Yoo Hye Jin, Jung Keum Ji, Kim Minkyung, Kim Minjoo, Kang Minsik, Jee Sun Ha, Choi Yoonjeong, Lee Jong Ho
National Leading Research Laboratory of Clinical Nutrigenetics/Nutrigenomics, Department of Food and Nutrition, College of Human Ecology, Yonsei University, Seoul, South Korea.
Research Center for Silver Science, Institute of Symbiotic Life-TECH, Yonsei University, Seoul, South Korea.
Front Physiol. 2019 Nov 19;10:1421. doi: 10.3389/fphys.2019.01421. eCollection 2019.
Liver cirrhosis (LC) is the final usual outcome of liver damage induced by various chronic liver diseases. Because of asymptomatic nature of LC, it is usually diagnosed at late and advanced stages, and patients are easy to miss the best timing for treatment. Thus, the early detection of LC is needed. In the prospective Korean Cancer Prevention Study-II (K-II), we aimed to identify valuable biomarkers for LC using metabolomics to distinguish subjects with incident LC (LC group) from subjects free from LC (control group) during a mean 7-year follow-up period. Metabolic alterations were investigated using baseline serum specimens acquired from 94 subjects with incident LC and 180 age- and sex-matched LC-free subjects via ultra-performance liquid chromatography (UPLC)-linear-trap quardrupole (LTQ)-Orbitrap mass spectrometry (MS). As a result of the metabolic analysis, 46 metabolites were identified. Among them, 11 and 18 metabolite level showed a significant increase and decrease, respectively, in the LC group compared to the control group. Nine metabolic pathways, including glyoxylate and dicarboxylate metabolism, amino acid metabolism, fatty acid metabolism, linoleic acid metabolism, α-linolenic acid metabolism, and arachidonic acid metabolism, were significantly different between the two groups. Logistic regression demonstrated that the LC emergence was independently affected by serum levels of myristic acid, palmitic acid, linoleic acid, eicosapentaenoic acid (EPA), lysophosphatidic acid (LPA) (18:1), glycolic acid, lysophosphatidylcholine (lysoPC) (22:6), and succinylacetone ( = 0.837, < 0.001). This prospective study revealed that dysregulation of various metabolism had the clinical relevance on the LC development. Moreover, myristic acid, palmitic acid, linoleic acid, EPA, LPA (18:1), glycolic acid, lysoPC (22:6), and succinylacetone were emerged as independent variables influencing the incidence of LC. The results support that the early biomarkers found in this study may useful for predicting and remedying the risk of LC.
肝硬化(LC)是各种慢性肝病导致肝损伤的最终常见结局。由于LC具有无症状的特性,通常在晚期和进展期才被诊断出来,患者很容易错过最佳治疗时机。因此,需要早期检测LC。在韩国前瞻性癌症预防研究II(K-II)中,我们旨在利用代谢组学确定有价值的LC生物标志物,以便在平均7年的随访期内区分新发LC患者(LC组)和无LC患者(对照组)。通过超高效液相色谱(UPLC)-线性离子阱四极杆(LTQ)-轨道阱质谱(MS),使用从94例新发LC患者和180例年龄及性别匹配的无LC受试者采集的基线血清标本,研究代谢改变。代谢分析结果显示,共鉴定出46种代谢物。其中,与对照组相比,LC组中分别有11种和18种代谢物水平显著升高和降低。两组之间有9条代谢途径存在显著差异,包括乙醛酸和二羧酸代谢、氨基酸代谢、脂肪酸代谢、亚油酸代谢、α-亚麻酸代谢和花生四烯酸代谢。逻辑回归分析表明,肉豆蔻酸、棕榈酸、亚油酸、二十碳五烯酸(EPA)、溶血磷脂酸(LPA)(18:1)、乙醇酸、溶血磷脂酰胆碱(lysoPC)(22:6)和琥珀酰丙酮的血清水平独立影响LC的发生( = 0.837, < 0.001)。这项前瞻性研究表明,各种代谢失调与LC的发展具有临床相关性。此外,肉豆蔻酸、棕榈酸、亚油酸、EPA、LPA(18:1)、乙醇酸、lysoPC(22:6)和琥珀酰丙酮成为影响LC发病的独立变量。这些结果支持本研究中发现的早期生物标志物可能有助于预测和补救LC风险。