Centre for Forensic Science, University of Technology Sydney, Sydney, New South Wales, Australia.
Climate Change Cluster, University of Technology Sydney, Sydney, New South Wales, Australia.
Dev Med Child Neurol. 2021 May;63(5):552-559. doi: 10.1111/dmcn.14774. Epub 2020 Dec 17.
To explore the cerebrospinal fluid (CSF) metabolite features in acute neuroinflammatory diseases and identify potential biomarkers to diagnose and monitor neuroinflammation.
A cohort of 14 patients (five females, nine males; mean [median] age 7y 9mo [9y], range 6mo-13y) with acute encephalitis (acute disseminated encephalomyelitis n=6, unknown suspected viral encephalitis n=3, enteroviral encephalitis n=2, seronegative autoimmune encephalitis n=2, herpes simplex encephalitis n=1) and age-matched non-inflammatory neurological disease controls (n=14) were investigated using an untargeted metabolomics approach. CSF metabolites were analyzed with liquid chromatography coupled to high resolution mass spectrometry, followed by subsequent multivariate and univariate statistical methods.
A total of 35 metabolites could be discriminated statistically between the groups using supervised orthogonal partial least squares discriminant analysis and analysis of variance. The tryptophan-kynurenine pathway contributed nine key metabolites. There was a statistical increase of kynurenine, quinolinic acid, and anthranilic acid in patients with encephalitis, whereas tryptophan, 3-hydroxyanthrnailic acid, and kynurenic acid were decreased. The nitric oxide pathway contributed four metabolites, with elevated asymmetric dimethylarginine and argininosuccinic acid, and decreased arginine and citrulline in patients with encephalitis. An increase in the CSF kynurenine/tryptophan ratio (p<0.001), anthranilic acid/3-hydroxyanthranilic acid ratio (p<0.001), asymmetric dimethylarginine/arginine ratio (p<0.001), and neopterin (p<0.001) strongly predicted neuroinflammation.
The combination of alterations in the tryptophan-kynurenine pathway, nitric oxide pathway, and neopterin represent a useful potential panel for neuroinflammation and holds potential for clinical translation practice.
The kynurenine/tryptophan and anthranilic acid/3-hydroxyanthranilic acid ratios hold great potential as biomarkers of neuroinflammation. Elevation of the asymmetric dimethylarginine/arginine ratio in acute brain inflammation shows dysregulation of the nitric oxide pathway.
探讨急性神经炎症性疾病中脑脊液(CSF)代谢物特征,并确定潜在的生物标志物以诊断和监测神经炎症。
本研究纳入了 14 名患者(女性 5 名,男性 9 名;平均[中位数]年龄 7 岁 9 个月[9 岁],范围 6 个月-13 岁),这些患者患有急性脑炎(急性播散性脑脊髓炎 n=6,病因不明疑似病毒性脑炎 n=3,肠道病毒性脑炎 n=2,血清阴性自身免疫性脑炎 n=2,单纯疱疹性脑炎 n=1),并与年龄匹配的非炎症性神经疾病对照组(n=14)进行了比较。采用非靶向代谢组学方法对患者的 CSF 代谢物进行分析,采用液相色谱与高分辨质谱联用,随后进行多变量和单变量统计分析。
采用正交偏最小二乘判别分析和方差分析对两组间的 35 种代谢物进行了统计学区分。色氨酸-犬尿氨酸途径贡献了 9 种关键代谢物。脑炎患者的犬尿氨酸、喹啉酸和邻氨基苯甲酸的水平升高,而色氨酸、3-羟基邻氨基苯甲酸和犬尿氨酸的水平降低。一氧化氮途径贡献了 4 种代谢物,其中脑炎患者的不对称二甲基精氨酸和精氨琥珀酸升高,而精氨酸和瓜氨酸降低。CSF 犬尿氨酸/色氨酸比值(p<0.001)、邻氨基苯甲酸/3-羟基邻氨基苯甲酸比值(p<0.001)、不对称二甲基精氨酸/精氨酸比值(p<0.001)和新蝶呤(p<0.001)升高强烈提示存在神经炎症。
色氨酸-犬尿氨酸途径、一氧化氮途径和新蝶呤的改变组合代表了神经炎症的一个有用的潜在标志物,具有转化为临床实践的潜力。
犬尿氨酸/色氨酸和邻氨基苯甲酸/3-羟基邻氨基苯甲酸比值具有作为神经炎症生物标志物的巨大潜力。急性脑炎症时不对称二甲基精氨酸/精氨酸比值升高表明一氧化氮途径失调。