Holm Nikolaj Normann, Le Thao Minh, Frølich Anne, Andersen Ove, Juul-Larsen Helle Gybel, Stockmarr Anders, Venkatesh Svetha
Department of Applied Mathematics and Computer Science, Technical University of Denmark, Kgs. Lyngby, Denmark.
Applied Artificial Intelligence Institute, Deakin University, Geelong, Australia.
Comput Biol Med. 2025 Mar;186:109632. doi: 10.1016/j.compbiomed.2024.109632. Epub 2025 Jan 16.
Multimorbidity, the co-occurrence of multiple chronic conditions within the same individual, is increasing globally. This is a challenge for the single patients, as these individuals are subject to a heavy disease and treatment burden, yet evidence on the epidemiology and consequences of multimorbidity remains underexplored. Historically, studies aiming to understand multimorbidity patterns predominantly utilized cross-sectional data, neglecting the essential temporal dynamics which shape multimorbidity progression. Other studies based their analyses on small datasets, or populations only targeting certain sectors of the healthcare system. In this study, we (1) introduce a novel two-step multimodal Variational Autoencoder-based approach for temporal disease-based clustering (i.e. discovering age-aware multimorbidity clusters); (2) provide quantitative experiments for the robustness of our approach and the extracted temporal clusters; and (3) demonstrate how the temporal disease clusters obtained from our model can provide novel understanding of the development of multiple conditions over time and thus generate new hypotheses for different stages of multimorbidity and their associations. We trained and evaluated our models on a dataset containing the entire adult population of Denmark in the period 1995-2015, focusing on individuals suffering from chronic heart disease, including 766,596 individuals.
共病,即同一个体内多种慢性病并存的情况,在全球范围内呈上升趋势。这对个体患者来说是一项挑战,因为这些人承受着沉重的疾病和治疗负担,然而关于共病的流行病学和后果的证据仍未得到充分探索。从历史上看,旨在了解共病模式的研究主要使用横断面数据,而忽略了影响共病进展的基本时间动态。其他研究则基于小数据集或仅针对医疗系统某些部门的人群进行分析。在本研究中,我们(1)引入了一种基于变分自编码器的新颖两步多模态方法,用于基于时间疾病的聚类(即发现年龄感知共病簇);(2)对我们的方法和提取的时间簇的稳健性进行定量实验;(3)展示从我们的模型中获得的时间疾病簇如何能够提供对多种疾病随时间发展的新理解,从而为共病的不同阶段及其关联产生新的假设。我们在一个包含1995 - 2015年丹麦全体成年人口的数据集上训练和评估我们的模型,重点关注患有慢性心脏病的个体,其中包括766,596人。