# Temporal patterns of multiple long-term conditions in individuals with intellectual disability living in Wales: an unsupervised clustering approach to disease trajectories

**Authors:** Rania Kousovista, Georgina Cosma, Emeka Abakasanga, Ashley Akbari, Francesco Zaccardi, Gyuchan Thomas Jun, Reza Kiani, Satheesh Gangadharan

PMC · DOI: 10.3389/fdgth.2025.1528882 · Frontiers in Digital Health · 2025-03-27

## TL;DR

This study explores how multiple long-term health conditions develop over time in people with intellectual disability in Wales, revealing patterns that vary by age and sex.

## Contribution

The paper introduces an unsupervised clustering method to identify distinct disease trajectory patterns in individuals with intellectual disability.

## Key findings

- Males under 45 had a cluster dominated by neurological conditions, while older males showed a cluster focused on circulatory issues.
- Females under 45 had a cluster centered on digestive conditions, and older females showed clusters involving circulatory and musculoskeletal conditions.
- Mental illness, epilepsy, and reflux disorders were common across all groups, highlighting shared health challenges.

## Abstract

Identifying and understanding the co-occurrence of multiple long-term conditions (MLTCs) in individuals with intellectual disability (ID) is crucial for effective healthcare management. Individuals with ID often experience earlier onset and higher prevalence of MLTCs compared to the general population, however, the specific patterns of co-occurrence and temporal progression of these conditions remain largely unexplored. This study presents an innovative unsupervised approach for examining and characterising clusters of MLTC in individuals with ID, based on their shared disease trajectories.

Using a dataset of electronic health records (EHRs) from 13,069 individuals with ID, encompassing primary and secondary care data in Wales from 2000 to 2021, this study analysed the time sequences of disease diagnoses. Significant pairwise disease associations were identified, and their temporal directionality assessed. Subsequently, an unsupervised clustering algorithm—spectral clustering—was applied to the shared disease trajectories, grouping them based on common temporal patterns.

The study population comprised 52.3% males and 47.7% females, with a mean of 4.5 ± 3 long-term conditions (LTCs) per patient. Distinct MLTC clusters were identified in both males and females, stratified by age groups (<45 and ≥45 years). For males under 45, a single cluster dominated by neurological conditions (32.4%), while three clusters were identified for older males, with the largest characterised by circulatory (51.8%). In females under 45, one cluster was found with digestive system conditions (24.6%) being most prevalent. For females ≥ 45 years, two clusters were identified: the first cluster was predominantly defined by circulatory (34.1%), while the second cluster by digestive (25.9%) and musculoskeletal (21.9%) system conditions. Mental illness, epilepsy, and reflux disorders were prevalent across all groups.

This study reveals complex multimorbidity patterns in individuals with ID, highlighting age and sex differences. The identified clusters provide new insights into disease progression and co-occurrence in this population. These findings can inform the development of targeted interventions and risk stratification strategies, potentially improving personalised healthcare for individuals with ID and MLTCs with the aim of improving health outcome for this vulnerable group of patients i.e. reducing frequency and length of hospital admissions and premature mortality.

## Linked entities

- **Diseases:** mental illness (MONDO:0002025), epilepsy (MONDO:0005027)

## Full-text entities

- **Diseases:** ID (MESH:D008607), reflux disorders (MESH:D005764), MLTCs (MESH:D000088562), Mental illness (MESH:D001523), epilepsy (MESH:D004827)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC11983499/full.md

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Source: https://tomesphere.com/paper/PMC11983499