Black-pigmented material in airway macrophages from healthy children: association with lung function and modeled PM10.

Epidemiologic studies in children suggest that chronic inhalation of carbonaceous particulate matter < or = 10 pm in aerodynamic diameter (PM10) attenuates the normal growth of lung function. However, the relation between markers of PM10 exposure and the quantity of particles entering the pediatric airway is unclear. Experimental studies have shown that particles entering the lower airway remain visible in the cytoplasm of airway macrophages (AMs) for several months. We hypothesized that particle loading of AMs, detected as black-pigmented material, reflects individual exposure of healthy children to PM10. In this study, we aimed to establish the relation between the median area of black material in AMs (measured as the two-dimensional area of black material ["black area"] per AM per child) and (1) lung function, and (2) level of primary PM10 at the child's home address as estimated by dispersion modeling (referred to as "modeled primary PM10"). We also performed a series of exploratory analyses assessing the association between the median black area in AMs and (1) variables that could modify individual exposure, and (2) airway inflammation. To achieve these aims, AMs were sampled using induced sputum from children in Leicestershire, United Kingdom, and lung function was determined by spirometry. Data from 64 of 116 children who provided adequate induced sputum samples were analyzed. The area of the black material in AMs was determined by an analysis of digitized light-microscopic images of 100 randomly chosen AMs per child. There was a significant inverse association between size of black area in AMs and lung function: each 1.0-microm2 increase in the area of the black material in AMs was associated with a 17.0% (95% confidence interval [CI], 5.6 to 28.4) reduction in forced expiratory volume in one second (FEV1), a 12.9% (95% CI, 0.9 to 24.8) reduction in forced vital capacity (FVC), and a 34.7% (95% CI, 11.3 to 58.1) reduction in forced expiratory flow between 25% and 75% of forced vital capacity (FEF25%-75%). These associations were not affected by bronchodilator treatment. There was also an association between modeled exposure to primary PM10 and area of black material in AMs: each 1.0-microg/m3 increase in primary PM10 was associated with an increase of 0.10 microm2 (95% CI, 0.01 to 0.18) in black area in AMs. There was no significant association between the median black area in AMs and age, height, weight, sex, activity level, and levels of neutrophilic airway inflammation in the induced sputum. We conclude that the median area of black material in AMs in children is a promising marker of individual exposure to carbonaceous PM10 and that our data strengthen the epidemiologic data suggesting that PM10 impairs the growth of lung function in children.

[1]  Lesley Rushton,et al.  Carbon in airway macrophages and lung function in children , 2006, European Respiratory Review.

[2]  P. Rufin [Pulmonary function testing in children]. , 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[3]  M. Cooke,et al.  Neutrophils in induced sputum from healthy children: role of interleukin-8 and oxidative stress. , 2007, Respiratory medicine.

[4]  G. Verleden,et al.  Fine Particles in Alveolar Macrophages and Their Association With Outdoor Particulate Air Pollution , 2007 .

[5]  A. Aggarwal,et al.  Comparison of Indian reference equations for spirometry interpretation , 2007, Respirology.

[6]  B. Brunekreef,et al.  Long-term personal exposure to PM2.5, Soot and NOx in children attending schools located near busy roads, a validation study , 2007 .

[7]  C. Henríquez-Roldán,et al.  Pediatric Respiratory and Systemic Effects of Chronic Air Pollution Exposure: Nose, Lung, Heart, and Brain Pathology , 2007, Toxicologic pathology.

[8]  L. Rushton,et al.  Locally generated particulate pollution and respiratory symptoms in young children , 2006, Thorax.

[9]  J. Schwartz,et al.  Characterization of particulate and gas exposures of sensitive subpopulations living in Baltimore and Boston. , 2005, Research report.

[10]  D. Behera,et al.  Applicability of commonly used Caucasian prediction equations for spirometry interpretation in India. , 2005, The Indian journal of medical research.

[11]  J. Grigg,et al.  Carbon loading of alveolar macrophages in adults and children exposed to biomass smoke particles. , 2005, The Science of the total environment.

[12]  K. Berhane,et al.  The effect of air pollution on lung development from 10 to 18 years of age. , 2004, The New England journal of medicine.

[13]  J. Schwartz Air pollution and children's health. , 2004, Pediatrics.

[14]  J. Ayres,et al.  Particulate air pollution and panel studies in children: a systematic review , 2004, Occupational and Environmental Medicine.

[15]  S. Salvi,et al.  Different airway inflammatory responses in asthmatic and healthy humans exposed to diesel , 2004, European Respiratory Journal.

[16]  R. Burnett,et al.  Cardiovascular Mortality and Long-Term Exposure to Particulate Air Pollution: Epidemiological Evidence of General Pathophysiological Pathways of Disease , 2003, Circulation.

[17]  Constantinos Sioutas,et al.  Controlled exposures of healthy and asthmatic volunteers to concentrated ambient particles in metropolitan Los Angeles. , 2003, Research report.

[18]  P. Gibson,et al.  Relationship between induced sputum eosinophils and the clinical pattern of childhood asthma , 2003, Thorax.

[19]  Tan Zhu,et al.  Chapter three: methodology of exposure modeling. , 2002, Chemosphere.

[20]  P. Gibson,et al.  Sputum induction in children , 2002, European Respiratory Journal.

[21]  J. Spengler,et al.  Particulate matter and lung function growth in children: a 3-yr follow-up study in Austrian schoolchildren , 2002, European Respiratory Journal.

[22]  B. Zielinska,et al.  EFFECTS OF SUBCHRONIC INHALATION EXPOSURE OF RATS TO EMISSIONS FROM A DIESEL ENGINE BURNING SOYBEAN OIL-DERIVED BIODIESEL FUEL , 2002, Inhalation toxicology.

[23]  J. Mauderly,et al.  Health effects of subchronic exposure to low levels of wood smoke in rats. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.

[24]  R. Hubbard,et al.  Living near a main road and the risk of wheezing illness in children. , 2001, American journal of respiratory and critical care medicine.

[25]  J. Foidart,et al.  Induced sputum: comparison between isotonic and hypertonic saline solution inhalation in patients with asthma. , 2001, Chest.

[26]  D. Dinsdale,et al.  Ultrafine particles in alveolar macrophages from normal children , 2001, Thorax.

[27]  S Viswanathan,et al.  Carbon monoxide modeling from transportation sources. , 2001, Chemosphere.

[28]  P. Gibson,et al.  The tolerability, safety, and success of sputum induction and combined hypertonic saline challenge in children. , 2001, American journal of respiratory and critical care medicine.

[29]  J. Hogg,et al.  Cytokines involved in the systemic inflammatory response induced by exposure to particulate matter air pollutants (PM(10)). , 2001, American journal of respiratory and critical care medicine.

[30]  R. Devlin,et al.  Canines as sentinel species for assessing chronic exposures to air pollutants: part 2. Cardiac pathology. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[31]  M. Brauer,et al.  Air quality in postunification Erfurt, East Germany: associating changes in pollutant concentrations with changes in emissions. , 2001, Environmental health perspectives.

[32]  C. J. Chung,et al.  Canines as sentinel species for assessing chronic exposures to air pollutants: part 1. Respiratory pathology. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.

[33]  P. Gibson,et al.  Noninvasive assessment of airway inflammation in children: induced sputum, exhaled nitric oxide, and breath condensate. , 2000, The European respiratory journal.

[34]  W G Kreyling,et al.  Daily mortality and fine and ultrafine particles in Erfurt, Germany part I: role of particle number and particle mass. , 2000, Research report.

[35]  R. Burnett,et al.  Identifying subgroups of the general population that may be susceptible to short-term increases in particulate air pollution: a time-series study in Montreal, Quebec. , 2000, Research report.

[36]  M. Silverman,et al.  Induced sputum in children: feasibility, repeatability, and relation of findings to asthma severity. , 2000, Thorax.

[37]  L. Kobzik,et al.  Alveolar macrophage-environmental particle interaction: analysis by flow cytometry. , 2000, Methods.

[38]  T. Sandström,et al.  Airway inflammation following exposure to diesel exhaust: a study of time kinetics using induced sputum. , 2000, The European respiratory journal.

[39]  R M Harrison,et al.  Particulate matter in the atmosphere: which particle properties are important for its effects on health? , 2000, The Science of the total environment.

[40]  S T Holgate,et al.  Acute exposure to diesel exhaust increases IL-8 and GRO-alpha production in healthy human airways. , 2000, American journal of respiratory and critical care medicine.

[41]  I. Pavord,et al.  Induced sputum inflammatory mediator concentrations in eosinophilic bronchitis and asthma. , 2000, American journal of respiratory and critical care medicine.

[42]  M. Cenci,et al.  Carbon and hemosiderin-laden macrophages in sputum of traffic policeman exposed to air pollution. , 1999, Archives of environmental health.

[43]  Y. Schwarz,et al.  Assessment of hazardous dust exposure by BAL and induced sputum. , 1999, Chest.

[44]  C. Holman Sources of Air Pollution , 1999 .

[45]  R. Devlin,et al.  Retention and intracellular distribution of instilled iron oxide particles in human alveolar macrophages. , 1998, American journal of respiratory cell and molecular biology.

[46]  B. Brunekreef,et al.  Childhood exposure to PM10: relation between personal, classroom, and outdoor concentrations. , 1997, Occupational and environmental medicine.

[47]  U. Costabel,et al.  Smoker's lung transplanted to a nonsmoker. Long-term detection of smoker's macrophages. , 1997, American journal of respiratory and critical care medicine.

[48]  B. Brunekreef,et al.  Motor vehicle exhaust and chronic respiratory symptoms in children living near freeways. , 1997, Environmental research.

[49]  Bert Brunekreef,et al.  Air Pollution from Truck Traffic and Lung Function in Children Living near Motorways , 1997, Epidemiology.

[50]  Mark A Pereira,et al.  A collection of Physical Activity Questionnaires for health-related research. , 1997, Medicine and science in sports and exercise.

[51]  M. Sagai,et al.  Biological effects of diesel exhaust particles (DEP). III. Pathogenesis of asthma like symptoms in mice. , 1996, Free radical biology & medicine.

[52]  U. Epa Air Quality Criteria for Particulate Matter , 1996 .

[53]  John L. Hankinson,et al.  Standardization of Spirometry, 1994 Update. American Thoracic Society. , 1995, American journal of respiratory and critical care medicine.

[54]  R. Harrison,et al.  The chemical composition of airborne particles in the UK atmosphere , 1995 .

[55]  M. Sagai,et al.  Biological effects of diesel exhaust particles (DEP). II. Acute toxicity of DEP introduced into lung by intratracheal instillation. , 1995, Toxicology.

[56]  L. C. Rainey,et al.  Characterization by scanning transmission electron microscopy of silica particles from alveolar macrophages of coal miners. , 1994, Environmental health perspectives.

[57]  P. de Vuyst,et al.  Comparative analysis of inhaled particles contained in human bronchoalveolar lavage fluids, lung parenchyma and lymph nodes. , 1994, Environmental health perspectives.

[58]  R K Griffiths,et al.  Hospital admissions for asthma in preschool children: relationship to major roads in Birmingham, United Kingdom. , 1994, Archives of environmental health.

[59]  U Keil,et al.  Self-reported wheezing and allergic rhinitis in children and traffic density on street of residence. , 1994, Annals of epidemiology.

[60]  M. Wjst,et al.  Road traffic and adverse effects on respiratory health in children. , 1993, BMJ.

[61]  M. Rosenthal,et al.  Lung function in white children aged 4 to 19 years: II--Single breath analysis and plethysmography. , 1993, Thorax.

[62]  A. Kriska,et al.  The epidemiology of leisure physical activity in an adolescent population. , 1993, Medicine and science in sports and exercise.

[63]  D. Strachan,et al.  Determinants of passive smoking in children in Edinburgh, Scotland. , 1992, American journal of public health.

[64]  C. Feyerabend,et al.  A rapid gas‐liquid chromatographic method for the determination of cotinine and nicotine in biological fluids , 1990, The Journal of pharmacy and pharmacology.

[65]  R. West,et al.  Saliva cotinine as an indicator of cigarette smoking in adolescents. , 1987, British journal of addiction.

[66]  Eisen Jd,et al.  Pulmonary function testing in children. , 1987, Clinics in chest medicine.

[67]  A. Nunn,et al.  A survey of ventilatory capacity in Chinese subjects in Hong Kong. , 1982, Annals of human biology.

[68]  G. Polgar,et al.  The functional development of the respiratory system from the period of gestation to adulthood. , 1979, The American review of respiratory disease.

[69]  A. Arstila,et al.  Pulmonary deposits of titanium dioxide in cytologic and lung biopsy specimens. Light and electron microscopic x-ray analysis. , 1975, Laboratory investigation; a journal of technical methods and pathology.