Clinical trial

Relationship Between Eating Patterns, Body Composition and the Detection of Fatty Liver in Children and Adolescents With Trisomy 21: LiverTy Project

Invitation only · Not applicable · 1 countries · Registry ID NCT06888570

Invitation onlyNot applicableObservational

What this study is about

Childhood obesity is a growing public health issue affecting millions of children worldwide, increasing the risk of metabolic and cardiovascular diseases in adulthood. This problem is particularly concerning in children and adolescents with Down syndrome (trisomy 21, T21), who have a higher predisposition to fat accumulation due to genetic, metabolic, and behavioral factors. However, assessing their nutritional status and body composition is challenging, as conventional tools such as body mass index (BMI) may not accurately reflect adiposity in this population. One of the most severe risks associated with obesity in children with T21 is non-alcoholic fatty liver disease (NAFLD). This condition is characterized by fat accumulation in the liver without significant alcohol consumption and is closely linked to insulin resistance, dyslipidemia, and pro-inflammatory states. If not detected early, NAFLD can progress to more severe liver diseases such as fibrosis or cirrhosis. In individuals with T21, the prevalence of NAFLD may be underestimated due to the difficulty in properly assessing body composition and metabolism. Since NAFLD diagnosis traditionally requires invasive procedures such as liver biopsy, this study proposes using non-invasive techniques, such as liver elastography, to assess liver health in children and adolescents with T21. Additionally, dietary habits will be analyzed using standardized tools to establish the relationship between nutrition, body composition, and NAFLD risk in this population. Study Hypothesis: The main hypothesis is that obesity and inadequate dietary patterns increase the risk of NAFLD in our participants with T21. The investigators also believe that liver elastography will enable the early detection of fat accumulation in the liver and other signs of liver disease, facilitating timely intervention. Study Objectives: The primary objective of this study is to evaluate the presence and severity of NAFLD in children and adolescents with T21 using non-invasive diagnostic techniques and nutritional assessment methods. Specifically, the study will analyze: * Liver health: Measurement of liver fat and stiffness using elastography. Body composition: Anthropometric evaluation and adiposity analysis. Dietary habits: 24-hour food recall and KIDMED questionnaire to assess adherence to the Mediterranean diet. * Relationship between obesity and NAFLD: Identification of metabolic and behavioral risk factors.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age5 Years to 22 Years
SexAll
Healthy volunteersAccepted
ConditionObesity Prevention, Pediatric Obesity, Trisomy 21, Down Syndrome (Trisomy 21), Elastography, Nutrition Assessment, Liver Diseases, Non Alcoholic Fatty Liver Disease, Body Composition

Full registry criteria

Inclusion Criteria: * Children (5-10 years), and adolescents (11-19) andyoung adults (20-22 years) of bothSexes * 5 to 22 years old * Diagnosis of trisomy 21 or other intellectual disability of genetic origin for the group of the cases. * BMI: 17-40 Kg/m2 * Signing of the informed consent by the parents or guardians. Exclusion Criteria: * Not meeting the inclusion criteria * Have previous liver pathology. * Be under any medical treatment that * Modify composition parameters Body: GLP-1 analogues and derivatives.

Treatments and study arms

To evaluate fat liver content in the cases/controls population.

Other

The studied population includes participants aged 5-22 years old with/without T21 Down Syndrome.

Primary outcomes

Liver fat content.3 months.

To estimate liver fat content with hepatic elastography (FibroScan), CAP measurement will be used. Control population CAP value would range between 160-184 db/m and cases ≥ 184 db/m.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Fundación Jerome Lejeune🇪🇸 Madrid, Madrid, Spain