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脑损伤患者脑脊液的骨诱导作用。

Osteoinductive effect of cerebrospinal fluid from brain-injured patients.

作者信息

Gautschi Oliver P, Toffoli Andrew M, Joesbury Karen A, Skirving Allan P, Filgueira Luis, Zellweger René

机构信息

Department of Orthopaedic and Trauma Surgery, Royal Perth Hospital, Wellington Street, Perth, 6000 WA, Australia.

出版信息

J Neurotrauma. 2007 Jan;24(1):154-62. doi: 10.1089/neu.2006.0166.

Abstract

Patients with traumatic brain injury (TBI) are predisposed to heterotopic ossification, which is believed to be due to osteoinductive factors released at the site of the brain injury. To date, little is known about the presence of such factors in human cerebrospinal fluid (CSF). This study investigated whether CSF of TBI patients is osteoinductive. In addition, known osteoinductive factors--such as bone morphogenetic protein (BMP)-2, BMP-4, and BMP-7, and S100B--were measured in CSF. Eighty-four consecutive patients were classified according to brain pathology: TBI (n = 11), non-traumatic brain pathology (NTBP) (n = 26), and no brain pathology (control group) (n = 47). The osteoinductive effect of CSF was measured repeatedly in proliferation assays using a fetal human osteoblast cell line. The mean proliferation rate (normalized to the internal negative control) of the TBI, NTBP, and control groups was 138.2% (SD 13.1), 110.0% (SD 22.1), and 118.8% (SD 16.9), respectively. The potentially confounding effect of age was investigated further by restricting the selection of patients for analysis to that of the oldest patient in the TBI group and use of multiple regression analysis. After implementation of both, it was shown that age is highly unlikely to account for the higher rates of proliferation observed among the TBI patients in this study. Of note, the TBI group had a significantly higher mean proliferation rate than the NTBP (p = 0.001) and the control group (p = 0.006). S100B and BMP-2, -4, or -7 concentrations were measured using enzyme-linked immunosorbent assay (ELISA). There was no correlation between proliferation rates and S100B (r = 0.023). Only three of 36 CSF samples had measurable levels of BMP-2 and -7, and none had detectable concentrations of BMP-4. Consequently, it is unlikely that S100B or BMP-2, -4, or -7 are the putative osteoinductive factors. The results indicate that CSF from TBI patients has an osteoinductive effect in vitro. However, the osteoinductive factor has still to be characterized.

摘要

创伤性脑损伤(TBI)患者易发生异位骨化,据信这是由于脑损伤部位释放的骨诱导因子所致。迄今为止,对于人类脑脊液(CSF)中此类因子的存在情况知之甚少。本研究调查了TBI患者的脑脊液是否具有骨诱导作用。此外,还对脑脊液中的已知骨诱导因子——如骨形态发生蛋白(BMP)-2、BMP-4、BMP-7和S100B进行了检测。根据脑部病理学对84例连续患者进行分类:TBI(n = 11)、非创伤性脑部病变(NTBP)(n = 26)和无脑部病变(对照组)(n = 47)。使用人胎儿成骨细胞系通过增殖试验反复测量脑脊液的骨诱导作用。TBI组、NTBP组和对照组的平均增殖率(相对于内部阴性对照进行标准化)分别为138.2%(标准差13.1)、110.0%(标准差22.1)和118.8%(标准差16.9)。通过将分析患者的选择限制为TBI组中年龄最大的患者并使用多元回归分析,进一步研究了年龄可能产生的混杂效应。在实施这两项措施后,结果表明年龄极不可能是本研究中TBI患者观察到的较高增殖率的原因。值得注意的是,TBI组的平均增殖率显著高于NTBP组(p = 0.001)和对照组(p = 0.006)。使用酶联免疫吸附测定(ELISA)测量S100B和BMP-2、-4或-7的浓度。增殖率与S100B之间无相关性(r = 0.023)。36份脑脊液样本中只有3份可检测到BMP-2和-7水平,且均未检测到BMP-4的浓度。因此,S100B或BMP-2、-4或-7不太可能是假定的骨诱导因子。结果表明,TBI患者的脑脊液在体外具有骨诱导作用。然而,骨诱导因子仍有待鉴定。

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