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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.
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页码:33 / 41
页数:9
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