Effect of aging on sputum inflammation and asthma control

被引:45
作者
Busse, Paula J. [1 ]
Birmingham, Janette M. [1 ]
Calatroni, Agustin [4 ]
Manzi, Joseph [1 ]
Goryachokovsky, Anna [1 ]
Fontela, Giselle [1 ]
Federman, Alex D. [2 ]
Wisnivesky, Juan P. [2 ,3 ]
机构
[1] Icahn Sch Med Mt Sinai, Div Clin Immunol, 1425 Madision Ave,Rm 11-20, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Div Gen Internal Med, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Div Pulm Crit Care & Sleep Med, New York, NY 10029 USA
[4] Fed Syst Div, Rho, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
Asthma; sputum; inflammation; sensitization; inner city; REGULATORY T-CELLS; INNER-CITY ASTHMA; OBSTRUCTIVE PULMONARY-DISEASE; QUALITY-OF-LIFE; AIRWAY NEUTROPHILIA; UNITED-STATES; RISK-FACTORS; HUMAN LUNG; IN-VIVO; AGE;
D O I
10.1016/j.jaci.2016.09.015
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Aged asthmatic patients experience increased morbidity and mortality. Knowledge of the aging effect on airway inflammation and asthma control is limited. Objective: We sought to compare airway inflammation and its relationship to asthma control in aged versus younger patients and determine whether differences are asthma specific or caused by "inflamm-aging." Methods: We performed a prospective study of aged (>60 years) and younger (21-40 years) inner-city patients with asthma. After a run-in period to control for inhaled corticosteroid use, induced sputum was collected. Age-matched nonasthmatic control subjects were included to measure age-related inflammatory changes. Results: Aged (mean age, 67.9 +/- 5.1 years; n = 35) compared with younger (mean age, 30.8 +/- 5.9 years; n = 37) asthmatic patients had significantly worse asthma control and lower FEV1. Aged asthmatic patients had higher sputum neutrophil (30.5 x 10(4)/mL and 23.1%) and eosinophil (7.0 x 10(4)/mL and 3.8%) numbers and percentages compared with younger patients (neutrophils, 13.0 x 10(4)/mL [P < .01] and 6.9% [P < .01]; eosinophils, 2.0 x 10(4)/mL [P < .01] and 1.2% [P < .01]). Aged asthmatic patients had higher sputum IL-6 (P < .01) and IL-8 (P = .01) levels. No significant inflammatory differences between aged and younger control subjects were observed. In aged asthmatic patients increased sputum IL-6 and macrophage inflammatory protein 3 alpha/CCL20 levels were significantly associated with decreased asthma control and increased sputum neutrophil numbers and IL-1 beta, IL-6, and macrophage inflammatory protein 3 alpha/CCL20 levels were associated with hospitalization. Conclusions: The inflammatory patterns of aged versus younger asthmatic patients are associated with increased sputum neutrophil and eosinophil values and cytokine levels related to neutrophil recruitment. Differences in airway inflammation can contribute to diminished asthma control in the aged. Further understanding of asthma pathophysiology in aged patients is needed to improve management of this vulnerable population.
引用
收藏
页码:1808 / +
页数:17
相关论文
共 94 条
[1]   Interleukins 1β and 6 but not transforming growth factor-β are essential for the differentiation of interleukin 17-producing human T helper cells [J].
Acosta-Rodriguez, Eva V. ;
Napolitani, Giorgio ;
Lanzavecchia, Antonio ;
Sallusto, Federica .
NATURE IMMUNOLOGY, 2007, 8 (09) :942-949
[2]   The biology of interleukin-27 reveals unique pro- and anti-inflammatory functions in immunity [J].
Aparicio-Siegmund, Samadhi ;
Garbers, Christoph .
CYTOKINE & GROWTH FACTOR REVIEWS, 2015, 26 (05) :579-586
[3]   Age-dependent interaction between atopy and eosinophils in asthma cases: results from NHANES 2005-2006 [J].
Arbes, S. J., Jr. ;
Calatroni, A. ;
Mitchell, H. E. ;
Gergen, P. J. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2013, 43 (05) :544-551
[4]   Mechanisms of T regulatory cell function [J].
Askenasy, Nadir ;
Kaminitz, Ayelet ;
Yarkoni, Shai .
AUTOIMMUNITY REVIEWS, 2008, 7 (05) :370-375
[5]   Asthma in the elderly - Mortality rate and associated risk factors for mortality [J].
Bellia, Vincenzo ;
Pedone, Claudio ;
Catalano, Filippo ;
Zito, Anna ;
Palange, Stefania ;
Forastiere, Francesco ;
Incalzi, Raffaele Antonelli .
CHEST, 2007, 132 (04) :1175-1182
[6]   Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells [J].
Bettelli, E ;
Carrier, YJ ;
Gao, WD ;
Korn, T ;
Strom, TB ;
Oukka, M ;
Weiner, HL ;
Kuchroo, VK .
NATURE, 2006, 441 (7090) :235-238
[7]   Relationship between airway neutrophilia and ageing in asthmatics and non-asthmatics [J].
Brooks, Collin R. ;
Gibson, Peter G. ;
Douwes, Jeroen ;
Van Dalen, Christine J. ;
Simpson, Jodie L. .
RESPIROLOGY, 2013, 18 (05) :857-865
[8]   CHARACTERISTICS OF ASTHMA AMONG ELDERLY ADULTS IN A SAMPLE OF THE GENERAL-POPULATION [J].
BURROWS, B ;
BARBEE, RA ;
CLINE, MG ;
KNUDSON, RJ ;
LEBOWITZ, MD .
CHEST, 1991, 100 (04) :935-942
[9]   Effect of ageing on pulmonary inflammation, airway hyperresponsiveness and T and B cell responses in antigen-sensitized and -challenged mice [J].
Busse, Paula J. ;
Zhang, Teng Fei ;
Srivastava, Kamal ;
Schofield, Brian ;
Li, Xiu-Min .
CLINICAL AND EXPERIMENTAL ALLERGY, 2007, 37 (09) :1392-1403
[10]   Frailty syndrome: an overview [J].
Chen, Xujiao ;
Mao, Genxiang ;
Leng, Sean X. .
CLINICAL INTERVENTIONS IN AGING, 2014, 9 :433-441