Genetic Determinants and Clinical Consequences of Early-onset Severe Obesity

Childhood Obesity Clinical Trial

— PeLi  

Official title:

Genetic Determinants and Clinical Consequences of Early-onset Severe Obesity

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT02645422
• Other study ID #: HUCH43/2015
• Status: Enrolling by invitation
• Start date: December 2015
• Est. completion date: December 31, 2023

Study information

• Verified date: September 2023
• Source: Helsinki University Central Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of the present study is to identify new obesity-related genetic defects and determine their association with clinical manifestations in families with childhood-onset severe obesity. The investigators hypothesize that by exploring children with severe early-onset obesity they can find new obesity-related genetic defects and by exploring obesity-associated clinical manifestations the investigators can elucidate the outcomes of severe childhood obesity.

Description:

Obesity is a complex disorder with many contributing genetic and environmental factors. The genetic causes and mechanisms for severe childhood obesity are still incompletely understood. It is acknowledged that obesity in some individuals could be a consequence of rare genetic variants with strong effect - these rare variants might be population specific. The aims of this study are to determine - inheritance patterns of early-onset obesity - new obesity-related genetic variants and disease-causing gene mutations - the association between obesity-related genetic defects and clinical manifestations - the association between obesity-related genetic defects and psychiatric symptoms in patients with early-onset obesity and their first-degree relatives Significant advancements in genetic methodology provide new tools to explore genetic defects underlying obesity. Family-based approach provides several advantages compared to cohort studies to investigate genetic determinants of complex diseases.The unique genetic composition of the Finnish population enables identification of novel genetic entities. Discovery of genetic defects associated with severe childhood-onset obesity will increase the investigators understanding of the pathogenesis of obesity and allows early detection, by genetic testing, of those at increased risk and optimal targeting of preventive measures.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 400
• Est. completion date: December 31, 2023
• Est. primary completion date: September 22, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 10 Years to 18 Years

Eligibility

Inclusion Criteria:

• children and adolescents age 10-18 years
• height-adjusted weight >60 % before the age of 7 years.
• Finnish descent

Exclusion Criteria:

• patients with a known endocrine or genetic disorder underlying obesity (e.g. Prader-Willi syndrome, hypercortisolism, hypothyroidism)

Related Conditions & MeSH terms

• Childhood Obesity
• Obesity
• Obesity, Morbid
• Pediatric Obesity

Locations

Country	Name	City	State
n/a

Sponsors (3)

Lead Sponsor	Collaborator
Helsinki University Central Hospital	Folkhälsan Researech Center, Karolinska Institutet

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of patients with gene mutations or genetic variants in children with early-onset severe obesity		Baseline, first day of enrollment