中国自闭症谱系障碍队列血斑的代谢组学分析:一项初步研究。
Metabolomic analysis of blood spots in a Chinese cohort with autism spectrum disorders: a pilot study.
作者信息
Wang Hui, Ding Li, Mao Zheng-Huan, Du Yu, Han Qing-Mei, Xu Jia-Yu, Peng Fei-Fei, Li Hai-Feng, Zou Chao-Chun
机构信息
Department of Rehabilitation, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang, China.
Department of Endocrinology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, No. 3333 Binsheng Road, Hangzhou, 310051, Zhejiang, China.
出版信息
Metab Brain Dis. 2025 Jun 20;40(6):230. doi: 10.1007/s11011-025-01635-5.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder with a strong genetic component that is becoming increasingly prevalent. The identification of plasma molecular biomarkers may provide potential insights into ASD and aid in early diagnosis. In this study, we characterized the metabolomic profiles of ASD children using blood spot samples collected at the Children's Hospital of Zhejiang University School of Medicine from children with ASD (n = 43) and typically developing (TD) children (n = 43). Our results highlight differences between children with ASD and TD controls. We identified possibly associations between ASD and a variety of metabolites, including carnosine (Car), glutaric acid, histidine (His), succinic acid, tryptophan, glutamine (Gln), asparagine, guanidinoacetic acid, sarcosine, kynurenine, glutamic acid (Glu) and cysteine (Cys). Metabolic pathway analysis demonstrated a possible imbalance in the amino acid metabolism of Glu/Gln, Car/His in ASD children. These findings may provide new insights into the molecular mechanisms that influence ASD risk and have possibility for the discovery of biomarkers.
自闭症谱系障碍(ASD)是一种具有强大遗传成分的神经发育障碍,且其发病率正日益上升。血浆分子生物标志物的识别可能为自闭症谱系障碍提供潜在的见解,并有助于早期诊断。在本研究中,我们使用从浙江大学医学院附属儿童医院收集的血斑样本,对自闭症谱系障碍儿童(n = 43)和发育正常(TD)儿童(n = 43)的代谢组学特征进行了表征。我们的结果突出了自闭症谱系障碍儿童与发育正常儿童之间的差异。我们确定了自闭症谱系障碍与多种代谢物之间可能存在的关联,包括肌肽(Car)、戊二酸、组氨酸(His)、琥珀酸、色氨酸、谷氨酰胺(Gln)、天冬酰胺、胍基乙酸、肌氨酸、犬尿氨酸、谷氨酸(Glu)和半胱氨酸(Cys)。代谢途径分析表明,自闭症谱系障碍儿童的谷氨酸/谷氨酰胺、肌肽/组氨酸氨基酸代谢可能存在失衡。这些发现可能为影响自闭症谱系障碍风险的分子机制提供新的见解,并有可能发现生物标志物。