Distribution of airway smooth muscle remodelling in asthma: Relation to airway inflammation

被引:63
作者
Elliot, John G. [1 ]
Jones, Robyn L. [1 ]
Abramson, Michael J. [3 ]
Green, Francis H. [6 ]
Mauad, Thais [8 ]
McKay, Karen O. [4 ,5 ]
Bai, Tony R. [7 ]
James, Alan L. [1 ,2 ]
机构
[1] Sir Charles Gairdner Hosp, West Australian Sleep Disorders Res Inst, Dept Pulm Physiol & Sleep Med, Perth, WA 6009, Australia
[2] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
[3] Monash Univ, Dept Epidemiol & Prevent Med, Melbourne, Vic 3004, Australia
[4] Childrens Hosp Westmead, Dept Resp Med, Sydney, NSW, Australia
[5] Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia
[6] Univ Calgary, Dept Pathol & Lab Med, Calgary, AB, Canada
[7] Univ British Columbia, James Hogg Res Ctr, Vancouver, BC V5Z 1M9, Canada
[8] Univ Sao Paulo, Sch Med, Dept Pathol, Sao Paulo, Brazil
基金
英国医学研究理事会;
关键词
airway smooth muscle; asthma; inflammation; remodelling; small airway; HE-3; MAGNETIC-RESONANCE; HETEROGENEITY; METHACHOLINE; HYPERTROPHY; HYPERPLASIA; ACTIVATION; EOSINOPHIL; LUNGS; CT;
D O I
10.1111/resp.12384
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background and objectivePathological phenotypes of asthma have been based predominantly on inflammation, rather than airway wall remodelling. Differences in the distribution of airway smooth muscle (ASM) remodelling between large and small airways may affect clinical outcomes in asthma. The aim of this study was to examine the distribution of ASM remodelling and its relation to airway inflammation. MethodsPost-mortem cases of asthma (n=68) were categorized by the distribution of increased thickness of the ASM layer (relative to nonasthmatic controls, n=37), into large only' (LO, n=15), small only' (SO, n=4) large/small' (LS, n=24) or no increase (NI, n=25). Subject characteristics, ASM and airway wall dimensions and inflammatory cell numbers were compared between groups. ResultsApart from reduced clinical severity of asthma in NI cases (P=0.002), subject characteristics did not distinguish asthma groups. Compared with control subjects, ASM cell number, reticular basement membrane thickness, airway wall thickness, percent muscle shortening and eosinophil number were increased (P< 0.05) in both large and small airways in LS cases and only the large airways in LO cases. Increased numbers of neutrophils were observed only in the small airways of LO cases. ConclusionsDistinct distributions of ASM remodelling are seen in asthma. Pathology limited to the small airways was uncommon. Increased thickness of the ASM layer was associated with airway remodelling and eosinophilia, but not neutrophilia. These data support the presence of distinct pathological phenotypes based on the site of increased ASM.
引用
收藏
页码:66 / 72
页数:7
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