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The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study
IMPORTANCE: The impact of long‐term burden of excessive body weight, beginning in childhood, on inflammatory status in adulthood has been poorly described. OBJECTIVE: To characterize the longitudinal body mass index (BMI) trajectory from childhood and examine its relationship with inflammatory statu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984006/ https://www.ncbi.nlm.nih.gov/pubmed/33778423 http://dx.doi.org/10.1002/ped4.12248 |
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author | Yan, Yinkun Li, Shengxu Liu, Yang Bazzano, Lydia He, Jiang Mi, Jie Chen, Wei |
author_facet | Yan, Yinkun Li, Shengxu Liu, Yang Bazzano, Lydia He, Jiang Mi, Jie Chen, Wei |
author_sort | Yan, Yinkun |
collection | PubMed |
description | IMPORTANCE: The impact of long‐term burden of excessive body weight, beginning in childhood, on inflammatory status in adulthood has been poorly described. OBJECTIVE: To characterize the longitudinal body mass index (BMI) trajectory from childhood and examine its relationship with inflammatory status in adulthood. METHODS: We included 1285 adults who had 4–15 repeat measurements of BMI from childhood to adulthood. The area under the curve (AUC) of growth curves was calculated to characterize long‐term burden (total AUC) and trends (incremental AUC) of BMI. RESULTS: After adjusting for covariates, higher values of BMI in terms of childhood and adulthood, as well as total and incremental AUC, were strongly associated with elevated levels of adult C‐reactive protein (CRP) in the four race‐sex groups. There were significant differences in linear and nonlinear curve parameters between the normal and high CRP groups for all race‐sex groups (P < 0.01). Compared with participants who had consistently low BMI in both childhood and adulthood, participants with high BMI in adulthood had higher CRP levels (P < 0.001), irrespective of their childhood BMI status; participants with high BMI in childhood but low BMI in adulthood had similar adult CRP levels. INTERPRETATION: The impact of excessive body weight on inflammation is cumulative and exacerbated over time. The influence of childhood overweight/obesity on inflammatory status in adulthood can be alleviated by reducing adiposity in adulthood. |
format | Online Article Text |
id | pubmed-7984006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79840062021-03-25 The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study Yan, Yinkun Li, Shengxu Liu, Yang Bazzano, Lydia He, Jiang Mi, Jie Chen, Wei Pediatr Investig Original Article IMPORTANCE: The impact of long‐term burden of excessive body weight, beginning in childhood, on inflammatory status in adulthood has been poorly described. OBJECTIVE: To characterize the longitudinal body mass index (BMI) trajectory from childhood and examine its relationship with inflammatory status in adulthood. METHODS: We included 1285 adults who had 4–15 repeat measurements of BMI from childhood to adulthood. The area under the curve (AUC) of growth curves was calculated to characterize long‐term burden (total AUC) and trends (incremental AUC) of BMI. RESULTS: After adjusting for covariates, higher values of BMI in terms of childhood and adulthood, as well as total and incremental AUC, were strongly associated with elevated levels of adult C‐reactive protein (CRP) in the four race‐sex groups. There were significant differences in linear and nonlinear curve parameters between the normal and high CRP groups for all race‐sex groups (P < 0.01). Compared with participants who had consistently low BMI in both childhood and adulthood, participants with high BMI in adulthood had higher CRP levels (P < 0.001), irrespective of their childhood BMI status; participants with high BMI in childhood but low BMI in adulthood had similar adult CRP levels. INTERPRETATION: The impact of excessive body weight on inflammation is cumulative and exacerbated over time. The influence of childhood overweight/obesity on inflammatory status in adulthood can be alleviated by reducing adiposity in adulthood. John Wiley and Sons Inc. 2021-03-22 /pmc/articles/PMC7984006/ /pubmed/33778423 http://dx.doi.org/10.1002/ped4.12248 Text en © 2021 Chinese Medical Association. Pediatric Investigation published by John Wiley & Sons Australia, Ltd on behalf of Futang Research Center of Pediatric Development. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Article Yan, Yinkun Li, Shengxu Liu, Yang Bazzano, Lydia He, Jiang Mi, Jie Chen, Wei The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study |
title | The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study |
title_full | The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study |
title_fullStr | The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study |
title_full_unstemmed | The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study |
title_short | The impact of body weight trajectory from childhood on chronic inflammation in adulthood: The Bogalusa Heart Study |
title_sort | impact of body weight trajectory from childhood on chronic inflammation in adulthood: the bogalusa heart study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984006/ https://www.ncbi.nlm.nih.gov/pubmed/33778423 http://dx.doi.org/10.1002/ped4.12248 |
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