Actively Recruiting
Metabolic Syndrome Among Polish Twins
Led by Poznan University of Medical Sciences · Updated on 2025-09-18
1500
Participants Needed
1
Research Sites
421 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Over a 5-year follow-up period, we aim to conduct a study among twins aged 15-44 years from the Polish population with the following objectives: 1. To determine the incidence and risk factors for the development of de novo metabolic dysfunction-associated steatotic liver disease (MASLD), liver fibrosis, or cirrhosis. We also intend to evaluate the progression of hepatic steatosis from early to advanced stages or toward fibrosis/cirrhosis. 2. To determine the prevalence and identify predictive factors for the onset and progression of features, diseases, or complications of metabolic syndrome (MS) other than liver disease, particularly within the spectrum of metabolic, nutritional, cardiovascular, endocrine, oncological, psychological, and other disorders typically associated with MS. 3. To assess the association between previous COVID-19 infection or long-COVID features and the occurrence of MASLD, liver fibrosis, or cirrhosis due to MASLD, as well as other features, diseases, or complications of MS. 4. To evaluate the prevalence of malignancies in a young twin population (aged 15-44 years) with MS or with risk factors for MS. 5. To investigate the contribution of genetic and environmental factors and gut microbiota composition to the development and progression of structural liver changes (steatosis, fibrosis, cirrhosis) in MASLD, as well as other features and complications of MS in twins discordant for the MS phenotype. 6. To assess the role of genetic and environmental components in the occurrence and severity of MS phenotype discordance in monozygotic twins.
CONDITIONS
Official Title
Metabolic Syndrome Among Polish Twins
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 15 and 44 years
- Provided informed consent to participate
- Have a living co-twin
- Positive family history of metabolic syndrome or its common complications in first- or second-degree relatives
You will not qualify if you...
- Co-twin does not consent to participate
- Unable to obtain medical history of biological family members
- Advanced liver fibrosis, cirrhosis, or liver cancer
- Known liver genetic disorders, autoimmune hepatitis, celiac disease, hemochromatosis, primary biliary cholangitis, primary sclerosing cholangitis, cystic fibrosis, or Wilson's disease
- Current or chronic alcohol consumption over 20 g/day in women or 30 g/day in men
- Short bowel syndrome
- Cyanotic congenital heart defect
- Myasthenia
- Central nervous system degenerative diseases such as Alzheimer's, Parkinson's, or Huntington's disease
- Storage diseases involving the liver
- Active malignant cancer under treatment (excluding certain skin cancers treated without drugs)
- Chronic kidney disease requiring renal replacement therapy
- History of organ or tissue transplantation requiring immunosuppression
- Pituitary, hypothalamic, or adrenal dysfunction requiring hormone therapy
- Addiction to psychoactive substances or drugs
- Other severe incurable diseases preventing participation
- Lack of cooperation during research center visits
- Acute infection, fever, or antibiotic use at recruitment (temporary exclusion)
- Vaccination within past 6 weeks (temporary exclusion)
- Pregnancy or up to 6 months postpartum (temporary exclusion)
- Within 3 months after breastfeeding cessation (temporary exclusion)
- Within 3 months after surgery (except minor procedures) (temporary exclusion)
- Untreated thyroid dysfunction (temporary exclusion until euthyroidism achieved)
- Significant recent weight change over 10% (temporary exclusion until stable)
- Within 6 months after stopping parenteral or enteral nutrition via feeding tube (temporary exclusion)
- Within 12 months after bariatric surgery (temporary exclusion)
- Recent systemic treatment with steroids, chemotherapy, immunosuppressants, or hepatotoxic biological therapy (temporary exclusion until 3 months after treatment completion)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Uniwersytecki Szpital Kliniczny
Poznan, Wielkopolska, Poland, 60-355
Actively Recruiting
Research Team
P
Piotr Eder, MD, Profesor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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