Morphometric analysis of bronchial cartilage in chronic obstructive pulmonary disease and bronchial asthma

被引:43
作者
Haraguchi, M [1 ]
Shimura, S [1 ]
Shirato, K [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Internal Med 1, Aoba Ku, Sendai, Miyagi 9808574, Japan
关键词
D O I
10.1164/ajrccm.159.3.9712144
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
To clarify the changes in bronchial cartilage in diseased airways, we performed morphometric analysis of airways in autopsied lungs of 16 patients with chronic bronchitis (Group CB), pulmonary emphysema (Group PE), and branchial asthma (Group BA), and in control patients without respiratory diseases (Group CN). Although degeneration of branchial cartilage was clearly observed in airways from all groups except Group CN, the most extreme change was seen in Group CB. Increased perichondrial fibrosis was observed in both Groups CB and BA, and the more extreme change was seen in Group BA. Both the area proportions of degenerated cartilage (Deg%) and perichondrial fibrosis (Fib%) to total cartilage in bronchi (3 to 8 mm in diameter), cut vertically in the cross-section profile, were measured with a digitizing tablet coupled to a computer. No significant differences in the area proportion of cartilage to bronchial wall were observed among the four study groups. The Deg% values of Groups CB (mean: 15.4%), BA (mean: 12.9%), and PE (mean: 9.6%) were significantly higher than those of Group CN (mean: 1.0%) (p < 0.01 in each case). The Deg% values correlated significantly with the number of neutrophils in the branchial walls (r = 0.63, p < 0.01). Both Group CB (mean: 28.5%) and Group BA (mean: 33.6%) showed significantly higher values of Fib% than did Group CN (mean: 18.5%) (p < 0.01, each), and the value for Group PE (mean: 21.8%) was slightly increased (p < 0.05). The values of Fib% correlated significantly with the number of eosinophils in the bronchial walls (r = 0.51, p < 0.05), thickness of basement membrane (r = 0.77, p < 0.0002), bronchial gland area (r = 0.56, p < 0.02), and goblet-cell area (r = 0.55, p < 0.02). Further, the values of Deg% correlated significantly with those of Fib% (r = 0.64, p < 0.01). These findings indicate that airways in chronic obstructive pulmonary disease and branchial asthma have both degenerative changes in the cartilage (chondrocytes) and increased perichondrial fibrosis, and that these alterations in bronchial cartilage may differ in chronic bronchitis and bronchial asthma.
引用
收藏
页码:1005 / 1013
页数:9
相关论文
共 40 条
[1]   MARKED GOBLET CELL HYPERPLASIA WITH MUCUS ACCUMULATION IN THE AIRWAYS OF PATIENTS WHO DIED OF SEVERE ACUTE ASTHMA ATTACK [J].
AIKAWA, T ;
SHIMURA, S ;
SASAKI, H ;
EBINA, M ;
TAKISHIMA, T .
CHEST, 1992, 101 (04) :916-921
[2]   MORPHOMETRIC ANALYSIS OF INTRALUMINAL MUCUS IN AIRWAYS IN CHRONIC OBSTRUCTIVE PULMONARY-DISEASE [J].
AIKAWA, T ;
SHIMURA, S ;
SASAKI, H ;
TAKISHIMA, T ;
YAEGASHI, H ;
TAKAHASHI, T .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (02) :477-482
[3]   MODIFICATION OF NA AND CL TRANSPORT IN CANINE TRACHEAL MUCOSA BY PROSTAGLANDINS [J].
ALBAZZAZ, F ;
YADAVA, VP ;
WESTENFELDER, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1981, 240 (02) :F101-F105
[4]   Adenosine receptor-mediated relaxation of rabbit airway smooth muscle: a role for nitric oxide [J].
Ali, S ;
Metzger, WJ ;
Olanrewaju, HA ;
Mustafa, SJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 273 (03) :L581-L587
[5]  
[Anonymous], 1987, AM REV RESPIR DIS, V136, P225
[6]  
AOKI T, 1984, AM REV RESPIR DIS, V129, P465
[7]  
BERGIN C, 1986, AM REV RESPIR DIS, V133, P541
[8]   MYOFIBROBLASTS AND SUBEPITHELIAL FIBROSIS IN BRONCHIAL-ASTHMA [J].
BREWSTER, CEP ;
HOWARTH, PH ;
DJUKANOVIC, R ;
WILSON, J ;
HOLGATE, ST ;
ROCHE, WR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1990, 3 (05) :507-511
[9]   EPIDEMIOLOGIC EVIDENCE FOR DIFFERENT TYPES OF CHRONIC AIR-FLOW OBSTRUCTION [J].
BURROWS, B .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 143 (06) :1452-1455
[10]   Airway structure and inflammatory cells in fatal attacks of asthma [J].
Carroll, N ;
Carello, S ;
Cooke, C ;
James, A .
EUROPEAN RESPIRATORY JOURNAL, 1996, 9 (04) :709-715