Evidence map›Paper›PMID 35415453›Full record

ArticleJournal of healthcare informatics research2021

Risk Factor Identification in Heterogeneous Disease Progression with L1-Regularized Multi-state Models.

Xuan Dang, Shuai Huang, Xiaoning Qian

Abstract read
In one paragraph

Article in Journal of healthcare informatics research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trial
  2. Article
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.

Xuan DangTexas A&M University, College Station, TX 77840 USA.ORCID 0000-0002-3896-9621
Shuai HuangUniversity of Washington, Seattle, WA 98195 USA.
Xiaoning QianTexas A&M University, College Station, TX 77840 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multi-state model (MSM) is a useful tool to analyze longitudinal data for modeling disease progression at multiple time points. While the regularization approaches to variable selection have been widely used, extending them to MSM remains largely unexplored. In this paper, we have developed the L1-regularized multi-state model (L1MSTATE) framework that enables parameter estimation and variable selection simultaneously. The regularized optimization problem was solved by deriving a one-step coordinate descent algorithm with great computational efficiency. The L1MSTATE approach was evaluated using extensive simulation studies, and it showed that L1MSTATE outperformed existing regularized multi-state models in terms of the accurate identification of risk factors. It also outperformed the un-regularized multi-state models (MSTATE) in terms of identifying the important risk factors in situations with small sample sizes. The power of L1MSTATE in predicting the transition probabilities comparing with MSTATE was demonstrated using the Europe Blood and Marrow Transplantation (EBMT) dataset. The L1MSTATE was implemented in the open-access R package '

Indexed as

L1-regularizationLongitudinal dataMulti-state modelRare transition predictionVariable selection

Identifiers

PMID35415453
PMCPMC8982743

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.