Novel eicosanoid signature in plasma provides diagnostic for metabolic dysfunction-associated steatotic liver disease.

IF 5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Lipid Research Pub Date : 2024-10-01 Epub Date: 2024-09-18 DOI:10.1016/j.jlr.2024.100647
Oswald Quehenberger, Aaron M Armando, Tiffany H Cedeno, Rohit Loomba, Arun J Sanyal, Edward A Dennis
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Abstract

There is a clinical need for a simple test implementable at the primary point of care to identify individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) in the population. Blood plasma samples from adult patients with varying phenotypes of MASLD were used to identify a minimal set of lipid analytes reflective of underlying histologically confirmed MASLD. Samples were obtained from the NIDDK Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) NAFLD Database prospective cohort study (MASLD group; N = 301). Samples of control subjects were obtained from cohort studies at the University of California San Diego (control group; N = 48). Plasma samples were utilized for targeted quantitation of circulating eicosanoids, related bioactive metabolites, and polyunsaturated fatty acids by ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) lipidomics analysis. Bioinformatic approaches were used to discover a panel of bioactive lipids that can be used as a diagnostic tool to identify MASLD. The final panel of fifteen lipid metabolites consists of 12 eicosanoid metabolites and 3 free fatty acids that were identified to be predictive for MASLD by multivariate area under the receiver operating characteristics curve (AUROC) analysis. The panel was highly predictive for MASLD with an AUROC of 0.999 (95% CI = 0.986-1.0) with only one control misclassified. A validation study confirmed the resulting MASLD LIPIDOMICS SCORE, which may require a larger-scale prospective study to optimize. This predictive model should guide the development of a non-invasive "point-of-care" test to identify MASLD patients requiring further evaluation for the presence of metabolic dysfunction-associated steatohepatitis.

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血浆中的新型类二十碳烷特征可诊断代谢功能障碍相关性脂肪肝。
临床上需要一种可在初级医疗点实施的简单检测方法来识别人群中患有代谢功能障碍相关性脂肪性肝病(MASLD)的个体。我们从具有不同表型的 MASLD 成年患者身上采集了血浆样本,用于鉴定一组反映组织学确诊的潜在 MASLD 的最基本脂质分析物。样本来自 NIDDK 非酒精性脂肪性肝炎临床研究网络(NASH CRN)非酒精性脂肪性肝病数据库前瞻性队列研究(MASLD 组;N = 301)。对照受试者样本来自加州大学圣地亚哥分校的队列研究(对照组;N = 48)。利用血浆样本,通过超高效液相色谱-质谱(UPLC-MS)脂质组学分析,对循环中的二十烷酸、相关生物活性代谢物和多不饱和脂肪酸进行定向定量。利用生物信息学方法发现了一组生物活性脂质,可用作鉴别 MASLD 的诊断工具。通过多变量接收者操作特征曲线下面积(AUROC)分析,最终确定了 15 种脂质代谢物,其中包括 12 种二十烷类代谢物和 3 种游离脂肪酸,它们对 MASLD 具有预测作用。该面板对 MASLD 有很高的预测性,AUROC 为 0.999(95% CI = 0.986-1.0),只有一个对照组被误诊。虽然包含了一项验证研究,但还需要与匹配对照进行更大规模的前瞻性研究,以优化由此产生的 MASLD LIPIDOMICS SCORE,使其成为一种非侵入性的 "护理点 "测试,用于识别需要进一步评估是否存在代谢功能障碍相关性脂肪性肝炎(MASH)的 MASLD 患者。
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来源期刊
Journal of Lipid Research
Journal of Lipid Research 生物-生化与分子生物学
CiteScore
11.10
自引率
4.60%
发文量
146
审稿时长
41 days
期刊介绍: The Journal of Lipid Research (JLR) publishes original articles and reviews in the broadly defined area of biological lipids. We encourage the submission of manuscripts relating to lipids, including those addressing problems in biochemistry, molecular biology, structural biology, cell biology, genetics, molecular medicine, clinical medicine and metabolism. Major criteria for acceptance of articles are new insights into mechanisms of lipid function and metabolism and/or genes regulating lipid metabolism along with sound primary experimental data. Interpretation of the data is the authors’ responsibility, and speculation should be labeled as such. Manuscripts that provide new ways of purifying, identifying and quantifying lipids are invited for the Methods section of the Journal. JLR encourages contributions from investigators in all countries, but articles must be submitted in clear and concise English.
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