.m.: 21.484 U/L and (c) IgA at 8 a.m.: 95.10 mg/dL, 2 p.m.: 88.55 mg/dL and 8 p.m.: 80.80 mg/dL. Significantly higher levels were demonstrated in children younger than 6 years and those with Pediatric Risk Index Score of Mortality ⩾8 upon admission. Disturbances in circadian rhythm were observed. Cortisol circadian rhythm disturbance was observed only in children with Pediatric Risk Index Score of Mortality score ⩾8 upon admission while maintaining normal α-amylase circadian rhythm, which was associated with less than 3 days hospitalization in pediatric intensive care unit. No daily variance in IgA was observed.
Salivary biomarkers may serve, in critically ill children, as a sensitive, non-invasive method, important for the early recognition of those at high risk and guiding intervention, before clinical deterioration, promoting the quality of health care in pediatric population.
测量唾液生物标志物可提供有关下丘脑 - 垂体 - 肾上腺轴在正常情况下以及对心理或身体应激反应时活动的重要信息。我们的目的是将唾液应激标志物,如皮质醇、α - 淀粉酶和免疫球蛋白A,与儿科重症监护病房收治儿童的儿科死亡风险指数评分、基础疾病(病理、创伤和术后)、机械通气/镇静需求以及发病至入院的时间间隔进行关联。
我们在两年期间纳入了79名儿科重症监护病房患者(2 - 14岁),这些患者符合纳入标准,但最终对65名患者进行了唾液生物标志物评估。在入院后24小时内的上午8点、下午2点和晚上8点采集唾液样本,以检查昼夜节律的潜在紊乱。
总体而言,唾液生物标志物升高;具体而言,中位数为:(a)上午8点皮质醇:50.04 nmol/L,下午2点:30.69 nmol/L,晚上8点:247.12 nmol/L;(b)α - 淀粉酶:上午8点:22.567 U/L,下午2点:22.702 U/L,晚上8点:21.484 U/L;(c)免疫球蛋白A上午8点:95.10 mg/dL,下午2点:88.55 mg/dL,晚上8点:80.80 mg/dL。6岁以下儿童以及入院时儿科死亡风险指数评分≥8的儿童中,这些标志物水平显著更高。观察到昼夜节律紊乱。仅在入院时儿科死亡风险指数评分≥8的儿童中观察到皮质醇昼夜节律紊乱,而α - 淀粉酶昼夜节律保持正常,这与在儿科重症监护病房住院少于3天相关。未观察到免疫球蛋白A的每日变化。
在危重症儿童中,唾液生物标志物可作为一种敏感、非侵入性的方法,对于在临床恶化前早期识别高危儿童并指导干预非常重要,有助于提高儿科人群的医疗保健质量。