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基线表观遗传学作为重度哮喘中美泊利单抗反应的生物标志物。

Baseline epigenetics as a biomarker of mepolizumab response in severe asthma.

作者信息

Zhang Hongmei, Jin Xin, Arshad Hasan, Kurukulaaratchy Ramesh J

机构信息

Division of Epidemiology, Biostatistics, Environmental Health, School of Public Health, University of Memphis, Memphis, TN, USA.

The David Hide Asthma and Allergy Research Centre, St. Mary's Hospital, Isle of Wight, UK.

出版信息

medRxiv. 2025 Sep 4:2025.09.02.25334098. doi: 10.1101/2025.09.02.25334098.

Abstract

Biologic treatment options have expanded considerably for severe asthma, transforming patient management, but only ~70% of patients respond to the treatment following standard criteria. This preliminary study utilized data collected in the Wessex AsThma CoHort of difficult asthma (WATCH) study. DNAm was measured in n=15 severe asthma patients at baseline, i.e., before mepolizumab (MEPO), an interleukin-5 receptor antagonist, was administered and the response to MEPO was analyzed. We aimed to assess the potential of DNA methylation as a feasible biomarker to predict responses to MEPO among severe asthma patients. Our preliminary findings suggested that pre-biologic DNA methylation as a predictor of a patient's response status may outperform pre-biologic blood eosinophils cell counts.

摘要

对于重度哮喘,生物治疗选择已大幅扩展,改变了患者管理方式,但按照标准标准,只有约70%的患者对治疗有反应。这项初步研究利用了在威塞克斯哮喘难治病队列(WATCH)研究中收集的数据。在n = 15名重度哮喘患者基线时,即给予白细胞介素-5受体拮抗剂美泊利单抗(MEPO)之前,测量了DNA甲基化,并分析了对MEPO的反应。我们旨在评估DNA甲基化作为一种可行生物标志物来预测重度哮喘患者对MEPO反应的潜力。我们的初步研究结果表明,生物治疗前的DNA甲基化作为患者反应状态的预测指标可能优于生物治疗前的血液嗜酸性粒细胞计数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6465/12425039/0be6f55e9301/nihpp-2025.09.02.25334098v1-f0001.jpg

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