Skip to content

The role and mechanisms of hyperglycemia in the progression of liver cirrhosis to acute-on-chronic liver failure and neutrophil dysfunction

The role and mechanisms of hyperglycemia in the progression of liver cirrhosis to acute-on-chronic liver failure and neutrophil dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104764
Enrollment
Unknown
Registered
2025-06-23
Start date
2024-12-22
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

End-stage liver diseases

Interventions

Control group (healthy individuals):NA
Liver cirrhosis group:NA
Acute-on-chronic liver failure (ACLF) group:NA

Sponsors

Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients aged 18-60 years with liver cirrhosis were enrolled, who voluntarily participated and signed informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with acute-on-chronic liver failure (ACLF) at admission; 2. A family history of diabetes mellitus and/or confirmed diagnosis of diabetes mellitus prior to the onset of liver disease; 3. Secondary diabetes caused by pituitary, adrenal, or thyroid disorders, or primary diabetes (particularly type 2 diabetes mellitus); 4. Concurrent hepatocellular carcinoma (HCC), hepatorenal syndrome (HRS), hepatic encephalopathy, or gastrointestinal bleeding at admission; 5. Coexisting hepatotropic viral hepatitis, drug-induced liver injury, or autoimmune-associated liver diseases; 6. Comorbidities including other malignancies, tuberculosis, or severe dysfunction of vital organs (heart, brain, lungs, kidneys); 7. Long-term use of immunosuppressants and/or glucocorticoids; 8. Active infection or antibiotic use within one week prior to hospitalization; 9. Acquired immune deficiency (e.g., HIV/AIDS); 10. Lactating or pregnant women; 11. Family history of glucose-6-phosphate dehydrogenase (G6PD) deficiency; 12. Hematologic disorders; 13. Incomplete clinical or biochemical data or loss to follow-up.

Design outcomes

Primary

MeasureTime frame
Complete blood count (CBC);Blood biochemistry;Glucose metabolism-related parameters;Neutrophil function assay;Endoplasmic reticulum (ER) stress-related protein detection;

Countries

China

Contacts

Public ContactSide Li

Affiliated Hospital of Zunyi Medical University

linshide6@hoemall.com+86 138 8525 4802

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026