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Improving the comprehension of sarcopenic state determinants: An multivariate approach involving hormonal, nutritional, lifestyle and genetic variables.

Authors :
da Silva JRD
Freire IV
Ribeiro ÍJS
Dos Santos CS
Casotti CA
Dos Santos DB
Barbosa AAL
Pereira R
Source :
Mechanisms of ageing and development [Mech Ageing Dev] 2018 Jul; Vol. 173, pp. 21-28. Date of Electronic Publication: 2018 May 25.
Publication Year :
2018

Abstract

It is known that sarcopenia is a multifaceted phenomenon, which involves genetic, nutritional, hormonal and living habits aspects. Then, an integrated analysis, as a multivariate approach, could improve the comprehension about the determinants of sarcopenic state in old adults. The present study aimed to investigate the interaction among serum vitamin D, daily caloric and protein intake, lifestyle habits, ACE I/D gene polymorphism and sarcopenic state in community-dwelling old adults. One hundred one community-dwelling old adults were clinically stratified as sarcopenic or non-sarcopenic. Serum vitamin D, daily caloric and protein intake, lifestyle habits (smoking, physical activity level and sedentary behavior) and ACE I/D gene polymorphism were recorded. A multivariate logistic regression technique was applied to investigate the interaction among the selected independent variables and the sarcopenic state. The independent variables age, smoking, serum Vitamin D and ACE I/D polymorphism achieved the statistical criteria to be inserted in the multivariate analysis. After a stepwise procedure from the multivariate logistic regression, the variables age, serum Vitamin D and ACE I/D polymorphism remained, together, in the final model. Sarcopenic state was significantly associated to older age, II-genotype and low serum Vitamin D in old adults from 60 years old.<br /> (Copyright © 2018 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-6216
Volume :
173
Database :
MEDLINE
Journal :
Mechanisms of ageing and development
Publication Type :
Academic Journal
Accession number :
29807051
Full Text :
https://doi.org/10.1016/j.mad.2018.05.008