Risk-period-cohort approach for averting identification problems in longitudinal models.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2019
2019
Historique:
received:
07
03
2019
accepted:
21
06
2019
entrez:
11
7
2019
pubmed:
11
7
2019
medline:
29
2
2020
Statut:
epublish
Résumé
In epidemiology, gerontology, human development and the social sciences, age-period-cohort (APC) models are used to study the variability in trajectories of change over time. A well-known issue exists in simultaneously identifying age, period and birth cohort effects, namely that the three characteristics comprise a perfectly collinear system. That is, since age = period-cohort, only two of these effects are estimable at a time. In this paper, we introduce an alternative framework for considering effects relating to age, period and birth cohort. In particular, instead of directly modeling age in the presence of period and cohort effects, we propose a risk modeling approach to characterize age-related risk (i.e., a hybrid of multiple biological and sociological influences to evaluate phenomena associated with growing older). The properties of this approach, termed risk-period-cohort (RPC), are described in this paper and studied by simulations. We show that, except for pathological circumstances where risk is uniquely determined by age, using such risk indices obviates the problem of collinearity. We also show that the size of the chronological age effect in the risk prediction model associates with the correlation between a risk index and chronological age and that the RPC approach can satisfactorily recover cohort and period effects in most cases. We illustrate the advantages of RPC compared to traditional APC analysis on 27496 individuals from NHANES survey data (2005-2016) to study the longitudinal variability in depression screening over time. Our RPC method has broad implications for examining processes of change over time in longitudinal studies.
Identifiants
pubmed: 31291339
doi: 10.1371/journal.pone.0219399
pii: PONE-D-19-06690
pmc: PMC6620014
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0219399Subventions
Organisme : NIA NIH HHS
ID : R01 AG055480
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK112905
Pays : United States
Déclaration de conflit d'intérêts
Adam Perzynski, PhD is a co-author on this manuscript and is a Editorial Board Member at PLOS ONE.
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