Balancing precision versus cohort transcriptomic analysis of acute and recovery phase of viral bronchiolitis.
Ruchir GuptaMara L LeimanisMarie AdamsAndré S BachmannKatie L UhlCaleb P BuppNicholas L HartogEric J KortRosemary OliveroSarah S ComstockDominic J SanfilippoSophia Y LuntJeremy W ProkopSurender RajasekaranPublished in: American journal of physiology. Lung cellular and molecular physiology (2021)
Viral infections affecting the lower respiratory tract place enormous burdens on hospitals. As neither vaccines nor antiviral agents exist for many viruses, understanding risk factors and outcomes in each patient using minimally invasive analysis, such as blood, can lead to improved health care delivery. A cohort of PAXgene RNA sequencing of infants admitted with moderate or severe acute bronchiolitis and respiratory syncytial virus were compared with case-control statistical analysis and cohort-based outlier mapping for precision transcriptomics. Patients with severe bronchiolitis had signatures connected to the immune system, interferon signaling, and cytokine signaling, with marked sex differences in XIST, RPS4Y1, KDM5D, and LINC00278 for severity. Several patients had unique secondary infections, cytokine activation, immune responses, biological pathways, and immune cell activation, highlighting the need for defining patient-level transcriptomic signatures. Balancing relative contributions of cohort-based biomarker discoveries with patient's biological responses is needed to understand the totality of mechanisms of adverse outcomes in viral bronchiolitis.
Keyphrases
- respiratory syncytial virus
- healthcare
- single cell
- case report
- respiratory tract
- sars cov
- minimally invasive
- risk factors
- immune response
- end stage renal disease
- chronic kidney disease
- case control
- ejection fraction
- newly diagnosed
- cell proliferation
- dendritic cells
- high intensity
- liver failure
- early onset
- peritoneal dialysis
- type diabetes
- inflammatory response
- patient reported outcomes
- dna methylation
- intensive care unit
- long noncoding rna
- acute respiratory distress syndrome
- health insurance
- glycemic control