Castellví Ivan, Castillo Diego, Corominas Hèctor, Mariscal Anaís, Orozco Sandra, Benito Natividad, Pomar Virginia, Baucells Andrés, Mur Isabel, de la Rosa-Carrillo David, Lobo David, Millan Ana Milena, Hernández de Sosa Nerea, Filella David, Matas Laia, Martínez-Martínez Laura, Juarez Cándido, Casademont Jordi, Domingo Pere
Department of Rheumatology and Systemic Autoimmune Diseases, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Department of Pneumology, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain.
Front Med (Lausanne). 2022 Aug 8;9:973918. doi: 10.3389/fmed.2022.973918. eCollection 2022.
Coronavirus disease 2019 (COVID-19) has rapidly expanded worldwide. Currently, there are no biomarkers to predict respiratory worsening in patients with mild to moderate COVID-19 pneumonia. Small studies explored the use of Krebs von de Lungen-6 circulating serum levels (sKL-6) as a prognostic biomarker of the worsening of COVID-19 pneumonia. We aimed at a large study to determine the prognostic value of sKL-6 in predicting evolving trends in COVID-19. We prospectively analyzed the characteristics of 836 patients with COVID-19 with mild lung disease on admission. sKL-6 was obtained in all patients at least at baseline and compared among patients with or without respiratory worsening. The receiver operating characteristic curve was used to find the optimal cutoff level. A total of 159 (19%) patients developed respiratory worsening during hospitalization. Baseline sKL-6 levels were not higher in patients who had respiratory worsening (median {IQR} 315.5 {209-469} vs. 306 {214-423} U/ml = 0.38). The last sKL-6 and the change between baseline and last sKL-6 were higher in the respiratory worsening group ( = 0.02 and < 0.0001, respectively). The best sKL-6 cutoff point for respiratory worsening was 497 U/ml (area under the curve 0.52; 23% sensitivity and 85% specificity). sKL-6 was not found to be an independent predictor of respiratory worsening. A conditional inference tree (CTREE) was not useful to discriminate patients at risk of worsening. We found that sKL-6 had a low sensibility to predict respiratory worsening in patients with mild-moderate COVID-19 pneumonia and may not be of use to assess the risk of present respiratory worsening in inpatients with COVID-19 pneumonia.
2019冠状病毒病(COVID-19)已在全球迅速蔓延。目前,尚无生物标志物可预测轻至中度COVID-19肺炎患者的呼吸状况恶化。小型研究探索了使用克雷布斯冯德吕根6循环血清水平(sKL-6)作为COVID-19肺炎恶化的预后生物标志物。我们旨在进行一项大型研究,以确定sKL-6在预测COVID-19病情发展趋势方面的预后价值。我们前瞻性分析了836例入院时患有轻度肺部疾病的COVID-19患者的特征。所有患者至少在基线时检测了sKL-6,并在有或无呼吸状况恶化的患者之间进行比较。采用受试者工作特征曲线来确定最佳临界值。共有159例(19%)患者在住院期间出现呼吸状况恶化。呼吸状况恶化的患者基线sKL-6水平并不更高(中位数{四分位间距}315.5{209 - 469}与306{214 - 423}U/ml,P = 0.38)。呼吸状况恶化组的末次sKL-6水平以及基线与末次sKL-6之间的变化更高(分别为P = 0.02和P < 0.0001)。预测呼吸状况恶化的最佳sKL-6临界值为497 U/ml(曲线下面积0.52;敏感度23%,特异度85%)。未发现sKL-6是呼吸状况恶化的独立预测因素。条件推断树(CTREE)对区分有恶化风险的患者并无帮助。我们发现,sKL-6预测轻至中度COVID-19肺炎患者呼吸状况恶化的敏感度较低,可能无法用于评估COVID-19肺炎住院患者当前呼吸状况恶化的风险。