School of Medical Sciences, Örebro University, 702 81 Örebro, Sweden.
Turku Bioscience Centre, University of Turku and Åbo Akademi University, FI-20520 Turku, Finland.
Int J Mol Sci. 2020 Feb 19;21(4):1395. doi: 10.3390/ijms21041395.
Recent evidence suggests that patients with traumatic brain injuries (TBIs) have a distinct circulating metabolic profile. However, it is unclear if this metabolomic profile corresponds to changes in brain morphology as observed by magnetic resonance imaging (MRI). The aim of this study was to explore how circulating serum metabolites, following TBI, relate to structural MRI (sMRI) findings. Serum samples were collected upon admission to the emergency department from patients suffering from acute TBI and metabolites were measured using mass spectrometry-based metabolomics. Most of these patients sustained a mild TBI. In the same patients, sMRIs were taken and volumetric data were extracted (138 metrics). From a pool of 203 eligible screened patients, 96 met the inclusion criteria for this study. Metabolites were summarized as eight clusters and sMRI data were reduced to 15 independent components (ICs). Partial correlation analysis showed that four metabolite clusters had significant associations with specific ICs, reflecting both the grey and white matter brain injury. Multiple machine learning approaches were then applied in order to investigate if circulating metabolites could distinguish between positive and negative sMRI findings. A logistic regression model was developed, comprised of two metabolic predictors (erythronic acid and -inositol), which, together with neurofilament light polypeptide (NF-L), discriminated positive and negative sMRI findings with an area under the curve of the receiver-operating characteristic of 0.85 (specificity = 0.89, sensitivity = 0.65). The results of this study show that metabolomic analysis of blood samples upon admission, either alone or in combination with protein biomarkers, can provide valuable information about the impact of TBI on brain structural changes.
最近的证据表明,创伤性脑损伤 (TBI) 患者具有独特的循环代谢特征。然而,目前尚不清楚这种代谢组学特征是否与磁共振成像 (MRI) 观察到的脑形态变化相对应。本研究旨在探讨 TBI 后循环血清代谢物与结构 MRI (sMRI) 结果的关系。在急诊科收治的急性 TBI 患者入院时采集血清样本,并使用基于质谱的代谢组学方法测量代谢物。这些患者大多患有轻度 TBI。在同一患者中进行 sMRI 检查并提取容积数据(138 个指标)。在 203 名符合筛选标准的患者中,有 96 名符合本研究的纳入标准。代谢物被总结为 8 个簇,sMRI 数据被简化为 15 个独立成分 (IC)。偏相关分析显示,4 个代谢物簇与特定的 IC 有显著关联,反映了灰质和白质的脑损伤。然后应用多种机器学习方法来研究循环代谢物是否可以区分 sMRI 阳性和阴性结果。建立了一个逻辑回归模型,由两个代谢预测因子(赤藓糖酸和肌醇)组成,与神经丝轻链蛋白 (NF-L) 一起,区分 sMRI 阳性和阴性结果的曲线下面积为 0.85(特异性 = 0.89,敏感性 = 0.65)。这项研究的结果表明,入院时血液样本的代谢组学分析,无论是单独分析还是与蛋白质生物标志物联合分析,都可以提供关于 TBI 对脑结构变化影响的有价值信息。