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特发性肺纤维化患者脂质代谢的改变及其与疾病严重程度和预后的关系:一项病例对照研究

Alteration of Lipid Metabolism in Patients with IPF and Its Association with Disease Severity and Prognosis: A Case-Control Study.

作者信息

Faverio Paola, Rebora Paola, Franco Giovanni, Amato Anna, Corti Nicole, Cattaneo Katya, Spiti Simona, Zanini Umberto, Maloberti Alessandro, Giannattasio Cristina, Luppi Fabrizio, Leoni Valerio

机构信息

U.O.C. di Pneumologia, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.

School of Medicine and Surgery, Università degli Studi di Milano-Bicocca, 20100 Milan, Italy.

出版信息

Int J Mol Sci. 2025 Jun 17;26(12):5790. doi: 10.3390/ijms26125790.

Abstract

The pathogenesis of idiopathic pulmonary fibrosis (IPF) involves complex interactions between epithelial, mesenchymal, immune, and endothelial cells, often aggravated by lipid metabolism dysfunction, mitochondrial, and peroxisomal abnormalities. Changes in lipid metabolism may drive fibrotic processes, suggesting the potential of lipid biomarkers for disease monitoring. We compared here the cholesterol metabolism and very-long-chain fatty acid profiles of patients with IPF with healthy controls. The IPF patients' lipidic profiles were also evaluated according to disease severity and progression rate. This prospective, observational study involved 50 IPF patients at disease diagnosis before antifibrotic treatment initiation and 50 age- and gender-matched healthy controls. Using a serum lipidomic profile, we focused on cholesterol synthesis, mitochondrial and peroxisomal markers, inflammatory lipids, and oxidative stress markers. Disease severity was evaluated using the Gender-Age-Physiology (GAP) index, while the prognosis was assessed by classifying patients as rapid or slow progressors based on a 24-month follow-up. IPF patients exhibited lower levels of cholesterol synthesis precursors (e.g., lathosterol), mitochondrial oxysterols, and inflammatory mediators (e.g., arachidonic acid) compared to controls. Reduced levels of these biomarkers were also associated with higher disease severity and rapid disease progression. Conversely, some peroxisomal markers (e.g., brassidic acid and nervonic acid) showed altered trends depending on disease severity. Our findings indicate that patients with IPF, compared to healthy controls, may show lipidomic alterations, particularly a reduction in cholesterol precursors and docosahexaenoic acids, which are also associated with IPF severity and progression. While preliminary, this study suggests lipidomics to be a promising tool to stratify IPF severity and prognosis.

摘要

特发性肺纤维化(IPF)的发病机制涉及上皮细胞、间充质细胞、免疫细胞和内皮细胞之间的复杂相互作用,脂质代谢功能障碍、线粒体和过氧化物酶体异常常常会加重这种相互作用。脂质代谢的变化可能会推动纤维化进程,这表明脂质生物标志物在疾病监测方面具有潜力。我们在此比较了IPF患者与健康对照者的胆固醇代谢和极长链脂肪酸谱。还根据疾病严重程度和进展速度对IPF患者的脂质谱进行了评估。这项前瞻性观察性研究纳入了50例在开始抗纤维化治疗前处于疾病诊断阶段的IPF患者以及50例年龄和性别匹配的健康对照者。利用血清脂质组学谱,我们重点关注了胆固醇合成、线粒体和过氧化物酶体标志物、炎性脂质以及氧化应激标志物。使用性别 - 年龄 - 生理学(GAP)指数评估疾病严重程度,而通过对患者进行24个月随访,将其分类为快速进展者或缓慢进展者来评估预后。与对照组相比,IPF患者的胆固醇合成前体(如羊毛甾醇)、线粒体氧化甾醇和炎性介质(如花生四烯酸)水平较低。这些生物标志物水平的降低也与更高的疾病严重程度和快速的疾病进展相关。相反,一些过氧化物酶体标志物(如芥酸和神经酸)根据疾病严重程度呈现出不同的变化趋势。我们的研究结果表明,与健康对照者相比,IPF患者可能存在脂质组学改变,尤其是胆固醇前体和二十二碳六烯酸的减少,这也与IPF的严重程度和进展相关。虽然本研究尚属初步,但表明脂质组学是一种有前景的工具,可用于对IPF的严重程度和预后进行分层。

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