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A prospective observational study for the diagnosis of non-alcoholic fatty liver disease with circulating natriuretic peptides

A prospective observational study for the diagnosis of fatty deposits and fibrosis in non-alcoholic fatty liver disease with circulating natriuretic peptides - Diagnosis of non-alcoholic fatty liver disease with circulating natriuretic peptides

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000048569
Enrollment
500
Registered
2022-09-01
Start date
2022-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Interventions

None listed

Sponsors

Sapporo Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who are diagnosed with fatty liver in the out-patient clinic or hospitalized at the Department of Gastroenterology, Sapporo Medical University Hospital, and provided written consent. 1. Patients who have already been diagnosed with fatty liver in a medical check-up and are scheduled for an abdominal ultrasound 2. Hospitalized patients who are pointed out with fatty liver by abdominal ultrasound or abdominal CT 3. Patients aged 18 years or older at the time of obtained consent 4. Patients who provided voluntary written consent from the patient or their legal representative after receiving sufficient explanation about participating in this study

Exclusion criteria

Exclusion criteria: 1. Patients with a history diagnosed or treated with heart failure 2. Patients with alcohol intake (ethanol conversion) of 30g/day for males and 20g/day for females 3. Patients diagnosed with liver cirrhosis 4. Patients who have a history of infection or who are treated with hepatitis B or hepatitis C 5. Patients with intrahepatic malignant tumors such as hepatocellular carcinoma 6. Patients with a diagnosis of any malignancy 7. Patients under treatment with steroids, immunosuppressants, anticancer drugs, etc. 8. Patients diagnosed with chronic inflammatory diseases, such as autoimmune hepatitis, inflammatory bowel disease 9. Patients who do not consent to this study 10. Patients who are judged to be inappropriate as research subjects by the research director

Design outcomes

Primary

MeasureTime frame
Correlation between the degree of hepatic steatosis/fibrosis by abdominal ultrasound and plasma ANP or BNP concentration

Secondary

MeasureTime frame
1. Comparison of the diagnostic accuracy of liver fibrosis between the conventional scoring system to predict liver fibrosis (Fib-4 index, NAFLD fibrosis score) and plasma ANP or BNP concentration 2. Correlation between the presence or absence of arteriosclerosis diagnosed by ABI (ankle brachial pressure index) and plasma ANP/BNP concentrations 3. Correlation between liver fibrosis, arteriosclerosis, and RAS/fibrosis/inflammatory biomarkers

Countries

Japan

Contacts

Public ContactTomoko Ichiki

Sapporo Medical University Department of General Medicine

Ichiki.tomoko@sapmed.ac.jp011-611-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026