居住在威尔士的智力残疾个体的多种长期状况的时间模式:疾病轨迹的无监督聚类方法。

IF 3.2 Q1 HEALTH CARE SCIENCES & SERVICES
Frontiers in digital health Pub Date : 2025-03-27 eCollection Date: 2025-01-01 DOI:10.3389/fdgth.2025.1528882
Rania Kousovista, Georgina Cosma, Emeka Abakasanga, Ashley Akbari, Francesco Zaccardi, Gyuchan Thomas Jun, Reza Kiani, Satheesh Gangadharan
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引用次数: 0

摘要

在智力残疾(ID)患者中识别和理解多种长期疾病(MLTCs)的共存对于有效的医疗管理至关重要。与一般人群相比,患有ID的个体通常会经历更早的发病和更高的MLTCs患病率,然而,这些疾病的共同发生和时间进展的具体模式在很大程度上仍未被探索。本研究提出了一种创新的无监督方法,基于他们共同的疾病轨迹来检查和表征ID个体的MLTC集群。方法:本研究使用来自13069名身份证患者的电子健康记录(EHRs)数据集,包括2000年至2021年威尔士的初级和二级保健数据,分析了疾病诊断的时间序列。发现了显著的成对疾病关联,并评估了它们的时间方向性。随后,将无监督聚类算法-谱聚类-应用于共享疾病轨迹,根据共同的时间模式对它们进行分组。结果:研究人群中男性占52.3%,女性占47.7%,平均每位患者有4.5±3个长期疾病(LTCs)。在男性和女性中都发现了不同的MLTC集群,按年龄组(≥45岁)分层。对于45岁以下的男性,单一集群以神经系统疾病为主(32.4%),而在老年男性中确定了三个集群,其中最大的特征是循环系统(51.8%)。在45岁以下的女性中,消化系统疾病(24.6%)最为普遍。对于≥45岁的女性,确定了两个集群:第一集群主要由循环系统(34.1%)定义,而第二集群主要由消化系统(25.9%)和肌肉骨骼系统(21.9%)定义。精神疾病、癫痫和反流障碍在所有人群中都很普遍。讨论:本研究揭示了ID患者复杂的多病模式,突出了年龄和性别差异。确定的群集为该人群的疾病进展和共发生提供了新的见解。这些发现可以为有针对性的干预措施和风险分层策略的制定提供信息,有可能改善ID和MLTCs患者的个性化医疗保健,目的是改善这一弱势患者群体的健康结果,即减少住院次数和住院时间,减少过早死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Temporal patterns of multiple long-term conditions in individuals with intellectual disability living in Wales: an unsupervised clustering approach to disease trajectories.

Introduction: 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.

Methods: 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.

Results: 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.

Discussion: 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.

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