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METHODS FOR THE PREDICTION OF ACUTE RESPIRATORY DISTRESS SYNDROME

机译:急性呼吸窘迫综合征的预测方法

摘要

The invention relates to a method for predicting the risk of developing acute respiratory distress syndrome (ARDS). Prediction of ARDS remains challenging despite available clinical scores. The inventors aimed to assess soluble isoforms and gene variants of the receptor for advanced glycation end-products (RAGE), as predictors of ARDS in a high-risk population. The inventors conducted a multicenter, prospective study including 500 adult patients with at least one ARDS risk factor upon admission to intensive care units. Plasma soluble RAGE (sRAGE) and endogenous secretory RAGE (esRAGE) were measured at baseline and 24 hours later, and four RAGE single nucleotide polymorphisms (SNPs). The primary outcome was ARDS development within seven days. Higher baseline and day one plasma sRAGE and the RAGE rs2070600 SNP were independently associated with an increased rate of ARDS development. Thus, the invention relates to a method for predicting the risk of having or developing ARDS in a patient in need thereof, comprising the step of determining the expression level of Plasma sRAGE and/or detecting RAGE SNP rs2070600 in a biological sample obtained from said patient.
机译:本发明涉及一种预测发生急性呼吸窘迫综合征(ARDS)的风险的方法。尽管可获得临床评分,但ARDS的预测仍然具有挑战性。发明人旨在评估晚期糖基化终产物(RAGE)的受体的可溶性同工型和基因变体,作为高危人群中ARDS的预测指标。发明人进行了一项多中心,前瞻性研究,研究对象包括500名成年患者,他们进入重症监护病房后至少具有一种ARDS危险因素。在基线和24小时后测量血浆可溶性RAGE(sRAGE)和内源性分泌RAGE(esRAGE),以及四个RAGE单核苷酸多态性(SNP)。主要结果是7天内ARDS发展。较高的基线和第一天血浆sRAGE和RAGE rs2070600 SNP与ARDS发生率增加独立相关。因此,本发明涉及一种用于预测有需要的患者患有或发展ARDS的风险的方法,其包括确定血浆sRAGE的表达水平和/或检测从所述患者获得的生物样品中的RAGE SNP rs2070600的步骤。 。

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