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Testing for differences in distribution tails to test for differences in 'maximum' lifespan

BACKGROUND: Investigators are actively testing interventions intended to increase lifespan and wish to test whether the interventions increase maximum lifespan. Based on the fact that one cannot be assured of observing population maximum lifespans in finite samples, in previous work, we constructed...

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Autores principales: Gao, Guimin, Wan, Wen, Zhang, Sijian, Redden, David T, Allison, David B
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529340/
https://www.ncbi.nlm.nih.gov/pubmed/18655712
http://dx.doi.org/10.1186/1471-2288-8-49
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author Gao, Guimin
Wan, Wen
Zhang, Sijian
Redden, David T
Allison, David B
author_facet Gao, Guimin
Wan, Wen
Zhang, Sijian
Redden, David T
Allison, David B
author_sort Gao, Guimin
collection PubMed
description BACKGROUND: Investigators are actively testing interventions intended to increase lifespan and wish to test whether the interventions increase maximum lifespan. Based on the fact that one cannot be assured of observing population maximum lifespans in finite samples, in previous work, we constructed and validated several tests of difference in the upper parts of lifespan distributions between a treatment group and a control group by testing whether the probabilities that observations are above some threshold defining 'old' or being in the tail of the survival distribution are equal in the two groups. However, a limitation of these tests is that they do not consider how much above the threshold any particular observation is. METHODS: In this article we propose new methods which improve upon our previous tests by considering not only whether an observation is above some threshold, but also the magnitudes by which observations exceed the threshold. RESULTS: Simulations show that the new methods control type I error rates quite well and that the power of the new methods is usually higher than that of the tests we previously proposed. In illustrative analyses of two real datasets involving rodents, when setting the threshold equal to 110 (100) weeks for the first (second) datasets, the new methods detected differences in 'maximum lifespan' between groups at nominal alpha levels of 0.01 (0.05) for the first (second) datasets and provided more significant results than competitor tests. CONCLUSION: The new methods not only have good performance in controlling the type I error rates but also improve the power compared with the tests we previously proposed.
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spelling pubmed-25293402008-09-05 Testing for differences in distribution tails to test for differences in 'maximum' lifespan Gao, Guimin Wan, Wen Zhang, Sijian Redden, David T Allison, David B BMC Med Res Methodol Research Article BACKGROUND: Investigators are actively testing interventions intended to increase lifespan and wish to test whether the interventions increase maximum lifespan. Based on the fact that one cannot be assured of observing population maximum lifespans in finite samples, in previous work, we constructed and validated several tests of difference in the upper parts of lifespan distributions between a treatment group and a control group by testing whether the probabilities that observations are above some threshold defining 'old' or being in the tail of the survival distribution are equal in the two groups. However, a limitation of these tests is that they do not consider how much above the threshold any particular observation is. METHODS: In this article we propose new methods which improve upon our previous tests by considering not only whether an observation is above some threshold, but also the magnitudes by which observations exceed the threshold. RESULTS: Simulations show that the new methods control type I error rates quite well and that the power of the new methods is usually higher than that of the tests we previously proposed. In illustrative analyses of two real datasets involving rodents, when setting the threshold equal to 110 (100) weeks for the first (second) datasets, the new methods detected differences in 'maximum lifespan' between groups at nominal alpha levels of 0.01 (0.05) for the first (second) datasets and provided more significant results than competitor tests. CONCLUSION: The new methods not only have good performance in controlling the type I error rates but also improve the power compared with the tests we previously proposed. BioMed Central 2008-07-25 /pmc/articles/PMC2529340/ /pubmed/18655712 http://dx.doi.org/10.1186/1471-2288-8-49 Text en Copyright © 2008 Gao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gao, Guimin
Wan, Wen
Zhang, Sijian
Redden, David T
Allison, David B
Testing for differences in distribution tails to test for differences in 'maximum' lifespan
title Testing for differences in distribution tails to test for differences in 'maximum' lifespan
title_full Testing for differences in distribution tails to test for differences in 'maximum' lifespan
title_fullStr Testing for differences in distribution tails to test for differences in 'maximum' lifespan
title_full_unstemmed Testing for differences in distribution tails to test for differences in 'maximum' lifespan
title_short Testing for differences in distribution tails to test for differences in 'maximum' lifespan
title_sort testing for differences in distribution tails to test for differences in 'maximum' lifespan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529340/
https://www.ncbi.nlm.nih.gov/pubmed/18655712
http://dx.doi.org/10.1186/1471-2288-8-49
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