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Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study
Familial longevity confers advantages in terms of health, functionality, and longevity. We sought to assess potential differences in frailty and sarcopenia in older adults according to a parental history of extraordinary longevity. A total of 176 community-dwelling subjects aged 65–80 years were rec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865421/ https://www.ncbi.nlm.nih.gov/pubmed/36674289 http://dx.doi.org/10.3390/ijerph20021534 |
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author | Belenguer-Varea, Angel Avellana-Zaragoza, Juan Antonio Inglés, Marta Cunha-Pérez, Cristina Cuesta-Peredo, David Borrás, Consuelo Viña, José Tarazona-Santabalbina, Francisco José |
author_facet | Belenguer-Varea, Angel Avellana-Zaragoza, Juan Antonio Inglés, Marta Cunha-Pérez, Cristina Cuesta-Peredo, David Borrás, Consuelo Viña, José Tarazona-Santabalbina, Francisco José |
author_sort | Belenguer-Varea, Angel |
collection | PubMed |
description | Familial longevity confers advantages in terms of health, functionality, and longevity. We sought to assess potential differences in frailty and sarcopenia in older adults according to a parental history of extraordinary longevity. A total of 176 community-dwelling subjects aged 65–80 years were recruited in this observational case–control study, pair-matched 1:1 for gender, age, and place of birth and residence: 88 centenarians’ offspring (case group) and 88 non-centenarians’ offspring (control group). The main variables were frailty and sarcopenia based on Fried’s phenotype and the European Working Group on Sarcopenia in Older People (EWGSOP) definitions, respectively. Sociodemographics, comorbidities, clinical and functional variables, the presence of geriatric syndromes, and laboratory parameters were also collected. Related sample tests were applied, and conditional logistic regression was performed. Cases had a higher percentage of robust patients (31.8% vs. 15.9%), lower percentages of frailty (9.1% vs. 21.6%) and pre-frailty (59.1% vs. 62.5%) (p = 0.001), and lower levels of IL-6 (p = 0.044) than controls. The robust adjusted OR for cases was 3.00 (95% CI = 1.06–8.47, p = 0.038). No significant differences in muscle mass were found. Familial longevity was also associated with less obesity, insomnia, pain, and polypharmacy and a higher education level and total and low-density lipoprotein cholesterol. The results suggest an inherited genetic component in the frailty phenotype, while the sarcopenia association with familial longevity remains challenging. |
format | Online Article Text |
id | pubmed-9865421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98654212023-01-22 Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study Belenguer-Varea, Angel Avellana-Zaragoza, Juan Antonio Inglés, Marta Cunha-Pérez, Cristina Cuesta-Peredo, David Borrás, Consuelo Viña, José Tarazona-Santabalbina, Francisco José Int J Environ Res Public Health Article Familial longevity confers advantages in terms of health, functionality, and longevity. We sought to assess potential differences in frailty and sarcopenia in older adults according to a parental history of extraordinary longevity. A total of 176 community-dwelling subjects aged 65–80 years were recruited in this observational case–control study, pair-matched 1:1 for gender, age, and place of birth and residence: 88 centenarians’ offspring (case group) and 88 non-centenarians’ offspring (control group). The main variables were frailty and sarcopenia based on Fried’s phenotype and the European Working Group on Sarcopenia in Older People (EWGSOP) definitions, respectively. Sociodemographics, comorbidities, clinical and functional variables, the presence of geriatric syndromes, and laboratory parameters were also collected. Related sample tests were applied, and conditional logistic regression was performed. Cases had a higher percentage of robust patients (31.8% vs. 15.9%), lower percentages of frailty (9.1% vs. 21.6%) and pre-frailty (59.1% vs. 62.5%) (p = 0.001), and lower levels of IL-6 (p = 0.044) than controls. The robust adjusted OR for cases was 3.00 (95% CI = 1.06–8.47, p = 0.038). No significant differences in muscle mass were found. Familial longevity was also associated with less obesity, insomnia, pain, and polypharmacy and a higher education level and total and low-density lipoprotein cholesterol. The results suggest an inherited genetic component in the frailty phenotype, while the sarcopenia association with familial longevity remains challenging. MDPI 2023-01-14 /pmc/articles/PMC9865421/ /pubmed/36674289 http://dx.doi.org/10.3390/ijerph20021534 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 Belenguer-Varea, Angel Avellana-Zaragoza, Juan Antonio Inglés, Marta Cunha-Pérez, Cristina Cuesta-Peredo, David Borrás, Consuelo Viña, José Tarazona-Santabalbina, Francisco José Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study |
title | Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study |
title_full | Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study |
title_fullStr | Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study |
title_full_unstemmed | Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study |
title_short | Effect of Familial Longevity on Frailty and Sarcopenia: A Case–Control Study |
title_sort | effect of familial longevity on frailty and sarcopenia: a case–control study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865421/ https://www.ncbi.nlm.nih.gov/pubmed/36674289 http://dx.doi.org/10.3390/ijerph20021534 |
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