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Nucleotide Polymorphism in ARDS Outcome

Nucleotide Polymorphism in ARDS Outcome: a Whole Exome Sequencing Association Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02644798
Enrollment
105
Registered
2016-01-01
Start date
2016-01-01
Completion date
2017-06-30
Last updated
2022-03-15

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

Conditions

ARDS

Keywords

ARDS, Nucleotide polymorphism

Brief summary

Acute respiratory distress syndrome (ARDS) is characterized by increased pulmonary vascular permeability and reduced aerated lung tissue. With an extremely high hospital mortality among 35 - 46%, current therapeutic strategies to increase ARDS survival are still limited. Advances in etiology and pathology of ARDS are urging. Numerous genetic variants were identified associated with ARDS outcome. By whole-exome sequencing association study, our goal was to explore the associations between genetic variants and ARDS outcome.

Detailed description

Acute respiratory distress syndrome (ARDS) is characterized by increased pulmonary vascular permeability and reduced aerated lung tissue. With an extremely high hospital mortality among 35 - 46%, current therapeutic strategies to increase ARDS survival are still limited. Advances in etiology and pathology of ARDS are urging. Numerous genetic variants were identified associated with ARDS outcome. Then a few genetic risk factors have been discovered by large-scale genotyping approaches, from in vivo or in vitro models of lung injury, which highlight the importance of identifying genetic biomarkers of ARDS outcome to further improve stratification. The mutational landscape and variability at single nucleotide polymorphisms (SNP) with ARDS outcome in Chinese is unknown, not to mention their associations. By whole-exome sequencing association study, our goal was to explore the associations between genetic variants and ARDS outcome.

Interventions

OTHERBaseline-recorded data recorded

Baseline-recorded data recorded. Peripheral blood samples were drawn.

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adult ARDS (according to Berlin definition) patients were enrolled in the trial. The diagnostic criteria included 1. within one week of a known clinical insult or new or worsening respiratory symptoms; 2. chest imaging showing that bilateral opacities-not fully explained by effusions, lobar/lung collapse, or nodules; 3. respiratory failure not fully explained by cardiac failure or fluid overload; 4. arterial partial pressure of oxygen / fraction of inspiration oxygen (PaO2/FiO2 ratio, P/F ratio) less than or equal to 300 mmHg.

Exclusion criteria

Patients refused to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Number of survived participantsthrough study completion, an average of 28 daySurvivors and non-survivors in ICU

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026