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Clinical Trials in China / NCT04964310
Recruiting Observational

Screening of Susceptibility Genes for APAP Induced Drug Induced LIver Injury in ChiNese Population: a Case-control Study

NCT04964310 · tracked via the Priya Life Science China tracker
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Phase
Observational
Started
2020-08-31
Last updated
2025-02-26

Condition(s) studied

AcetaminophenDrug-Induced Liver InjuryPharmacogeneticsChina

Investigational drug(s) / intervention(s)

genetic polymorphism

genetic polymorphism: Observe the genetic polymorphism frequency difference between case and control groups

Study summary

Acetaminophen (APAP) is the most commonly used NSAIDS in clinic, and it is also a common cause of drug-induced liver injury (DILI). In 2012, the proportion of DILI caused by APAP in the United States was 51%, while in Asia, it was only 7.10%. Previously, a small cohort study in the United States screened for some of the susceptibility genes for DILI due to APAP by the Genome wide association study (GWAS) method. However, the genetic susceptibility loci based on the US cohort were not applicable to the Chinese population. Therefore, we make a study design include Chinese population who ingested APAP and divided them into case group and control group according to the occurrence of DILI. We hope to be able to find the root of differences at the genetic level and explore new pathogenic mechanisms.

Eligibility

Sex
ALL
Min age
14 Years
Max age
Healthy volunteers
No
Inclusion criteria: * A clear history of acetaminophen (or acetaminophen-containing drugs) ingestion. * Plasma and/or urine testing for acetaminophen components if history of ingestion is unclear. * Monitoring of Alanine aminotransferase (ALT) or Aspartate Aminotransferase (AST) ≥ 1000 IU/L at any time after APAP administration and Roussel Uclaf Causality Assessment Method(RUCAM) score \> 6 * Age ≥ 14 years old * The subject or guardian agrees to participate in this project and signs an informed consent form. Exclusion criteria: * The use of drugs for which frequency of adverse reactions to liver damage is defined as "common or very common" (≥1%) in the instructions. * Concurrent use of herbs that are clearly susceptible to liver damage (see list of definitions in the Annex). * Have a known definite cause of liver damage: active viral hepatitis; alcoholic liver disease; autoimmune liver disease; primary or secondary liver tumors; and other underlying liver disease that has affected liver function. * Those who fail to provide complete general information and clinical information. * Subjects or guardians who do not agree to see this project do not sign the informed consent form.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital with Nanjing Medical University Nanjing Jiangsu Recruiting

More The First Affiliated Hospital with Nanjing Medical University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04964310 on ClinicalTrials.gov ↗ ← All trials in China