Evidence map›Paper›PMID 36730335›Full record

ArticlePloS one2023

A nonparametric alternative to the Cochran-Armitage trend test in genetic case-control association studies: The Jonckheere-Terpstra trend test.

Sydney E Manning, Hung-Chih Ku, Douglas F Dluzen, Chao Xing, Zhengyang Zhou

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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

  1. Pooled it
  2. Associations BetweenBiology · 2026
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  7. Are SNPs Linked to Somatic Cell Score Suitable Markers for the Susceptibility to Specific Mastitis Pathogens in Holstein Cows?Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Genetic Background of Acute Heart Rate Response to Exercise.International journal of molecular sciences · 2024
    Article
  13. Article
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.

Sydney E ManningDepartment of Pharmacotherapy, University of North Texas Health Science Center, Fort Worth, TX, United States of America.ORCID 0000-0003-1715-7891
Hung-Chih KuDepartment of Mathematical Sciences, DePaul University, Chicago, IL, United States of America.
Douglas F DluzenDepartment of Biology, Morgan State University, Baltimore, Maryland, MD, United States of America.
Chao XingMcDermott Center for Human Growth and Development and Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, United States of America.ORCID 0000-0002-1838-0502
Zhengyang ZhouDepartment of Biostatistics and Epidemiology, University of North Texas Health Science Center, Fort Worth, TX, United States of America.ORCID 0000-0002-8039-418X

Funding

Wastewater surveillance for addressing environmental health disparitiesU54MD013376 · NIMHD · MORGAN STATE UNIVERSITY · PI Ingrid K TULLOCH · 2019 to 2026
$33.5M
Genome-wide screen for dynamic gene-environment interactionsR03ES034138 · NIEHS · UT SOUTHWESTERN MEDICAL CENTER · PI XING, CHAO · 2022 to 2023
$174k
NIEHS NIH HHS R03 ES034138NIMHD NIH HHS U54 MD013376
6 · The paper itself

Abstract

Identifications of novel genetic signals conferring susceptibility to human complex diseases is pivotal to the disease diagnosis, prevention, and treatment. Genetic association study is a powerful tool to discover candidate genetic signals that contribute to diseases, through statistical tests for correlation between the disease status and genetic variations in study samples. In such studies with a case-control design, a standard practice is to perform the Cochran-Armitage (CA) trend test under an additive genetic model, which suffers from power loss when the model assumption is wrong. The Jonckheere-Terpstra (JT) trend test is an alternative method to evaluate association in a nonparametric way. This study compares the power of the JT trend test and the CA trend test in various scenarios, including different sample sizes (200-2000), minor allele frequencies (0.05-0.4), and underlying modes of inheritance (dominant genetic model to recessive genetic model). By simulation and real data analysis, it is shown that in general the JT trend test has higher, similar, and lower power than the CA trend test when the underlying mode of inheritance is dominant, additive, and recessive, respectively; when the sample size is small and the minor allele frequency is low, the JT trend test outperforms the CA trend test across the spectrum of genetic models. In sum, the JT trend test is a valuable alternative to the CA trend test under certain circumstances with higher statistical power, which could lead to better detection of genetic signals to human diseases and finer dissection of their genetic architecture.

Indexed as

Databases, GeneticModels, GeneticCase-Control StudiesComputer SimulationGenetic Association StudiesHumans

Identifiers

PMID36730335
PMCPMC9894441

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LicenceCC BY
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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.