Evidence map›Paper›PMID 36535980›Full record

ArticleScientific reports2022

Global patterns of prognostic biomarkers across disease space.

Neha Murad, Eugene Melamud

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Neha MuradCalico Life Sciences LLC, South San Francisco, CA, USA.
Eugene MelamudCalico Life Sciences LLC, South San Francisco, CA, USA. eugene@calicolabs.com.

Funding

Medical Research Council MC_PC_17228
6 · The paper itself

Abstract

There is a multitude of pathological conditions that affect human health, yet we currently lack a predictive model for most diseases, and underlying mechanisms that are shared by multiple diseases are poorly understood. We leveraged baseline clinical biomarker data and long-term disease outcomes in UK Biobank to build prognostic multivariate survival models for over 200 most common diseases. We construct a similarity map between biomarker-disease hazard ratios and demonstrate broad patterns of shared similarity in biomarker profiles across the entire disease space. Further aggregation of risk profiles through density based clustering showed that biomarker-risk profiles can be partitioned into few distinct clusters with characteristic patterns representative of broad disease categories. To confirm these risk patterns we built disease co-occurrence networks in the UK Biobank and US HCUP hospitalization databases, and compared similarity in biomarker risk profiles to disease co-occurrence. We show that proximity in the biomarker-disease space is strongly related to the occurrence of disease comorbidity, suggesting biomarker profile patterns can be used for both predicting future outcomes as well as a sensitive mechanism for detecting under-diagnosed disease states.

Indexed as

PrognosisBiomarkersComorbidityForecastingHumansProportional Hazards ModelsBiomarkers

Identifiers

PMID36535980
PMCPMC9763245

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.