Evidence map›Paper›PMID 30612522›Full record

ArticleStatistical methods in medical research2020

A multi-locus predictiveness curve and its summary assessment for genetic risk prediction.

Changshuai Wei, Ming Li, Yalu Wen, Chengyin Ye, Qing Lu

Open access · greenAbstract read
In one paragraph

Article in Statistical methods in medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 100% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 5 institutions in 3 countries.

Changshuai WeiCore Artificial Intelligence, Amazon.com Inc, Seattle, WA, USA.
Ming LiDepartment of Epidemiology and Biostatistics, Indiana University at Bloomington, Bloomington, IN, USA.
Yalu WenDepartment of Statistics, University of Auckland, Auckland, New Zealand.
Chengyin YeDepartment of Health Management, Hangzhou Normal University, Hangzhou, China.
Qing LuDepartment of Epidemiology and Biostatistics, Michigan State University, East Lansing, MI, USA.ORCID 0000-0002-7943-966X
Amazon (United States) · USHangzhou Normal University · CNIndiana University Bloomington · USMichigan State University · USUniversity of Auckland · NZ

Funding

Computational Efficient Statistical Tools for Analyzing Substance Dependence Sequencing DataR01DA043501 · NIDA · UNIVERSITY OF FLORIDA · PI LU, QING · 2017 to 2021
$2.1M
Methods and Software for High-dimensional Risk Prediction ResearchR01LM012848 · NLM · UNIVERSITY OF FLORIDA · PI LU, QING · 2018 to 2021
$1.2M
Random Field Modelling of genetic and epigenetic association underlying congenital heart defects in the presence of disease heterogeneityK01HL140333 · NHLBI · TRUSTEES OF INDIANA UNIVERSITY · PI LI, MING · 2018 to 2021
$724k
Gene-by-Gene and Gene-by-Environment Interactions Underlying Congenital Heart DefectsR03HD092854 · NICHD · TRUSTEES OF INDIANA UNIVERSITY · PI LI, MING · 2018 to 2019
$171k
NHLBI NIH HHS K01 HL140333NICHD NIH HHS R03 HD092854NIDA NIH HHS R01 DA043501NLM NIH HHS R01 LM012848
6 · The paper itself

Abstract

Genetic association studies using high-throughput genotyping and sequencing technologies have identified a large number of genetic variants associated with complex human diseases. These findings have provided an unprecedented opportunity to identify individuals in the population at high risk for disease who carry causal genetic mutations and hold great promise for early intervention and individualized medicine. While interest is high in building risk prediction models based on recent genetic findings, it is crucial to have appropriate statistical measurements to assess the performance of a genetic risk prediction model. Predictiveness curves were recently proposed as a graphic tool for evaluating a risk prediction model on the basis of a single continuous biomarker. The curve evaluates a risk prediction model for classification performance as well as its usefulness when applied to a population. In this article, we extend the predictiveness curve to measure the collective contribution of multiple genetic variants. We further propose a nonparametric, U-statistics-based measurement, referred to as the U-Index, to quantify the performance of a multi-locus predictiveness curve. In particular, a global U-Index and a partial U-Index can be used in the general population and a subpopulation of particular clinical interest, respectively. Through simulation studies, we demonstrate that the proposed U-Index has advantages over several existing summary statistics under various disease models. We also show that the partial U-Index can have its own uniqueness when rare variants have a substantial contribution to disease risk. Finally, we use the proposed predictiveness curve and its corresponding U-Index to evaluate the performance of a genetic risk prediction model for nicotine dependence.

Indexed as

Genetic Predisposition to DiseaseModels, GeneticModels, StatisticalBiomarkersGenetic VariationGenome-Wide Association StudyGenotypeHumansPredictive Value of TestsRisk AssessmentTobacco Use DisorderBiomarkersgenetic risk predictionHigh-dimensional datanicotine dependenceU-statistics

Identifiers

PMID30612522
PMCPMC6612460
OpenAlexW2909393468

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

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 Socratic graph.