Evidence map›Paper›PMID 39349692›Full record

ArticleNPJ digital medicine2024

Talking about diseases; developing a model of patient and public-prioritised disease phenotypes.

Karin Slater, Paul N Schofield, James Wright, Paul Clift, Anushka Irani, William Bradlow, Furqan Aziz, Georgios V Gkoutos

Abstract read
In one paragraph

Article in NPJ digital medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Karin SlaterInstitute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK. k.slater@bham.ac.uk.
Paul N SchofieldDepartment of Physiology, Development, and Neuroscience, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-5111-7263
James WrightWhite Swan Charity, London, UK.
Paul CliftUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Anushka IraniNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
William BradlowUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Furqan AzizCentre for Health Data Science, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-0906-1323
Georgios V GkoutosInstitute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0002-2061-091X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deep phenotyping describes the use of standardised terminologies to create comprehensive phenotypic descriptions of biomedical phenomena. These characterisations facilitate secondary analysis, evidence synthesis, and practitioner awareness, thereby guiding patient care. The vast majority of this knowledge is derived from sources that describe an academic understanding of disease, including academic literature and experimental databases. Previous work indicates a gulf between the priorities, perspectives, and perceptions held by different healthcare stakeholders. Using social media data, we develop a phenotype model that represents a public perspective on disease and compare this with a model derived from a combination of existing academic phenotype databases. We identified 52,198 positive disease-phenotype associations from social media across 311 diseases. We further identified 24,618 novel phenotype associations not shared by the biomedical and literature-derived phenotype model across 304 diseases, of which we considered 14,531 significant. Manifestations of disease affecting quality of life, and concerning endocrine, digestive, and reproductive diseases were over-represented in the social media phenotype model. An expert clinical review found that social media-derived associations were considered similarly well-established to those derived from literature, and were seen significantly more in patient clinical encounters. The phenotype model recovered from social media presents a significantly different perspective than existing resources derived from biomedical databases and literature, providing a large number of associations novel to the latter dataset. We propose that the integration and interrogation of these public perspectives on the disease can inform clinical awareness, improve secondary analysis, and bridge understanding and priorities across healthcare stakeholders.

Identifiers

PMID39349692
PMCPMC11443070

What Socratic 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 Socratic graph.