Evidence map›Paper›PMID 37893003›Full record

ArticleBiomedicines2023

Detection of Amyotrophic Lateral Sclerosis (ALS) Comorbidity Trajectories Based on Principal Tree Model Analytics.

Yang-Sheng Wu, David Taniar, Kiki Adhinugraha, Li-Kai Tsai, Tun-Wen Pai

Abstract read
In one paragraph

Article in Biomedicines, 2023. 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. Review
  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

5 authors.

Yang-Sheng WuDepartment of Computer Science and Information Engineering, National Taipei University of Technology, Taipei 106, Taiwan.
David TaniarDepartment of Software Systems & Cybersecurity, Monash University, Melbourne, VIC 3800, Australia.ORCID 0000-0002-8862-3960
Kiki AdhinugrahaDepartment of Computer Science and Information Technology, La Trobe University, Melbourne, VIC 3086, Australia.ORCID 0000-0001-5884-1409
Li-Kai TsaiDepartment of Neurology and Stroke Center, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei 100, Taiwan.
Tun-Wen PaiDepartment of Computer Science and Information Engineering, National Taipei University of Technology, Taipei 106, Taiwan.ORCID 0000-0002-2869-4169

Funding

National Science and Technology Council MOST 111-2221-E-027 -113 -MY2
6 · The paper itself

Abstract

The multifaceted nature and swift progression of Amyotrophic Lateral Sclerosis (ALS) pose considerable challenges to our understanding of its evolution and interplay with comorbid conditions. This study seeks to elucidate the temporal dynamics of ALS progression and its interaction with associated diseases. We employed a principal tree-based model to decipher patterns within clinical data derived from a population-based database in Taiwan. The disease progression was portrayed as branched trajectories, each path representing a series of distinct stages. Each stage embodied the cumulative occurrence of co-existing diseases, depicted as nodes on the tree, with edges symbolizing potential transitions between these linked nodes. Our model identified eight distinct ALS patient trajectories, unveiling unique patterns of disease associations at various stages of progression. These patterns may suggest underlying disease mechanisms or risk factors. This research re-conceptualizes ALS progression as a migration through diverse stages, instead of the perspective of a sequence of isolated events. This new approach illuminates patterns of disease association across different progression phases. The insights obtained from this study hold the potential to inform doctors regarding the development of personalized treatment strategies, ultimately enhancing patient prognosis and quality of life.

Indexed as

Amyotrophic Lateral Sclerosis (ALS)clinical datadisease progressiondisease trajectoryprincipal tree

Identifiers

PMID37893003
PMCPMC10604752

What OpenQuestion holds

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Registered trials

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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.