Amirsardari Zahra, Moghadam Ehsan Aghaei, Mohebbi Ali, Fanos Vassilios, Ayati Aryan, Portman Michael A, Tahghighi Fatemeh, Ziaee Vahid
School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Cardiogenetic Research Center, Rajaie Cardiovascular Institute, Tehran, Iran.
J Cardiovasc Transl Res. 2025 Jul 18. doi: 10.1007/s12265-025-10648-5.
We investigated the metabolomic profile of Kawasaki disease(KD) and its association with the development of coronary artery aneurysms (CAA) and resistance to intravenous immunoglobulin(IVIG) therapy. Metabolomic profiling was performed on 26 patients with KD. A total of 44 metabolites-including 12 amino acids, L-carnitine, and 31 acylcarnitines-were analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) after IVIG administration. Methylglutarylcarnitine, a medium-chain acylcarnitine, was identified as a differentially expressed metabolite in KD patients with CAA. Additionally, C2, C3, C14, C16, C16OH, C18:2, and C18:2OH were differentially expressed between IVIG-resistant and IVIG-responsive patients. Pathway analysis using the KEGG database revealed that arginine biosynthesis and alanine, aspartate, and glutamate metabolism were among the most affected pathways in KD patients with CAA. This study demonstrated several differentially expressed metabolites in KD patients with CAA and IVIG resistance. These findings provide new insights into the metabolic pathways underlying KD complications.
我们研究了川崎病(KD)的代谢组学特征及其与冠状动脉瘤(CAA)发生和静脉注射免疫球蛋白(IVIG)治疗抵抗的关系。对26例KD患者进行了代谢组学分析。在给予IVIG后,使用液相色谱 - 串联质谱(LC-MS/MS)分析了总共44种代谢物,包括12种氨基酸、L-肉碱和31种酰基肉碱。中链酰基肉碱甲基戊二酰肉碱被鉴定为患有CAA的KD患者中差异表达的代谢物。此外,IVIG抵抗患者和IVIG反应患者之间C2、C3、C14、C16、C16OH、C18:2和C18:2OH存在差异表达。使用KEGG数据库进行的通路分析表明,精氨酸生物合成以及丙氨酸、天冬氨酸和谷氨酸代谢是患有CAA的KD患者中受影响最大的通路。这项研究证明了患有CAA和IVIG抵抗的KD患者中几种差异表达的代谢物。这些发现为KD并发症的潜在代谢途径提供了新的见解。