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Role of New Adipokines and Hepatokines in Prediction of Patients With Metabolic Syndrome or NAFLD

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02285218
Enrollment
200
Registered
2014-11-06
Start date
2014-04-30
Completion date
2019-03-31
Last updated
2019-03-18

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

Conditions

Metabolic Syndrome, Non-alcoholic Fatty Liver Disease, Type 2 Diabetes

Brief summary

To investigate the predictive roles of adipokines and hepatokines to detect non-alcoholic fatty liver disease (NAFLD), diabetes, or dyslipidmia. To examine the association or effects of clinical and biochemical factors (lab results and medication, etc.) on serum levels of adipokines and hepatokines in certain subjects with non-alcoholic fatty liver disease (NAFLD), diabetes, or dyslipidmia.

Interventions

OTHERserum blood sampling

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. dyslipidemia 1. serum triglyceride≥150mg/dl, or taking medication to lower triglyceride levels (e.g. fibrates, niacin, omega-3, etc.) or 2. serum LDL-C≥100mg/dl, or taking medication to lower LDL-C levels (e.g. statin, ezetimibe, etc.) 2. type 2 diabetes 1. defined according to the ADA guideline (DM definition) or 2. taking any anti-diabetic medications 3. non-alcoholic fatty liver disease (NAFLD) 1. diagnosed as having fatty liver by ultrasonogram or 2. diagnosed as having fatty liver by transient elastogram (Fibroscan) or 3. diagnosed as having fatty liver by abdomina CT scan 4. Normal control 1. should not be included in other groups as above and 2. not taking any medication related to diabetes and dyslipidemia and 3. BMI \<25kg/m2

Exclusion criteria

1. subjects who refused to agree with informed consents 2. subjects with organ-transplantation 3. serum creatinine ≥1.5mg/dl 4. pregnant women 5. liver cancer or pancreatic cancer 6. subjects with chronic hepatitis B or C virus infection 7. for NAFLD group, subjects with excessive alcohol consumption (men: ≥210g of alcohol per week, women: ≥140g of alcohol per week)

Design outcomes

Primary

MeasureTime frameDescription
new adipokinesTo 8h fasting blood sampleseveral candidate adipokines and hepatokines to predict diseases will be measured using ELISA
new hepatokinesTo 8h fasting blood sampleseveral candidate adipokines and hepatokines to predict diseases will be measured using ELISA

Countries

South Korea

Contacts

Primary ContactBong Soo Cha, MD
bscha@yuhs.ac+82-2-2228-1932

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026