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Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease

Despite being largely preventable, cardiovascular disease (CVD) is still the leading cause of death globally. Recent studies suggest that the immune system, particularly a form of systemic chronic inflammation (SCI), is involved in the mechanisms leading to CVD; thus, targeting SCI may help prevent...

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Autores principales: Dioum, El Hadji M., Schneider, Kevin L., Vigerust, David J., Cox, Bryan D., Chu, YiFang, Zachwieja, Jeffery J., Furman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656573/
https://www.ncbi.nlm.nih.gov/pubmed/36364734
http://dx.doi.org/10.3390/nu14214471
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author Dioum, El Hadji M.
Schneider, Kevin L.
Vigerust, David J.
Cox, Bryan D.
Chu, YiFang
Zachwieja, Jeffery J.
Furman, David
author_facet Dioum, El Hadji M.
Schneider, Kevin L.
Vigerust, David J.
Cox, Bryan D.
Chu, YiFang
Zachwieja, Jeffery J.
Furman, David
author_sort Dioum, El Hadji M.
collection PubMed
description Despite being largely preventable, cardiovascular disease (CVD) is still the leading cause of death globally. Recent studies suggest that the immune system, particularly a form of systemic chronic inflammation (SCI), is involved in the mechanisms leading to CVD; thus, targeting SCI may help prevent or delay the onset of CVD. In a recent placebo-controlled randomized clinical trial, an oat product providing 3 g of β-Glucan improved cholesterol low-density lipoprotein (LDL) levels and lowered cardiovascular risk in adults with borderline high cholesterol. Here, we conducted a secondary measurement of the serum samples to test whether the oat product has the potential to reduce SCI and improve other clinical outcomes related to healthy aging. We investigated the effects of the oat product on a novel metric for SCI called Inflammatory Age(®) (iAge(®)), derived from the Stanford 1000 Immunomes Project. The iAge(®) predicts multimorbidity, frailty, immune decline, premature cardiovascular aging, and all-cause mortality on a personalized level. A beneficial effect of the oat product was observed in subjects with elevated levels of iAge(®) at baseline (>49.6 iAge(®) years) as early as two weeks post-treatment. The rice control group did not show any significant change in iAge(®). Interestingly, the effects of the oat product on iAge(®) were largely driven by a decrease in the Eotaxin-1 protein, an aging-related chemokine, independent of a person’s gender, body mass index, or chronological age. Thus, we describe a novel anti-SCI role for oats that could have a major impact on functional, preventative, and personalized medicine.
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spelling pubmed-96565732022-11-15 Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease Dioum, El Hadji M. Schneider, Kevin L. Vigerust, David J. Cox, Bryan D. Chu, YiFang Zachwieja, Jeffery J. Furman, David Nutrients Article Despite being largely preventable, cardiovascular disease (CVD) is still the leading cause of death globally. Recent studies suggest that the immune system, particularly a form of systemic chronic inflammation (SCI), is involved in the mechanisms leading to CVD; thus, targeting SCI may help prevent or delay the onset of CVD. In a recent placebo-controlled randomized clinical trial, an oat product providing 3 g of β-Glucan improved cholesterol low-density lipoprotein (LDL) levels and lowered cardiovascular risk in adults with borderline high cholesterol. Here, we conducted a secondary measurement of the serum samples to test whether the oat product has the potential to reduce SCI and improve other clinical outcomes related to healthy aging. We investigated the effects of the oat product on a novel metric for SCI called Inflammatory Age(®) (iAge(®)), derived from the Stanford 1000 Immunomes Project. The iAge(®) predicts multimorbidity, frailty, immune decline, premature cardiovascular aging, and all-cause mortality on a personalized level. A beneficial effect of the oat product was observed in subjects with elevated levels of iAge(®) at baseline (>49.6 iAge(®) years) as early as two weeks post-treatment. The rice control group did not show any significant change in iAge(®). Interestingly, the effects of the oat product on iAge(®) were largely driven by a decrease in the Eotaxin-1 protein, an aging-related chemokine, independent of a person’s gender, body mass index, or chronological age. Thus, we describe a novel anti-SCI role for oats that could have a major impact on functional, preventative, and personalized medicine. MDPI 2022-10-25 /pmc/articles/PMC9656573/ /pubmed/36364734 http://dx.doi.org/10.3390/nu14214471 Text en © 2022 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 Article
Dioum, El Hadji M.
Schneider, Kevin L.
Vigerust, David J.
Cox, Bryan D.
Chu, YiFang
Zachwieja, Jeffery J.
Furman, David
Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease
title Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease
title_full Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease
title_fullStr Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease
title_full_unstemmed Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease
title_short Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease
title_sort oats lower age-related systemic chronic inflammation (iage) in adults at risk for cardiovascular disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656573/
https://www.ncbi.nlm.nih.gov/pubmed/36364734
http://dx.doi.org/10.3390/nu14214471
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