Ventilation heterogeneity is associated with airway responsiveness in asthma but not COPD

被引:19
作者
Hardaker, Kate M. [1 ,2 ,3 ]
Downie, Sue R. [1 ,2 ,3 ]
Kermode, Jessica A. [1 ,2 ,3 ]
Berend, Norbert [1 ,2 ,3 ]
King, Gregory G. [1 ,2 ,3 ,4 ]
Salome, Cheryl M. [1 ,2 ,3 ]
机构
[1] Woolcock Inst Med Res, Glebe, NSW 2050, Australia
[2] Univ Sydney, Darlington, Durham, Australia
[3] Cooperat Res Ctr Asthma & Airways, Glebe, NSW, Australia
[4] Royal N Shore Hosp, Dept Resp Med, St Leonards, NSW 2065, Australia
关键词
Aging; Airway hyperresponsiveness; Chronic obstructive pulmonary disease; Physiology; Pulmonary mechanics; OBSTRUCTIVE PULMONARY-DISEASE; EXHALED NITRIC-OXIDE; LUNG-FUNCTION; BRONCHIAL HYPERRESPONSIVENESS; METHACHOLINE RESPONSIVENESS; FLOW OBSTRUCTION; SMOKERS; EOSINOPHILS; POPULATION; PREDICTORS;
D O I
10.1016/j.resp.2013.07.009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Airway hyperresponsiveness (AHR) occurs in both asthma and COPD. In older people with asthma, AHR is associated with increased acinar ventilation heterogeneity, but it is unknown if this association exists in COPD. Thirty one COPD and 19 age-matched asthmatic subjects had measures of spirometry, lung volumes, exhaled nitric oxide, ventilation heterogeneity, and methacholine challenge. Indices of acinar (Sacin) and conducting (Scond) airway ventilation heterogeneity were calculated from the multiple breath nitrogen washout. Predictors of AHR were then determined. In COPD, AHR was predicted by lower Sacin and lower PVC (model r(2)=0.35, p=0.001). In asthma, AHR as predicted by higher Sacin and higher residual volume (model r(2)=0.62, p<0.001). These findings suggest that airway responsiveness in COPD and asthma is determined by underlying disease-specific processes, rather than a common pattern of physiological abnormality. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:106 / 111
页数:6
相关论文
共 39 条
[1]   ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005 [J].
American Thoracic Society ;
European Respiratory Society .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (08) :912-930
[2]   How to interpret reduced forced expiratory volume in 1 s (FEV1)/vital capacity ratio with normal FEV1 [J].
Barisione, G. ;
Crimi, E. ;
Bartolini, S. ;
Saporiti, R. ;
Copello, F. ;
Pellegrino, R. ;
Brusasco, V. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 33 (06) :1396-1402
[3]   Against the Dutch hypothesis: Asthma and chronic obstructive pulmonary disease are distinct diseases [J].
Barnes, Peter J. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (03) :240-243
[4]   DISTRIBUTION OF BRONCHIAL NONSPECIFIC REACTIVITY IN THE GENERAL-POPULATION [J].
CERVERI, I ;
BRUSCHI, C ;
ZOIA, MC ;
ZANON, P ;
MACCARINI, L ;
GRASSI, M ;
RAMPULLA, C .
CHEST, 1988, 93 (01) :26-30
[5]  
CRAPO RO, 1982, B EUR PHYSIOPATH RES, V18, P419
[6]  
CRAPO RO, 1981, AM REV RESPIR DIS, V123, P185
[7]  
Crapo RO, 2000, AM J RESP CRIT CARE, V161, P309
[8]   Changes in FVC during methacholine-induced bronchoconstriction in elderly patients with asthma - Bronchial hyperresponsiveness and aging [J].
Cuttitta, G ;
Cibella, F ;
Bellia, V ;
Grassi, V ;
Cossi, S ;
Bucchieri, S ;
Bonsignore, G .
CHEST, 2001, 119 (06) :1685-1690
[9]   Exhaled nitric oxide as a diagnostic test for asthma - Online versus offline techniques and effect of flow rate [J].
Deykin, A ;
Massaro, AF ;
Drazen, JM ;
Israel, E .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (12) :1597-1601
[10]   Ventilation heterogeneity is a major determinant of airway hyperresponsiveness in asthma, independent of airway inflammation [J].
Downie, Sue R. ;
Salome, Cheryl M. ;
Verbanck, Sylvia ;
Thompson, Bruce ;
Berend, Norbert ;
King, Gregory G. .
THORAX, 2007, 62 (08) :684-689