Evidence map›Paper›PMID 38991683›Full record

ArticleBMJ open2024

Trajectories in long-term condition accumulation and mortality in older adults: a group-based trajectory modelling approach using the English Longitudinal Study of Ageing.

Christos V Chalitsios, Cornelia Santoso, Yvonne Nartey, Nusrat Khan, Glenn Simpson, Nazrul Islam, Beth Stuart, Andrew Farmer, Hajira Dambha-Miller

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Article in BMJ open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Christos V ChalitsiosPrimary Care Research Centre, University of Southampton, Southampton, UK.ORCID 0000-0002-0836-9385
Cornelia SantosoPrimary Care Research Centre, University of Southampton, Southampton, UK.
Yvonne NarteyPrimary Care Research Centre, University of Southampton, Southampton, UK.
Nusrat KhanPrimary Care Research Centre, University of Southampton, Southampton, UK.
Glenn SimpsonPrimary Care Research Centre, University of Southampton, Southampton, UK.
Nazrul IslamPrimary Care Research Centre, University of Southampton, Southampton, UK.
Beth StuartQueen Mary University of London, London, UK.ORCID 0000-0001-5432-7437
Andrew FarmerNuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-6170-4402
Hajira Dambha-MillerPrimary Care Research Centre, University of Southampton, Southampton, UK H.Dambha-Miller@soton.ac.uk.ORCID 0000-0003-0175-443X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo classify older adults into clusters based on accumulating long-term conditions (LTC) as trajectories, characterise clusters and quantify their associations with all-cause mortality.

designWe conducted a longitudinal study using the English Longitudinal Study of Ageing over 9 years (n=15 091 aged 50 years and older). Group-based trajectory modelling was used to classify people into clusters based on accumulating LTC over time. Derived clusters were used to quantify the associations between trajectory memberships, sociodemographic characteristics and all-cause mortality by conducting regression models.

resultsFive distinct clusters of accumulating LTC trajectories were identified and characterised as: 'no LTC' (18.57%), 'single LTC' (31.21%), 'evolving multimorbidity' (25.82%), 'moderate multimorbidity' (17.12%) and 'high multimorbidity' (7.27%). Increasing age was consistently associated with a larger number of LTCs. Ethnic minorities (adjusted OR=2.04; 95% CI 1.40 to 3.00) were associated with the 'high multimorbidity' cluster. Higher education and paid employment were associated with a lower likelihood of progression over time towards an increased number of LTCs. All the clusters had higher all-cause mortality than the 'no LTC' cluster.

conclusionsThe development of multimorbidity in the number of conditions over time follows distinct trajectories. These are determined by non-modifiable (age, ethnicity) and modifiable factors (education and employment). Stratifying risk through clustering will enable practitioners to identify older adults with a higher likelihood of worsening LTC over time to tailor effective interventions to prevent mortality.

Indexed as

MultimorbidityAgedAged, 80 and overAgingChronic DiseaseCluster AnalysisEnglandFemaleHumansLongitudinal StudiesMaleMiddle AgedMortalityRisk Factorsepidemiologygeriatric medicinepublic health

Identifiers

PMID38991683
PMCPMC11243147

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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.