Growth of the small airways and alveoli from childhood to the adult lung measured by aerosol-derived airway morphometry.

Understanding the human development of pulmonary air spaces is important for calculating the dose from exposure to inhaled materials as a function of age. We have measured, in vivo, the air space caliber of the small airways and alveoli at their natural full distension [total lung capacity (TLC)] by aerosol-derived airway morphometry in 53 children of age 6-22 yr and 59 adults of age 23-80 yr. Aerosol-derived airway morphometry utilizes the gravitational settling time of inhaled inert particles to infer the vertical distance necessary to produce the observed loss of particles to the airway surfaces at sequential depths into the lung. Previously, we identified anatomical features of the lung: the caliber of the transitional bronchioles [transitional effective air space dimension (EADtrans)]; the mean linear dimension of the alveoli (EADmin); and a measure of conducting airway volume [volumetric lung depth (VLDtrans)]. In the present study, we found that EADmin increased with age, from 184 microm at age 6 to 231 microm at age 22, generally accounting for the increase in TLC observed over this age range. EADtrans did not increase with TLC, averaging 572 microm, but increased with subject age and height when the entire age range of 6-80 yr is included {EADtrans (microm)=0.012[height (cm)]x[age (yr)]+508; P=0.007}. VLDtrans scaled linearly with lung volume, but VLDtrans relative to TLC did not change with age, averaging 7.04+/-1.55% of TLC. The data indicate that from childhood (age of 6 yr) to adulthood a constant number of respiratory units is maintained while both the smallest bronchioles and alveoli expand in size to produce the increased lung volume with increased age and height.

[1]  W. Thurlbeck The internal surface area of nonemphysematous lungs. , 2015, The American review of respiratory disease.

[2]  N. Rosenblum,et al.  Genetic Regulation of Branching Morphogenesis: Lessons Learned from Loss-of-Function Phenotypes , 2003, Pediatric Research.

[3]  S. Schulman,et al.  Effects of maternal nicotine exposure on branching morphogenesis of mouse fetal lung: in vivo and in vitro studies. , 2003, Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi.

[4]  A. Hislop,et al.  Lung development-the effects of chronic hypoxia. , 2003, Seminars in neonatology : SN.

[5]  P. Pharoah,et al.  Lung function and respiratory health in adolescents of very low birth weight , 2003, Archives of disease in childhood.

[6]  W. Bennett,et al.  In vivo characterization of the transitional bronchioles by aerosol-derived airway morphometry. , 1999, Journal of applied physiology.

[7]  R. Crapo,et al.  Effects of nutrition, growth hormone disturbances, training, altitude and sleep on lung volumes. , 1997, The European respiratory journal.

[8]  S. Isomae,et al.  Hydrogen passivation of iron‐related hole traps in silicon , 1996 .

[9]  P. Quanjer,et al.  Human lung growth: A review , 1996, Pediatric pulmonology.

[10]  A. Numa,et al.  Anatomic dead space in infants and children. , 1996, Journal of applied physiology.

[11]  J. Heyder,et al.  Aerosol derived airway morphometry in healthy subjects. , 1995, The European respiratory journal.

[12]  J. Heyder,et al.  Aerosol-derived lung morphometry: comparisons with a lung model and lung function indexes. , 1991, Journal of applied physiology.

[13]  J. Stocks,et al.  Compilation of reference values for lung function measurements in children. , 1989, The European respiratory journal. Supplement.

[14]  E R Weibel,et al.  Morphometry of the human pulmonary acinus , 1988, The Anatomical record.

[15]  W. Stahlhofen,et al.  Particle Deposition of Inhaled Aerosol Boluses in the Upper Human Airways , 1987 .

[16]  P. Burri,et al.  The postnatal development and growth of the human lung. II. Morphology. , 1987, Respiration physiology.

[17]  H. Kusaka,et al.  Trachea and lung dimensions in nonsmoking twins: morphological and functional studies. , 1986, Journal of applied physiology.

[18]  S. Dilly Scanning electron microscope study of the development of the human respiratory acinus. , 1984, Thorax.

[19]  M. Lebowitz,et al.  Changes in the normal maximal expiratory flow-volume curve with growth and aging. , 1983, The American review of respiratory disease.

[20]  W. Thurlbeck Postnatal human lung growth. , 1982, Thorax.

[21]  O. Raabe,et al.  Structure of the human respiratory acinus. , 1981, The American journal of anatomy.

[22]  J. Heyder,et al.  Use of aerosols to estimate pulmonary air-space dimensions. , 1981, Journal of applied physiology: respiratory, environmental and exercise physiology.

[23]  C. Carrington,et al.  Morphometry of the Human Lung , 1965, The Yale Journal of Biology and Medicine.

[24]  M C Hart,et al.  Relation between anatomic respiratory dead space and body size and lung volume , 1963, Journal of applied physiology.

[25]  M. Dunnill,et al.  Postnatal Growth of the Lung , 1962 .

[26]  Matthias Ochs,et al.  The number of alveoli in the human lung. , 2004, American journal of respiratory and critical care medicine.

[27]  Nobuyuki Itoh,et al.  Tube or not tube: remodeling epithelial tissues by branching morphogenesis. , 2003, Developmental cell.

[28]  W. Bennett,et al.  Measuring alveolar dimensions at total lung capacity by aerosol-derived airway morphometry. , 1995, Journal of aerosol medicine : the official journal of the International Society for Aerosols in Medicine.

[29]  J. Heyder,et al.  Aerosol Derived Airway Morphometry at Different Levels of Lung Inflation , 1993 .

[30]  J. Heyder Assessment of Airway Geometry with Inert Aerosols , 1989 .

[31]  F. Rosenthal Aerosol recovery following breathholding derived from the distribution of chordlengths in pulmonary tissue , 1989 .