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New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology

Statistically, the concentration of antibodies against parasites decreases with the duration of infection. This can result in false-negative outcomes of diagnostic tests for subjects with old infections. When a property of seronegative and seropositive subjects is compared under these circumstances,...

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Autores principales: Flegr, Jaroslav, Tureček, Petr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994960/
https://www.ncbi.nlm.nih.gov/pubmed/31953266
http://dx.doi.org/10.1242/bio.045948
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author Flegr, Jaroslav
Tureček, Petr
author_facet Flegr, Jaroslav
Tureček, Petr
author_sort Flegr, Jaroslav
collection PubMed
description Statistically, the concentration of antibodies against parasites decreases with the duration of infection. This can result in false-negative outcomes of diagnostic tests for subjects with old infections. When a property of seronegative and seropositive subjects is compared under these circumstances, the statistical tests can detect no difference between these two groups of subjects, despite the fact that they differ. When the effect of the infection has a cumulative character and subjects with older infections are affected to a greater degree, we may even get paradoxical results of the comparison – the seropositive subjects have, on average, a higher value of certain traits despite the infection having a negative effect on those traits. A permutation test for the contaminated data implemented, e.g. in the program Treept or available as a comprehensibly commented R function at https://github.com/costlysignalling/Permutation_test_for_contaminated_data, can be used to reveal and to eliminate the effect of false negatives. A Monte Carlo simulation in the program R showed that our permutation test is a conservative test – it could provide false negative, but not false positive, results if the studied population contains no false-negative subjects. A new R version of the test was expanded by skewness analysis, which helps to estimate the proportion of false-negative subjects based on the assumption of equal data skewness in groups of healthy and infected subjects. Based on the results of simulations and our experience with empirical studies we recommend the usage of a permutation test for contaminated data whenever seronegative and seropositive individuals are compared.
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spelling pubmed-69949602020-02-03 New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology Flegr, Jaroslav Tureček, Petr Biol Open Research Article Statistically, the concentration of antibodies against parasites decreases with the duration of infection. This can result in false-negative outcomes of diagnostic tests for subjects with old infections. When a property of seronegative and seropositive subjects is compared under these circumstances, the statistical tests can detect no difference between these two groups of subjects, despite the fact that they differ. When the effect of the infection has a cumulative character and subjects with older infections are affected to a greater degree, we may even get paradoxical results of the comparison – the seropositive subjects have, on average, a higher value of certain traits despite the infection having a negative effect on those traits. A permutation test for the contaminated data implemented, e.g. in the program Treept or available as a comprehensibly commented R function at https://github.com/costlysignalling/Permutation_test_for_contaminated_data, can be used to reveal and to eliminate the effect of false negatives. A Monte Carlo simulation in the program R showed that our permutation test is a conservative test – it could provide false negative, but not false positive, results if the studied population contains no false-negative subjects. A new R version of the test was expanded by skewness analysis, which helps to estimate the proportion of false-negative subjects based on the assumption of equal data skewness in groups of healthy and infected subjects. Based on the results of simulations and our experience with empirical studies we recommend the usage of a permutation test for contaminated data whenever seronegative and seropositive individuals are compared. The Company of Biologists Ltd 2020-01-23 /pmc/articles/PMC6994960/ /pubmed/31953266 http://dx.doi.org/10.1242/bio.045948 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Flegr, Jaroslav
Tureček, Petr
New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology
title New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology
title_full New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology
title_fullStr New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology
title_full_unstemmed New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology
title_short New approach and new permutation tests with R programs for analyses of false-negative-contaminated data in medicine and biology
title_sort new approach and new permutation tests with r programs for analyses of false-negative-contaminated data in medicine and biology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994960/
https://www.ncbi.nlm.nih.gov/pubmed/31953266
http://dx.doi.org/10.1242/bio.045948
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