{"title":"Assessment of Frailty in Animal Models.","authors":"Susan E Howlett","doi":"10.1159/000381131","DOIUrl":null,"url":null,"abstract":"<p><p>Animal models have contributed greatly to our understanding of the biology of aging and have been used to test new potential interventions to enhance survival. However, whether these interventions can modify frailty in animals is not yet clear, in part because until recently, frailty had not been considered in animal studies of aging. This review is focused on investigations that have attempted to address the issue of frailty, or aspects of frailty, in animal models, including invertebrate and vertebrate models. Some studies have used skeletal muscle weakness or sarcopenia as a surrogate for frailty in aging animals. Others have used genetically altered mice, in which components of human frailty such as inflammation are enhanced. This review also explores a novel approach to quantify frailty with a 'frailty index' based on deficit accumulation in aging animals. The concept of the frailty index is well established in the clinical literature, but recent work suggests that this approach can also be used to measure frailty in aging animals. The ability to quantify frailty in animals is a major step forward in the effort to understand the biology of frailty and to develop new clinical interventions.</p>","PeriodicalId":37866,"journal":{"name":"Interdisciplinary topics in gerontology and geriatrics","volume":"41 ","pages":"15-25"},"PeriodicalIF":0.0000,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000381131","citationCount":"24","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interdisciplinary topics in gerontology and geriatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000381131","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2015/7/17 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 24
Abstract
Animal models have contributed greatly to our understanding of the biology of aging and have been used to test new potential interventions to enhance survival. However, whether these interventions can modify frailty in animals is not yet clear, in part because until recently, frailty had not been considered in animal studies of aging. This review is focused on investigations that have attempted to address the issue of frailty, or aspects of frailty, in animal models, including invertebrate and vertebrate models. Some studies have used skeletal muscle weakness or sarcopenia as a surrogate for frailty in aging animals. Others have used genetically altered mice, in which components of human frailty such as inflammation are enhanced. This review also explores a novel approach to quantify frailty with a 'frailty index' based on deficit accumulation in aging animals. The concept of the frailty index is well established in the clinical literature, but recent work suggests that this approach can also be used to measure frailty in aging animals. The ability to quantify frailty in animals is a major step forward in the effort to understand the biology of frailty and to develop new clinical interventions.
期刊介绍:
At a time when interest in the process of aging is driving more and more research, ''Interdisciplinary Topics in Gerontology and Geriatrics'' offers investigators a way to stay at the forefront of developments. This series represents a comprehensive and integrated approach to the problems of aging and presents pertinent data from studies in animal and human gerontology. In order to provide a forum for a unified concept of gerontology, both the biological foundations and the clinical and sociological consequences of aging in humans are presented. Individual volumes are characterized by an analytic overall view of the aging process, novel ideas, and original approaches to healthy aging as well as age-related functional decline.