Evidence map›Paper›PMID 32773372›Full record

ArticleJournal of medical Internet research2020

Personal Health Information Inference Using Machine Learning on RNA Expression Data from Patients With Cancer: Algorithm Validation Study.

Solbi Kweon, Jeong Hoon Lee, Younghee Lee, Yu Rang Park

Abstract readValidation Study
In one paragraph

Article in Journal of medical Internet research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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4 · The record

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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.

Solbi Kweon *Department of Biomedical System Informatics, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-8021-9605
Jeong Hoon Lee *Department of Biomedical System Informatics, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-1789-8270
Younghee LeeDepartment of Biomedical Informatics, University of Utah School of Medicine, Salt Lake City, UT, United States.ORCID 0000-0002-6850-0082
Yu Rang ParkDepartment of Biomedical System Informatics, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-4210-2094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs the need for sharing genomic data grows, privacy issues and concerns, such as the ethics surrounding data sharing and disclosure of personal information, are raised.

objectiveThe main purpose of this study was to verify whether genomic data is sufficient to predict a patient's personal information.

methodsRNA expression data and matched patient personal information were collected from 9538 patients in The Cancer Genome Atlas program. Five personal information variables (age, gender, race, cancer type, and cancer stage) were recorded for each patient. Four different machine learning algorithms (support vector machine, decision tree, random forest, and artificial neural network) were used to determine whether a patient's personal information could be accurately predicted from RNA expression data. Performance measurement of the prediction models was based on the accuracy and area under the receiver operating characteristic curve. We selected five cancer types (breast carcinoma, kidney renal clear cell carcinoma, head and neck squamous cell carcinoma, low-grade glioma, and lung adenocarcinoma) with large samples sizes to verify whether predictive accuracy would differ between them. We also validated the efficacy of our four machine learning models in analyzing normal samples from 593 cancer patients.

resultsIn most samples, personal information with high genetic relevance, such as gender and cancer type, could be predicted from RNA expression data alone. The prediction accuracies for gender and cancer type, which were the best models, were 0.93-0.99 and 0.78-0.94, respectively. Other aspects of personal information, such as age, race, and cancer stage, were difficult to predict from RNA expression data, with accuracies ranging from 0.0026-0.29, 0.76-0.96, and 0.45-0.79, respectively. Among the tested machine learning methods, the highest predictive accuracy was obtained using the support vector machine algorithm (mean accuracy 0.77), while the lowest accuracy was obtained using the random forest method (mean accuracy 0.65). Gender and race were predicted more accurately than other variables in the samples. On average, the accuracy of cancer stage prediction ranged between 0.71-0.67, while the age prediction accuracy ranged between 0.18-0.23 for the five cancer types.

conclusionsWe attempted to predict patient information using RNA expression data. We found that some identifiers could be predicted, but most others could not. This study showed that personal information available from RNA expression data is limited and this information cannot be used to identify specific patients.

Indexed as

Support Vector MachineAdolescentAdultAgedAged, 80 and overAlgorithmsChildFemaleHealth Records, PersonalHigh-Throughput Nucleotide SequencingHumansMachine LearningMaleMiddle AgedNeoplasmsNeural Networks, ComputerRNAcancermachine learningpersonal informationpredictionprivacy issueRNA sequencing

Identifiers

PMID32773372
PMCPMC7445622

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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.