Evidence map›Paper›PMID 31808976›Full record

ArticleStatistics in medicine2020

An empirical comparison of two novel transformation models.

Yuqi Tian, Torsten Hothorn, Chun Li, Frank E Harrell, Bryan E Shepherd

Abstract read
In one paragraph

Article in Statistics in medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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

6 citing papers in PubMed.

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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

5 authors.

Yuqi TianDepartment of Biostatistics, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0003-0601-3454
Torsten HothornInstitut für Epidemiologie, Biostatistik und Prävention, Universität Zürich, Zürich, Switzerland.ORCID 0000-0001-8301-0471
Chun LiDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, Ohio.
Frank E HarrellDepartment of Biostatistics, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0002-8271-5493
Bryan E ShepherdDepartment of Biostatistics, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0002-3758-5992

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Koethe · 2015 to 2026
$27.5M
VIROLOGY COREP30AI054999 · NIAID · VANDERBILT UNIVERSITY · PI D'AQUILA, RICHARD · 2003 to 2011
$10.3M
Statistical Methods for Ordinal Variables in HIV/AIDS StudiesR01AI093234 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Chun Li, Bryan Earl Shepherd · 2011 to 2026
$4.9M
Oxidant Stress and Antioxidants during HIV TherapyK23AT002508 · NCCIH · VANDERBILT UNIVERSITY · PI HULGAN, TODD M · 2004 to 2007
$473k
NCATS NIH HHS UL1 TR000445NCCIH NIH HHS K23 AT002508NIAID NIH HHS P30 AI054999NIAID NIH HHS P30 AI110527NIAID NIH HHS R01 AI093234United States National Institutes of Health K23100700United States National Institutes of Health K23AT002508United States National Institutes of Health P30AI110527United States National Institutes of Health P30AI54999,United States National Institutes of Health R01AI093234United States National Institutes of Health UL1TR000445
6 · The paper itself

Abstract

Continuous response variables are often transformed to meet modeling assumptions, but the choice of the transformation can be challenging. Two transformation models have recently been proposed: semiparametric cumulative probability models (CPMs) and parametric most likely transformation models (MLTs). Both approaches model the cumulative distribution function and require specifying a link function, which implicitly assumes that the responses follow a known distribution after some monotonic transformation. However, the two approaches estimate the transformation differently. With CPMs, an ordinal regression model is fit, which essentially treats each continuous response as a unique category and therefore nonparametrically estimates the transformation; CPMs are semiparametric linear transformation models. In contrast, with MLTs, the transformation is parameterized using flexible basis functions. Conditional expectations and quantiles are readily derived from both methods on the response variable's original scale. We compare the two methods with extensive simulations. We find that both methods generally have good performance with moderate and large sample sizes. MLTs slightly outperformed CPMs in small sample sizes under correct models. CPMs tended to be somewhat more robust to model misspecification and outcome rounding. Except in the simplest situations, both methods outperform basic transformation approaches commonly used in practice. We apply both methods to an HIV biomarker study.

Indexed as

Likelihood FunctionsHumansLinear ModelsSample SizeHIVnonparametric maximum likelihood estimationordinal regression modeltransformation model

Identifiers

PMID31808976
PMCPMC7537829

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Registered trials

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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.