Evidence map›Paper›PMID 24465432›Full record

ArticlePloS one2014

Linear mixed effects models under inequality constraints with applications.

Laura Farnan, Anastasia Ivanova, Shyamal D Peddada

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  6. Elevated plasma 8-iso-prostaglandin FFree radical biology & medicine · 2018
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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

3 authors at 3 institutions in 1 country.

Laura FarnanLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Anastasia IvanovaDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Shyamal D PeddadaBiostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America.
National Institute of Environmental Health Sciences · USUNC Lineberger Comprehensive Cancer CenterUniversity of North Carolina at Chapel Hill · US

Funding

Statistical Methods with Applications to Toxicology and Microarray dataZIAES101744 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI PEDDADA, SHYAMAL · 2009 to 2017
$4.2M
Microarray and Genome InformaticsZ01ES102345 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI BUSHEL, PIERRE · 2007 to 2008
$2.5M
Current Design Issues in Oncology TrialsR01CA120082 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI IVANOVA, ANASTASIA · 2006 to 2008
$403k
Intramural NIH HHS Z01 ES102345NCI NIH HHS R01 CA120082NCI NIH HHS R01 CA120082-01A1NIEHS NIH HHS Z01 ES102345-04
6 · The paper itself

Abstract

Constraints arise naturally in many scientific experiments/studies such as in, epidemiology, biology, toxicology, etc. and often researchers ignore such information when analyzing their data and use standard methods such as the analysis of variance (ANOVA). Such methods may not only result in a loss of power and efficiency in costs of experimentation but also may result poor interpretation of the data. In this paper we discuss constrained statistical inference in the context of linear mixed effects models that arise naturally in many applications, such as in repeated measurements designs, familial studies and others. We introduce a novel methodology that is broadly applicable for a variety of constraints on the parameters. Since in many applications sample sizes are small and/or the data are not necessarily normally distributed and furthermore error variances need not be homoscedastic (i.e. heterogeneity in the data) we use an empirical best linear unbiased predictor (EBLUP) type residual based bootstrap methodology for deriving critical values of the proposed test. Our simulation studies suggest that the proposed procedure maintains the desired nominal Type I error while competing well with other tests in terms of power. We illustrate the proposed methodology by re-analyzing a clinical trial data on blood mercury level. The methodology introduced in this paper can be easily extended to other settings such as nonlinear and generalized regression models.

Indexed as

Analysis of VarianceAntidotesChelating AgentsComputer SimulationHumansLinear ModelsMercuryMercury PoisoningResearch DesignSuccimerAntidotesChelating AgentsMercurySuccimer

Identifiers

PMID24465432
PMCPMC3897384
OpenAlexW2034410940

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

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.