Viz-Lasheras Sandra, Gómez-Carballa Alberto, Pardo-Seco Jacobo, Bello Xabier, Rivero-Calle Irene, Dacosta Ana Isabel, Kaforou Myrsini, Habgood-Coote Dominic, Cunnington Aubrey J, Emonts Marieke, Herberg Jethro A, Wright Victoria J, Carrol Enitan D, Paulus Stephane C, Zenz Werner, Kohlfürst Daniela S, Van der Flier Michiel, de Groot Ronald, Schlapbach Luregn J, Agyeman Philipp, Pollard Andrew J, Fink Colin, Kuijpers Taco T, Anderson Suzanne, Calvo Cristina, Martínez-Padilla María Del Carmen, Pérez-Aragón Ana, Gómez-Sánchez Esteban, Valencia-Ramos Juan, Giménez-Sánchez Francisco, Alonso-Quintela Paula, Moreno-Galarraga Laura, von Both Ulrich, Pokorn Marko, Zavadska Dace, Tsolia María, Vermont Clementien L, Moll Henriëtte A, Levin Michael, Martinón-Torres Federico, Salas Antonio
Unidade de Xenética, Instituto de Ciencias Forenses, Facultade de Medicina, Universidade de Santiago de Compostela, and Genética de Poblaciones en Biomedicina (GenPoB) Research Group, Instituto de Investigación Sanitaria (IDIS), 15706 Hospital Clínico Universitario de Santiago (SERGAS), Galicia, Spain.
Genetics, Vaccines and Infections Research Group (GenViP), Instituto de Investigación Sanitaria de Santiago, 15706 Universidade de Santiago de Compostela, Santiago de Compostela, Galicia, Spain.
iScience. 2025 Jan 4;28(2):111747. doi: 10.1016/j.isci.2025.111747. eCollection 2025 Feb 21.
Pneumonia stands as the primary cause of death among children under five, yet current diagnosis methods often result in inadequate or unnecessary treatments. Our research seeks to address this gap by identifying host transcriptomic biomarkers in the blood of children with definitive viral and bacterial pneumonia. We performed RNA sequencing on 192 prospectively collected whole blood samples, including 38 controls and 154 pneumonia cases, uncovering a 5-transcript signature (genes , , , , and ) that effectively distinguishes bacterial from viral pneumonia (area under the curve (AUC): 0.95 [0.88-1.00]). Initial validation using combined definitive and probable cases yielded an AUC of 0.87 [0.77-0.97], while full validation in a new prospective cohort of 32 patients achieved an AUC of 0.92 [0.83-1.00]. This robust signature holds significant potential to enhance diagnostics accuracy for pediatric pneumonia, reducing diagnostic delays and unnecessary treatments and potentially transforming clinical practice.
肺炎是五岁以下儿童死亡的主要原因,但目前的诊断方法常常导致治疗不足或不必要。我们的研究旨在通过识别确诊为病毒性和细菌性肺炎儿童血液中的宿主转录组生物标志物来填补这一空白。我们对192份前瞻性收集的全血样本进行了RNA测序,其中包括38份对照样本和154份肺炎病例样本,发现了一个由5个转录本组成的特征(基因、、、和),可有效区分细菌性肺炎和病毒性肺炎(曲线下面积(AUC):0.95 [0.88 - 1.00])。使用确诊病例和可能病例组合进行的初步验证得出的AUC为0.87 [0.77 - 0.97],而在一个新的32例患者的前瞻性队列中进行的全面验证得出的AUC为0.92 [0.83 - 1.00]。这一强大的特征对于提高儿童肺炎的诊断准确性具有巨大潜力,可减少诊断延误和不必要的治疗,并有可能改变临床实践。