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Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls

Background and objectives: The human immune system is an ever-changing composition of innumerable cells and proteins, continually ready to respond to pathogens or insults. The cost of maintaining this state of immunological readiness is rarely considered. In this paper we aim to discern a cost to no...

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Autores principales: Shattuck-Heidorn, Heather, Reiches, Meredith W., Prentice, Andrew M., Moore, Sophie E., Ellison, Peter T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381351/
https://www.ncbi.nlm.nih.gov/pubmed/28003312
http://dx.doi.org/10.1093/emph/eow034
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author Shattuck-Heidorn, Heather
Reiches, Meredith W.
Prentice, Andrew M.
Moore, Sophie E.
Ellison, Peter T.
author_facet Shattuck-Heidorn, Heather
Reiches, Meredith W.
Prentice, Andrew M.
Moore, Sophie E.
Ellison, Peter T.
author_sort Shattuck-Heidorn, Heather
collection PubMed
description Background and objectives: The human immune system is an ever-changing composition of innumerable cells and proteins, continually ready to respond to pathogens or insults. The cost of maintaining this state of immunological readiness is rarely considered. In this paper we aim to discern a cost to non-acute immune function by investigating how low levels of C-reactive protein (CRP) relate to other energetic demands and resources in adolescent Gambian girls. Methodology: Data from a longitudinal study of 66 adolescent girls was used to test hypotheses around investment in immune function. Non-acute (under 2 mg/L) CRP was used as an index of immune function. Predictor variables include linear height velocity, adiposity, leptin, and measures of energy balance. Results: Non-acute log CRP was positively associated with adiposity (β = 0.16, P < 0.001, R(2 )= 0.17) and levels of the adipokine leptin (β = 1.17, P = 0.006, R(2 )= 0.09). CRP was also negatively associated with increased investment in growth, as measured by height velocity (β = −0.58, P < 0.001, R(2 )= 0.13) and lean mass deposition β = −0.42, P = 0.005, R(2 )= 0.08). Relationships between adiposity and growth explained some, but not all, of this association. We do not find that CRP was related to energy balance. Conclusions and implications: These data support a hypothesis that investment in non-acute immune function is facultative, and sensitive to energetic resources and demands. We also find support for an adaptive association between the immune system and adipose tissue.
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spelling pubmed-53813512017-04-10 Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls Shattuck-Heidorn, Heather Reiches, Meredith W. Prentice, Andrew M. Moore, Sophie E. Ellison, Peter T. Evol Med Public Health Original Research Article Background and objectives: The human immune system is an ever-changing composition of innumerable cells and proteins, continually ready to respond to pathogens or insults. The cost of maintaining this state of immunological readiness is rarely considered. In this paper we aim to discern a cost to non-acute immune function by investigating how low levels of C-reactive protein (CRP) relate to other energetic demands and resources in adolescent Gambian girls. Methodology: Data from a longitudinal study of 66 adolescent girls was used to test hypotheses around investment in immune function. Non-acute (under 2 mg/L) CRP was used as an index of immune function. Predictor variables include linear height velocity, adiposity, leptin, and measures of energy balance. Results: Non-acute log CRP was positively associated with adiposity (β = 0.16, P < 0.001, R(2 )= 0.17) and levels of the adipokine leptin (β = 1.17, P = 0.006, R(2 )= 0.09). CRP was also negatively associated with increased investment in growth, as measured by height velocity (β = −0.58, P < 0.001, R(2 )= 0.13) and lean mass deposition β = −0.42, P = 0.005, R(2 )= 0.08). Relationships between adiposity and growth explained some, but not all, of this association. We do not find that CRP was related to energy balance. Conclusions and implications: These data support a hypothesis that investment in non-acute immune function is facultative, and sensitive to energetic resources and demands. We also find support for an adaptive association between the immune system and adipose tissue. Oxford University Press 2016-12-21 /pmc/articles/PMC5381351/ /pubmed/28003312 http://dx.doi.org/10.1093/emph/eow034 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Shattuck-Heidorn, Heather
Reiches, Meredith W.
Prentice, Andrew M.
Moore, Sophie E.
Ellison, Peter T.
Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls
title Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls
title_full Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls
title_fullStr Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls
title_full_unstemmed Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls
title_short Energetics and the immune system: Trade-offs associated with non-acute levels of CRP in adolescent Gambian girls
title_sort energetics and the immune system: trade-offs associated with non-acute levels of crp in adolescent gambian girls
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381351/
https://www.ncbi.nlm.nih.gov/pubmed/28003312
http://dx.doi.org/10.1093/emph/eow034
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