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Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound

BACKGROUND: Obesity in adolescents is increasing worldwide and associated with an elevated cardiovascular risk later in life. In a group-comparative study, we investigated the association between adiposity in adolescents and signs of vascular aging and inflammation. METHODS: Thirty-nine adolescents...

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Autores principales: Naessen, Tord, Bergsten, Peter, Lundmark, Tobias, Forslund, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Open Academia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254329/
https://www.ncbi.nlm.nih.gov/pubmed/35846851
http://dx.doi.org/10.48101/ujms.v127.8676
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author Naessen, Tord
Bergsten, Peter
Lundmark, Tobias
Forslund, Anders
author_facet Naessen, Tord
Bergsten, Peter
Lundmark, Tobias
Forslund, Anders
author_sort Naessen, Tord
collection PubMed
description BACKGROUND: Obesity in adolescents is increasing worldwide and associated with an elevated cardiovascular risk later in life. In a group-comparative study, we investigated the association between adiposity in adolescents and signs of vascular aging and inflammation. METHODS: Thirty-nine adolescents (10–18 years old), 19 with obesity and 20 with normal weight, were enrolled. The intima thickness and intima/media thickness ratio (I/M) were assessed using high-resolution ultrasound in the common carotid artery (center frequency 22 MHz) and the distal radial artery (RA; 50 MHz). Increased intima and high I/M are signs of vascular aging. Body characteristics, high-sensitivity C-reactive protein (hs-CRP), plasma lipids, and glycemic parameters were measured. RESULTS: Adolescents with obesity, compared to normal-weight peers, had elevated plasma lipid, insulin c-peptide, and hs-CRP levels, the latter increasing exponentially with increasing adiposity. Obese adolescents had a thicker RA intima layer [0.005 mm; 95% confidence intervals (0.000, 0.009); P = 0.043] and a higher RA I/M [0.10; (0.040, 0.147); P < 0.0007]. Group differences for the RA I/M remained significant after adjustment for age, sex, fasting plasma insulin, and body mass index, both separately and together (P = 0.032). The RA I/M was correlated with hs-CRP, and both were correlated with the analyzed cardiovascular risk factors. Receiver operating curve c-values for RA I/M (0.86) and hs-CRP (0.90) strongly indicated correct placement in the obese or non-obese group. CONCLUSIONS: Adolescents with obesity had significantly more extensive vascular aging in the muscular RA, than normal-weight peers. The findings support an inflammatory link between obesity and vascular aging in adolescents.
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spelling pubmed-92543292022-07-14 Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound Naessen, Tord Bergsten, Peter Lundmark, Tobias Forslund, Anders Ups J Med Sci Original Article BACKGROUND: Obesity in adolescents is increasing worldwide and associated with an elevated cardiovascular risk later in life. In a group-comparative study, we investigated the association between adiposity in adolescents and signs of vascular aging and inflammation. METHODS: Thirty-nine adolescents (10–18 years old), 19 with obesity and 20 with normal weight, were enrolled. The intima thickness and intima/media thickness ratio (I/M) were assessed using high-resolution ultrasound in the common carotid artery (center frequency 22 MHz) and the distal radial artery (RA; 50 MHz). Increased intima and high I/M are signs of vascular aging. Body characteristics, high-sensitivity C-reactive protein (hs-CRP), plasma lipids, and glycemic parameters were measured. RESULTS: Adolescents with obesity, compared to normal-weight peers, had elevated plasma lipid, insulin c-peptide, and hs-CRP levels, the latter increasing exponentially with increasing adiposity. Obese adolescents had a thicker RA intima layer [0.005 mm; 95% confidence intervals (0.000, 0.009); P = 0.043] and a higher RA I/M [0.10; (0.040, 0.147); P < 0.0007]. Group differences for the RA I/M remained significant after adjustment for age, sex, fasting plasma insulin, and body mass index, both separately and together (P = 0.032). The RA I/M was correlated with hs-CRP, and both were correlated with the analyzed cardiovascular risk factors. Receiver operating curve c-values for RA I/M (0.86) and hs-CRP (0.90) strongly indicated correct placement in the obese or non-obese group. CONCLUSIONS: Adolescents with obesity had significantly more extensive vascular aging in the muscular RA, than normal-weight peers. The findings support an inflammatory link between obesity and vascular aging in adolescents. Open Academia 2022-06-03 /pmc/articles/PMC9254329/ /pubmed/35846851 http://dx.doi.org/10.48101/ujms.v127.8676 Text en © 2022 The Author(s). Published by Upsala Medical Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Naessen, Tord
Bergsten, Peter
Lundmark, Tobias
Forslund, Anders
Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
title Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
title_full Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
title_fullStr Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
title_full_unstemmed Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
title_short Obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
title_sort obesity in adolescents associated with vascular aging – a study using ultra-high-resolution ultrasound
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254329/
https://www.ncbi.nlm.nih.gov/pubmed/35846851
http://dx.doi.org/10.48101/ujms.v127.8676
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