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What Cure Models Can Teach us About Genome-Wide Survival Analysis
The aim of logistic regression is to estimate genetic effects on disease risk, while survival analysis aims to determine effects on age of onset. In practice, genetic variants may affect both types of outcomes. A cure survival model analyzes logistic and survival effects simultaneously. The aim of t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751180/ https://www.ncbi.nlm.nih.gov/pubmed/26552795 http://dx.doi.org/10.1007/s10519-015-9764-0 |
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author | Stringer, Sven Denys, Damiaan Kahn, René S. Derks, Eske M. |
author_facet | Stringer, Sven Denys, Damiaan Kahn, René S. Derks, Eske M. |
author_sort | Stringer, Sven |
collection | PubMed |
description | The aim of logistic regression is to estimate genetic effects on disease risk, while survival analysis aims to determine effects on age of onset. In practice, genetic variants may affect both types of outcomes. A cure survival model analyzes logistic and survival effects simultaneously. The aim of this simulation study is to assess the performance of logistic regression and traditional survival analysis under a cure model and to investigate the benefits of cure survival analysis. We simulated data under a cure model and varied the percentage of subjects at risk for disease (cure fraction), the logistic and survival effect sizes, and the contribution of genetic background risk factors. We then computed the error rates and estimation bias of logistic, Cox proportional hazards (PH), and cure PH analysis, respectively. The power of logistic and Cox PH analysis is sensitive to the cure fraction and background heritability. Our results show that traditional Cox PH analysis may erroneously detect age of onset effects if no such effects are present in the data. In the presence of genetic background risk even the cure model results in biased estimates of both the odds ratio and the hazard ratio. Cure survival analysis takes cure fractions into account and can be used to simultaneously estimate the effect of genetic variants on disease risk and age of onset. Since genome-wide cure survival analysis is not computationally feasible, we recommend this analysis for genetic variants that are significant in a traditional survival analysis. |
format | Online Article Text |
id | pubmed-4751180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-47511802016-02-22 What Cure Models Can Teach us About Genome-Wide Survival Analysis Stringer, Sven Denys, Damiaan Kahn, René S. Derks, Eske M. Behav Genet Original Research The aim of logistic regression is to estimate genetic effects on disease risk, while survival analysis aims to determine effects on age of onset. In practice, genetic variants may affect both types of outcomes. A cure survival model analyzes logistic and survival effects simultaneously. The aim of this simulation study is to assess the performance of logistic regression and traditional survival analysis under a cure model and to investigate the benefits of cure survival analysis. We simulated data under a cure model and varied the percentage of subjects at risk for disease (cure fraction), the logistic and survival effect sizes, and the contribution of genetic background risk factors. We then computed the error rates and estimation bias of logistic, Cox proportional hazards (PH), and cure PH analysis, respectively. The power of logistic and Cox PH analysis is sensitive to the cure fraction and background heritability. Our results show that traditional Cox PH analysis may erroneously detect age of onset effects if no such effects are present in the data. In the presence of genetic background risk even the cure model results in biased estimates of both the odds ratio and the hazard ratio. Cure survival analysis takes cure fractions into account and can be used to simultaneously estimate the effect of genetic variants on disease risk and age of onset. Since genome-wide cure survival analysis is not computationally feasible, we recommend this analysis for genetic variants that are significant in a traditional survival analysis. Springer US 2015-11-09 2016 /pmc/articles/PMC4751180/ /pubmed/26552795 http://dx.doi.org/10.1007/s10519-015-9764-0 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Stringer, Sven Denys, Damiaan Kahn, René S. Derks, Eske M. What Cure Models Can Teach us About Genome-Wide Survival Analysis |
title | What Cure Models Can Teach us About Genome-Wide Survival Analysis |
title_full | What Cure Models Can Teach us About Genome-Wide Survival Analysis |
title_fullStr | What Cure Models Can Teach us About Genome-Wide Survival Analysis |
title_full_unstemmed | What Cure Models Can Teach us About Genome-Wide Survival Analysis |
title_short | What Cure Models Can Teach us About Genome-Wide Survival Analysis |
title_sort | what cure models can teach us about genome-wide survival analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751180/ https://www.ncbi.nlm.nih.gov/pubmed/26552795 http://dx.doi.org/10.1007/s10519-015-9764-0 |
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