Research agenda for frailty in older adults: Toward a better understanding of physiology and etiology: Summary from the American Geriatrics Society/National institute on aging research conference on frailty in older adults

被引:1142
作者
Walston, Jeremy
Hadley, Evan C.
Ferrucci, Luigi
Guralnik, Jack M.
Newman, Anne B.
Studenski, Stephanie A.
Ershler, William B.
Harris, Tamara
Fried, Linda P.
机构
[1] Johns Hopkins Med Inst, Dept Med, Baltimore, MD 21205 USA
[2] NIA, Bethesda, MD 20892 USA
[3] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA USA
[4] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA USA
[5] Ctr Geriatr Res Educ & Clin, Dept Vet Affairs Pittsburgh Healthcare Ctr, Pittsburgh, PA USA
[6] Natl Geriatr Resource Consortium, Inst Adv Studies Aging & Geriatr Med, Washington, DC USA
关键词
frailty; multisystem decline; pathophysiology;
D O I
10.1111/j.1532-5415.2006.00745.x
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Evolving definitions of frailty, and improved understanding of molecular and physiological declines in multiple systems that may increase vulnerability in frail, older adults has encouraged investigators from many disciplines to contribute to this emerging field of research. This article reports on the results of the 2004 American Geriatrics Society/National Institute on Aging conference on a Research Agenda on Frailty in Older Adults, which brought together a diverse group of clinical and basic scientists to encourage further investigation in this area. This conference was primarily focused on physical and physiological aspects of frailty. Although social and psychological aspects of frailty are critically important and merit future research, these topics were largely beyond the scope of this meeting. Included in this article are sections on the evolving conceptualization and definitions of frailty; physiological underpinnings of frailty, including the potential contributions of inflammatory, endocrine, skeletal muscle, and neurologic system changes; potential molecular and genetic contributors; proposed animal models; and integrative, system biology approaches that may help to facilitate future frailty research. In addition, several specific recommendations as to future directions were developed from suggestions put forth by participants, including recommendations on definition and phenotype development, methodological development to perform clinical studies of individual-system and multiple-system vulnerability to stressors, development of animal and cellular models, application of population-based studies to frailty research, and the development of large collaborative networks in which populations and resources can be shared. This meeting and subsequent article were not meant to be a comprehensive review of frailty research; instead, they were and are meant to provide a more-targeted research agenda-setting process.
引用
收藏
页码:991 / 1001
页数:11
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