Clusters of Severe Eosinophilic Asthma in a Korean Asthma Cohort

Author:

Lee Ji-Hyang,An Jin,Won Ha-Kyeong,Seo Bomi,Kim Jung-Hyun,Park So-Young,Kim Min-Hye,Shin Yoo Seob,Jung Jae-Woo,Song Woo-Jung,Lee Taehoon,Kwon Hyouk-Soo,Lee Jae Hyun,Kim Joo-Hee,Kim Sae-Hoon,Chang Yoon-Seok,Cho You Sook,Nahm Dong-HoORCID,Jang An-Soo,Park Jung-Won,Yoon Ho-JooORCID,Cho Sang-Heon,Cho Young-Joo,Choi Byoung Whui,Moon Hee-Bom,Kim Tae-Bum,

Abstract

Background: Targeted therapies have broadened the available treatment options for patients with severe eosinophilic asthma (SEA). However, differences in the magnitude of treatment responses among patients indicate the presence of various underlying pathophysiological processes and patient subgroups. Objectives: We aimed to describe the characteristics of SEA and identify its patient subgroups. Methods: Clinical data from the Cohort for Reality and Evolution of Adult Asthma in Korea were analyzed. Cluster analysis was performed among those with SEA using 5 variables, namely, prebronchodilator forced expiratory volume in 1 s, body mass index, age at symptom onset, smoking amount, and blood eosinophil counts. Results: Patients with SEA showed prevalent sensitization to aeroallergens, decreased lung function, and poor asthma control status. Cluster analysis revealed 3 distinctive subgroups among patients with SEA. Cluster 1 (n = 177) consisted of patients reporting the lowest blood eosinophils (median, 346.8 cells/μL) and modest severe asthma with preserved lung function during the 12-month treatment period. Cluster 2 (n = 42) predominantly included smoking males with severe persistent airway obstruction and moderate eosinophilia (median, 451.8 cells/μL). Lastly, cluster 3 (n = 95) included patients with the most severe asthma, the highest eosinophil levels (median, 817.5 cells/μL), and good treatment response in terms of improved lung function and control status. Conclusions: Three subgroups were identified in SEA through the cluster analysis. The distinctive features of each cluster may help physicians predict patients who will respond to biologics with greater magnitude of clinical improvement. Further research regarding the underlying pathophysiology and clinical importance of each subgroup is warranted.

Publisher

S. Karger AG

Subject

Pulmonary and Respiratory Medicine

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