Evidence map›Paper›PMID 27917508›Full record

ArticleStatistics in medicine2017

Estimating personalized diagnostic rules depending on individualized characteristics.

Ying Liu, Yuanjia Wang, Chaorui Huang, Donglin Zeng

Abstract read
In one paragraph

Article in Statistics in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

1 citing paper in PubMed.

  1. Incentivizing adherence to pre-exposure prophylaxis for HIV prevention: a randomized pilot trial among male sex workers in Mexico.The European journal of health economics : HEPAC : health economics in prevention and care · 2025
    Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ying LiuDivision of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, 53226, WI, U.S.A.
Yuanjia WangDepartment of Biostatistics, Mailman School of Public Health, Columbia University, New York, NY, 10027, U.S.A.
Chaorui HuangBrain and Mind Research Institute, Weill Cornell Medical College, NY, 10065, U.S.A.
Donglin ZengDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, 27514, NC, U.S.A.

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TSIATIS, ANASTASIOS A · 2010 to 2019
$21.3M
Statistical Methods for Integrating Mixed-type Biomarkers and Phenotypes in Neurodegenerative Disease ModelingR01NS073671 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WANG, YUANJIA · 2011 to 2025
$3.9M
Identifying Huntington's disease markers by modern statistical learning methods.U01NS082062 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WANG, YUANJIA · 2014 to 2016
$1.1M
NCI NIH HHS P01 CA142538NINDS NIH HHS R01 NS073671NINDS NIH HHS U01 NS082062
6 · The paper itself

Abstract

There is an increasing demand for personalization of disease screening based on assessment of patient risk and other characteristics. For example, in breast cancer screening, advanced imaging technologies have made it possible to move away from 'one-size-fits-all' screening guidelines to targeted risk-based screening for those who are in need. Because diagnostic performance of various imaging modalities may vary across subjects, applying the most accurate modality to the patients who would benefit the most requires personalized strategy. To address these needs, we propose novel machine learning methods to estimate personalized diagnostic rules for medical screening or diagnosis by maximizing a weighted combination of sensitivity and specificity across subgroups of subjects. We first develop methods that can be applied when competing modalities or screening strategies that are observed on the same subject (paired design). Next, we present methods for studies where not all subjects receive both modalities (unpaired design). We study theoretical properties including consistency and risk bound of the personalized diagnostic rules and conduct simulation studies to examine performance of the proposed methods. Lastly, we analyze data collected from a brain imaging study of Parkinson's disease using positron emission tomography and diffusion tensor imaging with paired and unpaired designs. Our results show that in some cases, a personalized modality assignment is estimated to improve empirical area under the receiver operating curve compared with a 'one-size-fits-all' assignment strategy. Copyright © 2016 John Wiley & Sons, Ltd.

Indexed as

DiagnosisIndividualityPrecision MedicineBrainDecision Support TechniquesDiffusion Tensor ImagingHumansMachine LearningModels, StatisticalParkinson DiseasePositron-Emission TomographyRisk FactorsROC CurveStatistics as TopicParkinson's diseasepersonalized screeningweighted support vector machine

Identifiers

PMID27917508
PMCPMC5334177

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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.