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The Mechanism of lncRNA NEAT1 in Alleviating Acute Respiratory Distress Syndrome Through miR-27b Regulated Nrf2 Pathway

The Mechanism of lncRNA NEAT1 in Alleviating Acute Respiratory Distress Syndrome Through miR-27b Regulated Nrf2 Pathway

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04937855
Enrollment
425
Registered
2021-06-24
Start date
2021-07-01
Completion date
2023-12-31
Last updated
2021-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome, Inflammation

Keywords

long non-coding RNA NEAT1, microRNA-27b, nuclear factor E2-related factor 2

Brief summary

The acute respiratory distress syndrome, formerly known as the acute lung injury (ARDS/ALI), is a critical illness with high mortality due to the lack of effective treatment. The pathogenesis of ARDS/ALI has not been fully elucidated. Nuclear factor E2-related factor 2 (Nrf2) plays a key role in regulating lung inflammation and oxidative stress which are closely related to lung injury in ARDS/ALI, but its regulatory mechanism remains unclear. The investigator's provious study shown that microRNA-27b (miR-27b) downregulated Nrf2 to aggravate lung inflammation and histological injury. Furthermore, in lipopolysaccharide (LPS)-induced cell (J774A.1) inflammation model, miR-27b was upregulated while the long non-coding RNA (lncRNA) NEAT1 was downregulated, the putative binding sites of lncRNA NEAT1 and miR-27b were successfully predicted by bioinformatics approach. Thus, the investigators propose that NEAT1 plays as a competing endogenous RNA (ceRNA) to adsorb miR-27b and liberate Nrf2, therefore, to attenuate lung inflammation and related lung injury in ARDS/ALI. This project aims to explore the role of the lncRNA NEAT1/ mir-27b /Nrf2 signal axis in the development and treatment of ARDS/ALI in patients, as well as in LPS-induced ALI animal and cell models by using bioinformatics, molecular biology, histomorphology and clinical phenotype approaches, and to clarify the new mechanism in ARDS/ALI development and to provide new therapeutic targets.

Detailed description

Collect blood and BALF from 400 ARDS patients at different time (at check-in, 24, 48 and 72 h after check-in the hospital) and 25 gender and age matching healthy controls. Use RT-PCR to detect the expression of lncRNA NEAT1、miR-27b and Nrf2 in blood and BALF of ARDS patients and health controls. The expressions of inflammatory and oxidative stress associated factors (NLRP3、NF-κB-P65、 p-P65、IκB、p-IκB、HO-1、NQO1、caspase-1、IL-1β、IL-6、IL-18、TNF-α) will be detected by western blot、ELISA and RT-PCR. Moreover, flow cytometry will be adopted to measure the numbers and kinds of cells in BALF. Then, analyze the differences of the expressions of lncRNA NEAT1、miR-27b and Nrf2 in the groups. To explore the correlation of expressions of lncRNA NEAT1、miR-27b and Nrf2 with inflammation and oxidative stress in the groups. Finally, to declare the relative of lncRNA NEAT1、miR-27b and Nrf2 with the time of mechanical ventilation, severity and mortality in 28 days of ARDS patients.

Interventions

OTHERno intervention

no intervention

Sponsors

Beijing Anzhen Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

We included patients with acute respiratory distress according to 2012 ARDS Berlin new definition (Acute Respiratory Distress Syndrome: The Berlin Definition. JAMA, 2012, 307(23):2526). * Acute or progressive dyspnea within 1 week with identify cause; * Chest radiograph/chest CT showed double lung infiltration, which could not be fully explained by pleural effusion, atelectasis, or nodules; * Respiratory failure cannot be fully explained by heart failure and fluid overload; * Hypoxemia, partial pressure of oxygen in arterial blood (PaO2)/oxygen fraction in air (FIO2) \<150 mm Hg under PEEP ≥5 cm H2O, (mild ARDS: 200mmHg\<PaO2/FiO2≤300mmHg, moderate ARDS: 100mmHg\<PaO2/FiO2≤200mmHg, severe ARDS: PaO2/FiO2≤100mmHg); * 18\ 70 years old; * Agree to participate in the trial, and sign the informed consent.

Exclusion criteria

* Age less than 18 years old; * Time of hospital stay \<24 h; * Pregnancy; * Using V-V ECOM; * Cardiac index \<1.5L·ml.min-1.m-2; * Pulmonary resection; * Pulmonary embolism ; * Refused to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
the mortality in 28 days of ARDS patientsup to 28 dayRecord the mortality in 28 days of ARDS patients
The kinds of inflammatory cells in BALF and blood in all groupsup to 3 dayUse flow cytometry to detect the kinds of inflammatory cells(neutrophile、macrophage、 lymphocyte) in BALF and blood in all groups
The time of mechanical ventilation of patients in ARDS groupsup to28 dayRecord the time of mechanical ventilation of patients in ARDS groups
The severity of ARDS patients in ARDS groupsup to 28 dayRecord the severity(PaO2/FiO2、OI、S/F、OSI) of ARDS patients in ARDS groups
The expression of lncRNA NEAT1 in blood and BALF in all groupsup to 24 dayUse RT-PCR to measure the expression of lncRNA NEAT1 in blood and BALF in all groups
The expression of miR-27b in blood and BALF in all groupsup to 3 dayUse RT-PCR to measure the expression of miR-27b in blood and BALF in all groups
The expression of Nrf2 in blood and BALF in all groupsup to 3 dayUse RT-PCR and Wsetern blot to measure the expression of Nrf2 in blood and BALF in all groups
The expression of inflammatory factors(IL-1β、IL-6、IL-18、TNF-α) in blood and BALF in all groupsup to 3 dayUse RT-PCR and ELISA to measure the expression of inflammatory factors(IL-1β、IL-6、IL-18、TNF-α) in blood and BALF in all groups
The expression of oxidative stress associated factors in blood and BALF in all groupsup to 3 dayUse Western blot to measure the expression of oxidative stress associated factors(NLRP3、NF-κB-P65、 p-P65、IκB、p-IκB、HO-1、NQO1、caspase-1) in blood and BALF in all groups
The numbers and kinds of inflammatory cells in BALF and blood in all groupsup to 3 dayUse flow cytometry to detect the number of inflammatory cells in BALF and blood in all groups

Secondary

MeasureTime frameDescription
The correlation of expressions of lncRNA NEAT1、miR-27b and Nrf2 with inflammation and oxidative stress in the groups.up to 28 dayTo explore the correlation of expressions of lncRNA NEAT1、miR-27b and Nrf2 with inflammation and oxidative stress in the groups.
The relative of lncRNA NEAT1、miR-27b and Nrf2 with the time of mechanical ventilation, severity and mortality in 28 days of ARDS patientsup to 28 dayTo declare the relative of lncRNA NEAT1、miR-27b and Nrf2 with the time of mechanical ventilation, severity and mortality in 28 days of ARDS patients
The differences and correlation of the expressions of lncRNA NEAT1、miR-27b and Nrf2 in the groupsup to 28 dayAnalyse the differences of the expressions of lncRNA NEAT1、miR-27b and Nrf2 in the groups, and to explore the relations between the three(lncRNA NEAT1、miR-27b and Nrf2) in different groups.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026