Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, London, UK; Department of Neonatal Intensive Care, Università degli Studi della Campania Luigi Vanvitelli, Naples, Italy.
Centre for Perinatal Neuroscience, Department of Brain Sciences, Imperial College London, London, UK.
EBioMedicine. 2020 Feb;52:102663. doi: 10.1016/j.ebiom.2020.102663. Epub 2020 Feb 12.
Although thalamic magnetic resonance (MR) spectroscopy (MRS) accurately predicts adverse outcomes after neonatal encephalopathy, its utility in infants without MR visible deep brain nuclei injury is not known. We examined thalamic MRS metabolite perturbations in encephalopathic infants with white matter (WM) injury with or without cortical injury and its associations with adverse outcomes.
We performed a subgroup analysis of all infants recruited to the MARBLE study with isolated WM or mixed WM/cortical injury, but no visible injury to the basal ganglia/thalamus (BGT) or posterior limb of the internal capsule (PLIC). We used binary logistic regression to examine the association of MRS biomarkers with three outcomes (i) WM injury score (1 vs. 2/3); (ii) cortical injury scores (0/1 vs. 2/3); and (iii) adverse outcomes (defined as death, moderate/severe disability) at two years (yes/no). We also assessed the accuracy of MRS for predicting adverse outcome.
Of the 107 infants included in the analysis, five had adverse outcome. Reduced thalamic N-acetylaspartate concentration [NAA] (odds ratio 0.4 (95% CI 0.18-0.93)) and elevated thalamic Lactate/NAA peak area ratio (odds ratio 3.37 (95% CI 1.45-7.82)) were significantly associated with higher WM injury scores, but not with cortical injury. Thalamic [NAA] (≤5.6 mmol/kg/wet weight) had the best accuracy for predicting adverse outcomes (sensitivity 1.00 (95% CI 0.16-1.00); specificity 0.95 (95% CI 0.84-0.99)).
Thalamic NAA is reduced in encephalopathic infants without MR visible deep brain nuclei injury and may be a useful predictor of adverse outcomes.
The National Institute for Health Research (NIHR).
尽管丘脑磁共振波谱(MRS)能准确预测新生儿脑病后的不良预后,但它在无明显深部脑核损伤的婴儿中的应用尚不清楚。我们研究了伴有或不伴有皮质损伤的白质(WM)损伤脑病婴儿的丘脑 MRS 代谢物变化及其与不良预后的关系。
我们对 MARBLE 研究中所有招募的单纯 WM 或 WM 合并皮质损伤、但基底节/丘脑(BGT)或内囊后肢(PLIC)无明显损伤的婴儿进行了亚组分析。我们使用二项逻辑回归分析 MRS 生物标志物与 3 个结局的相关性(i)WM 损伤评分(1 比 2/3);(ii)皮质损伤评分(0/1 比 2/3);和(iii)2 年时的不良结局(定义为死亡、中重度残疾)。我们还评估了 MRS 预测不良结局的准确性。
在纳入分析的 107 名婴儿中,有 5 名出现不良结局。较低的丘脑 N-乙酰天冬氨酸浓度[NAA](比值比 0.4(95%CI 0.18-0.93))和较高的丘脑乳酸/NAA 峰面积比(比值比 3.37(95%CI 1.45-7.82))与较高的 WM 损伤评分显著相关,但与皮质损伤无关。丘脑[NAA](≤5.6mmol/kg/湿重)对预测不良结局的准确性最高(敏感性 1.00(95%CI 0.16-1.00);特异性 0.95(95%CI 0.84-0.99))。
在无明显深部脑核损伤的脑病婴儿中,丘脑 NAA 减少,可能是不良预后的有用预测指标。
英国国家健康研究所(NIHR)。