Sociodemographic characteristics and longitudinal progression of multimorbidity: A multistate modelling analysis of a large primary care records dataset in England

Sida Chen*, Tom Marshall, Christopher Jackson, Jennifer Cooper, Francesca Crowe, Krish Nirantharakumar, Catherine L. Saunders, Paul Kirk, Sylvia Richardson, Duncan Edwards, Simon Griffin, Christopher Yau, Jessica K. Barrett

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

67 Downloads (Pure)

Abstract

Background: Multimorbidity, characterised by the coexistence of multiple chronic conditions in an individual, is a rising public health concern. While much of the existing research has focused on cross-sectional patterns of multimorbidity, there remains a need to better understand the longitudinal accumulation of diseases. This includes examining the associations between important sociodemographic characteristics and the rate of progression of chronic conditions.

Methods and findings: We utilised electronic primary care records from 13.48 million participants in England, drawn from the Clinical Practice Research Datalink (CPRD Aurum), spanning from 2005 to 2020 with a median follow-up of 4.71 years (IQR: 1.78, 11.28). The study focused on 5 important chronic conditions: cardiovascular disease (CVD), type 2 diabetes (T2D), chronic kidney disease (CKD), heart failure (HF), and mental health (MH) conditions. Key sociodemographic characteristics considered include ethnicity, social and material deprivation, gender, and age. We employed a flexible spline-based parametric multistate model to investigate the associations between these sociodemographic characteristics and the rate of different disease transitions throughout multimorbidity development. Our findings reveal distinct association patterns across different disease transition types. Deprivation, gender, and age generally demonstrated stronger associations with disease diagnosis compared to ethnic group differences. Notably, the impact of these factors tended to attenuate with an increase in the number of preexisting conditions, especially for deprivation, gender, and age. For example, the hazard ratio (HR) (95% CI; p-value) for the association of deprivation with T2D diagnosis (comparing the most deprived quintile to the least deprived) is 1.76 ([1.74, 1.78]; p < 0.001) for those with no preexisting conditions and decreases to 0.95 ([0.75, 1.21]; p = 0.69) with 4 preexisting conditions. Furthermore, the impact of deprivation, gender, and age was typically more pronounced when transitioning from an MH condition. For instance, the HR (95% CI; p-value) for the association of deprivation with T2D diagnosis when transitioning from MH is 2.03 ([1.95, 2.12], p < 0.001), compared to transitions from CVD 1.50 ([1.43, 1.58], p < 0.001), CKD 1.37 ([1.30, 1.44], p < 0.001), and HF 1.55 ([1.34, 1.79], p < 0.001). A primary limitation of our study is that potential diagnostic inaccuracies in primary care records, such as underdiagnosis, overdiagnosis, or ascertainment bias of chronic conditions, could influence our results.

Conclusions: Our results indicate that early phases of multimorbidity development could warrant increased attention. The potential importance of earlier detection and intervention of chronic conditions is underscored, particularly for MH conditions and higher-risk populations. These insights may have important implications for the management of multimorbidity.
Original languageEnglish
Article numbere1004310
Number of pages21
JournalPLoS Medicine
Volume20
Issue number11
DOIs
Publication statusPublished - 3 Nov 2023

Bibliographical note

Funding:
This work is part of the Bringing Innovative Research Methods to Clustering Analysis of Multimorbidity (BIRM-CAM) project funded by the UKRI. SC is funded by the MRC/NIHR grant MR/S027602/1 (BIRM-CAM). TM is supported by the National Institute for Health Research Collaboration Applied Research Collaboration West Midlands (NIHR ARC WM). CJ was funded by the Medical Research Council programme number MRC_MC_UU_00002/11. TM, KN, FC and CY are partly funded by National Institute for Health Research (NIHR) Intelligence for Multiple Long-Term Conditions (AIM) funded project. OPTIMising therapies, disease trajectories, and AI assisted clinical management for patients Living with complex multimorbidity (OPTIMAL study) Award ID: NIHR202632 https://fundingawards.nihr.ac.uk/award/NIHR202632. CY is also funded by a UKRI Turing AI Fellowship (EP/V023233/2). PK, SR, JB are funded by the Medical Research Council as part of the Precision Medicine and Inference for Complex Outcomes theme of the MRC Biostatistics Unit. PK was funded by MRC unit programme MC_UU_00002/13. SR was funded by MRC unit programme MC_UU_00002/10. JB was funded by MRC unit programme MC_UU_00002/5. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Fingerprint

Dive into the research topics of 'Sociodemographic characteristics and longitudinal progression of multimorbidity: A multistate modelling analysis of a large primary care records dataset in England'. Together they form a unique fingerprint.

Cite this