Lipidomics for diagnosis and prognosis of pulmonary hypertension.

Natalie Bordag, Bence Miklos Nagy, Elmar Zügner, Helga Ludwig, Vasile Foris, Chandran Nagaraj, Valentina Biasin, Ulrich Bodenhofer, Christoph Magnes, Bradley A Maron, Silvia Ulrich, Tobias J Lange, Konrad Hötzenecker, Thomas Pieber, Horst Olschewski, Andrea Olschewski
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Abstract

Background: Pulmonary hypertension (PH) poses a significant health threat with high morbidity and mortality, necessitating improved diagnostic tools for enhanced management. Current biomarkers for PH lack functionality and comprehensive diagnostic and prognostic capabilities. Therefore, there is a critical need to develop biomarkers that address these gaps in PH diagnostics and prognosis.

Methods: To address this need, we employed a comprehensive metabolomics analysis in 233 blood based samples coupled with machine learning analysis. For functional insights, human pulmonary arteries (PA) of idiopathic pulmonary arterial hypertension (PAH) lungs were investigated and the effect of extrinsic FFAs on human PA endothelial and smooth muscle cells was tested in vitro.

Results: PA of idiopathic PAH lungs showed lipid accumulation and altered expression of lipid homeostasis-related genes. In PA smooth muscle cells, extrinsic FFAs caused excessive proliferation and endothelial barrier dysfunction in PA endothelial cells, both hallmarks of PAH.In the training cohort of 74 PH patients, 30 disease controls without PH, and 65 healthy controls, diagnostic and prognostic markers were identified and subsequently validated in an independent cohort. Exploratory analysis showed a highly impacted metabolome in PH patients and machine learning confirmed a high diagnostic potential. Fully explainable specific free fatty acid (FFA)/lipid-ratios were derived, providing exceptional diagnostic accuracy with an area under the curve (AUC) of 0.89 in the training and 0.90 in the validation cohort, outperforming machine learning results. These ratios were also prognostic and complemented established clinical prognostic PAH scores (FPHR4p and COMPERA2.0), significantly increasing their hazard ratios (HR) from 2.5 and 3.4 to 4.2 and 6.1, respectively.

Conclusion: In conclusion, our research confirms the significance of lipidomic alterations in PH, introducing innovative diagnostic and prognostic biomarkers. These findings may have the potential to reshape PH management strategies.

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脂质组学在肺动脉高压诊断和预后中的应用。
肺动脉高压(PH)是一种严重的血液动力学、进展性疾病,与高发病率和死亡率相关,早期和微创诊断可以至关重要地改善管理。需要具有功能性、诊断性和预后的PH生物标志物。我们使用了一种广泛的代谢组学方法,结合机器学习分析和特异性游离脂肪酸(FFA)/脂质比率来开发诊断和预后PH生物标志物。在一个由74名PH患者、30名无PH的疾病对照组和65名健康对照组组成的训练队列中,我们确定了在64名受试者的独立队列中验证的诊断和预后标志物。基于亲脂性代谢物的标记物比基于亲水性代谢物的更坚固。在训练和验证队列中,FFA/脂质比率为PH提供了极好的诊断准确性,AUC分别高达0.89和0.90。这些比率提供了与年龄无关的预后信息,并且与已确定的临床评分相结合,FPHR4p和COMPERA2的风险比(HR)分别从2.5增加到4.3和从3.3增加到5.6。特发性PAH(IPAH)肺的肺动脉(PA)表现出脂质积聚和脂质稳态相关基因表达的改变,这可能解释了这种积聚。我们对肺动脉内皮细胞和平滑肌细胞的功能研究表明,FFA水平升高会导致过度增殖和肺动脉内皮屏障功能障碍,这两种都是肺动脉高压(PAH)的特征。总之,PH的脂质组学变化提供了新的诊断和预后生物标志物,并可能指向新的代谢治疗靶点。
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