Distinct Phenotypes of Smokers with Fixed Airflow Limitation Identified by Cluster Analysis of Severe Asthma

被引:47
|
作者
Konno, Satoshi [1 ]
Taniguchi, Natsuko [1 ]
Makita, Hironi [1 ]
Nakamaru, Yuji [2 ]
Shimizu, Kaoruko [1 ]
Shijubo, Noriharu [3 ]
Fuke, Satoshi [4 ]
Takeyabu, Kimihiro [5 ]
Oguri, Mitsuru [6 ]
Kimura, Hirokazu [1 ]
Maeda, Yukiko [1 ]
Suzuki, Masaru [1 ]
Nagai, Katsura [1 ]
Ito, Yoichi M. [7 ]
Wenzel, Sally E. [8 ]
Nishimura, Masaharu [1 ]
机构
[1] Hokkaido Univ, Sch Med, Dept Med 1, Sapporo, Hokkaido, Japan
[2] Hokkaido Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Sapporo, Hokkaido, Japan
[3] Japan Railways Sapporo Hosp, Dept Resp Med, Sapporo, Hokkaido, Japan
[4] KKR Sapporo Med Ctr, Dept Resp Med, Sapporo, Hokkaido, Japan
[5] Otaru Kyokai Hosp, Dept Resp Med, Otaru, Hokkaido, Japan
[6] Oji Gen Hosp, Dept Resp Med, Tomakomai, Japan
[7] Hokkaido Univ, Grad Sch Med, Dept Biostat, Sapporo, Hokkaido, Japan
[8] Univ Pittsburgh, Med Ctr, Asthma Inst, Sch Med, Pittsburgh, PA 15260 USA
关键词
severe asthma; smoking; cluster analysis; phenotypes; eosinophils; CHRONIC RHINOSINUSITIS; SMOKING ASTHMATICS; OBESE INDIVIDUALS; RESEARCH-PROGRAM; INFLAMMATION; OSTEOPONTIN; BIOMARKERS; DISEASE;
D O I
10.1513/AnnalsATS.201701-065OC
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Rationale: Smoking may have multifactorial effects on asthma phenotypes, particularly in severe asthma. Cluster analysis has been applied to explore novel phenotypes, which are not based on any a priori hypotheses. Objectives: To explore novel severe asthma phenotypes by cluster analysis when including smoking patients with asthma. Methods: We recruited a total of 127 subjects with severe asthma, including 59 current or ex-smokers, from our university hospital and its 29 affiliated hospitals/pulmonary clinics. Clinical variables obtained during a 2-day hospital stay were used for cluster analysis. After clustering using clinical variables, the sputum levels of 14 molecules were measured to biologically characterize the clinical clusters. Results: Five clinical clusters, including two characterized by low forced expiratory volume in 1 second/forced vital capacity, were identified. When characteristics of smoking subjects in these two clusters were compared, there were marked differences between the two groups: one had high levels of circulating eosinophils, high immunoglobulin E levels, and a high sinus score, and the other was characterized by low levels of the same parameters. Sputum analysis revealed intriguing differences of cytokine/chemokine pattern in these two groups. The other three clusters were similar to those previously reported: young onset/atopic, nonsmoker/less eosinophilic, and female/obese. Key clinical variables were confirmed to be stable and consistent 3 years later. Conclusions: This study reveals two distinct phenotypes with potentially different biological pathways contributing to fixed airflow limitation in cigarette smokers with severe asthma.
引用
收藏
页码:33 / 41
页数:9
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