TY - JOUR
T1 - Measures of healthspan as indices of aging in Mice-A recommendation
AU - Richardson, Arlan
AU - Fischer, Kathleen E.
AU - Speakman, John R.
AU - De Cabo, Rafael
AU - Mitchell, Sarah J.
AU - Peterson, Charlotte A.
AU - Rabinovitch, Peter
AU - Chiao, Ying A.
AU - Taffet, George
AU - Miller, Richard A.
AU - Rentería, René C.
AU - Bower, James
AU - Ingram, Donald K.
AU - Ladiges, Warren C.
AU - Ikeno, Yuji
AU - Sierra, Felipe
AU - Austad, Steven N.
N1 - Publisher Copyright:
©The Author 2015. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Over the past decade, a large number of discoveries have shown that interventions (genetic, pharmacological, and nutritional) increase the lifespan of invertebrates and laboratory rodents. Therefore, the possibility of developing antiaging interventions for humans has gone from a dream to a reality. However, it has also become apparent that we need more information than just lifespan to evaluate the translational potential of any proposed antiaging intervention to humans. Information is needed on how an intervention alters the "healthspan" of an animal, that is, how the physiological functions that change with age are altered. In this report, we describe the utility and the limitations of assays in mice currently available for measuring a wide range of physiological functions that potentially impact quality of life. We encourage investigators and reviewers alike to expect at minimum an overall assessment of health in several domains across several ages before an intervention is labeled as "increasing healthspan." In addition, it is important that investigators indicate any tests in which the treated group did worse or did not differ statistically from controls because overall health is a complex phenotype, and no intervention discovered to date improves every aspect of health. Finally, we strongly recommend that functional measurements be performed in both males and females so that sex differences in the rate of functional decline in different domains are taken into consideration.
AB - Over the past decade, a large number of discoveries have shown that interventions (genetic, pharmacological, and nutritional) increase the lifespan of invertebrates and laboratory rodents. Therefore, the possibility of developing antiaging interventions for humans has gone from a dream to a reality. However, it has also become apparent that we need more information than just lifespan to evaluate the translational potential of any proposed antiaging intervention to humans. Information is needed on how an intervention alters the "healthspan" of an animal, that is, how the physiological functions that change with age are altered. In this report, we describe the utility and the limitations of assays in mice currently available for measuring a wide range of physiological functions that potentially impact quality of life. We encourage investigators and reviewers alike to expect at minimum an overall assessment of health in several domains across several ages before an intervention is labeled as "increasing healthspan." In addition, it is important that investigators indicate any tests in which the treated group did worse or did not differ statistically from controls because overall health is a complex phenotype, and no intervention discovered to date improves every aspect of health. Finally, we strongly recommend that functional measurements be performed in both males and females so that sex differences in the rate of functional decline in different domains are taken into consideration.
KW - Age
KW - Healthspan
KW - Lifespan
KW - Physiological function
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U2 - 10.1093/gerona/glv080
DO - 10.1093/gerona/glv080
M3 - Review article
C2 - 26297941
AN - SCOPUS:84964890856
SN - 1079-5006
VL - 71
SP - 427
EP - 430
JO - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
JF - Journals of Gerontology - Series A Biological Sciences and Medical Sciences
IS - 4
ER -