María Isabel Serrano-Tomás, Paulina Contreras-Romero, Mara Parellada, Javier Chaves-Cordero, Javier Zamora, Martha Hengst, Patricia Pozo, Rosa Del Campo, Sheyla Guzmán-Salas
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引用次数: 0
摘要
近年来,肠脑轴及其微生物代谢物作为自闭症谱系障碍(ASDs)的潜在病因或生理病理因子受到了广泛关注。有机化合物对甲酚(p-cresol)在不同的ASD儿童群体中水平升高,这表明它可能被证实是与微生物群相关的ASD生物标志物。本研究的目的是对对甲酚在ASD中的应用进行系统回顾,并进行荟萃分析,以阐明其作为生物标志物潜力的科学证据。方法:于2024年5月在PubMed、Web of Science和Scopus数据库中进行检索。Axis关键评价工具用于评价纳入本综述的研究的方法学质量。三名独立审查员检查了已识别的记录并进行了数据提取。结果:系统评价共产生15篇文章,其中只有6篇最终用于meta分析。ASD患者尿中对甲酚水平明显高于健康对照组,而在粪便中没有观察到显著差异。结论:本荟萃分析验证了ASD患者尿液中对甲酚水平升高,这可能代表了疾病发病机制中微生物群进化评估的标志。然而,该代谢物的作用与ASD的病理生理之间是否存在因果关系,并验证其临床应用,还需要进一步的研究。
Recognition of the microbial metabolite p-cresol in autism spectrum disorder: systematic review and meta-analysis.
Introduction: In recent years, research has focused on the gut-brain axis and its microbial metabolites as potential etiological or physiopathological agents of autism spectrum disorders (ASDs). Elevated levels of the organic compound para-cresol (p-cresol) have been reported in various populations of children with ASD, suggesting that it could be validated as a possible ASD biomarker related to microbiota. The aim of this study was to perform a systematic review of p-cresol in ASD along with a meta-analysis to elucidate the scientific evidence of its potential as a biomarker.
Methods: A search was performed in the PubMed, Web of Science and Scopus databases in May 2024. The Axis critical appraisal tool was used to evaluate the methodological quality of the studies included in the review. Three independent reviewers examined the identified records and performed data extraction.
Results: The systematic review yielded 15 articles, of which only 6 were ultimately used for the meta-analysis. Urinary p-cresol levels were significantly higher in those with ASD than in healthy controls, whereas no significant differences were observed in feces.
Conclusion: This meta-analysis validates that in ASD an increased level of p-cresol is detected in urine, which could represent a marker of microbiota evolution assessment in the pathogenesis of the disease. However, further research is needed to determine whether there is a causal relationship between the role of this metabolite and the pathophysiology of ASD and to validate its clinical utility.
期刊介绍:
Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.