Evidence map›Paper›PMID 36749789›Full record

ArticlePLoS genetics2023

PRSet: Pathway-based polygenic risk score analyses and software.

Shing Wan Choi, Judit García-González, Yunfeng Ruan, Hei Man Wu, Christian Porras, Jessica Johnson, Bipolar Disorder Working group of the Psychiatric Genomics Consortium, Clive J Hoggart, Paul F O'Reilly

Abstract read
In one paragraph

Article in PLoS genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing 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

78 citing papers in PubMed.

  1. Article
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  5. Genetic basis of Asian diabetes.Journal of diabetes investigation · 2026
    Review
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18 more citing papers are in PubMed but not listed here.

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

9 authors.

Shing Wan ChoiDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.
Judit García-GonzálezDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.ORCID 0000-0001-6245-740X
Yunfeng RuanThe Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-3213-8309
Hei Man WuDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.
Christian PorrasDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.ORCID 0000-0002-2621-6753
Jessica JohnsonDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.ORCID 0000-0002-4519-3120
Bipolar Disorder Working group of the Psychiatric Genomics Consortium
Clive J HoggartDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.ORCID 0000-0002-0482-0052
Paul F O'ReillyDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York City, New York, United States of America.ORCID 0000-0001-7515-0845

Funding

Next-generation, pathway-specific, polygenic risk scoresR01MH122866 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI O'REILLY, PAUL FRANCIS · 2020 to 2024
$3.1M
Big Omics Data Engine 2 SupercomputerS10OD026880 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2019 to 2019
$2.0M
Medical Research Council MR/N015746/1NIH HHS S10 OD026880NIMH NIH HHS R01 MH122866
6 · The paper itself

Abstract

Polygenic risk scores (PRSs) have been among the leading advances in biomedicine in recent years. As a proxy of genetic liability, PRSs are utilised across multiple fields and applications. While numerous statistical and machine learning methods have been developed to optimise their predictive accuracy, these typically distil genetic liability to a single number based on aggregation of an individual's genome-wide risk alleles. This results in a key loss of information about an individual's genetic profile, which could be critical given the functional sub-structure of the genome and the heterogeneity of complex disease. In this manuscript, we introduce a 'pathway polygenic' paradigm of disease risk, in which multiple genetic liabilities underlie complex diseases, rather than a single genome-wide liability. We describe a method and accompanying software, PRSet, for computing and analysing pathway-based PRSs, in which polygenic scores are calculated across genomic pathways for each individual. We evaluate the potential of pathway PRSs in two distinct ways, creating two major sections: (1) In the first section, we benchmark PRSet as a pathway enrichment tool, evaluating its capacity to capture GWAS signal in pathways. We find that for target sample sizes of >10,000 individuals, pathway PRSs have similar power for evaluating pathway enrichment as leading methods MAGMA and LD score regression, with the distinct advantage of providing individual-level estimates of genetic liability for each pathway -opening up a range of pathway-based PRS applications, (2) In the second section, we evaluate the performance of pathway PRSs for disease stratification. We show that using a supervised disease stratification approach, pathway PRSs (computed by PRSet) outperform two standard genome-wide PRSs (computed by C+T and lassosum) for classifying disease subtypes in 20 of 21 scenarios tested. As the definition and functional annotation of pathways becomes increasingly refined, we expect pathway PRSs to offer key insights into the heterogeneity of complex disease and treatment response, to generate biologically tractable therapeutic targets from polygenic signal, and, ultimately, to provide a powerful path to precision medicine.

Indexed as

GenomicsMultifactorial InheritanceGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansRisk FactorsSoftware

Identifiers

PMID36749789
PMCPMC9937466

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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.