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Association of latent class analysis-derived multimorbidity clusters with adverse health outcomes in patients with multiple long-term conditions: comparative results across three UK cohorts

Krauth, Stefanie J.; Steell, Lewis; Ahmed, Sayem; McIntosh, Emma; Dibben, Grace O.; Hanlon, Peter; Lewsey, Jim; Nicholl, Barbara I.; McAllister, David A.; Smith, Susan M.; Evans, Rachael; Ahmed, Zahira; Dean, Sarah; Greaves, Colin; Barber, Shaun; Doherty, Patrick; Gardiner, Nikki; Ibbotson, Tracy; Jolly, Kate; Ormandy, Paula; Simpson, Sharon A.; Taylor, Rod S.; Singh, Sally J.; Mair, Frances S.; Jani, Bhautesh Dinesh

Association of latent class analysis-derived multimorbidity clusters with adverse health outcomes in patients with multiple long-term conditions: comparative results across three UK cohorts Thumbnail


Authors

Stefanie J. Krauth

Lewis Steell

Sayem Ahmed

Emma McIntosh

Grace O. Dibben

Peter Hanlon

Jim Lewsey

Barbara I. Nicholl

David A. McAllister

Susan M. Smith

Rachael Evans

Zahira Ahmed

Sarah Dean

Colin Greaves

Shaun Barber

Patrick Doherty

Nikki Gardiner

Tracy Ibbotson

Kate Jolly

Sharon A. Simpson

Rod S. Taylor

Sally J. Singh

Frances S. Mair

Bhautesh Dinesh Jani



Abstract

Background
It remains unclear how to meaningfully classify people living with multimorbidity (multiple long-term conditions (MLTCs)), beyond counting the number of conditions. This paper aims to identify clusters of MLTCs in different age groups and associated risks of adverse health outcomes and service use.

Methods
Latent class analysis was used to identify MLTCs clusters in different age groups in three cohorts: Secure Anonymised Information Linkage Databank (SAIL) (n = 1,825,289), UK Biobank (n = 502,363), and the UK Household Longitudinal Study (UKHLS) (n = 49,186). Incidence rate ratios (IRR) for MLTC clusters were computed for: all-cause mortality, hospitalisations, and general practice (GP) use over 10 years, using <2 MLTCs as reference. Information on health outcomes and service use were extracted for a ten year follow up period (between 01st Jan 2010 and 31st Dec 2019 for UK Biobank and UKHLS, and between 01st Jan 2011 and 31st Dec 2020 for SAIL).

Findings
Clustering MLTCs produced largely similar results across different age groups and cohorts. MLTC clusters had distinct associations with health outcomes and service use after accounting for LTC counts, in fully adjusted models. The largest associations with mortality, hospitalisations and GP use in SAIL were observed for the “Pain+” cluster in the age-group 18–36 years (mortality IRR = 4.47, hospitalisation IRR = 1.84; GP use IRR = 2.87) and the “Hypertension, Diabetes & Heart disease” cluster in the age-group 37–54 years (mortality IRR = 4.52, hospitalisation IRR = 1.53, GP use IRR = 2.36). In UK Biobank, the “Cancer, Thyroid disease & Rheumatoid arthritis” cluster in the age group 37–54 years had the largest association with mortality (IRR = 2.47). Cardiometabolic clusters across all age groups, pain/mental health clusters in younger groups, and cancer and pulmonary related clusters in older age groups had higher risk for all outcomes. In UKHLS, MLTC clusters were not significantly associated with higher risk of adverse outcomes, except for the hospitalisation in the age-group 18–36 years.

Interpretation
Personalising care around MLTC clusters that have higher risk of adverse outcomes may have important implications for practice (in relation to secondary prevention), policy (with allocation of health care resources), and research (intervention development and targeting), for people living with MLTCs.

Funding
This study was funded by the National Institute for Health and Care Research (NIHR; Personalised Exercise-Rehabilitation FOR people with Multiple long-term conditions (multimorbidity)—NIHR202020).

Citation

Krauth, S. J., Steell, L., Ahmed, S., McIntosh, E., Dibben, G. O., Hanlon, P., …Jani, B. D. (in press). Association of latent class analysis-derived multimorbidity clusters with adverse health outcomes in patients with multiple long-term conditions: comparative results across three UK cohorts. #Journal not on list, 74, 102703. https://doi.org/10.1016/j.eclinm.2024.102703

Journal Article Type Article
Acceptance Date Jun 7, 2024
Online Publication Date Jun 28, 2024
Deposit Date Jul 8, 2024
Publicly Available Date Jul 8, 2024
Journal eClinicalMedicine
Peer Reviewed Peer Reviewed
Volume 74
Pages 102703
DOI https://doi.org/10.1016/j.eclinm.2024.102703

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