Cross-population validation of statistical distance as a measure of physiological dysregulation during aging

被引:44
作者
Cohen, Alan A. [1 ]
Milot, Emmanuel [1 ]
Li, Qing [1 ]
Legault, Veronique [1 ]
Fried, Linda P. [2 ]
Ferrucci, Luigi [3 ]
机构
[1] Univ Sherbrooke, CHUS Fleurimont, Dept Family Med, Grp Rech PRIMUS, Sherbrooke, PQ J1H 5N4, Canada
[2] Columbia Univ, Mailman Sch Publ Hlth, New York, NY 10032 USA
[3] NIA, Translat Gerontol Branch, Longitudinal Studies Sect, NIH,MedStar Harbor Hosp, Baltimore, MD 21225 USA
基金
加拿大自然科学与工程研究理事会;
关键词
Physiological dysregulation; Aging; WHAS; InCHIANTI; Biomarker; Mahalanobis distance; ALLOSTATIC LOAD; ELDERLY-PEOPLE; OLDER-ADULTS; FRAILTY; DECLINE; STRESS;
D O I
10.1016/j.exger.2014.04.016
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
Measuring physiological dysregulation during aging could be a key tool both to understand underlying aging mechanisms and to predict clinical outcomes in patients. However, most existing indices are either circular or hard to interpret biologically. Recently, we showed that statistical distance of 14 common blood biomarkers (a measure of how strange an individual's biomarker profile is) was associated with age and mortality in the WHAS II data set, validating its use as a measure of physiological dysregulation. Here, we extend the analyses to other data sets (WHAS I and InCHIANTI) to assess the stability of the measure across populations. We found that the statistical criteria used to determine the original 14 biomarkers produced diverging results across populations; in other words, had we started with a different data set, we would have chosen a different set of markers. Nonetheless, the same 14 markers (or the subset of 12 available for InCHIANTI) produced highly similar predictions of age and mortality. We include analyses of all combinatorial subsets of the markers and show that results do not depend much on biomarker choice or data set, but that more markers produce a stronger signal. We conclude that statistical distance as a measure of physiological dysregulation is stable across populations in Europe and North America. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
相关论文
共 24 条
[1]  
[Anonymous], 1995, WOMENS HLTH AGING ST
[2]   Frailty in elderly people [J].
Clegg, Andrew ;
Young, John ;
Iliffe, Steve ;
Rikkert, Marcel Olde ;
Rockwood, Kenneth .
LANCET, 2013, 381 (9868) :752-762
[3]   A novel statistical approach shows evidence for multi-system physiological dysregulation during aging [J].
Cohen, Alan A. ;
Milot, Emmanuel ;
Yong, Jian ;
Seplaki, Christopher L. ;
Fueloep, Tamas ;
Bandeen-Roche, Karen ;
Fried, Linda P. .
MECHANISMS OF AGEING AND DEVELOPMENT, 2013, 134 (3-4) :110-117
[4]   Physiological regulatory networks: ecological roles and evolutionary constraints [J].
Cohen, Alan A. ;
Martin, Lynn B. ;
Wingfield, John C. ;
McWilliams, Scott R. ;
Dunne, Jennifer A. .
TRENDS IN ECOLOGY & EVOLUTION, 2012, 27 (08) :428-435
[5]   Age differences in allostatic load: an index of physiological dysregulation [J].
Crimmins, EM ;
Johnston, M ;
Hayward, M ;
Seeman, T .
EXPERIMENTAL GERONTOLOGY, 2003, 38 (07) :731-734
[6]   The Mahalanobis distance [J].
De Maesschalck, R ;
Jouan-Rimbaud, D ;
Massart, DL .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2000, 50 (01) :1-18
[7]   Subsystems contributing to the decline in ability to walk: Bridging the gap between epidemiology and geriatric practice in the InCHIANTI study [J].
Ferrucci, L ;
Bandinelli, S ;
Benvenuti, E ;
Di Iorio, A ;
Macchi, C ;
Harris, TB ;
Guralnik, JM .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2000, 48 (12) :1618-1625
[8]  
Fried Linda P, 2005, Sci Aging Knowledge Environ, V2005, ppe24, DOI 10.1126/sageke.2005.31.pe24
[9]   Frailty in older adults: Evidence for a phenotype [J].
Fried, LP ;
Tangen, CM ;
Walston, J ;
Newman, AB ;
Hirsch, C ;
Gottdiener, J ;
Seeman, T ;
Tracy, R ;
Kop, WJ ;
Burke, G ;
McBurnie, MA .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2001, 56 (03) :M146-M156
[10]  
Fried LP, 2000, J GERONTOL A-BIOL, V55, pM43