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Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty
Frailty (FI) and metabolic syndrome (MS) are each associated with adverse health outcomes. A relationship between FI and MS has previously been described in adults. We considered the prevalence of a metabolically unhealthy phenotype (MUP) in malnourished children with neurological impairment and in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293425/ https://www.ncbi.nlm.nih.gov/pubmed/34287378 http://dx.doi.org/10.3390/pediatric13030042 |
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author | Calcaterra, Valeria Cena, Hellas Ruggieri, Annamaria Zuccotti, Gianvincenzo De Silvestri, Annalisa Bonalumi, Gianni Pelizzo, Gloria |
author_facet | Calcaterra, Valeria Cena, Hellas Ruggieri, Annamaria Zuccotti, Gianvincenzo De Silvestri, Annalisa Bonalumi, Gianni Pelizzo, Gloria |
author_sort | Calcaterra, Valeria |
collection | PubMed |
description | Frailty (FI) and metabolic syndrome (MS) are each associated with adverse health outcomes. A relationship between FI and MS has previously been described in adults. We considered the prevalence of a metabolically unhealthy phenotype (MUP) in malnourished children with neurological impairment and in subjects with obesity in comparison to a group of elderly individuals at risk of FI, and we did so in order to define the potential similarities that may underline the risk of FI in specific children. We considered 50 undernourished (defined as having a body mass index of BMI ≤ 2, standard deviation score, SDS, according to World Health Organization) disabled children; 50 children with obesity (BMI ≥ 2 SDS); 50 children who were a normal weight (−1 SDS ≤ BMI ≤ +1 SDS); 21 patients who were >75 years old. MUP was defined as the presence of at least one of the following risk factors: hypertension, hyperglycemia or diabetes, hypercholesterolemia, and hypertriglyceridemia. In children with a disability and obesity, a higher prevalence (p < 0.001) and risk (disability OR 54.88, obesity OR 13.37) of MUP was noted compared to children of a normal weight. Compared to elderly patients, the prevalence of MUP did not differ in disabled children. On the contrary, MUP was lower in children with obesity (p < 0.001) and in pediatric subjects of a normal weight (p < 0.01). MS might play a key role in “pediatric” frailty. The extremities of the aging process and malnutrition are likely key factors in the development of FI. A multidisciplinary approach to FI may represent an important milestone for pediatric care. |
format | Online Article Text |
id | pubmed-8293425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82934252021-07-22 Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty Calcaterra, Valeria Cena, Hellas Ruggieri, Annamaria Zuccotti, Gianvincenzo De Silvestri, Annalisa Bonalumi, Gianni Pelizzo, Gloria Pediatr Rep Communication Frailty (FI) and metabolic syndrome (MS) are each associated with adverse health outcomes. A relationship between FI and MS has previously been described in adults. We considered the prevalence of a metabolically unhealthy phenotype (MUP) in malnourished children with neurological impairment and in subjects with obesity in comparison to a group of elderly individuals at risk of FI, and we did so in order to define the potential similarities that may underline the risk of FI in specific children. We considered 50 undernourished (defined as having a body mass index of BMI ≤ 2, standard deviation score, SDS, according to World Health Organization) disabled children; 50 children with obesity (BMI ≥ 2 SDS); 50 children who were a normal weight (−1 SDS ≤ BMI ≤ +1 SDS); 21 patients who were >75 years old. MUP was defined as the presence of at least one of the following risk factors: hypertension, hyperglycemia or diabetes, hypercholesterolemia, and hypertriglyceridemia. In children with a disability and obesity, a higher prevalence (p < 0.001) and risk (disability OR 54.88, obesity OR 13.37) of MUP was noted compared to children of a normal weight. Compared to elderly patients, the prevalence of MUP did not differ in disabled children. On the contrary, MUP was lower in children with obesity (p < 0.001) and in pediatric subjects of a normal weight (p < 0.01). MS might play a key role in “pediatric” frailty. The extremities of the aging process and malnutrition are likely key factors in the development of FI. A multidisciplinary approach to FI may represent an important milestone for pediatric care. MDPI 2021-07-01 /pmc/articles/PMC8293425/ /pubmed/34287378 http://dx.doi.org/10.3390/pediatric13030042 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Calcaterra, Valeria Cena, Hellas Ruggieri, Annamaria Zuccotti, Gianvincenzo De Silvestri, Annalisa Bonalumi, Gianni Pelizzo, Gloria Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty |
title | Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty |
title_full | Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty |
title_fullStr | Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty |
title_full_unstemmed | Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty |
title_short | Metabolically Unhealthy Phenotype: A Key Factor in Determining “Pediatric” Frailty |
title_sort | metabolically unhealthy phenotype: a key factor in determining “pediatric” frailty |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8293425/ https://www.ncbi.nlm.nih.gov/pubmed/34287378 http://dx.doi.org/10.3390/pediatric13030042 |
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