Evidence map›Paper›PMID 39569347›Full record

ArticleRoyal Society open science2024

Data-driven Huntington's disease progression modelling and estimation of societal cost in the UK.

Andrew Pollard, Danica Greetham, James Myatt, Hugh Rickards, Cath Stanley, Dave Dungate

Abstract read
In one paragraph

Article in Royal Society open science, 2024. 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

6 authors.

Andrew PollardHybrid Intelligence, Capgemini Engineering, Stevenage, UK.
Danica GreethamHybrid Intelligence, Capgemini Engineering, Stevenage, UK.ORCID https://orcid.org/0000-0003-3822-7908
James MyattHybrid Intelligence, Capgemini Engineering, Stevenage, UK.
Hugh RickardsHuntington's Disease Association (England and Wales), Liverpool, UK.
Cath StanleyHuntington's Disease Association (England and Wales), Liverpool, UK.
Dave DungateHybrid Intelligence, Capgemini Engineering, Stevenage, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We develop a Huntington's disease (HD) progression model and integrate this with a novel economic model, accounting for the major factors of the HD's societal cost. Data from the Enroll-HD observational study were used to fit a continuous-time hidden Markov disease progression model, which identified five distinct states. The number of disease states was determined using a cross-validated maximum likelihood approach. A novel data augmentation method was used to correct the biased life expectancy of the progression model. Multiple sources of cost data were then mapped to Enroll-HD variables using expert experience. A simulation of a synthetic patient population was used to show the feasibility of the approach in estimating population costs and the impact of hypothetical intervention scenarios. Our results confirm that early cognitive decline, which is not captured by the total functional capacity score currently used by clinicians but flagged up in HD integrated staging system, can be quantified from participants' visits. Finally, the results of the UK cost modelling show that indirect costs of HD such as state benefits and lost gross domestic product contribution could be the driving factors for the societal cost, over and above health and social care costs.

Indexed as

disease progressionhealth costsHuntington diseaseMarkov process

Identifiers

PMID39569347
PMCPMC11576117

What OpenQuestion holds

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LicenceCC BY
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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.