Single-Cell and Spatial Transcriptomics Analysis of Steatotic Donor Liver Susceptibility to Post-Transplant Injury

Air Force Military Medical University of People's Liberation Army

Status: Completed

Conditions: Postoperative Complications; Fatty Liver; Liver Transplant; Complications; Liver Failure; End Stage Liver Disease; Ischaemia Reperfusion Injury of Liver

Study type: Observational

Funder types: Other

Identifiers

NCT07362745

KY20252571-C-1

Details and patient eligibility

About

The goal of this observational study is to understand why liver transplants from donors with fatty liver disease (steatotic donor livers) are more vulnerable to post-transplant injury, analyzing historical clinical data and collected tissue samples using advanced genetic techniques.

The main questions it aims to answer are:

• Which specific cell types and their spatial interactions contribute to increased post-transplant injury susceptibility in steatotic donor livers?
• What are the key molecular differences in gene expression between steatotic and normal donor livers following transplantation?

Researchers will compare 300 historical liver transplant cases from 2015-2025, including 50 cases with archived tissue samples available for molecular analysis, and 250 cases with clinical data only. Donor liver steatosis was assessed by histopathology when tissue was available, or by donor clinical data when tissue was not available. The two groups (steatotic donor liver recipients vs. normal donor liver recipients) will be matched based on donor age, ischemia time, recipient scores, and other key clinical parameters to control for potential confounding variables.

This is a retrospective analysis of existing data and archived biospecimens; no prospective participant enrollment or additional sample collection will occur.

Enrollment: 300 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Recipient Criteria:

• Participant (or legal representative if unable to read/sign) provides written informed consent
• Age 18-80 years (inclusive) at time of enrollment
• Clinical diagnosis of liver failure requiring liver transplantation
• Stable vital signs and deemed medically fit to tolerate liver transplantation surgery

Donor Criteria:

• Fatty degeneration range: Macrovesicular steatosis 0-30%
• Donor age: ≤60 years
• Cold ischemia time (CIT): ≤12 hours for deceased donors
• Liver function: ALT/AST <5 times upper limit of normal

Exclusion criteria

Recipient Criteria:

• Pregnant or lactating women
• Prior history of non-autologous (allogeneic) bone marrow or stem cell transplantation
• Blood transfusion within 7 days prior to tissue sampling
• Radical cancer treatment within 3 years prior to enrollment
• Use of anti-tumor medications within 30 days prior to enrollment
• Known bleeding diathesis or coagulation disorder
• Active autoimmune disease
• Concurrent malignancy or multiple primary tumors

Donor Criteria:

• Fibrosis: Any degree of hepatic fibrosis
• Steatohepatitis: Presence of lobular inflammation or hepatocyte ballooning
• Active infection: HBV, HCV, or HIV positive
• Severe fatty liver-related comorbidities: Uncontrolled diabetes (HbA1c>8%), severe hyperlipidemia

Trial design

300 participants in 2 patient groups

Steatotic Donor Liver Recipients

Description:

Liver transplant recipients receiving donor livers with macrovesicular steatosis ≥5% (steatotic donor liver). Participants undergo standard liver transplantation with two small liver tissue samples collected during surgery (during graft preparation and before abdominal closure) followed by postoperative monitoring.

Normal Donor Liver Recipients

Description:

Liver transplant recipients receiving donor livers with \<5% steatosis (normal donor liver). Participants undergo standard liver transplantation with two small liver tissue samples collected during surgery (during graft preparation and before abdominal closure) followed by postoperative monitoring.