Zdanowicz Katarzyna, Bobrus-Chcociej Anna, Pogodzinska Karolina, Blachnio-Zabielska Agnieszka, Zelazowska-Rutkowska Beata, Lebensztejn Dariusz Marek, Daniluk Urszula
Department of Pediatrics, Gastroenterology, Hepatology, Nutrition and Allergology, Medical University of Bialystok, 15-274 Bialystok, Poland.
Department of Hygiene, Epidemiology and Metabolic Disorders, Medical University of Bialystok, 15-22 Bialystok, Poland.
J Clin Med. 2022 Sep 23;11(19):5613. doi: 10.3390/jcm11195613.
(1) Background: Disturbances in the sphingolipid profile are observed in many diseases. There are currently no data available on the evaluation of sphingolipids and ceramides in cholelithiasis in children. The aim of this study was to evaluate the concentrations of sphingolipids in the sera of pediatric patients with gallstones. We determined their relationship with anthropometric and biochemical parameters. (2) Methods: The concentrations of sphingolipids in serum samples were evaluated using a quantitative method, ultra-high-performance liquid chromatography-tandem mass spectrometry. (3) Results: The prospective study included 48 children and adolescents diagnosed with gallstones and 38 controls. Serum concentrations of total cholesterol (TC); sphinganine (SPA); ceramides-C14:0-Cer, C16:0-Cer, C18:1-Cer, C18:0-Cer, C20:0-Cer and C24:1-Cer; and lactosylceramides-C16:0-LacCer, C18:0-LacCer, C18:1-LacCer, C24:0-LacCer and C24:1-LacCer differed significantly between patients with cholelithiasis and without cholelithiasis. After adjusting for age, gender, obesity and TC and TG levels, we found the best differentiating sphingolipids for cholelithiasis in the form of decreased SPA, C14:0-Cer, C16:0-Cer, C24:1-LacCer and C24:0-LacCer concentration and increased C20:0-Cer, C24:1-Cer, C16:0-LacCer and C18:1-LacCer. The highest area under the curve (AUC), specificity and sensitivity were determined for C16:0-Cer with cholelithiasis diagnosis. (4) Conclusions: Our results suggest that serum sphingolipids may be potential biomarkers in pediatric patients with cholelithiasis.
(1) 背景:在许多疾病中都观察到鞘脂谱的紊乱。目前尚无关于儿童胆结石中鞘脂和神经酰胺评估的可用数据。本研究的目的是评估小儿胆结石患者血清中鞘脂的浓度。我们确定了它们与人体测量和生化参数的关系。(2) 方法:采用定量方法,即超高效液相色谱 - 串联质谱法评估血清样本中鞘脂的浓度。(3) 结果:前瞻性研究纳入了48名诊断为胆结石的儿童和青少年以及38名对照。胆结石患者和无胆结石患者之间的血清总胆固醇(TC)、鞘氨醇(SPA)、神经酰胺 - C14:0 - Cer、C16:0 - Cer、C18:1 - Cer、C18:0 - Cer、C20:0 - Cer和C24:1 - Cer以及乳糖基神经酰胺 - C16:0 - LacCer、C18:0 - LacCer、C18:1 - LacCer、C24:0 - LacCer和C24:1 - LacCer浓度存在显著差异。在调整年龄、性别、肥胖以及TC和TG水平后,我们发现胆结石的最佳鉴别鞘脂表现为SPA、C14:0 - Cer、C16:0 - Cer、C24:1 - LacCer和C24:0 - LacCer浓度降低,以及C20:0 - Cer、C24:1 - Cer、C16:0 - LacCer和C18:1 - LacCer浓度升高。对于胆结石诊断,C16:0 - Cer的曲线下面积(AUC)、特异性和敏感性最高。(4) 结论:我们的结果表明,血清鞘脂可能是小儿胆结石患者的潜在生物标志物。