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CHEST Guidelines
Comorbidity-Based-Clusters-Contain-Chaos-in-COPD_c
Comorbidity-Based-Clusters-Contain-Chaos-in-COPD_c
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Pdf Summary
This editorial, published in CHEST, discusses recent research aimed at understanding the heterogeneity within Chronic Obstructive Pulmonary Disease (COPD) through comorbidity-based clustering. COPD, a leading cause of death globally, exhibits diverse clinical and pathological features, complicating its diagnosis and treatment. Efforts to identify subtypes using unsupervised clustering methods, like k-means clustering, have yielded varied results, leading to concerns about their external validity and reproducibility across different populations. <br /><br />In a study by Tiew and colleagues, clusters based on clinical features, comorbidities, and demographic details were identified in a Chinese cohort with COPD. Five clusters emerged: (1) prior primary TB, (2) coexisting diabetes, (3) low comorbidity, low risk, (4) low comorbidity, high risk, and (5) coexisting cardiovascular disease. The study highlighted increased mortality in the cardiovascular and prior TB clusters and attempted to biologically validate these findings through cytokine profiles.<br /><br />Strengths of Tiew's study include its focus on an understudied demographic with significant comorbid conditions like TB and its methodical validation of findings in a separate cohort. However, it faces limitations in terms of generalizability due to the specific population studied. Furthermore, the study doesn't integrate COPD medication use, which might affect cluster-specific outcomes.<br /><br />The editorial emphasizes the need for future studies to enhance the understanding of COPD heterogeneity by incorporating multiomic data and supervised clustering techniques. This approach could lead to more nuanced subtyping of COPD, offering tailored treatment strategies and better prognostication. While these clustering efforts have advanced knowledge, the challenge remains to establish consistent subtypes across diverse populations and clinical settings.
Keywords
COPD
comorbidity-based clustering
k-means clustering
heterogeneity
Tiew study
Chinese cohort
cytokine profiles
multiomic data
supervised clustering
subtyping
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