TY - JOUR
T1 - A novel, population-specific approach to define frailty
AU - Montesanto, Alberto
AU - Lagani, Vincenzo
AU - Martino, Cinzia
AU - Dato, Serena
AU - De Rango, Francesco
AU - Berardelli, Maurizio
AU - Corsonello, Andrea
AU - Mazzei, Bruno
AU - Mari, Vincenzo
AU - Lattanzio, Fabrizia
AU - Conforti, Domenico
AU - Passarino, Giuseppe
N1 - Generated from Scopus record by KAUST IRTS on 2023-09-23
PY - 2010/9/1
Y1 - 2010/9/1
N2 - The description of frailty, a syndrome of the elderly due to the decline of homeostatic capacities, has opened new opportunities in the study of the biological basis of human aging. However, the noticeable heterogeneity for this trait in different geographic areas makes it difficult to use standardized methods for measuring the quality of aging in different populations. Consequently, the necessity to carry out population-specific surveys to define tools which are able to highlight groups of subjects with homogeneous aging phenotype within each population has emerged. We carried out an extensive monitoring of the status of the elderly population in Calabria, southern Italy, performing a geriatric multidimensional evaluation of 680 subjects (age range 65-108 years). Then, in order to classify the subjects, we applied a cluster analysis which considered physical, cognitive, and psychological parameters such as classification variables. We identified groups of subjects homogeneous for the aging phenotypes. The diagnostic and predictive soundness of our classification was confirmed by a 3-year longitudinal study. In fact, both Kaplan-Meier estimates of the survival functions and Cox proportional hazard models indicate higher survival chance for subjects characterized by lower frailty. The availability of operative frailty phenotypes allows a reappraisal of the biological basis of healthy aging as it regards both biomarkers correlated with the frail phenotype and the genetic variability associated with the phenotypes identified. Indeed, we found that the frailty phenotype is strongly correlated with clinical parameters associated with the nutritional status. © 2010 American Aging Association, Media.
AB - The description of frailty, a syndrome of the elderly due to the decline of homeostatic capacities, has opened new opportunities in the study of the biological basis of human aging. However, the noticeable heterogeneity for this trait in different geographic areas makes it difficult to use standardized methods for measuring the quality of aging in different populations. Consequently, the necessity to carry out population-specific surveys to define tools which are able to highlight groups of subjects with homogeneous aging phenotype within each population has emerged. We carried out an extensive monitoring of the status of the elderly population in Calabria, southern Italy, performing a geriatric multidimensional evaluation of 680 subjects (age range 65-108 years). Then, in order to classify the subjects, we applied a cluster analysis which considered physical, cognitive, and psychological parameters such as classification variables. We identified groups of subjects homogeneous for the aging phenotypes. The diagnostic and predictive soundness of our classification was confirmed by a 3-year longitudinal study. In fact, both Kaplan-Meier estimates of the survival functions and Cox proportional hazard models indicate higher survival chance for subjects characterized by lower frailty. The availability of operative frailty phenotypes allows a reappraisal of the biological basis of healthy aging as it regards both biomarkers correlated with the frail phenotype and the genetic variability associated with the phenotypes identified. Indeed, we found that the frailty phenotype is strongly correlated with clinical parameters associated with the nutritional status. © 2010 American Aging Association, Media.
UR - http://link.springer.com/10.1007/s11357-010-9136-x
UR - http://www.scopus.com/inward/record.url?scp=77956182854&partnerID=8YFLogxK
U2 - 10.1007/s11357-010-9136-x
DO - 10.1007/s11357-010-9136-x
M3 - Article
SN - 0161-9152
VL - 32
SP - 385
EP - 395
JO - Age
JF - Age
IS - 3
ER -