Evidence map›Paper›PMID 36996020›Full record

ArticlePLOS digital health2023

Modelling and classifying joint trajectories of self-reported mood and pain in a large cohort study.

Rajenki Das, Mark Muldoon, Mark Lunt, John McBeth, Belay Birlie Yimer, Thomas House

Abstract read
In one paragraph

Article in PLOS digital health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rajenki DasDepartment of Mathematics, University of Manchester, Manchester, United Kingdom.ORCID https://orcid.org/0000-0002-6225-4247
Mark MuldoonDepartment of Mathematics, University of Manchester, Manchester, United Kingdom.
Mark LuntCentre for Epidemiology Versus Arthritis, University of Manchester, Manchester, United Kingdom.
John McBethCentre for Epidemiology Versus Arthritis, University of Manchester, Manchester, United Kingdom.
Belay Birlie YimerCentre for Epidemiology Versus Arthritis, University of Manchester, Manchester, United Kingdom.
Thomas HouseDepartment of Mathematics, University of Manchester, Manchester, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is well-known that mood and pain interact with each other, however individual-level variability in this relationship has been less well quantified than overall associations between low mood and pain. Here, we leverage the possibilities presented by mobile health data, in particular the "Cloudy with a Chance of Pain" study, which collected longitudinal data from the residents of the UK with chronic pain conditions. Participants used an App to record self-reported measures of factors including mood, pain and sleep quality. The richness of these data allows us to perform model-based clustering of the data as a mixture of Markov processes. Through this analysis we discover four endotypes with distinct patterns of co-evolution of mood and pain over time. The differences between endotypes are sufficiently large to play a role in clinical hypothesis generation for personalised treatments of comorbid pain and low mood.

Identifiers

PMID36996020
PMCPMC10062665

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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.