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Trajectories of multiple long-term conditions and mortality in older adults: A retrospective cohort study using English Longitudinal Study of Ageing (ELSA)

OBJECTIVES: To classify older adults with MLTC into clusters based on accumulating conditions as trajectories over time, characterise clusters and quantify associations between derived clusters and all-cause mortality. DESIGN: We conducted a retrospective cohort study using the English Longitudinal...

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Detalles Bibliográficos
Autores principales: Chalitsios, Christos V., Santoso, Cornelia, Nartey, Yvonne, Khan, Nusrat, Simpson, Glenn, Islam, Nazrul, Stuart, Beth, Farmer, Andrew, Dambha-Miller, Hajira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246039/
https://www.ncbi.nlm.nih.gov/pubmed/37292869
http://dx.doi.org/10.1101/2023.05.18.23290151
Descripción
Sumario:OBJECTIVES: To classify older adults with MLTC into clusters based on accumulating conditions as trajectories over time, characterise clusters and quantify associations between derived clusters and all-cause mortality. DESIGN: We conducted a retrospective cohort study using the English Longitudinal Study of Ageing (ELSA) over nine years (n=15,091 aged 50 years and older). Group-based trajectory modelling was used to classify people into MLTC clusters based on accumulating conditions over time. Derived clusters were used to quantify the associations between MLTC trajectory memberships, sociodemographic characteristics, and all-cause mortality. RESULTS: Five distinct clusters of MLTC trajectories were identified and characterised as: “no-LTC” (18.57%), “single-LTC” (31.21%), “evolving MLTC” (25.82%), “moderate MLTC” (17.12%), and “high MLTC” (7.27%). Increasing age was consistently associated with an increased number of MLTC. Female sex (aOR = 1.13; 95%CI 1.01 to 1.27) and ethnic minority (aOR = 2.04; 95%CI 1.40 to 3.00) were associated with the “moderate MLTC” and “high MLTC” clusters, respectively. Higher education and paid employment were associated with a lower likelihood of progression over time towards an increased number of MLTC. All the clusters had higher all-cause mortality than the “no-LTC” cluster. CONCLUSIONS: The development of MLTC and the increase in the number of conditions over time follow distinct trajectories. These are determined by non-modifiable (age, sex, ethnicity) and modifiable factors (education and employment). Stratifying risk through clustering will enable practitioners to identify older adults with a higher likelihood of worsening MLTC over time to tailor effective interventions.