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Biological Age Assessment in Adults With Prader-Willi Syndrome (ETABIOLPWS)

Biological Age Assessment in Adults With Prader-Willi Syndrome Undergoing an Integrated Multidisciplinary Metabolic Rehabilitation Program

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05778032
Acronym
ETABIOLPWS
Enrollment
30
Registered
2023-03-21
Start date
2022-05-25
Completion date
2025-12-31
Last updated
2024-10-02

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

Conditions

Prader-Willi Syndrome

Keywords

Prader-Willi syndrome, Obesity, Biological age, Metabolic rehabilitation

Brief summary

The primary objective of the study is to compare, in a cohort of obese subjects with PWS hospitalized at the Division of Auxology, Istituto Auxologico Italiano, Piancavallo (VB), Italy, the age acceleration calculated at study entry (T0) with the age acceleration measured at the end of a 3-week multidisciplinary metabolic rehabilitation program (T1). Secondary objectives are to correlate the biological age with the anthropometric characteristics (with particular reference to the body composition), the glycometabolic picture, the main parameters and cardiovascular risk factors, the therapy (previous and concomitant) with rhGH and the cognitive function (mainly, the IQ).

Detailed description

Methods Thirty adults affected by clinically diagnosed and genetically confirmed PWS are recruited, regardless of the treatment (previous or concomitant) with rhGH (F/M = 15/15; age: ≥ 18 years; BMI \> 35 kg/m2), hospitalized for a period of integrated multidisciplinary metabolic rehabilitation at the Division of Auxology, Istituto Auxologico Italiano, Piancavallo (VB), Italy. After verifying the inclusion criteria, clinical and anthropometric data will be collected, including the evaluation of body composition with bioimpedance analysis. Cognitive function will be assessed with a psychometric scale (Wechsler Adult Intelligence Scale). Blood samples will be taken from each patient upon admission to the hospital (T0) and after 3 weeks of rehabilitation hospitalization (at the same time to reduce circadian variability) for the determination of the basal glycometabolic profile (glucose, insulin, HOMA-IR, glycated Hb , triglycerides, total cholesterol, LDL, HDL, and hsPCR), as well as circulating levels of leptin, IL-6, and TNF-α. The samples taken will be used for DNA extraction. DNA methylation will be performed by treatment with sodium bisulphite and PCR-Pyrosequencing. Biological age measurement Biological (epigenetic) age will be measured using the two algorithms of Zbiec-Piekarska (9) and Daunay (10), based on the level of DNA methylation in specific gene loci. To have an estimate of the epigenetic (biological) age that is independent of the chronological age, we will use a measure defined as age acceleration, from which, with statistical inference, we will calculate the age acceleration. To calculate it, a linear regression model with the chronological age as the independent variable and the epigenetic age as the dependent variable will be applied; the difference between the observed value and the one predicted by the model will constitute the age acceleration due to epigenetic effects. In the event that the epigenetic age is greater than the chronological age, the age acceleration will have a positive value expressed in years, negative if vice versa.

Interventions

OTHERMultidisciplinary metabolic rehabilitation program

Multidisciplinary metabolic rehabilitation program with a duration of 3 weeks

Sponsors

Istituto Auxologico Italiano
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult patients with PWS, clinically diagnosed and genetically confirmed, regardless of rhGH treatment (previous or concomitant) * age: ≥ 18 years * BMI \> 35 kg/m2 * hospitalization for integrated multidisciplinary metabolic rehabilitation program

Exclusion criteria

* age \< 18 years * BMI \< 35 kg/m2

Design outcomes

Primary

MeasureTime frameDescription
DNA methylationBaseline and at the end of the rehabilitation program (21 days)Change in level of DNA methylation

Secondary

MeasureTime frameDescription
Body fat massBaseline and at the end of the rehabilitation program (21 days)Change in body fat mass - bioimpedance analysis
Glycometabolic profile: glucoseBaseline and at the end of the rehabilitation program (21 days)Change in glycometabolic profile - glucose levels
Glycometabolic profile: insulinBaseline and at the end of the rehabilitation program (21 days)Change in glycometabolic profile - insulin levels
Body weightBaseline and at the end of the rehabilitation program (21 days)Change in body weight
Body mass indexBaseline and at the end of the rehabilitation program (21 days)Change in body mass index
Body fat free massBaseline and at the end of the rehabilitation program (21 days)Change in body fat free mass - bioimpedance analysis

Countries

Italy

Outcome results

None listed

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