Potential of circulating lncRNA CASC2 as a biomarker in reflecting the inflammatory cytokines, multi-organ dysfunction, disease severity, and mortality in sepsis patients.


Journal

Journal of clinical laboratory analysis
ISSN: 1098-2825
Titre abrégé: J Clin Lab Anal
Pays: United States
ID NLM: 8801384

Informations de publication

Date de publication:
Aug 2022
Historique:
revised: 06 06 2022
received: 10 05 2022
accepted: 11 06 2022
pubmed: 28 6 2022
medline: 25 8 2022
entrez: 27 6 2022
Statut: ppublish

Résumé

Long noncoding RNA (lncRNA) cancer susceptibility candidate gene 2 (CASC2) inhibits inflammation and multi-organ dysfunction in various ways. The present study was intended to explore the potency of blood lncRNA CASC2 as a biomarker for sepsis management. Totally, 184 sepsis patients and 30 healthy controls were enrolled. The reverse transcription-quantitative polymerase chain reaction was used to detect lncRNA CASC2 expression in peripheral blood mononuclear cell samples from the subjects. Mortality during 28 days was recorded in sepsis patients. LncRNA CASC2 was decreased in sepsis patients [median (interquartile range [IQR]): 0.473 (0.241-0.773)] by comparison to healthy controls [median (IQR): 1.019 (0.676-1.685)] (p < 0.001). In sepsis patients, lncRNA CASC2 was negatively correlated with Acute Physiology and Chronic Health Evaluation II (APACHE II) (p = 0.001), Sequential Organ Failure Assessment (SOFA) (p < 0.001), SOFA-respiratory system (p = 0.010), SOFA-coagulation (p = 0.020), SOFA-liver (p = 0.019), and SOFA-renal (p = 0.010) scores, but was not related to SOFA-nervous (p = 0.466) and SOFA-cardio vascular system (p = 0.059) scores. Additionally, lncRNA CASC2 was negatively related to tumor necrosis factor-α (p = 0.024), interleukin (IL)-1β (p = 0.013), and IL-17A (p = 0.002), but was not linked to IL-6 (p = 0.112) or IL-10 (p = 0.074). Furthermore, lncRNA CASC2 was lower in sepsis deaths [median (IQR): 0.286 (0.166-0.475)] than in survivors [median (IQR): 0.534 (0.296-0.811)] (p < 0.001). Simultaneously, Kaplan-Meier (KM) curve analysis also observed that lncRNA CASC2 was inversely related to accumulating mortality in sepsis patients (p = 0.003). While lncRNA CASC2 could independently predict lower mortality risk. Circulating lncRNA CASC2 inadequacy indicates the release of inflammatory cytokines, severe multi-organ injuries, and increased mortality in sepsis patients.

Sections du résumé

BACKGROUND BACKGROUND
Long noncoding RNA (lncRNA) cancer susceptibility candidate gene 2 (CASC2) inhibits inflammation and multi-organ dysfunction in various ways. The present study was intended to explore the potency of blood lncRNA CASC2 as a biomarker for sepsis management.
METHODS METHODS
Totally, 184 sepsis patients and 30 healthy controls were enrolled. The reverse transcription-quantitative polymerase chain reaction was used to detect lncRNA CASC2 expression in peripheral blood mononuclear cell samples from the subjects. Mortality during 28 days was recorded in sepsis patients.
RESULTS RESULTS
LncRNA CASC2 was decreased in sepsis patients [median (interquartile range [IQR]): 0.473 (0.241-0.773)] by comparison to healthy controls [median (IQR): 1.019 (0.676-1.685)] (p < 0.001). In sepsis patients, lncRNA CASC2 was negatively correlated with Acute Physiology and Chronic Health Evaluation II (APACHE II) (p = 0.001), Sequential Organ Failure Assessment (SOFA) (p < 0.001), SOFA-respiratory system (p = 0.010), SOFA-coagulation (p = 0.020), SOFA-liver (p = 0.019), and SOFA-renal (p = 0.010) scores, but was not related to SOFA-nervous (p = 0.466) and SOFA-cardio vascular system (p = 0.059) scores. Additionally, lncRNA CASC2 was negatively related to tumor necrosis factor-α (p = 0.024), interleukin (IL)-1β (p = 0.013), and IL-17A (p = 0.002), but was not linked to IL-6 (p = 0.112) or IL-10 (p = 0.074). Furthermore, lncRNA CASC2 was lower in sepsis deaths [median (IQR): 0.286 (0.166-0.475)] than in survivors [median (IQR): 0.534 (0.296-0.811)] (p < 0.001). Simultaneously, Kaplan-Meier (KM) curve analysis also observed that lncRNA CASC2 was inversely related to accumulating mortality in sepsis patients (p = 0.003). While lncRNA CASC2 could independently predict lower mortality risk.
CONCLUSION CONCLUSIONS
Circulating lncRNA CASC2 inadequacy indicates the release of inflammatory cytokines, severe multi-organ injuries, and increased mortality in sepsis patients.

Identifiants

pubmed: 35754113
doi: 10.1002/jcla.24569
pmc: PMC9396177
doi:

Substances chimiques

Biomarkers 0
Cytokines 0
RNA, Long Noncoding 0
Tumor Suppressor Proteins 0
long non-coding RNA CASC2, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e24569

Subventions

Organisme : Protective Effects of oxymatrine on sepsis in rats
ID : No. 204106107

Informations de copyright

© 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.

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Auteurs

Rui Wang (R)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Jinglin Zhao (J)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Qi Wei (Q)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Hao Wang (H)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Chao Zhao (C)

Department of Pharmacology, Cangzhou Medical College, Cangzhou, China.

Caihong Hu (C)

Department of Pharmacology, Cangzhou Medical College, Cangzhou, China.

Yu Han (Y)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Zhi Hui (Z)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Long Yang (L)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Qingchun Dai (Q)

Department of Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, China.

Cuicui Liu (C)

Department of Pharmacology, Cangzhou Medical College, Cangzhou, China.

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Classifications MeSH