- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06647095
New Non-invasive Biomarkers of Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD)
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:
- Can a method find participants with higher liver fat than healthy participants?
- 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
Status
Conditions
Intervention / Treatment
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:
- analyzing the fasting spectrum of serum bile acids using liquid chromatography-mass spectrometry
- analyzing the disease-specific spectroscopy patterns given by vibrational and chiroptical spectroscopy of blood plasma
- 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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Liberec, Czech Republic, 46001
- Regional Hospital Liberec
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Praha 2, Czech Republic, 12800
- General University Hospital in Prague
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy controls
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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
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|
MASH
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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
|
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Steatosis
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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
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A single day during within the data collection period = between September 2021 and September 2024
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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
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To access the effect of serum bile acid concentrations on intergroup discrimination in a discriminant model as measured by model parameters and ROC
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A single day during within the data collection period = between September 2021 to September 2024
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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)
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Concentrations of VOC in fasting exhaled breath expressed in ppbv
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Single measurement on one day within 6 weeks (from mid-February 2023 to the end of March 2023)
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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)
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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
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Baseline, at 150min after capsules ingestion - both on one day within 6 weeks (from mid-February 2023 to the end of March 2023)
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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)
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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
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On one day within 6 weeks (from mid-February 2023 to the end of March 2023)
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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)
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A maximum concentration of d-Limonene and TMA in exhaled breath post-ingestion of d-Limonene and TMA-containing capsules, expressed in ppbv
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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)
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Spectroscopic patterns of blood plasma
Time Frame: Based on single peripheral blood uptake within the data collection period = between September 2021 and September 2024
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Disease-specific patterns of blood plasma expressed as differences in spectra (their normalized intensity (a.u.)) and regions between the aim groups
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Based on single peripheral blood uptake within the data collection period = between September 2021 and September 2024
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Collaborators and Investigators
Investigators
- Principal Investigator: Barbora Nováková, MD, General University Hospital in Prague
Publications and helpful links
General Publications
- Zizalova K, Novakova B, Vecka M, Petrtyl J, Lanska V, Pelinkova K, Smid V, Bruha R, Vitek L, Lenicek M. Serum concentration of taurochenodeoxycholic acid predicts clinically significant portal hypertension. Liver Int. 2023 Apr;43(4):888-895. doi: 10.1111/liv.15481. Epub 2022 Nov 25.
- WED-280 Spectroscopy of blood plasma has the potential to differentiate metabolic dysfunction-associated steatohepatitis from steatosis Nováková, Barbora et al. Journal of Hepatology, Volume 80, S539 - S540
- Puri P, Daita K, Joyce A, Mirshahi F, Santhekadur PK, Cazanave S, Luketic VA, Siddiqui MS, Boyett S, Min HK, Kumar DP, Kohli R, Zhou H, Hylemon PB, Contos MJ, Idowu M, Sanyal AJ. The presence and severity of nonalcoholic steatohepatitis is associated with specific changes in circulating bile acids. Hepatology. 2018 Feb;67(2):534-548. doi: 10.1002/hep.29359. Epub 2017 Dec 23.
- Spanel P, Smith D. Quantification of volatile metabolites in exhaled breath by selected ion flow tube mass spectrometry, SIFT-MS. Clin Mass Spectrom. 2020 Feb 13;16:18-24. doi: 10.1016/j.clinms.2020.02.001. eCollection 2020 Apr.
- Sinha R, Lockman KA, Homer NZM, Bower E, Brinkman P, Knobel HH, Fallowfield JA, Jaap AJ, Hayes PC, Plevris JN. Volatomic analysis identifies compounds that can stratify non-alcoholic fatty liver disease. JHEP Rep. 2020 Jun 15;2(5):100137. doi: 10.1016/j.jhepr.2020.100137. eCollection 2020 Oct.
- Ten-Doménech I, Rienda I, Pérez-Rojas J, et al. Progress and challenges of mid-infrared spectroscopy for liver characterization focusing on steatosis, fibrosis and cancer. Applied Spectroscopy Reviews. 2024;59(4):578-599
- Targher G, Byrne CD, Tilg H. MASLD: a systemic metabolic disorder with cardiovascular and malignant complications. Gut. 2024 Mar 7;73(4):691-702. doi: 10.1136/gutjnl-2023-330595.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GUHPrague83/21
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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