Lipidomics reveals the serum profiles of pediatric allergic rhinitis and its severity

Abstract Allergic rhinitis (AR) is a prevalent upper airway chronic inflammatory disease in children worldwide. The role of bioactive lipids in the regulation of AR has been recognized, but the underlying serum lipidomic basis of its pathology remains unclear. We utilized ultra‐performance liquid chromatography (UPLC)‐Q‐Exactive Orbitrap/mass spectrometry (MS) to investigate the serum lipidomic profiles of children with AR. The lipidomic analysis identified 42 lipids that were differentially expressed ( p < 0.05, fold change > 2) between the AR ( n = 75) and normal control groups ( n = 44). Specifically, the serum levels of diacylglycerol (DG), triacylglycerol (TG), fatty acid (FA), lysophosphatidylcholine (LPC), lysophosphatidylethanolamine, phosphatidyl‐ethanolamine, and cardiolipins were significantly higher in the AR group. The diagnostic potential of the identified lipids was further evaluated using receiver operating characteristic curve analysis. The analysis revealed that five lipids, including FA 30:7, LPC O‐18:1, LPC 18:0, LPC 16:0, and DG 34:0, had area under the curve values greater than 0.9 ( p < 0.05). Furthermore, serum levels of IgE and IL‐33, markers of AR severity, were found to have a significant positive correlation ( p < 0.05) with DGs, LPCs, TGs, and FAs in AR patients. This study revealed the lipid disorders associated with AR and its severity, providing new insights into the pathological process of AR.