A quantile frailty index without dichotomization

Garrett Stubbings, Kenneth Rockwood, Arnold Mitnitski, Andrew Rutenberg

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Summary measures of health quantify the aging process of individuals. They should be interpretable, associated with future adverse outcomes, and straightforward to assemble. We use the rank-ordering of risk within a population to construct a quantile frailty index (QFI) that avoids dichotomization, is convenient and interpretable, and is associated with adverse outcomes. We show that the QFI outperforms previous frailty index (FI) measures on cross-sectional laboratory data (NHANES, CSHA, and ELSA). We construct the QFI by ranking the risk of individuals with respect to a reference population. Sex-specific reference populations narrow male–female FI differences as a function of age, and improve predictive performance. With a fixed reference population of 80–85 year olds, our QFI appears similar to earlier FI measures. With an age-matched reference population for each individual, we obtain a QFI that contains very little age information and that has similar predictive performance as other age-controlled FI measures. Adding age as an auxiliary variable leads to significantly better performance. We conclude that age should be controlled for when evaluating the predictive performance of summary measures of health. This is straight-forward to do with the QFI.

Original languageEnglish
Article number111570
JournalMechanisms of Ageing and Development
Volume199
DOIs
Publication statusPublished - Oct 2021

Bibliographical note

Funding Information:
ADR thanks the Natural Sciences and Engineering Research Council (NSERC) for an operating Grant (RGPIN 2019-05888). KR has operational funding from the Canadian Institutes of Health Research (PJT-156114) and personal support from the Dalhousie Medical Research Foundation as the Kathryn Allen Weldon Professor of Alzheimer Research.

Publisher Copyright:
© 2021 Elsevier B.V.

ASJC Scopus Subject Areas

  • Ageing
  • Developmental Biology

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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