Evidence map›Paper›PMID 34468045›Full record

ArticleGenetic epidemiology2021

Block coordinate descent algorithm improves variable selection and estimation in error-in-variables regression.

Célia Escribe, Tianyuan Lu, Julyan Keller-Baruch, Vincenzo Forgetta, Bowei Xiao, J Brent Richards, Sahir Bhatnagar, Karim Oualkacha, Celia M T Greenwood

Abstract 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
–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

5 citing papers in PubMed.

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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

9 authors.

Célia EscribeLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.
Tianyuan LuLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.ORCID 0000-0002-5664-5698
Julyan Keller-BaruchLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.
Vincenzo ForgettaLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.
Bowei XiaoLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.
J Brent RichardsLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.
Sahir BhatnagarDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Québec, Canada.
Karim OualkachaDépartement de Mathématiques, Université du Québec à Montréal, Montreal, Québec, Canada.ORCID 0000-0002-9911-079X
Celia M T GreenwoodLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Québec, Canada.ORCID 0000-0002-2427-5696

Funding

CIHR PJT-148620Medical Research Council MC_PC_17228Medical Research Council MC_QA137853
6 · The paper itself

Abstract

Medical research increasingly includes high-dimensional regression modeling with a need for error-in-variables methods. The Convex Conditioned Lasso (CoCoLasso) utilizes a reformulated Lasso objective function and an error-corrected cross-validation to enable error-in-variables regression, but requires heavy computations. Here, we develop a Block coordinate Descent Convex Conditioned Lasso (BDCoCoLasso) algorithm for modeling high-dimensional data that are only partially corrupted by measurement error. This algorithm separately optimizes the estimation of the uncorrupted and corrupted features in an iterative manner to reduce computational cost, with a specially calibrated formulation of cross-validation error. Through simulations, we show that the BDCoCoLasso algorithm successfully copes with much larger feature sets than CoCoLasso, and as expected, outperforms the naïve Lasso with enhanced estimation accuracy and consistency, as the intensity and complexity of measurement errors increase. Also, a new smoothly clipped absolute deviation penalization option is added that may be appropriate for some data sets. We apply the BDCoCoLasso algorithm to data selected from the UK Biobank. We develop and showcase the utility of covariate-adjusted genetic risk scores for body mass index, bone mineral density, and lifespan. We demonstrate that by leveraging more information than the naïve Lasso in partially corrupted data, the BDCoCoLasso may achieve higher prediction accuracy. These innovations, together with an R package, BDCoCoLasso, make error-in-variables adjustments more accessible for high-dimensional data sets. We posit the BDCoCoLasso algorithm has the potential to be widely applied in various fields, including genomics-facilitated personalized medicine research.

Indexed as

AlgorithmsModels, GeneticHumansResearch Designestimation accuracyhigh dimensionLassomeasurement errorvariable selection

Identifiers

PMID34468045
PMCPMC9292988

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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.