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卒中后血清神经丝重链的超急性检测:一过性标志。

Hyperacute detection of neurofilament heavy chain in serum following stroke: a transient sign.

机构信息

Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Ismaninger Str 22, 81675 Munich, Germany.

出版信息

Neurochem Res. 2011 Dec;36(12):2287-91. doi: 10.1007/s11064-011-0553-8. Epub 2011 Jul 27.

DOI:10.1007/s11064-011-0553-8
PMID:21792676
Abstract

Serological biomarkers which enable quick and reliable diagnosis or measurement of the extent of irreversible brain injury early in the course of stroke are eagerly awaited. Neurofilaments (Nf) are a group of proteins integrated into the scaffolding of the neuronal and axonal cytoskeleton and an established biomarker of neuro-axonal damage. The Nf heavy chain (NfH(SMI35)) was assessed together with brain-specific astroglial proteins GFAP and S100B in hyperacute stroke (6 and 24 h from symptom onset) and daily for up to 6 days. Twenty-two patients with suspected stroke (median NIHSS 8) were recruited in a prospective observational study. Evidence for an ischaemic or haemorrhagic lesion on neuroimaging was found in 18 (ischaemia n = 16, intracerebral haemorrhage n = 2). Serum NfH(SMI35) levels became detectable within 24 h post-stroke (P < 0.0001) and elevated levels persisted over the study course. While GFAP was not detectable during the entire course, S100B levels peaked at the end of the observation period. The data indicate that significant in vivo information on the pathophysiology of stroke may be obtained by the determination of NfH(SMI35). Further studies are required to evaluate whether NfH(SMI35) in hyperacute stroke reflects the extent of focal ischaemic injury seen on neuroimaging or is a consequence of more diffuse neuro-axonal damage.

摘要

人们急切地期待能够快速、可靠地诊断或测量中风病程早期的不可逆转脑损伤程度的血清生物标志物。神经丝(Nf)是一组整合到神经元和轴突细胞骨架支架中的蛋白质,是神经轴突损伤的既定生物标志物。在超急性期(发病后 6 小时和 24 小时)以及每天最多 6 天的时间内,评估了神经丝重链(NfH(SMI35))与脑特异性星形胶质蛋白 GFAP 和 S100B 的关系。在一项前瞻性观察研究中,共招募了 22 名疑似中风的患者(中位数 NIHSS 为 8)。在神经影像学上发现 18 例(缺血性 n = 16,脑内出血 n = 2)有缺血或出血性病变的证据。中风后 24 小时内可检测到血清 NfH(SMI35)水平(P < 0.0001),并且在研究过程中持续升高。虽然整个研究过程中均未检测到 GFAP,但 S100B 水平在观察期结束时达到峰值。这些数据表明,通过测定 NfH(SMI35),可以获得有关中风病理生理学的重要信息。需要进一步的研究来评估超急性期中风中的 NfH(SMI35)是否反映了神经影像学上所见的局灶性缺血性损伤的程度,还是更广泛的神经轴突损伤的结果。

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