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The Influence of Autophagy on Fatty Liver

The Influence of Autophagy on Nonalcoholic Fatty Liver Disease

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01988441
Enrollment
800
Registered
2013-11-20
Start date
2013-09-30
Completion date
2025-08-31
Last updated
2023-09-14

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

Conditions

Non-alcoholic Fatty Liver Disease, Obesity

Keywords

autophagy, children, polymorphism

Brief summary

Non-alcoholic fatty liver disease (NAFLD) is one of the most common causes of chronic liver disease worldwide. It is not known why only some obese subjects develop NAFLD. In recent years, a growing body of evidence showed a crucial role of autophagy in in the regulation of liver fat storage. The purpose of this study is to determine whether autophagy pathway-related genetic polymorphisms affect NAFLD.

Detailed description

The investigators will perform a prospective comparison of the genotype distribution of autophagy pathway-related genetic polymorphisms between those with and without NAFLD in a cohort of obese children and adolescents. \[Subjects\] Obesity is defined as the BMI value \> 95 percentile by different age- and gender groups according to the standards of the Department of Health in Taiwan. \[Data collection\] The following data were obtained for each subject: age, gender, BMI, waist and hip circumference. The investigators will measure total serum bilirubin, alanine aminotransferase, aspartate aminotransferase, γ-glutamyltransferase fasting glucose, triglyceride, total cholesterol, and high-density lipoprotein cholesterol, insulin, glucose, and adiponectin. \[Liver ultrasonography\] All participants will receive an ultrasonographic study of the liver. NAFLD is defined as the presence of an ultrasonographic pattern consistent with the following criteria: liver-kidney echo discrepancy, attenuated echo penetration and visibility of diaphragm, and obscure hepatic vessel structures. \[Genotyping\] Genomic DNA will be extracted from 3 cc venous blood from each participant. After extraction, the genomic DNA will be immediately stored at -80°C. The TaqMan genotyping assays will be performed for selected SNPs genotyping on ABI 7300 Real-Time PCR System (Applied Biosystems). \[Sample size\] Sample size was estimated by Epi InfoTM 7 (CDC, USA) program. Because there was no previous data regarding to the effect of autophagy related gene on NAFLD, the investigators estimate the odds ratio to vary between 60-80%. The investigators used a confidence level of 95%, power of 80%, the ratio of controls to NAFLD cases of 25%, percent of controls exposed of 25-35%, the samples size required would be a total of 291-872 subjects.

Interventions

None listed

Sponsors

Ministry of Science and Technology, Taiwan
CollaboratorOTHER_GOV
Far Eastern Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Age 6-18 years old * Obesity definition: BMI \> 95% according to the age- and gender-specific standard by National Health Institute in Taiwan * Willing to give written informed consent

Exclusion criteria

* Alcohol consumption * Chronic liver diseases, including hepatitis B, hepatitis C, Wilson disease and autoimmune hepatitis * Major systemic diseases, including cardiopulmonary disease, renal failure, cancer, and psychotic disorder

Design outcomes

Primary

MeasureTime frameDescription
The genotype distribution of autophagy pathway-related genetic polymorphisms between those with and without NAFLDOne yearThe genotype distribution of autophagy pathway-related genetic polymorphisms between those with and without NAFLD

Countries

Taiwan

Contacts

Primary ContactYu-Cheng Lin, M.D., Ph.D.
q92421006@ntu.edu.tw+886-89667000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026