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代谢组学:自闭症谱系障碍临床应用的展望。

Metabolomics: Perspectives on Clinical Employment in Autism Spectrum Disorder.

机构信息

Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.

Child Neurology and Psychiatry Unit, Department of Neurosciences, Policlinico Tor Vergata Hospital, Viale Oxford 81, 00133 Rome, Italy.

出版信息

Int J Mol Sci. 2023 Aug 29;24(17):13404. doi: 10.3390/ijms241713404.

Abstract

Precision medicine is imminent, and metabolomics is one of the main actors on stage. We summarize and discuss the current literature on the clinical application of metabolomic techniques as a possible tool to improve early diagnosis of autism spectrum disorder (ASD), to define clinical phenotypes and to identify co-occurring medical conditions. A review of the current literature was carried out after PubMed, Medline and Google Scholar were consulted. A total of 37 articles published in the period 2010-2022 was included. Selected studies involve as a whole 2079 individuals diagnosed with ASD (1625 males, 394 females; mean age of 10, 9 years), 51 with other psychiatric comorbidities (developmental delays), 182 at-risk individuals (siblings, those with genetic conditions) and 1530 healthy controls (TD). Metabolomics, reflecting the interplay between genetics and environment, represents an innovative and promising technique to approach ASD. The metabotype may mirror the clinical heterogeneity of an autistic condition; several metabolites can be expressions of dysregulated metabolic pathways thus liable of leading to clinical profiles. However, the employment of metabolomic analyses in clinical practice is far from being introduced, which means there is a need for further studies for the full transition of metabolomics from clinical research to clinical diagnostic routine.

摘要

精准医学迫在眉睫,代谢组学是舞台上的主要角色之一。我们总结和讨论了代谢组学技术在临床应用方面的现有文献,这些技术可能有助于改善自闭症谱系障碍(ASD)的早期诊断,定义临床表型,并识别共发的医疗状况。在查阅了 PubMed、Medline 和 Google Scholar 后,对现有文献进行了综述。共纳入了 2010 年至 2022 年期间发表的 37 篇文章。选定的研究总共涉及 2079 名被诊断为 ASD 的个体(1625 名男性,394 名女性;平均年龄为 10.9 岁),51 名患有其他精神共病(发育迟缓),182 名高危个体(兄弟姐妹,有遗传条件)和 1530 名健康对照组(TD)。代谢组学反映了遗传和环境之间的相互作用,是一种创新且有前途的方法,可用于研究 ASD。代谢特征可能反映了自闭症状况的临床异质性;几种代谢物可以是代谢途径失调的表达,因此可能导致临床表型。然而,代谢组学分析在临床实践中的应用还远远没有得到普及,这意味着需要进一步的研究,以实现代谢组学从临床研究向临床诊断常规的全面转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c912/10487559/848031a5e331/ijms-24-13404-g001.jpg

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