New Non-invasive Biomarkers of Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD)

October 30, 2024 updated by: Barbora Nováková, MD, General University Hospital, Prague

Identification of New Non-invasive Biomarkers of Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) in Patients by Blood Plasma Spectroscopy, Breath Volatile Organic Compounds Analysis and Serum Bile Acids Analysis

The goal of this observational study is to learn if some components of blood or exhaled breath can diagnose people having more fat in their livers than is normal, because of their poorer metabolic health (for example, because of obesity and diabetes). The main questions it aims to answer are:

  1. Can a method find participants with higher liver fat than healthy participants?
  2. Can a method find participants in whom higher liver fat was a cause of liver inflammation or stiffness?

Participants will:

  • fast overnight
  • have a routine blood draw
  • easily exhale a few times into a special device or a plastic bag and fill in a short dietary questionnaire (if participating in a breath test)
  • optionally swallow capsules with an orange peel extract and fish oil before exhaling, which can help get better results from breath (capsules will be medically safe and approved)

Study Overview

Detailed Description

Patients with MASLD and healthy volunteers will be offered an observational study evaluating the diagnostic role of new non-invasive experimental methods (serum bile acids, breath VOC, and plasmatic spectroscopic patterns) assessing the presence and severity of liver fibrosis and steatosis.

First, this study aims to differentiate patients with metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) from healthy controls (or simple steatosis) using three experimental methods.

Second, the investigators aim to stratify patients with MASLD according to the presence/grade of steatosis and fibrosis (any, significant F2-3, advanced F3, cirrhosis F4) using the same methods.

Experimental methods tested in this study include:

  1. analyzing the fasting spectrum of serum bile acids using liquid chromatography-mass spectrometry
  2. analyzing the disease-specific spectroscopy patterns given by vibrational and chiroptical spectroscopy of blood plasma
  3. analyzing trace concentrations of volatile organic compounds (VOC) in exhaled human breath using the Selected ion flow tube mass spectrometry. This contains the so-called stress test to monitor breath VOC (d-Limonene and triethylamine) after their regulated ingestion in the form of capsules

These parameters may eventually be combined with anthropometric and laboratory parameters (such as age or BMI).

Clinical examinations, blood sampling, ultrasound examinations of the liver, and liver elastography will be performed as part of routine care.

The results of the blood parameters can be retrospectively evaluated.

Approximately 60-80 participants in total were anticipated for each method. For patients who participate in breath tests, adequate insurance must be guaranteed.

Statistical processing: individual parameters will be evaluated in an exploratory and a validation group or by the PLS-DA algorithm with repeated cross-validation. A difference of p <0.05 will be considered a statistically significant change.

Study Type

Observational

Enrollment (Actual)

172

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Liberec, Czech Republic, 46001
        • Regional Hospital Liberec
      • Praha 2, Czech Republic, 12800
        • General University Hospital in Prague

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Patients with MASLD of primary care clinic, healthy volunteers

Description

Inclusion Criteria for Participants with MASLD:

  • Presence of liver steatosis (detected either by hepatic ultrasonography/CAP/histologically) or MASH/simple steatosis confirmed by liver biopsy
  • Absence of secondary causes of fat accumulation in the liver and other liver disease: ruled out other etiologies of liver disease, such as viral hepatitis, drug-induced liver disease, autoimmune liver disease, biliary tract disease, and hereditary metabolic diseases

Inclusion Criteria for Negative Controls:

  • Absence of liver disease
  • For breath analysis: absence of liver steatosis (normal liver ultrasound image and CAP less than 248 dB/m)
  • For plasma spectroscopy and bile acid analysis: Body Mass Index ≤ 25 and waist-hip ratio ≤ 0.95 plus normal liver ultrasound
  • Absence of diabetes mellitus and metabolic syndrome
  • Normal liver function tests, lipid spectrum, fasting glycemia
  • Alcohol intake less than 20 g/ day (women) or 30 g/ day (men)

Exclusion Criteria:

  • Non-compliance with the investigation program
  • Failure to sign the informed consent form
  • Liver biopsy/clinic discrepancy
  • For LMN a TMA "stress test": fish, see fruit and citrus fruit allergy
  • Pregnancy
  • For bile acid analysis: Treatment with BA or BA sequestrants
  • For bile acid analysis: Portal hypertension (does not apply for MASH patients)
  • For bile acid analysis: Cirrhosis (does not apply for MASH patients)
  • For plasma spectroscopy: Cirrhosis
  • Anamnesis of alcohol abuse (based on GGT, carbohydrate-deficient transferrin, urinary ethyl-glucuronide, and patient's history)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Healthy controls
Capsules containing d-Limonene will be optionally given during the breath test to all participants of all groups
Capsules containing fish oil will be optionally given during the breath test to all participants of all groups
MASH
Capsules containing d-Limonene will be optionally given during the breath test to all participants of all groups
Capsules containing fish oil will be optionally given during the breath test to all participants of all groups
Steatosis
Capsules containing d-Limonene will be optionally given during the breath test to all participants of all groups
Capsules containing fish oil will be optionally given during the breath test to all participants of all groups

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Serum bile acids concentrations in the MASH/ Steatosis/ Healthy controls
Time Frame: A single day during within the data collection period = between September 2021 and September 2024
Individual bile acid concentrations in blood serum accessed by LC-MS/MS, measured in µmol/L or expressed as detectable or undetectable
A single day during within the data collection period = between September 2021 and September 2024
The effect of serum bile acids in the MASH/ Steatosis/ Healthy controls discrimination
Time Frame: A single day during within the data collection period = between September 2021 to September 2024
To access the effect of serum bile acid concentrations on intergroup discrimination in a discriminant model as measured by model parameters and ROC
A single day during within the data collection period = between September 2021 to September 2024
Native breath concentrations of volatile organic compounds in the aim groups
Time Frame: Single measurement on one day within 6 weeks (from mid-February 2023 to the end of March 2023)
Concentrations of VOC in fasting exhaled breath expressed in ppbv
Single measurement on one day within 6 weeks (from mid-February 2023 to the end of March 2023)
A change in d-Limonene and TMA concentrations before and after the ingestion of capsules containing d-LMN, TMA, ppbv
Time Frame: Baseline, at 150min after capsules ingestion - both on one day within 6 weeks (from mid-February 2023 to the end of March 2023)
A change in concentration of d-Limonene and TMA in exhaled breath after an overnight fast/ post-ingestion of d-Limonene and TMA-containing capsules, expressed in ppbv
Baseline, at 150min after capsules ingestion - both on one day within 6 weeks (from mid-February 2023 to the end of March 2023)
The effect of concentrations of volatile organic compounds in exhaled breath, native and post-ingestion, on the discrimination of the aim groups
Time Frame: On one day within 6 weeks (from mid-February 2023 to the end of March 2023)
To access the effect of VOC concentrations in exhaled breath, native and after the ingestion of d-Limonene and TMA-containing capsules, on intergroup discrimination in a discriminant model as measured by model parameters and ROC
On one day within 6 weeks (from mid-February 2023 to the end of March 2023)
Peak of d-LMN, and TMA concentration after the ingestion of capsules in the aim groups
Time Frame: At an individually specific time point for each participant that occurs within 4 hours after ingestion of d-Limonene and TMA-containing capsules on a single day within 6 weeks (from mid-February 2023 to the end of March 2023)
A maximum concentration of d-Limonene and TMA in exhaled breath post-ingestion of d-Limonene and TMA-containing capsules, expressed in ppbv
At an individually specific time point for each participant that occurs within 4 hours after ingestion of d-Limonene and TMA-containing capsules on a single day within 6 weeks (from mid-February 2023 to the end of March 2023)
Spectroscopic patterns of blood plasma
Time Frame: Based on single peripheral blood uptake within the data collection period = between September 2021 and September 2024
Disease-specific patterns of blood plasma expressed as differences in spectra (their normalized intensity (a.u.)) and regions between the aim groups
Based on single peripheral blood uptake within the data collection period = between September 2021 and September 2024

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Barbora Nováková, MD, General University Hospital in Prague

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2021

Primary Completion (Actual)

September 1, 2022

Study Completion (Actual)

September 1, 2024

Study Registration Dates

First Submitted

October 15, 2024

First Submitted That Met QC Criteria

October 15, 2024

First Posted (Actual)

October 17, 2024

Study Record Updates

Last Update Posted (Estimated)

November 1, 2024

Last Update Submitted That Met QC Criteria

October 30, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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