Identification of sleep phenotypes in COPD using machine learning-based cluster analysis

被引:0
|
作者
Razjouyan, Javad [1 ,2 ,3 ,4 ]
Hanania, Nicola A. [4 ]
Nowakowski, Sara [1 ,2 ,3 ,4 ]
Agrawal, Ritwick [4 ,5 ]
Sharafkhaneh, Amir [4 ,5 ,6 ]
机构
[1] Michael E DeBakey VA Med Ctr, Ctr Innovat Qual Effectiveness & Safety, VAs Hlth Serv Res & Dev Serv HSR &D, Houston, TX 77030 USA
[2] VA Off Res & Dev, Big Data Scientist Training Enhancement Program, Washington, DC 20420 USA
[3] Michael E DeBakey VA Med Ctr, VA Qual Scholars Coordinating Ctr, IQuESt, Houston, TX 77030 USA
[4] Baylor Coll Med, Dept Med, Sect Pulm & Crit Care Med, Houston, TX 77030 USA
[5] Michael E DeBakey VA Med Ctr, Crit Care & Sleep Med Sect, Pulm, Houston, TX 77030 USA
[6] 2002 Holcombe Blvd, Houston, TX 77030 USA
关键词
COPD; Sleep disorders; Phenotypes; Comorbidities; OBSTRUCTIVE PULMONARY-DISEASE; DISORDERS; MORTALITY; POLYSOMNOGRAPHY;
D O I
10.1016/j.rmed.2024.107641
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Disturbed sleep in patients with COPD impact quality of life and predict adverse outcomes. Research question: To identify distinct phenotypic clusters of patients with COPD using objective sleep parameters and evaluate the associations between clusters and all-cause mortality to inform risk stratification. Study design and methods: A longitudinal observational cohort study using nationwide Veterans Health Administration data of patients with COPD investigated for sleep disorders. Sleep parameters were extracted from polysomnography physician interpretation using a validated natural language processing algorithm. We performed cluster analysis using an unsupervised machine learning algorithm (K-means) and examined the association between clusters and mortality using Cox regression analysis, adjusted for potential confounders, and visualized with Kaplan-Meier estimates. Results: Among 9992 patients with COPD and a clinically indicated baseline polysomnogram, we identified five distinct clusters based on age, comorbidity burden and sleep parameters. Overall mortality increased from 9.4 % to 42 % and short -term mortality (<5.3 years) ranged from 3.4 % to 24.3 % in Cluster 1 to 5. In Cluster 1 younger age, in 5 high comorbidity burden and in the other three clusters, total sleep time and sleep efficiency had significant associations with mortality. Interpretation: We identified five distinct clinical clusters and highlighted the significant association between total sleep time and sleep efficiency on mortality. The identified clusters highlight the importance of objective sleep parameters in determining mortality risk and phenotypic characterization in this population.
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页数:7
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