Evidence map›Paper›PMID 23023008›Full record

ArticleEpidemiology (Cambridge, Mass.)2012

Correction of phenotype misclassification based on high-discrimination genetic predictive risk models.

John P A Ioannidis, Yi Yu, Johanna M Seddon

Abstract read
In one paragraph

Article in Epidemiology (Cambridge, Mass.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
  2. Host genomics in infectious diseases.Infection & chemotherapy · 2013
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

John P A IoannidisDepartment of Medicine, Stanford Prevention Research Center, Stanford University School of Medicine, Stanford, CA 94305, USA. jioannid@stanford.edu
Yi Yu
Johanna M Seddon

Funding

ETIOLOGIC STUDIES OF AGE-RELATED MACULAR DEGENERATIONR01EY011309 · NEI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SEDDON, JOHANNA M · 2003 to 2017
$9.3M
NEI NIH HHS R01 EY011309NEI NIH HHS R01-EY11309
6 · The paper itself

Abstract

Misclassification of phenotype status can seriously affect accuracy in association studies, including studies of genetic risk factors. A common problem is the classification of participants as nondiseased because of insufficient diagnostic workup or because participants have not been followed up long enough to develop disease. Some validated predictive models may have high discrimination in predicting disease. We suggest that information from such models can be used to predict the risk that a nondiseased participant will eventually develop disease and to recode the status of participants predicted to be at highest risk. We evaluate conditions under which recoding results in a maximal net improvement in the accuracy of phenotype classification. Net improvement is expected only when the positive likelihood ratio of the predictive model is larger than the inverse of the odds of disease among apparently nondiseased controls. We conducted simulations to probe the impact of reclassification on the power to detect new risk factors under several scenarios of classification accuracy of the previously developed models. We also apply this framework to a validated model of progression to advanced age-related macular degeneration that uses genetic and nongenetic variables (area under the curve = 0.915). In the training cohort (n = 2,937) and a separate validation cohort (n = 1,227), 195-272 and 78-91 nonprogressor participants, respectively, were reclassified as progressors. Correction of phenotype misclassification based on highly informative predictive models may be helpful in identifying additional genetic and other risk factors, when there are validated risk factors that provide strong discriminating ability.

Indexed as

PhenotypePolymorphism, Single NucleotideRisk AssessmentAgedAged, 80 and overAge of OnsetArea Under CurveCase-Control StudiesCohort StudiesDiscriminant AnalysisDisease ProgressionFollow-Up StudiesHumansMacular DegenerationMedical ErrorsMiddle Aged

Identifiers

PMID23023008
PMCPMC12124723

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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.