Cargando…
The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is a genetic disorder characterized by hyperphagia with progressive, severe obesity, and an increased risk of obesity-related comorbidities in adult life. Although low dietary vitamin D intake and low 25-hydroxy vitamin D (25OHD) levels are commonly reported in PWS in the...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230761/ https://www.ncbi.nlm.nih.gov/pubmed/32316673 http://dx.doi.org/10.3390/nu12041132 |
_version_ | 1783535031396859904 |
---|---|
author | Barrea, Luigi Muscogiuri, Giovanna Pugliese, Gabriella Aprano, Sara de Alteriis, Giulia Di Somma, Carolina Colao, Annamaria Savastano, Silvia |
author_facet | Barrea, Luigi Muscogiuri, Giovanna Pugliese, Gabriella Aprano, Sara de Alteriis, Giulia Di Somma, Carolina Colao, Annamaria Savastano, Silvia |
author_sort | Barrea, Luigi |
collection | PubMed |
description | Prader–Willi syndrome (PWS) is a genetic disorder characterized by hyperphagia with progressive, severe obesity, and an increased risk of obesity-related comorbidities in adult life. Although low dietary vitamin D intake and low 25-hydroxy vitamin D (25OHD) levels are commonly reported in PWS in the context of bone metabolism, the association of low 25OHD levels with fat mass has not been extensively evaluated in PWS adults. The aims of this study were to investigate the following in PWS adults: (1) 25OHD levels and the dietary vitamin D intake; (2) associations among 25OHD levels with anthropometric measurements and fat mass; (3) specific cut-off values for body mass index (BMI) and fat mass predictive of the 25OHD levels. In this cross-sectional, single-center study we enrolled 30 participants, 15 PWS adults (age 19–41 years and 40% males) and 15 control subjects matched by age, sex, and BMI from the same geographical area (latitude 40° 49’ N; elevation 17 m). Fat mass was assessed using a bioelectrical impedance analysis (BIA) phase-sensitive system. The 25OHD levels were determined by a direct competitive chemiluminescence immunoassay. Dietary vitamin D intake data was collected by three-day food records. The 25OHD levels in the PWS adults were constantly lower across all categories of BMI and fat mass compared with their obese counterpart. The 25OHD levels were negatively associated with BMI (p = 0.04), waist circumference (p = 0.03), fat mass (p = 0.04), and dietary vitamin D intake (p < 0.001). During multiple regression analysis, dietary vitamin D intake was entered at the first step (p < 0.001), thus explaining 84% of 25OHD level variability. The threshold values of BMI and fat mass predicting the lowest decrease in the 25OHD levels were found at BMI ≥ 42 kg/m(2) (p = 0.01) and fat mass ≥ 42 Kg (p = 0.003). In conclusion, our data indicate that: (i) 25OHD levels and dietary vitamin D intake were lower in PWS adults than in the control, independent of body fat differences; (ii) 25OHD levels were inversely associated with BMI, waist circumference, and fat mass, but low dietary vitamin D intake was the major determinant of low vitamin D status in these patients; (iii) sample-specific cut-off values of BMI and fat mass might help to predict risks of the lowest 25OHD level decreases in PWS adults. The presence of trained nutritionists in the integrated care teams of PWS adults is strongly suggested in order to provide an accurate nutritional assessment and tailored vitamin D supplementations. |
format | Online Article Text |
id | pubmed-7230761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72307612020-05-22 The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome Barrea, Luigi Muscogiuri, Giovanna Pugliese, Gabriella Aprano, Sara de Alteriis, Giulia Di Somma, Carolina Colao, Annamaria Savastano, Silvia Nutrients Article Prader–Willi syndrome (PWS) is a genetic disorder characterized by hyperphagia with progressive, severe obesity, and an increased risk of obesity-related comorbidities in adult life. Although low dietary vitamin D intake and low 25-hydroxy vitamin D (25OHD) levels are commonly reported in PWS in the context of bone metabolism, the association of low 25OHD levels with fat mass has not been extensively evaluated in PWS adults. The aims of this study were to investigate the following in PWS adults: (1) 25OHD levels and the dietary vitamin D intake; (2) associations among 25OHD levels with anthropometric measurements and fat mass; (3) specific cut-off values for body mass index (BMI) and fat mass predictive of the 25OHD levels. In this cross-sectional, single-center study we enrolled 30 participants, 15 PWS adults (age 19–41 years and 40% males) and 15 control subjects matched by age, sex, and BMI from the same geographical area (latitude 40° 49’ N; elevation 17 m). Fat mass was assessed using a bioelectrical impedance analysis (BIA) phase-sensitive system. The 25OHD levels were determined by a direct competitive chemiluminescence immunoassay. Dietary vitamin D intake data was collected by three-day food records. The 25OHD levels in the PWS adults were constantly lower across all categories of BMI and fat mass compared with their obese counterpart. The 25OHD levels were negatively associated with BMI (p = 0.04), waist circumference (p = 0.03), fat mass (p = 0.04), and dietary vitamin D intake (p < 0.001). During multiple regression analysis, dietary vitamin D intake was entered at the first step (p < 0.001), thus explaining 84% of 25OHD level variability. The threshold values of BMI and fat mass predicting the lowest decrease in the 25OHD levels were found at BMI ≥ 42 kg/m(2) (p = 0.01) and fat mass ≥ 42 Kg (p = 0.003). In conclusion, our data indicate that: (i) 25OHD levels and dietary vitamin D intake were lower in PWS adults than in the control, independent of body fat differences; (ii) 25OHD levels were inversely associated with BMI, waist circumference, and fat mass, but low dietary vitamin D intake was the major determinant of low vitamin D status in these patients; (iii) sample-specific cut-off values of BMI and fat mass might help to predict risks of the lowest 25OHD level decreases in PWS adults. The presence of trained nutritionists in the integrated care teams of PWS adults is strongly suggested in order to provide an accurate nutritional assessment and tailored vitamin D supplementations. MDPI 2020-04-17 /pmc/articles/PMC7230761/ /pubmed/32316673 http://dx.doi.org/10.3390/nu12041132 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Barrea, Luigi Muscogiuri, Giovanna Pugliese, Gabriella Aprano, Sara de Alteriis, Giulia Di Somma, Carolina Colao, Annamaria Savastano, Silvia The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome |
title | The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome |
title_full | The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome |
title_fullStr | The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome |
title_full_unstemmed | The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome |
title_short | The Sun’s Vitamin in Adult Patients Affected by Prader–Willi Syndrome |
title_sort | sun’s vitamin in adult patients affected by prader–willi syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230761/ https://www.ncbi.nlm.nih.gov/pubmed/32316673 http://dx.doi.org/10.3390/nu12041132 |
work_keys_str_mv | AT barrealuigi thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT muscogiurigiovanna thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT pugliesegabriella thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT apranosara thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT dealteriisgiulia thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT disommacarolina thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT colaoannamaria thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT savastanosilvia thesunsvitamininadultpatientsaffectedbypraderwillisyndrome AT barrealuigi sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT muscogiurigiovanna sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT pugliesegabriella sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT apranosara sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT dealteriisgiulia sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT disommacarolina sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT colaoannamaria sunsvitamininadultpatientsaffectedbypraderwillisyndrome AT savastanosilvia sunsvitamininadultpatientsaffectedbypraderwillisyndrome |