Evidence map›Paper›PMID 33836648›Full record

ArticleBMC gastroenterology2021

Distinct clinical phenotypes for Crohn's disease derived from patient surveys.

Tianyun Liu, Lichy Han, Mera Tilley, Lovisa Afzelius, Mateusz Maciejewski, Scott Jelinsky, Chao Tian, Matthew McIntyre, 23andMe Research Team, Nan Bing and 2 more

Abstract read
In one paragraph

Article in BMC gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
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

12 authors.

Tianyun LiuDepartment of Bioengineering, Stanford University, Shriram Room 209, MC: 4245, 443 Via Ortega Drive, Stanford, CA, 94305-4145, USA.
Lichy HanBiomedical Informatics Training Program, Stanford University, Stanford, CA, USA.
Mera TilleyInflammation and Immunology, Pfizer Inc., Cambridge, MA, USA.
Lovisa AfzeliusInflammation and Immunology, Pfizer Inc., Cambridge, MA, USA.
Mateusz MaciejewskiInflammation and Immunology, Pfizer Inc., Cambridge, MA, USA.
Scott JelinskyInflammation and Immunology, Pfizer Inc., Cambridge, MA, USA.
Chao Tian23andMe Research Team, 23andMe Inc., Sunnyvale, CA, USA.
Matthew McIntyre23andMe Research Team, 23andMe Inc., Sunnyvale, CA, USA.
23andMe Research Team
Nan BingInflammation and Immunology, Pfizer Inc., Cambridge, MA, USA.
Kenneth HungInflammation and Immunology, Pfizer Inc., Cambridge, MA, USA.
Russ B AltmanDepartment of Bioengineering, Stanford University, Shriram Room 209, MC: 4245, 443 Via Ortega Drive, Stanford, CA, 94305-4145, USA. russ.altman@stanford.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDefining clinical phenotypes provides opportunities for new diagnostics and may provide insights into early intervention and disease prevention. There is increasing evidence that patient-derived health data may contain information that complements traditional methods of clinical phenotyping. The utility of these data for defining meaningful phenotypic groups is of great interest because social media and online resources make it possible to query large cohorts of patients with health conditions.

methodsWe evaluated the degree to which patient-reported categorical data is useful for discovering subclinical phenotypes and evaluated its utility for discovering new measures of disease severity, treatment response and genetic architecture. Specifically, we examined the responses of 1961 patients with inflammatory bowel disease to questionnaires in search of sub-phenotypes. We applied machine learning methods to identify novel subtypes of Crohn's disease and studied their associations with drug responses.

resultsUsing the patients' self-reported information, we identified two subpopulations of Crohn's disease; these subpopulations differ in disease severity, associations with smoking, and genetic transmission patterns. We also identified distinct features of drug response for the two Crohn's disease subtypes. These subtypes show a trend towards differential genotype signatures.

conclusionOur findings suggest that patient-defined data can have unplanned utility for defining disease subtypes and may be useful for guiding treatment approaches.

Indexed as

Crohn DiseaseInflammatory Bowel DiseasesGenotypeHumansPhenotypeSurveys and QuestionnairesClassificationCrohn’s diseasePatient-reported dataPhenotypesSubtypes

Identifiers

PMID33836648
PMCPMC8034169

What OpenQuestion holds

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LicenceCC BY
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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.