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Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults

Background and Objectives: This study focused on investigating sarcopenic factors and immune cells in older adulthood. To achieve this, the variables related to sarcopenia and immune cells in people living in the same community were analyzed. Materials and Methods: A total of 433 elderly individuals...

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Autores principales: Heo, Seung-Jae, Jee, Yong-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607932/
https://www.ncbi.nlm.nih.gov/pubmed/37893417
http://dx.doi.org/10.3390/medicina59101700
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author Heo, Seung-Jae
Jee, Yong-Seok
author_facet Heo, Seung-Jae
Jee, Yong-Seok
author_sort Heo, Seung-Jae
collection PubMed
description Background and Objectives: This study focused on investigating sarcopenic factors and immune cells in older adulthood. To achieve this, the variables related to sarcopenia and immune cells in people living in the same community were analyzed. Materials and Methods: A total of 433 elderly individuals aged 61 to 85 years were randomly categorized as follows in 5-year intervals: 68 in the youngest-old group (aged 61–65), 168 in the young-old group (aged 66–70), 127 in the middle-old group (aged 71–75), 46 in the old-old group (aged 76–80), and 19 in the oldest-old group (aged 81–85). Results: With the progression of age, calf circumference (−8.4 to −11.05%; p = 0.001) and grip strength (−9.32 to −21.01%; p = 0.001) exhibited a noticeable reduction with each successive 5-year age bracket. Conversely, the capability to complete the five-time chair stand demonstrated a clear incline (32.49 to 56.81%; p = 0.001), starting from the middle-aged group. As for appendicular skeletal muscle mass, there was an evident tendency for it to decrease (−7.08 to −26.62%; p = 0.001) with increasing age. A gradual decline in natural killer cells became apparent within the old-old and oldest-old groups (−9.28 to −26.27%; p = 0.001). The results of the post hoc test revealed that CD3 T cells showcased their peak levels in both the youngest-old and young-old groups. This was followed by the middle-old and old-old groups, with slightly lower levels. This pattern was similarly observed in CD4 T cells, CD8 T cells, and CD19 B cells. Conclusions: This study reaffirmed that sarcopenia and immune cell function decline with each successive 5-year increase in age. Considering these findings, the importance of implementing programs aimed at ensuring a high-quality extension of life for the elderly is strongly underscored.
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spelling pubmed-106079322023-10-28 Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults Heo, Seung-Jae Jee, Yong-Seok Medicina (Kaunas) Article Background and Objectives: This study focused on investigating sarcopenic factors and immune cells in older adulthood. To achieve this, the variables related to sarcopenia and immune cells in people living in the same community were analyzed. Materials and Methods: A total of 433 elderly individuals aged 61 to 85 years were randomly categorized as follows in 5-year intervals: 68 in the youngest-old group (aged 61–65), 168 in the young-old group (aged 66–70), 127 in the middle-old group (aged 71–75), 46 in the old-old group (aged 76–80), and 19 in the oldest-old group (aged 81–85). Results: With the progression of age, calf circumference (−8.4 to −11.05%; p = 0.001) and grip strength (−9.32 to −21.01%; p = 0.001) exhibited a noticeable reduction with each successive 5-year age bracket. Conversely, the capability to complete the five-time chair stand demonstrated a clear incline (32.49 to 56.81%; p = 0.001), starting from the middle-aged group. As for appendicular skeletal muscle mass, there was an evident tendency for it to decrease (−7.08 to −26.62%; p = 0.001) with increasing age. A gradual decline in natural killer cells became apparent within the old-old and oldest-old groups (−9.28 to −26.27%; p = 0.001). The results of the post hoc test revealed that CD3 T cells showcased their peak levels in both the youngest-old and young-old groups. This was followed by the middle-old and old-old groups, with slightly lower levels. This pattern was similarly observed in CD4 T cells, CD8 T cells, and CD19 B cells. Conclusions: This study reaffirmed that sarcopenia and immune cell function decline with each successive 5-year increase in age. Considering these findings, the importance of implementing programs aimed at ensuring a high-quality extension of life for the elderly is strongly underscored. MDPI 2023-09-22 /pmc/articles/PMC10607932/ /pubmed/37893417 http://dx.doi.org/10.3390/medicina59101700 Text en © 2023 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
Heo, Seung-Jae
Jee, Yong-Seok
Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults
title Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults
title_full Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults
title_fullStr Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults
title_full_unstemmed Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults
title_short Characteristics of Age Classification into Five-Year Intervals to Explain Sarcopenia and Immune Cells in Older Adults
title_sort characteristics of age classification into five-year intervals to explain sarcopenia and immune cells in older adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607932/
https://www.ncbi.nlm.nih.gov/pubmed/37893417
http://dx.doi.org/10.3390/medicina59101700
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