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Metabolic Syndrome Among Polish Twins

Multimorbidity in Metabolic Syndrome: A Longitudinal Cohort Study in TWINS.PL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07181018
Acronym
TWINSPL
Enrollment
1500
Registered
2025-09-18
Start date
2025-09-01
Completion date
2033-09-30
Last updated
2025-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome, Twins

Brief summary

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.

Interventions

OTHERTrial within cohort (TWIC)

Educational intervention based on a protocol specifically developed for the TWINS.PL cohort, aimed at activating and engaging the participant in the intervention process. Intervention group: Phenotypically concordant participants from the TWINS.PL STUDY cohort, randomized to receive an educational intervention designed to actively engage them in modifying selected health-relevant endpoints. Control group: The co-twin of the participant randomized to the intervention arm, serving as the control. 1. TWINS-TWIC HL: Research Question: Does participation in a structured, participant-activating educational intervention program influence health literacy indicators among participants of the TWINS.PL study? Study Design: A randomized controlled trial embedded within a prospective observational twin cohort (TWiC study in a twin cohort). 2. TWINS-TWIC DIET Research Question: Does participation in a structured, participant-activating educational intervention focused on dietary habits influence the

Sponsors

Poznan University of Medical Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 44 Years
Healthy volunteers
No

Inclusion criteria

1\. Age between 15 and 44 years. 2. Provision of informed consent to participate in the study. 3. Twin with a living co-twin. 4. Positive family history in first- and second-degree relatives of metabolic syndrome (MS), associated diseases, or the most common complications of the syndrome. \_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_

Exclusion criteria

Permanent

Design outcomes

Primary

MeasureTime frameDescription
De novo occurrence of metabolic steatosis, hepatic fibrosis, or cirrhosis.Baseline up to approximately 5 yearsDe novo occurrence of metabolic steatosis, hepatic fibrosis, or cirrhosis based on assessment by magnetic resonance imaging-proton density fat fraction (MRI-PDFF) and/or transient elastography.
Progression of hepatic steatosis or fibrosis to more advanced stages or cirrhosis.Baseline up to approximately 5 yearsProgression of hepatic steatosis or fibrosis to more advanced stages or cirrhosis, as assessed by magnetic resonance imaging and dynamic elastography, using the following evaluation scales: * The hepatic steatosis grading scale based on magnetic resonance imaging-proton density fat fraction (MRI-PDFF); * The hepatic steatosis grading scale based on dynamic elastography using the Controlled Attenuation Parameter (CAP) technique; * The liver fibrosis grading scale assessed by dynamic elastography using liver stiffness (LS) measurement, according to the METAVIR scoring system

Secondary

MeasureTime frameDescription
First-time occurrence of Prediabetes or type 2 diabetes mellitus (T2DM)Baseline to approximately 5 yearsFirst diagnosis of prediabetes or type 2 diabetes mellitus (T2DM), confirmed by standard laboratory criteria (fasting plasma glucose, HbA1c, or oral glucose tolerance test) in accordance with current ADA/EASD guidelines
The assessment of HOMA-IRBaseline to approximately 5 yearsFirst-time occurrence of HOMA-IR \>5
First-time occurrence of Pancreatic steatosisBaseline to approximately 5 yearsVisualization of pancreatic steatosis during abdominal ultrasound and/or MRI-PDFF
First-time occurrence of Hypertension (HTN)Baseline to approximately 5 yearsDiagnosis of arterial hypertension according to the ESC/ESH definition
First-time occurrence of Acute coronary syndrome, the need for coronary artery bypass grafting (CABG), any percutaneous coronary intervention (PCI), or detection of regional wall motion abnormalities on echocardiographyBaseline to approximately 5 yearsAll outcome events will be confirmed through review of medical records, including hospitalization reports, procedural documentation, and echocardiographic findings, in accordance with the most recent ESC guidelines on Acute Coronary Syndromes.
First-time occurrence of Systolic heart failure with a reduced left ventricular ejection fraction of less than 45%Baseline to approximately 5 yearsDiagnosis of systolic heart failure confirmed by echocardiographic assessment showing a left ventricular ejection fraction (LVEF) \<45%.
First-time occurrence of Atrial fibrillation/flutterBaseline to approximately 5 yearsFirst documented episode of atrial fibrillation (paroxysmal, persistent, or permanent) or atrial flutter, confirmed by ECG or other cardiac monitoring, or the need for pulmonary vein isolation and/or cavotricuspid isthmus ablation.
First-time occurrence of Requirement for angioplasty, stenting, or surgery of the aorta or any other arteries (excluding trauma-related causes)Baseline to approximately 5 yearsFirst requirement for angioplasty, stent placement, or surgical intervention of the aorta or other arteries (excluding trauma-related procedures), confirmed by medical records and procedural documentation.
First-time occurrence of overweight or obesityBaseline to approximately 5 yearsOverweight will be defined as a BMI of 25 to \<30 kg/m², and obesity as a BMI of ≥30 kg/m²
First-time occurrence of Transient ischemic attack (TIA) or ischemic strokeBaseline to approximately 5 yearsFirst documented occurrence of transient ischemic attack (TIA) or ischemic stroke, confirmed by neurological assessment and/or neuroimaging, in accordance with current ESC guidelines.
First-time occurrence of Hashimoto's thyroiditisBaseline to approximately 5 yearsIncrease of at least one anti-thyroid autoantibody - anti-thyroid peroxidase and/or anti-thyroglobulin, accompanied by typical ultrasound picture suggesting Hashimoto's thyroiditis, namely irregular, decreased echogenicity of thyroid parenchyma, signs of fibrosis and decreased vascularity on Color Doppler examination
First-time occurrence of Focal thyroid lesions detected on ultrasoundBaseline to approximately 5 yearsFocal thyroid lesions detected on ultrasound (≥1 lesion with a diameter \>5 mm)
First-time occurrence of Adrenal incidentalomaBaseline to approximately 5 yearsAdrenal lesion \>10 mm in diameter
First-time occurrence of Malignancy with a known potential association with insulin resistanceBaseline to approximately 5 yearse.g., colorectal, thyroid, breast, endometrial, hepatic, pancreatic, renal, gallbladder, esophageal, or ovarian cancer
First-time occurrence of Long COVID-19 syndromeBaseline to approximately 5 yearsDefined as persistent (over 12 weeks) symptoms (listed in the questionnaire filled out by the patient), which appeared after COVID-19 infection and their occurrence cannot be explained by other causes
Death from non-accidental causesBaseline to approximately 5 yearsThe number of deaths from non accidental causes during the observation period
The assessment of HbA1cBaseline to approximately 5 yearsFirst-time occurrence of HbA1c \>5.7%
First-time occurrence of Implantation of a cardiac electronic deviceBaseline to approximately 5 yearsFirst implantation of a cardiac electronic device (e.g., pacemaker, ICD, or CRT) indicated for sick sinus syndrome, advanced atrioventricular conduction abnormalities, or ischemic heart disease, as confirmed by procedural documentation.
First-time occurrence of an increase in visceral adipose tissueBaseline to approximately 5 yearsIncrease in visceral adipose tissue \>10%, as assessed by DEXA or BIA

Countries

Poland

Contacts

Primary ContactPiotr Eder, MD, Profesor
piotreder@ump.edu.pl+(48) 618691343

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026