TY - JOUR
T1 - Evaluating Health Span in Preclinical Models of Aging and Disease
T2 - Guidelines, Challenges, and Opportunities for Geroscience
AU - Huffman, Derek M.
AU - Justice, Jamie N.
AU - Stout, Michael B.
AU - Kirkland, James L.
AU - Barzilai, Nir
AU - Austad, Steven N.
N1 - Funding Information:
This work was supported by the National Institutes of Health grant R24 AG044396 (J.L.K., S.N.A., and N.B.).
Publisher Copyright:
© 2016 The Author 2016. Published by Oxford University Press on behalf of The Gerontological Society of America.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Life extension is no longer considered sufficient evidence of delayed aging in research animals. It must also be demonstrated that a broad swathe of health indicators have been extended. During a retreat of the Geroscience Network, a consortium of basic and clinical aging researchers, potential measures of mouse health were considered for their potential as easily standardized, highly informative metrics. Major health domains considered were neuromuscular, cognitive, cardiovascular, metabolic, and inflammatory functions as well as body composition and energetics and a multitude of assays interrogating these domains. A particularly sensitive metric of health is the ability to respond to, and recover, from stress. Therefore, the Network also considered stresses of human relevance that could be implemented in mouse models to assess frailty and resilience. Mouse models already exist for responses to forced immobility, cancer chemotherapy, infectious diseases, dietary challenges, and surgical stress, and it was felt that these could be employed to determine whether putative senescence-retarding interventions increased and extended organismal robustness. The Network discussed challenges in modeling age-related human chronic diseases and concluded that more attention needs to be paid to developing disease models with later age of onset, models of co- and multimorbidity, diversifying the strains and sexes commonly used in aging research, and considering additional species.
AB - Life extension is no longer considered sufficient evidence of delayed aging in research animals. It must also be demonstrated that a broad swathe of health indicators have been extended. During a retreat of the Geroscience Network, a consortium of basic and clinical aging researchers, potential measures of mouse health were considered for their potential as easily standardized, highly informative metrics. Major health domains considered were neuromuscular, cognitive, cardiovascular, metabolic, and inflammatory functions as well as body composition and energetics and a multitude of assays interrogating these domains. A particularly sensitive metric of health is the ability to respond to, and recover, from stress. Therefore, the Network also considered stresses of human relevance that could be implemented in mouse models to assess frailty and resilience. Mouse models already exist for responses to forced immobility, cancer chemotherapy, infectious diseases, dietary challenges, and surgical stress, and it was felt that these could be employed to determine whether putative senescence-retarding interventions increased and extended organismal robustness. The Network discussed challenges in modeling age-related human chronic diseases and concluded that more attention needs to be paid to developing disease models with later age of onset, models of co- and multimorbidity, diversifying the strains and sexes commonly used in aging research, and considering additional species.
KW - Health span
KW - aging
KW - animal models
KW - longevity
KW - preclinical studies
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U2 - 10.1093/gerona/glw106
DO - 10.1093/gerona/glw106
M3 - Article
C2 - 27535967
AN - SCOPUS:84994424579
SN - 1079-5006
VL - 71
SP - 1395
EP - 1406
JO - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
JF - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
IS - 11
ER -