Blood long non‐coding RNA intersectin 1–2 is highly expressed and links with increased Th17 cells, inflammation, multiple organ dysfunction, and mortality risk in sepsis patients. Issue 4 (4th March 2022)

• Record Type: Journal Article
• Authors: Huang, Qinghe; Wang, Yibin; He, Fuyun
• Is Part Of: Journal of clinical laboratory analysis. Volume 36:Issue 4(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-03-04
• Subjects: inflammation -- lncRNA ITSN1‐2 -- multiple organ dysfunction -- sepsis -- Th1 and Th17 cells; Diagnosis, Laboratory -- Periodicals; Medical laboratory technology -- Periodicals; 616
• DOI: 10.1002/jcla.24330
• Languages: English
• ISSNs: 0887-8013

Abstract

Abstract: Background: Long non‐coding RNA intersectin 1–2 (lnc‐ITSN1‐2) exacerbates inflammation and promotes T‐helper (Th) cell differentiation, also serves as a biomarker in critical illness diseases. However, its clinical role in sepsis remains obscure. Hence, the study aimed to explore the relationship of lnc‐ITSN1‐2 with Th cells, inflammation, disease severity, multiple organ dysfunction, and mortality risk in sepsis. Methods: Peripheral blood mononuclear cells (PBMC) were isolated from 95 sepsis patients and 50 health controls, followed by lnc‐ITSN1‐2 evaluation using RT‐qPCR. PBMC Th1, Th17 cells and their secreted cytokines in serum were detected by flow cytometry and ELISA, respectively. Results: Lnc‐ITSN1‐2 in sepsis patients was higher than it in health controls ( Z = −7.328, p < 0.001). Lnc‐ITSN1‐2 correlated with increased interferon‐gamma ( p = 0.009), Th17 cells ( p = 0.022), and interleukin‐17A ( p = 0.006), but not Th1 cells ( p = 0.169) in sepsis patients. Moreover, lnc‐ITSN1‐2 had a positive connection with C‐reactive protein ( p = 0.001), acute pathologic and chronic health evaluation (APACHE) II ( p = 0.024), and sequential organ failure assessment (SOFA) scores ( p = 0.022). Regarding SOFA subscales, lnc‐ITSN1‐2 linked with elevated respiratory system score ( p = 0.005), cardiovascular system score ( p = 0.007), and renal system score ( p = 0.004) but no other subscales. Besides, lnc‐ITSN1‐2 had an increasing trend, but no statistical difference, in septic deaths compared to survivors ( Z = −1.852, p = 0.064). Conclusion: Lnc‐ITSN1‐2 reflects sepsis progression and unfavorable prognosis to some extent, which may serve as a potential biomarker to improve the management of sepsis patients. Abstract : Long non‐coding RNA intersectin 1‐2 (lnc‐ITSN1‐2) exacerbates inflammation and promotes T‐helper (Th) cell differentiation, also serves as biomarker in critical illness diseases. However, its clinical role in sepsis remains obscure. The findings of this study indicates that lnc‐ITSN1‐2 reflects sepsis progression and unfavorable prognosis to some extent, which may serve as a potential biomarker to improve the management of sepsis patients.