Evidence map›Paper›PMID 34245595›Full record

ArticleGenetic epidemiology2021

A novel transcriptional risk score for risk prediction of complex human diseases.

Nayang Shan, Yuhan Xie, Shuang Song, Wei Jiang, Zuoheng Wang, Lin Hou

Open access · greenAbstract read
In one paragraph

Article in Genetic epidemiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Nayang ShanCenter for Statistical Science, Department of Industrial Engineering, Tsinghua University, Beijing, China.
Yuhan XieDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.
Shuang SongCenter for Statistical Science, Department of Industrial Engineering, Tsinghua University, Beijing, China.
Wei JiangDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.
Zuoheng WangDepartment of Biostatistics, Yale School of Public Health, New Haven, Connecticut, USA.
Lin HouCenter for Statistical Science, Department of Industrial Engineering, Tsinghua University, Beijing, China.ORCID 0000-0002-4283-8501
Tsinghua University · CNYale University · US

Funding

Novel Methods for Longitudinal Study of Gene-Environment Interplay in AlcoholismK01AA023321 · NIAAA · YALE UNIVERSITY · PI WANG, ZUOHENG · 2015 to 2019
$863k
NIAAA NIH HHS K01 AA023321Wellcome Trust
6 · The paper itself

Abstract

Recently polygenetic risk score (PRS) has been successfully used in the risk prediction of complex human diseases. Many studies incorporated internal information, such as effect size distribution, or external information, such as linkage disequilibrium, functional annotation, and pleiotropy among multiple diseases, to optimize the performance of PRS. To leverage on multiomics datasets, we developed a novel flexible transcriptional risk score (TRS), in which messenger RNA expression levels were imputed and weighted for risk prediction. In simulation studies, we demonstrated that single-tissue TRS has greater prediction power than LDpred, especially when there is a large effect of gene expression on the phenotype. Multitissue TRS improves prediction accuracy when there are multiple tissues with independent contributions to disease risk. We applied our method to complex traits, including Crohn's disease, type 2 diabetes, and so on. The single-tissue TRS method outperformed LDpred and AnnoPred across the tested traits. The performance of multitissue TRS is trait-dependent. Moreover, our method can easily incorporate information from epigenomic and proteomic data upon the availability of reference datasets.

Indexed as

Diabetes Mellitus, Type 2HumansModels, GeneticPolymorphism, Single NucleotideProteomicsRisk Factorsgene imputationmultiomicsrisk predictiontranscriptional risk scores

Identifiers

PMID34245595
PMCPMC8604733
OpenAlexW3182177360

What OpenQuestion holds

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Registered trials

None linked

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.