S-100β in chronic subdural haematoma: Prospective cohort study

被引:3
作者
Thomas, Piers A. W. [1 ,2 ]
Moffatt, Claire E. [3 ]
Rudd, Donna [4 ]
Marshman, Laurence A. G. [1 ,2 ]
机构
[1] Townsville Hosp, Dept Neurosurg, Townsville, Qld 4810, Australia
[2] James Cook Univ, Sch Med & Dent, Townsville, Qld 4810, Australia
[3] James Cook Univ, Dept Psychol, Townsville, Qld 4810, Australia
[4] James Cook Univ, Dept Physiol, Townsville, Qld 4810, Australia
关键词
Chronic; Subdural haematoma; S-100; beta; Traumatic brain injury; RISK-FACTORS; S100B; SERUM;
D O I
10.1016/j.jocn.2019.05.058
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic subdural haematoma (CSDH) is invariably classified as 'neurotrauma'. However, whilst a history of trauma/fall is frequent, it is usually distant, mild or even absent. Serum S-100 beta > 1.38 mu g/L is associated with a 100% specificity for mortality/poor outcome acutely after moderate-severe neurotrauma. Serum S-100 beta > 0.10 mu g/L is used to screen mild neurotrauma cases for emergent neuro-imaging. Serum S-100 in controls is 0.057 mu g/L. S-100 beta in serum or CSDH fluid (CSDHf) has not been studied. No normal 'subdural fluid' exists to compare CSDHf. We measured serum and CSDHf S-100 beta at surgical drainage in a novel prospective single-centre cohort. Of n = 86/86 (100%, M65, age 73 +/- 13 yrs), n = 66 (76%) reported mild trauma/fall 31 +/- 23 days previously. N = 54 (63%) presented with good clinical Markwalder Grade (MG: 0-1). Paired serum and CSDHf S-100 beta samples were obtained in n = 45. CSDHf S-100 beta (n = 80) was elevated (0.9 +/- 0.6 mu g/L), was significantly higher than serum S-100 beta (n = 51) (0.33 +/- 0.05 mu g/L, P = 0.002), and was significantly correlated with midline-shift (r = 0.43, P = 0.005) and CSDH volume (r = 0.225, P = 0.046). CSDHf S-100 beta was not significantly associated with any demographic factor, co-morbidity or outcome measure. Conclusions: Despite expectations, S-100 beta was elevated in serum CSDH, but was significantly higher in CSDHf. Indeed, CSDHf S-100 beta approached serum levels associated with a poor prognosis after acute-neurotrauma. However, CSDHf S-100 beta did not represent a biomarker for trauma nor functional outcome. Whilst the non-traumatic source for on-going S-100 beta release could not be determined, prolonged compression of an atrophic brain, subsequent CSF leakage, or 'subdural-space' meningeal disruption/proliferation, represent theoretical possibilities. Elevated S-100 beta may therefore not be specific for mild-moderate-severe acute neurotrauma. Alternative non-traumatic intra-cranial mechanisms evidently also exist. Crown Copyright (C) 2019 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:145 / 150
页数:6
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