Beyond the factor indeterminacy problem using genome-wide association data

Margaret L. Clapp Sullivan*, Ted Schwaba, K. Paige Harden, Andrew D. Grotzinger, Michel G. Nivard, Elliot M. Tucker-Drob

*Corresponding author for this work

Research output: Contribution to JournalReview articleAcademicpeer-review

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Abstract

Latent factors, such as general intelligence, depression and risk tolerance, are invoked in nearly all social science research where a construct is measured via aggregation of symptoms, question responses or other measurements. Because latent factors cannot be directly observed, they are inferred by fitting a specific model to empirical patterns of correlations among measured variables. A long-standing critique of latent factor theories is that the correlations used to infer latent factors can be produced by alternative data-generating mechanisms that do not include latent factors. This is referred to as the factor indeterminacy problem. Researchers have recently begun to overcome this problem by using information on the associations between individual genetic variants and measured variables. We review historical work on the factor indeterminacy problem and describe recent efforts in genomics to rigorously test the validity of latent factors, advancing the understanding of behavioural science constructs.

Original languageEnglish
Pages (from-to)205-218
Number of pages14
JournalNature Human Behaviour
Volume8
Issue number2
Early online date15 Jan 2024
DOIs
Publication statusPublished - Feb 2024

Bibliographical note

Publisher Copyright:
© Springer Nature Limited 2024.

Funding

We thank M. Rhemtulla (University of California Davis), B. Domingue (Stanford University), K. Kanopka (New York University), S. Trejo (Princeton University), D. Londono-Correa (University of Texas at Austin) and C. Williams (University of Texas at Austin) for their invaluable feedback on earlier versions of this work. This research was supported by National Institutes of Health (NIH) grants R01MH120219 and RF1AG073593. E.M.T.-D. is a member of the Population Research Center and Center on Aging and Population Sciences at the University of Texas at Austin, which are supported by NIH grants P2CHD042849 and P30AG066614, respectively. We thank M. Rhemtulla (University of California Davis), B. Domingue (Stanford University), K. Kanopka (New York University), S. Trejo (Princeton University), D. Londono-Correa (University of Texas at Austin) and C. Williams (University of Texas at Austin) for their invaluable feedback on earlier versions of this work. This research was supported by National Institutes of Health (NIH) grants R01MH120219 and RF1AG073593. E.M.T.-D. is a member of the Population Research Center and Center on Aging and Population Sciences at the University of Texas at Austin, which are supported by NIH grants P2CHD042849 and P30AG066614, respectively.

FundersFunder number
Population Research Center and Center on Aging and Population SciencesP30AG066614, P2CHD042849
National Institutes of HealthR01MH120219, RF1AG073593
Stanford University
New York University
University of Texas at Austin

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