LncRNA HOTTIP as a diagnostic biomarker for acute respiratory distress syndrome in patients with sepsis and to predict the short-term clinical outcome: a case-control study

• Published in: BMC anesthesiology Vol. 24; no. 1; pp. 30 - 13
• Main Authors: Shi, Weitao, Zhu, Wang, Yu, Jiani, Shi, Yingjun, Zhao, Yuliang
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 18-01-2024; BioMed Central; BMC
• Subjects: Acute respiratory distress syndrome; Antisense RNA; ARDS; Biomarkers; Case-Control Studies; Diagnostic; Diagnostic equipment (Medical); Genes; HOTTIP; Humans; Infections; Inflammation; Medical prognosis; Medical research; Medicine, Experimental; MicroRNA; MicroRNAs; MicroRNAs - genetics; miRNA; Mortality; Non-coding RNA; Patient outcomes; Patients; Predicts; Prognosis; Pulmonary fibrosis; Respiratory distress syndrome; Respiratory Distress Syndrome - diagnosis; Respiratory Distress Syndrome - epidemiology; Risk factors; RNA, Long Noncoding - genetics; ROC Curve; Scandals; Sepsis; Sepsis - diagnosis; Sepsis - genetics; Taiwan; United Kingdom; United Kingdom; Taiwan; Diagnostic; Sepsis; Predicts; HOTTIP; ARDS
• ISSN: 1471-2253; 1471-2253
• DOI: 10.1186/s12871-024-02405-z

The present research aims to investigate the clinical diagnostic value of LncRNA HOXA distal transcript antisense RNA (HOTTIP) in acute respiratory distress syndrome (ARDS) of sepsis and its predictive significance for mortality.
One hundred eighteenth patients with sepsis and 96 healthy individuals were enrolled. RT-qPCR to examine HOTTIP levels. The incidence of ARDS and death was recorded. The diagnostic significance of HOTTIP in sepsis ARDS was examined using ROC and logistic regression analysis. The correlation between HOTTIP and disease severity was evaluated using Pearson's coefficients. Kaplan-Meier analysis and COX regression were employed to examine the predictive significance of mortality. Validation of HOTTIP target miRNA by dual-luciferase assay.
HOTTIP was persistently up-regulated in patients with ARDS sepsis than in patients without ARDS patients (P < 0.05). HOTTIP was a risk factor for the development of ARDS, which could be diagnosed in ARDS patients from non-ARDS patients (AUC = 0.847). Both the SOFA score (r = 0.6793) and the APACHE II score (r = 0.6384) were positively correlated with the HOTTIP levels. Furthermore, serum HOTTIP was an independent predictor of short-term mortality (HR = 4.813. 95%CI: 1.471-15.750, P = 0.009) and noticeably predicted the occurrence of short-term death (log rank = 0.020). miR-574-5p, a target miRNA for HOTTIP, was reduced in patients with sepsis ARDS and negatively correlated with HOTTIP.
The presence of HOTTIP serves as a diagnostic biomarker for the occurrence of ARDS, exhibits correlation with disease severity, and provides predictive value of short-term mortality in sepsis patients. HOTTIP may be involved in ARDS progression by targeting miR-574-5p.