Department of Biostatistics and Computational Biology, University of Rochester School Medicine, Rochester, NY, USA.
Department of Pediatrics, University of Rochester School Medicine, Rochester, NY, USA.
BMC Med Genomics. 2021 Feb 25;14(1):57. doi: 10.1186/s12920-021-00913-2.
A substantial number of infants infected with RSV develop severe symptoms requiring hospitalization. We currently lack accurate biomarkers that are associated with severe illness.
We defined airway gene expression profiles based on RNA sequencing from nasal brush samples from 106 full-tem previously healthy RSV infected subjects during acute infection (day 1-10 of illness) and convalescence stage (day 28 of illness). All subjects were assigned a clinical illness severity score (GRSS). Using AIC-based model selection, we built a sparse linear correlate of GRSS based on 41 genes (NGSS1). We also built an alternate model based upon 13 genes associated with severe infection acutely but displaying stable expression over time (NGSS2).
NGSS1 is strongly correlated with the disease severity, demonstrating a naïve correlation (ρ) of ρ = 0.935 and cross-validated correlation of 0.813. As a binary classifier (mild versus severe), NGSS1 correctly classifies disease severity in 89.6% of the subjects following cross-validation. NGSS2 has slightly less, but comparable, accuracy with a cross-validated correlation of 0.741 and classification accuracy of 84.0%.
Airway gene expression patterns, obtained following a minimally-invasive procedure, have potential utility for development of clinically useful biomarkers that correlate with disease severity in primary RSV infection.
相当数量的 RSV 感染婴儿会出现需要住院治疗的严重症状。目前我们缺乏与严重疾病相关的准确生物标志物。
我们基于 106 名足月健康 RSV 感染婴儿急性感染(发病第 1-10 天)和恢复期(发病第 28 天)时鼻拭子样本的 RNA 测序,定义了气道基因表达谱。所有患儿均被分配临床疾病严重程度评分(GRSS)。采用基于 AIC 的模型选择,我们基于 41 个基因(NGSS1)建立了一个与 GRSS 呈稀疏线性相关的模型。我们还建立了一个基于 13 个与急性严重感染相关但随时间表达稳定的基因的替代模型(NGSS2)。
NGSS1 与疾病严重程度高度相关,表现出幼稚相关(ρ)ρ=0.935 和交叉验证相关 0.813。作为二元分类器(轻症与重症),NGSS1 在交叉验证后正确分类 89.6%的患儿的疾病严重程度。NGSS2 的准确性略低,但相当,交叉验证相关 0.741,分类准确率 84.0%。
通过微创程序获得的气道基因表达模式,可能对开发与原发性 RSV 感染疾病严重程度相关的临床有用的生物标志物具有潜在的应用价值。