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).
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.
Study Type
OBSERVATIONAL
Enrollment
30
Multidisciplinary metabolic rehabilitation program with a duration of 3 weeks
Istituto Auxologico Italiano IRCCS, Site Piancavallo
Oggebbio, Verbania, Italy
DNA methylation
Change in level of DNA methylation
Time frame: Baseline and at the end of the rehabilitation program (21 days)
Glycometabolic profile: glucose
Change in glycometabolic profile - glucose levels
Time frame: Baseline and at the end of the rehabilitation program (21 days)
Glycometabolic profile: insulin
Change in glycometabolic profile - insulin levels
Time frame: Baseline and at the end of the rehabilitation program (21 days)
Body fat mass
Change in body fat mass - bioimpedance analysis
Time frame: Baseline and at the end of the rehabilitation program (21 days)
Body fat free mass
Change in body fat free mass - bioimpedance analysis
Time frame: Baseline and at the end of the rehabilitation program (21 days)
Body weight
Change in body weight
Time frame: Baseline and at the end of the rehabilitation program (21 days)
Body mass index
Change in body mass index
Time frame: Baseline and at the end of the rehabilitation program (21 days)
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