检验医学 ›› 2026, Vol. 41 ›› Issue (4): 380-385.DOI: 10.3969/j.issn.1673-8640.2026.04.011

• 论著 • 上一篇    下一篇

儿童特应性皮炎非靶向代谢组学分析

林慧1, 陈祥1, 李胜2, 唐满玲1()   

  1. 1 株洲市中心医院检验医学中心湖南 株洲 412000
    2 株洲市中心医院肾内科湖南 株洲 412000
  • 收稿日期:2024-08-01 修回日期:2025-08-05 出版日期:2026-04-30 发布日期:2026-05-07
  • 通讯作者: 唐满玲,E-mail:tangmaal678@126.com
  • 作者简介:林 慧,女,1993年生,硕士,主管技师,主要从事过敏性疾病的机制研究。
  • 基金资助:
    湖南省自然科学基金项目(2023JJ50218)

Non-targeted metabolomics analysis of atopic dermatitis in children

LIN Hui1, CHEN Xiang1, LI Sheng2, TANG Manling1()   

  1. 1 Laboratory Medicine CenterZhuzhou Central HospitalZhuzhou 412000,Hunan, China
    2 Department of NephrologyZhuzhou Central HospitalZhuzhou 412000,Hunan, China
  • Received:2024-08-01 Revised:2025-08-05 Online:2026-04-30 Published:2026-05-07

摘要:

目的 通过非靶向代谢组学技术分析特应性皮炎(AD)患儿代谢变化。方法 选取2023年1月1日—6月30日株洲市中心医院AD患儿37例(AD组)、非健康体检儿童18例(HMDB对照组)。检测所有患儿血清中的代谢物质,并筛选差异代谢物。采用京都基因与基因组(KEGG)数据库和HMDB数据库进行代谢通路分析,采用受试者工作特征(ROC)曲线分析差异代谢物中可用于诊断AD的潜在生物标志物。结果 AD患儿有87种代谢物显著上调,46种代谢物显著下调;上调居前5位的代谢物为鸟氨酸、甘氨酰脯氨酸、没食子酸、次黄嘌呤和同型半胱氨酸,下调居前5位的代谢物为D-甘露糖、(S)-甲基丙二酸半醛、(2R_3S)-2_3-苹果酸二甲酯、(S)-脱落酸和2-氧代戊酸;涉及的代谢通路包括精氨酸和脯氨酸代谢,D-氨基酸代谢,甘氨酸、丝氨酸和苏氨酸代谢,蛋白质消化和吸收,精氨酸生物合成,癌症中的中心碳代谢等。鸟氨酸、次黄嘌呤、同型半胱氨酸、D-甘露糖、(2R_3S)-2_3-苹果酸二甲酯诊断AD的曲线下面积(AUC)均为1,甘氨酰脯氨酸、没食子酸、(S)-甲基丙二酸半醛、(S)-脱落酸、2-氧代戊酸诊断AD的AUC分别为0.950、0.960、0.990、0.940、0.940。结论 儿童AD涉及的代谢通路包括氨基酸代谢、蛋白质消化吸收、癌症中的中心碳代谢,可能与发病机制相关。

关键词: 代谢组学, 发病机制, 氨基酸代谢, 特应性皮炎, 儿童

Abstract:

Objective To investigate the metabolic changes of atopic dermatitis(AD)in children using non-targeted metabolomics technology. Methods A total of 37 children with AD(AD group)and 17 healthy children (control group)were enrolled from Zhuzhou Central Hospital from January 1,2023 to June 30,2023. The metabolites in the serum were determined,and the differentially expressed metabolites were screened. Metabolic pathways were analyzed using the Kyoto Encyclopedia of Genes and Genomes(KEGG)and the Human Metabolome Database(HMDB),and potential biomarkers in the differentially expressed metabolites for the diagnosis of AD were evaluated by receiver operating characteristic(ROC)curve. Results Totally,87 metabolites in AD patients were upregulated(the top 5 were or nithine,glycylproline,gallic acid,hypoxanthine and homocystine),and 46 metabolites were downregulated [the top 5 were D-mannose,(S)-methylmalonyl semialdehyde,(2R_3S)-2_3-malic dimethyl ester,(S)-abscisic acid and 2-oxopentanoic acid]. The involved metabolic pathways included arginine and proline metabolism,D-amino acid metabolism,glycine,serine,threonine metabolism,protein digestion and absorption,arginine biosynthesis and central carbon metabolism in cancer. The areas under curves (AUC) of ornithine,hypoxanthine,homocysteine,D-mannose,(2R_3S)-2_3-malic dimethyl ester,glycylproline,gallic acid,(S)-methylmalonyl semialdehyde,(S)-abscisic acid and 2-oxopentanoic acid were 1.000,1.000,1.000,1.000,1.000,0.950,0.960,0.990,0.940 and 0.940,respectively. Conclusions The metabolic pathways involved in AD patients include amino acid metabolism,protein digestion and absorption and cancer central carbon metabolism,which may be related to the pathogenesis of childhood AD.

Key words: Metabolomics, Pathogenesis, Amino acid metabolism, Atopic dermatitis, children

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