Prediction of the neurological outcome with intrathecal high mobility group box 1 and S100B in cardiac arrest victims: A pilot study

被引:41
作者
Oda, Yasutaka [1 ]
Tsuruta, Ryosuke [1 ]
Fujita, Motoki [2 ]
Kaneda, Kotaro [1 ]
Kawamura, Yoshikatsu [1 ]
Izumi, Tomonori [2 ]
Kasaoka, Shunji [2 ]
Maruyama, Ikuro [3 ]
Maekawa, Tsuyoshi [1 ,2 ]
机构
[1] Yamaguchi Univ, Adv Med Emergency & Crit Care Ctr, Ube, Yamaguchi 7558505, Japan
[2] Yamaguchi Univ, Grad Sch Med, Dept Stress & Bioresponse Med, Ube, Yamaguchi 7558505, Japan
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Lab & Vasc Med, Kagoshima 8908544, Japan
关键词
Ischemia reperfusion injury; Cardiopulmonary arrest; Prognosis; Cerebrospinal fluid; Biomarker; CHROMATIN PROTEIN HMGB1; NEURON-SPECIFIC ENOLASE; IMMUNE-RESPONSES; BRAIN-DAMAGE; ISCHEMIA; RELEASE; S-100; RESUSCITATION; ACTIVATION; MARKERS;
D O I
10.1016/j.resuscitation.2012.01.030
中图分类号
R4 [临床医学];
学科分类号
100218 [急诊医学];
摘要
Objectives: To investigate whether high mobility group box 1 (HMGB1) and S100B in cerebrospinal fluid (CSF) and the serum predict the neurological outcome in patients resuscitated from out-of-hospital cardiac arrest (OHCA). Materials and methods: This study was designed as a prospective observational study. Twenty-five patients, who received standard cardiopulmonary resuscitation and post-resuscitation intensive care, were enrolled in this study. The patients were divided into two groups according to Glasgow-Pittsburgh Cerebral Performance categories (CPCs) at 6 months after return of spontaneous circulation (ROSC), Group G (n = 7, CPC 1 or 2) and Group P (n = 18, CPC = 3). Their blood samples were taken at 6, 24, and 48 h after ROSC. The patients, whose CSF was sampled at 48 h, were also divided into either sub-Group G (n = 6) or sub-Group P (n = 8) at 6 months after ROSC. Results: HMGB1 and S100B in CSF in sub-Group P were significantly higher than those in sub-Group G (HMGB1, <1.0 vs. 12.4 ng/ml, P = 0.009; S100B, 2.68 vs. 84.2 ng/ml, P = 0.007, respectively). HMGB1 in CSF was strongly correlated with S100B (sigma = 0.81, P = 0.001). HMGB1 was elevated in serum at 6 h and normalized within 48 h after ROSC without any significant differences between the two groups. Serum S100B in Group P was significantly higher than that in Group G at each time point. Conclusions: The significant elevations of HMGB1 and S100B in CSF, and S100B in serum are associated with the neurologically poor outcome in OHCA patients. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1006 / 1012
页数:7
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