Evidence map›Paper›PMID 29048458›Full record

ArticleBioinformatics (Oxford, England)2018

A probabilistic pathway score (PROPS) for classification with applications to inflammatory bowel disease.

Lichy Han, Mateusz Maciejewski, Christoph Brockel, William Gordon, Scott B Snapper, Joshua R Korzenik, Lovisa Afzelius, Russ B Altman

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. Pathway and network embedding methods for prioritizing psychiatric drugs.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2020
    Article
  17. Review
  18. Big data in IBD: a look into the future.Nature reviews. Gastroenterology & hepatology · 2019
    Review
  19. 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

8 authors.

Lichy HanBiomedical Informatics Training Program, Stanford University, Stanford, CA 94305, USA.
Mateusz MaciejewskiInflammation & Immunology, Pfizer Inc., Cambridge, MA 02139, USA.
Christoph BrockelHill's Pet Nutrition, Topeka, KS 66617, USA.
William GordonInflammation & Immunology, Pfizer Inc., Cambridge, MA 02139, USA.
Scott B SnapperDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Joshua R KorzenikDepartment of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Lovisa AfzeliusInflammation & Immunology, Pfizer Inc., Cambridge, MA 02139, USA.
Russ B AltmanDepartment of Genetics.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007365 · NIGMS · STANFORD UNIVERSITY · PI CHUA, KATRIN F · 1985 to 2021
$33.8M
STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Undergraduate Summer Research Experiences Support for Combining systems biology and structural biology to find new therapeuticsR01GM102365 · NIGMS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2012 to 2021
$3.0M
Systems Pharmacological Analysis of Drug Efficacy in Inflammatory Bowel DiseaseF30AI124553 · NIAID · STANFORD UNIVERSITY · PI HAN, LICHY · 2017 to 2019
$120k
NIAID NIH HHS F30 AI124553NIDDK NIH HHS P30 DK034854NIGMS NIH HHS R01 GM102365NIGMS NIH HHS T32 GM007365
6 · The paper itself

Abstract

Summary: Gene-based supervised machine learning classification models have been widely used to differentiate disease states, predict disease progression and determine effective treatment options. However, many of these classifiers are sensitive to noise and frequently do not replicate in external validation sets. For complex, heterogeneous diseases, these classifiers are further limited by being unable to capture varying combinations of genes that lead to the same phenotype. Pathway-based classification can overcome these challenges by using robust, aggregate features to represent biological mechanisms. In this work, we developed a novel pathway-based approach, PRObabilistic Pathway Score, which uses genes to calculate individualized pathway scores for classification. Unlike previous individualized pathway-based classification methods that use gene sets, we incorporate gene interactions using probabilistic graphical models to more accurately represent the underlying biology and achieve better performance. We apply our method to differentiate two similar complex diseases, ulcerative colitis (UC) and Crohn's disease (CD), which are the two main types of inflammatory bowel disease (IBD). Using five IBD datasets, we compare our method against four gene-based and four alternative pathway-based classifiers in distinguishing CD from UC. We demonstrate superior classification performance and provide biological insight into the top pathways separating CD from UC. Availability and Implementation: PROPS is available as a R package, which can be downloaded at http://simtk.org/home/props or on Bioconductor. Contact: rbaltman@stanford.edu. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Metabolic Networks and PathwaysSupervised Machine LearningAdultChildColitis, UlcerativeComputational BiologyCrohn DiseaseDiagnosis, DifferentialDisease ProgressionGene Regulatory NetworksHumansModels, BiologicalProtein Interaction Maps

Identifiers

PMID29048458
PMCPMC5860179

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.