Evidence map›Paper›PMID 36125235›Full record

ArticleBiometrics2023

Penalized estimation of frailty-based illness-death models for semi-competing risks.

Harrison T Reeder, Junwei Lu, Sebastien Haneuse

Abstract read
In one paragraph

Article in Biometrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. High-Dimensional Survival Analysis: Methods and Applications.Annual review of statistics and its application · 2023
    Article
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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

3 authors.

Harrison T ReederBiostatistics, Massachusetts General Hospital, Boston, Massachusetts, USA.ORCID 0000-0001-8813-9127
Junwei LuDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.ORCID 0000-0003-3743-6855
Sebastien HaneuseDepartment of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, Massachusetts, USA.ORCID 0000-0003-4963-0655

Funding

The Boston Lung Cancer Survival CohortU01CA209414 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI David C Christiani · 2017 to 2026
$12.2M
Unraveling the Complexities of Risk and Mechanism in CancerR35CA220523 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2018 to 2024
$6.0M
Joint Interdisciplinary Training Program in Biostatistics & Computational BiologyT32GM074897 · NIGMS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI HUTTENHOWER, CURTIS, LIN, XIHONG · 2005 to 2019
$3.7M
Statistical and Quantitative Training in Big Data Health ScienceT32LM012411 · NLM · HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2016 to 2020
$1.4M
Methods for High-Dimensional Statistical Inference and Individualized Risk Prediction under Semi-Competing RisksF31HD102159 · NICHD · HARVARD SCHOOL OF PUBLIC HEALTH · PI REEDER, HARRISON · 2020 to 2021
$74k
NCI NIH HHS R35 CA220523NCI NIH HHS R35CA220523NCI NIH HHS U01 CA209414NCI NIH HHS U01CA209414NICHD NIH HHS F31 HD102159NIGMS NIH HHS T32 GM074897NIGMS NIH HHS T32GM074897NLM NIH HHS T32 LM012411
6 · The paper itself

Abstract

Semi-competing risks refer to the time-to-event analysis setting, where the occurrence of a non-terminal event is subject to whether a terminal event has occurred, but not vice versa. Semi-competing risks arise in a broad range of clinical contexts, including studies of preeclampsia, a condition that may arise during pregnancy and for which delivery is a terminal event. Models that acknowledge semi-competing risks enable investigation of relationships between covariates and the joint timing of the outcomes, but methods for model selection and prediction of semi-competing risks in high dimensions are lacking. Moreover, in such settings researchers commonly analyze only a single or composite outcome, losing valuable information and limiting clinical utility-in the obstetric setting, this means ignoring valuable insight into timing of delivery after preeclampsia has onset. To address this gap, we propose a novel penalized estimation framework for frailty-based illness-death multi-state modeling of semi-competing risks. Our approach combines non-convex and structured fusion penalization, inducing global sparsity as well as parsimony across submodels. We perform estimation and model selection via a pathwise routine for non-convex optimization, and prove statistical error rate results in this setting. We present a simulation study investigating estimation error and model selection performance, and a comprehensive application of the method to joint risk modeling of preeclampsia and timing of delivery using pregnancy data from an electronic health record.

Indexed as

FrailtyPre-EclampsiaComputer SimulationFemaleHumansModels, StatisticalPregnancymulti-state modelrisk predictionsemi-competing risksstructured sparsitytime-to-event analysisvariable selection

Identifiers

PMID36125235
PMCPMC10025166

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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.