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使用与年龄相关的脑脊液代谢组学特征来确认神经代谢诊断。

Confirmation of neurometabolic diagnoses using age-dependent cerebrospinal fluid metabolomic profiles.

机构信息

Department of Laboratory Medicine, Translational Metabolic Laboratory (TML), Radboud University Medical Center, Nijmegen, The Netherlands.

Department of Neurology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.

出版信息

J Inherit Metab Dis. 2020 Sep;43(5):1112-1120. doi: 10.1002/jimd.12253. Epub 2020 May 23.

Abstract

Timely diagnosis is essential for patients with neurometabolic disorders to enable targeted treatment. Next-Generation Metabolic Screening (NGMS) allows for simultaneous screening of multiple diseases and yields a holistic view of disturbed metabolic pathways. We applied this technique to define a cerebrospinal fluid (CSF) reference metabolome and validated our approach with patients with known neurometabolic disorders. Samples were measured using ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry followed by (un)targeted analysis. For the reference metabolome, CSF samples from patients with normal general chemistry results and no neurometabolic diagnosis were selected and grouped based on sex and age (0-2/2-5/5-10/10-15 years). We checked the levels of known biomarkers in CSF from seven patients with five different neurometabolic disorders to confirm the suitability of our method for diagnosis. Untargeted analysis of 87 control CSF samples yielded 8036 features for semiquantitative analysis. No sex differences were found, but 1782 features (22%) were different between age groups (q < 0.05). We identified 206 diagnostic metabolites in targeted analysis. In a subset of 20 high-intensity metabolites and 10 biomarkers, 17 (57%) were age-dependent. For each neurometabolic patient, ≥1 specific biomarker(s) could be identified in CSF, thus confirming the diagnosis. In two cases, age-matching was essential for correct interpretation of the metabolomic profile. In conclusion, NGMS in CSF is a powerful tool in defining a diagnosis for neurometabolic disorders. Using our database with many (age-dependent) features in CSF, our untargeted approach will facilitate biomarker discovery and further understanding of mechanisms of neurometabolic disorders.

摘要

及时诊断对于神经代谢疾病患者至关重要,以便能够进行针对性治疗。下一代代谢筛查 (NGMS) 允许同时筛查多种疾病,并全面了解代谢途径的紊乱。我们应用该技术定义了脑脊液 (CSF) 参考代谢组,并通过已知神经代谢疾病患者对我们的方法进行了验证。使用超高效液相色谱-四极杆飞行时间质谱法进行样品测量,然后进行(非)靶向分析。对于参考代谢组,选择具有正常常规化学结果且无神经代谢诊断的患者的 CSF 样本,并根据性别和年龄(0-2/2-5/5-10/10-15 岁)进行分组。我们检查了来自七个患有五种不同神经代谢疾病的患者的 CSF 中已知生物标志物的水平,以确认我们的方法是否适合诊断。对 87 份对照 CSF 样本进行非靶向分析,得出 8036 个半定量分析特征。未发现性别差异,但年龄组之间存在 1782 个特征(22%)存在差异(q < 0.05)。我们在靶向分析中鉴定了 206 种诊断代谢物。在 20 种高浓度代谢物和 10 种生物标志物的子集中,有 17 种(57%)与年龄有关。对于每位神经代谢患者,均可在 CSF 中鉴定出≥1 种特异性生物标志物,从而确认诊断。在两种情况下,年龄匹配对于正确解释代谢组学特征至关重要。总之,CSF 中的 NGMS 是为神经代谢疾病定义诊断的有力工具。使用我们的数据库,该数据库具有 CSF 中许多(与年龄相关)特征,我们的非靶向方法将有助于生物标志物的发现,并进一步了解神经代谢疾病的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b736/7540372/220d997ad270/JIMD-43-1112-g001.jpg

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