Evidence map›Paper›PMID 33400061›Full record

ArticleBehavior genetics2021

Best Practices for Binary and Ordinal Data Analyses.

Brad Verhulst, Michael C Neale

Abstract read
In one paragraph

Article in Behavior genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Brad VerhulstDepartment of Psychiatry, Texas A&M University, College Station, USA. verhulst@tamu.edu.ORCID http://orcid.org/0000-0001-5369-9757
Michael C NealeVirginia Commonwealth University, Richmond, USA.

Funding

Examining Brain Development, Context, and Culture as Mediators and Moderators of the Relation between Adverse Childhood Experiences (ACEs) and Substance (Ab)useU01DA051037 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI James M Bjork, MICHAEL CHURTON NEALE · 2020 to 2026
$11.0M
Psychometric and Genetic Assessments of Substance UseR01DA018673 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2004 to 2019
$2.3M
Extensions of Mendelian Randomization Methodology for Combined Genomic and Methylomic AnalysisR01DA049867 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEALE, MICHAEL CHURTON · 2020 to 2024
$1.9M
NIDA NIH HHS R01 DA018673NIDA NIH HHS R01 DA049867NIDA NIH HHS U01 DA051037
6 · The paper itself

Abstract

The measurement of many human traits, states, and disorders begins with a set of items on a questionnaire. The response format for these questions is often simply binary (e.g., yes/no) or ordered (e.g., high, medium or low). During data analysis, these items are frequently summed or used to estimate factor scores. In clinical applications, such assessments are often non-normally distributed in the general population because many respondents are unaffected, and therefore asymptomatic. As a result, in many cases these measures violate the statistical assumptions required for subsequent analyses. To reduce the influence of the non-normality and quasi-continuous assessment, variables are frequently recoded into binary (affected-unaffected) or ordinal (mild-moderate-severe) diagnoses. Ordinal data therefore present challenges at multiple levels of analysis. Categorizing continuous variables into ordered categories typically results in a loss of statistical power, which represents an incentive to the data analyst to assume that the data are normally distributed, even when they are not. Despite prior zeitgeists suggesting that, e.g., variables with more than 10 ordered categories may be regarded as continuous and analyzed as if they were, we show via simulation studies that this is not generally the case. In particular, using Pearson product-moment correlations instead of maximum likelihood estimates of polychoric correlations biases the estimated correlations towards zero. This bias is especially severe when a plurality of the observations fall into a single observed category, such as a score of zero. By contrast, estimating the ordinal correlation by maximum likelihood yields no estimation bias, although standard errors are (appropriately) larger. We also illustrate how odds ratios depend critically on the proportion or prevalence of affected individuals in the population, and therefore are sub-optimal for studies where comparisons of association metrics are needed. Finally, we extend these analyses to the classical twin model and demonstrate that treating binary data as continuous will underestimate genetic and common environmental variance components, and overestimate unique environment (residual) variance. These biases increase as prevalence declines. While modeling ordinal data appropriately may be more computationally intensive and time consuming, failing to do so will likely yield biased correlations and biased parameter estimates from modeling them.

Indexed as

Data AnalysisBiasComputer SimulationHumansLikelihood FunctionsModels, StatisticalOdds RatioPractice Guidelines as TopicStatistics as TopicOdds ratioOrdinal dataPearson product-moment correlationPoint biserial correlationPolychoric correlationPrevalenceTetrachoric correlation

Identifiers

PMID33400061
PMCPMC8096648

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Registered trials

None linked

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.