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Identification of immune targets related to sepsis based on multi-omics Mendelian randomization analysis

Identification of immune targets related to sepsis based on multi-omics Mendelian randomization analysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129359
Enrollment
Unknown
Registered
2026-08-04
Start date
2026-08-05
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

sepsis

Interventions

Transcriptome, proteome:none

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Significantly related to exposure: SNPS must be associated with target exposure (expression of a specific gene or abundance of a specific protein) It is significantly correlated at the whole-genome level (eQTL usually p<5×10^-8, pQTL commonly p<5×10^-6). 2. Genetic independence: There is no linkage disequilibrium among the selected SNPs (usually r^2<0.001 within 10,000 kb) to ensure that each instrumental variable provides independent information. 3. Instrumental variable strength: The F-statistic of each SNP should be greater than 10 to avoid weak instrumental variable bias. "F-statistics" The formula for calculating the quantity is: F = (Beta^2/ SE^2). 4. Data Availability: The SNP must be present in both the exposure and outcome GWAS summary data, and the allelic side Be consistent.

Exclusion criteria

Exclusion criteria: 1. Palindromic sequences and chain ambiguity SNPs: Exclude those A/T or C/G SNPs whose positive chains cannot be determined to avoid alleles Matching error. 2. Outlier SNPS: In sensitivity analyses (such as MR-PRESSO), they are identified as having a disproportionately significant impact on the results Abnormal SNPS with loud noises will be excluded. 3. SNPS with significant pleiotropy: Discovered through methods such as MR-Egger regression and PhenoScanner database query Now, pleiotropic SNPS significantly associated with known sepsis confounding factors (such as smoking, obesity, and other autoimmune diseases) will be excluded. 4. Low frequency of secondary alleles: Rare variations with MAF<0.01 are usually excluded to ensure the stability of the results.

Design outcomes

Primary

MeasureTime frame
Risk of Sepsis, Exposure data, outcome data, validation and functional analysis data;

Countries

China

Contacts

Public ContactLi Yuling

The First Affiliated Hospital of Dalian Medical University

liyuling@firsthosp-dmu.com+86 411 83635963

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026