Evidence map›Paper›PMID 28780665›Full record

ArticleBehavior genetics2017

Sum Scores in Twin Growth Curve Models: Practicality Versus Bias.

Justin M Luningham, Daniel B McArtor, Meike Bartels, Dorret I Boomsma, Gitta H Lubke

Abstract read
In one paragraph

Article in Behavior genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Justin M LuninghamDepartment of Psychology, University of Notre Dame, 220 C Haggar Hall, Notre Dame, IN, 46556, USA. jluningh@nd.edu.
Daniel B McArtorDepartment of Psychology, University of Notre Dame, 220 C Haggar Hall, Notre Dame, IN, 46556, USA.
Meike BartelsDepartment of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Dorret I BoomsmaDepartment of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Gitta H LubkeDepartment of Psychology, University of Notre Dame, 220 C Haggar Hall, Notre Dame, IN, 46556, USA.

Funding

Psychometric and Genetic Assessments of Substance UseR37DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2005 to 2014
$3.7M
Psychometric and Genetic Assessments of Substance UseR01DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2004 to 2019
$2.3M
European Commission FP7-602768Nederlandse Organisatie voor Wetenschappelijk Onderzoek 451-04-034Nederlandse Organisatie voor Wetenschappelijk Onderzoek 463-06-001Nederlandse Organisatie voor Wetenschappelijk Onderzoek 480-04-004NIDA NIH HHS R01 DA018673NIDA NIH HHS R37 DA018673ZonMw 904-61-090ZonMw 904-61-193ZonMw 985-10-002ZonMw Middelgroot-911-09-032
6 · The paper itself

Abstract

To study behavioral or psychiatric phenotypes, multiple indices of the behavior or disorder are often collected that are thought to best reflect the phenotype. Combining these items into a single score (e.g. a sum score) is a simple and practical approach for modeling such data, but this simplicity can come at a cost in longitudinal studies, where the relevance of individual items often changes as a function of age. Such changes violate the assumptions of longitudinal measurement invariance (MI), and this violation has the potential to obfuscate the interpretation of the results of latent growth models fit to sum scores. The objectives of this study are (1) to investigate the extent to which violations of longitudinal MI lead to bias in parameter estimates of the average growth curve trajectory, and (2) whether absence of MI affects estimates of the heritability of these growth curve parameters. To this end, we analytically derive the bias in the estimated means and variances of the latent growth factors fit to sum scores when the assumption of longitudinal MI is violated. This bias is further quantified via Monte Carlo simulation, and is illustrated in an empirical analysis of aggression in children aged 3-12 years. These analyses show that measurement non-invariance across age can indeed bias growth curve mean and variance estimates, and our quantification of this bias permits researchers to weigh the costs of using a simple sum score in longitudinal studies. Simulation results indicate that the genetic variance decomposition of growth factors is, however, not biased due to measurement non-invariance across age, provided the phenotype is measurement invariant across birth-order and zygosity in twins.

Indexed as

Models, StatisticalAdolescentAggressionChildChild, PreschoolFemaleHumansLongitudinal StudiesMaleModels, GeneticMonte Carlo MethodTwinsTwin Studies as TopicAggressionGrowth curve modelsMeasurement invarianceSum scoresTwin models

Identifiers

PMID28780665
PMCPMC5719894

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.