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)
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
172
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
Regional Hospital Liberec
Liberec, Czech Republic, Czechia
General University Hospital in Prague
Prague, Czech Republic, Czechia
Serum bile acids concentrations in the MASH/ Steatosis/ Healthy controls
Individual bile acid concentrations in blood serum accessed by LC-MS/MS, measured in µmol/L or expressed as detectable or undetectable
Time frame: 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
To access the effect of serum bile acid concentrations on intergroup discrimination in a discriminant model as measured by model parameters and ROC
Time frame: 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
Concentrations of VOC in fasting exhaled breath expressed in ppbv
Time frame: 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
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
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)
The effect of concentrations of volatile organic compounds in exhaled breath, native and post-ingestion, on the discrimination of the aim groups
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
Time frame: 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
A maximum concentration of d-Limonene and TMA in exhaled breath post-ingestion of d-Limonene and TMA-containing capsules, expressed in ppbv
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)
Spectroscopic patterns of blood plasma
Disease-specific patterns of blood plasma expressed as differences in spectra (their normalized intensity (a.u.)) and regions between the aim groups
Time frame: Based on single peripheral blood uptake within the data collection period = between September 2021 and September 2024
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