Source:http://linkedlifedata.com/resource/pubmed/id/14566921
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
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pubmed:dateCreated |
2003-10-20
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pubmed:abstractText |
Logistic regression is widely used to estimate relative risks (odds ratios) from case-control studies, but when the study exposure is continuous, standard parametric models may not accurately characterize the exposure-response curve. Semi-parametric generalized linear models provide a useful extension. In these models, the exposure of interest is modelled flexibly using a regression spline or a smoothing spline, while other variables are modelled using conventional methods. When coupled with a model-selection procedure based on minimizing a cross-validation score, this approach provides a non-parametric, objective, and reproducible method to characterize the exposure-response curve by one or several models with a favourable bias-variance trade-off. We applied this approach to case-control data to estimate the dose-response relationship between alcohol consumption and risk of oral cancer among African Americans. We did not find a uniquely 'best' model, but results using linear, cubic, and smoothing splines were consistent: there does not appear to be a risk-free threshold for alcohol consumption vis-à-vis the development of oral cancer. This finding was not apparent using a standard step-function model. In our analysis, the cross-validation curve had a global minimum and also a local minimum. In general, the phenomenon of multiple local minima makes it more difficult to interpret the results, and may present a computational roadblock to non-parametric generalized additive models of multiple continuous exposures. Nonetheless, the semi-parametric approach appears to be a practical advance.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0277-6715
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pubmed:author | |
pubmed:copyrightInfo |
Published in 2003 by John Wiley & Sons, Ltd.
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3369-81
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:14566921-African Americans,
pubmed-meshheading:14566921-Alcohol Drinking,
pubmed-meshheading:14566921-Case-Control Studies,
pubmed-meshheading:14566921-Dose-Response Relationship, Drug,
pubmed-meshheading:14566921-Humans,
pubmed-meshheading:14566921-Models, Statistical,
pubmed-meshheading:14566921-Mouth Neoplasms,
pubmed-meshheading:14566921-Regression Analysis,
pubmed-meshheading:14566921-Risk Assessment,
pubmed-meshheading:14566921-Risk Factors,
pubmed-meshheading:14566921-Statistics, Nonparametric,
pubmed-meshheading:14566921-United States
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pubmed:year |
2003
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pubmed:articleTitle |
Quantifying epidemiologic risk factors using non-parametric regression: model selection remains the greatest challenge.
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pubmed:affiliation |
National Cancer Institute, Division of Cancer Epidemiology and Genetics, Biostatistics Branch, 6120 Executive Boulevard, EPS 7006, Rockville, MD 20852, USA. philip_rosenberg@nih.gov
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pubmed:publicationType |
Journal Article
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