Division of Medicine, "Division of Rehabilitation, Misasa Medical Center, Okayama University Medical and Dental School

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35 Low attenation area in asthma and Difference in low attenuation area (LAA) of the lungs on high resolution computed tomography (HRCT) between asthma and in relation to cigarette smoking Fumihiro Mitsunobu, Yasuhiro Hosaki, Kozo Ashida, Naofumi Iwagaki, Takuya Nagata, Makoto Fujii, Shingo Takata, Tadashi Yokoi ' ', Masanori Hamada ' ', and Yoshiro Tanizaki Division of Medicine, "Division of Rehabilitation, Misasa Medical Center, Okayama University Medical and Dental School Abstract : The low attenuation area (LAA) of the lungs on high resolution computed tomography (HRCT) was evaluated in 20 asthmatics (10 ex- smokers and 10 never - smokers) and 10 patients with (all s) by ventilatory function, lung volume, DLco, and a ratio of expiratory Winspiratory LAA. 1. The %LAA of the lungs on HRCT was significantly larger in patients with (PE) than in those with asthma, but there was not significant difference in %LAA between s and s of asthmatics. 2. A ratio of expiratory Winspiratory LAA was significantly higher in patients with PE than in those with asthma, and the ratio was significantly higher in s of asthmatics than in s (p<0.05). 3. The difference in %residual volume and %DLco was significant between asthma and PE, and between ex - smokers and never - smokers of asthmatics (%RV : p<0.05, DLco : p<0.05). 4. The difference in the values of %FVC, %FEVl.O, and FEV1.0% was significant between asthma and PE, but not sig- nificant between ex- smokers and never- smokers of asthmatics. The results suggest that the difference in a ratio of expiratory W inspiratory LAA, %RV and %DLco was significant between ex - smokers and never - smokers of asthmatics, and cigarette smoking induces more irreversible changes of the lungs. Key words : low attenuation area, asthma,, cigarette smoking, residual volume, DLco

Low attenation area in asthma and Introduction Subjects and Methods Asthma is a disease characterized by transient wheezing and dyspnea elicited by narrowing of the airways due to bronchoconstriction, edema of mucous membrane, and hypersecretion. The main pathogenesis of onset mechanisms of the disease is well known to be airway inflammation, in which IgE-mediated allergy play an important role, and an increase in muscle mass, mucous gland hypertrophy, and reorganization of the extracellular matrix, have been found in the inflammatory process. Furthermore, airway reconstruction such as bronchial wall thickening, bronchiectasis, tous changes' 3', and mosaic patterns of lung attenuation has been found by high resolution computed tomography (HRCT) in patients with asthma4. 5'. It has been shown that asthmatics with abnormal HRCT findings demonstrate poorer lung function and less hyperresponsive bronchi than those with normal HRCT findings6'. In contrast, low attenuation area (LAA) < -950 Hounsfield Units (HU) of the lungs on HRCT scans obtained at full inspiration is an objective measure of 7.''. A previous study suggested that the percentage of pixels below -900 HU is significantly correlated with function, and reflects air trapping in patients with asthmag'. However, the significance of the %LAA of the lungs on HRCT scans in asthma has not been determined. In the present study, the significance of %LAA of the lungs on HRCT in asthma was examined by comparing the %LAA of asthmatics with the %LAA in patients with, and further by comparing the %LAA of s of asthmatics with the %LAA of s in relation to function. The subjects of this study were 20 asthmatics and 10 patients with (PE). Of 20 asthmatics, 10 were s (5 females and 5 males, mean age 66.3 years), and the residual 10 were s (all males, mean age 71.2 years with a smoking history of 28.6 pack-years). Ten patients with PE were all s (all males, 68.8 years with a smoking history of 46. 7 pack-years). Diagnosis of PE was made by clinical symptoms, function, chest radiography and CT findings'''. All subjects had a modified HRCT scan of the lungs with a Toshiba Xpeed scanner (Toshiba Co) using the thin section (2 mm collimation) technique and a high-resolution reconstruction algorithm. An intravenous contrast medium was not administered. The scanning time was 2.7 seconds, tube current was 200 ma, and voltage was 120 kvp. Maximal inspiratory and maximal expiratory HRCT scans were obtained at the following three selected anatomic levels as described by Miniati et a1. "' : (1) top of the aortic arch, (2) origin of the lower lobe bronchus, and (3) 3cm abovgt the top of the diaphragm. In this study, the relative area of the lungs with an attenuation value lower than -950 HU at the second level (origin of the lower lobe bronchus) was obtained both at full inspiration (inspiratory LAA) and full expiration (expiratory LAA). The ratio of expiratory LAA to inspiratory LAA was also calculated. Spirometry was performed by means of a CHESTAC 33 (Chest Co) linked to a computer when their symptoms were stable. The following measurements were performed in all subjects : forced vital capacity (FVC), forced expiratory volume in one second (FEV1.O), and FEV1. O/ FVC (FEV1.0%). Residual volume (RV) was

37 Low attenation area in asthma and measured by body plethysmography (Autobox 2800, Chest Co). The di fusing capacity for carbon monoxide (DLco) was measured by the single breath technique using a CHESTAC 33. The actual DLco values were corrected for hemoglobin and carbon monoxide levels. The FVC, FEV1.O, RV, and DLco measurements for each patient were expressed as a percent of the predicted values. Serum IgE was measured by radioimmunosorbent test (RIST), and serum IgE antibodies specific to aeroallergens including house dust mite, pollens. Moulds, and animal danders were measured using the Pharmacia CAP system (Pharmacia Diagnostics SAB). Statistically significant differences of the mean were estimated using the unpaired Student's t test. A p value of <0.05 was regarded as significant. s than in s of asthmatics (p<o. 05) (Fig. 2 ). Fig.1. %Low attenuation area (LAA) of the lung on high-resolution computed tomography (HRCT) in patients with asthma and in those with. a:p<o.oz, b:p<0.001. Results The mean serum IgE level was 298 IU/ml (range 30-925 IU/ml) in s, 279 IU/ml (33-839 IU/ml) in s of asthmatics, and 580 IU/ml (15-2298 IU/ml) in patients with PE. A positive RAST score against inhalant allergens was observed in 3 of 10 neversmokers, 7 of 10 s of asthmatics, and 6 of 10 patients with PE. The %LAA of the lungs on HRCT, ratio of expiratory LAA to inspiratory LAA, %FVC, %FEV1.0, FEV1.0%, %RV, and %DLco, were significantly different between asthmatics and patients with PE. The %LAA of the lungs on HRCT was significantly larger in patients with PE than in asthmatics, however, the dierence in the %LAA was not significant between s and s of asthmatics (Fig. 1 ). In contrast, a ratio of expiratory LAA to inspiratory LAA was significantly higher in Fig.2. A ratio of LAA (expiratory/inspiratory)in patients with asthma and in those with. a:p0.05, b:p<0.001. A significant difference between s and s of asthmatics was observed in %RV (p<0.05) (Fig. 3 ) and %DLco (p< 0.05) (Fig. 4 ). However, a difference in %FIX, %FEVl.0 and FEV1.0% values was not significant between s and exsmokers in asthma (Fig. 5, 6, 7 ).

Low attenation area in asthma and loo "1 0 pulm~nary exsmoker Fig.3. %Residual dume (%RV) in patients with asthma and in those with. a:p<0.05, b:p<0.001. Fig.6. 46FEV1.0 in patients with asthma and in those with. a:p<0.001, b:p<o.ol. Fig.4. %DLco in patients with asthma and in those with. a:p<0.05. b:p<0.001. Fig.7. never-srndrw FEVI.O% in patients with asthma and in those with. a:p<o.ol, b:p<o.ol. Discussion Fig.5. %FVC in patients with asthma and in those with. a:p<0.001, b:p<0.01. Pulmonary is defined in structural terms as 'a condition of the lung characterized by abnormal, permanent enlargement of the airspaces distal to the terminal bronchiole, accompanied by destruction of their walls'"'. Regarding the evaluation of PE, it has been suggested that the diagnosis of PE by pathologic examination is correlated with HRCT scan find- ing~'~-'". The LAA <-950 HU of the lungs on HRCT scans at full inspiration is an objective measure

39 Low attenation area in asthma and of the extent of PE7. '.I5'. The qualitative analy- sis of has been carried out according to a visual score introduced by Sakai, et a1. 16' based on the assessment of two aspects of : severity and extent. Severity was graded on a 4-point scale : 0, no ; 1, low attenuation areas < 5 mm in diameter (type 1) ; 2, circumscribed low attenuation areas > 5 mm in diameter with intervening normal lung (type 2) ; 3, diise low attenuation areas without intervening normal lung (type 3) as shown in Fig. 8. The extent of was on a 4-point scale : 1, <25% of the lung involvement ; 2,25% to 50% lung involvement ; 3, 50 to 75% lung in-volvemment ; 4, >75% lung involvement. / 1. LAA<S mm in diameter (type 1) I 1 lung 2. Circumscribed LAA>5 mm in diameter with intervening normal lung (type 2) 3. Diffuse LAA without intervening normal (type 3) Fig. 8. Severity of low attenuation area (LAA) < -950 HU of the lung on HRCT The extent of %LAA of the lungs on HRCT was significantly larger in patients with PE than in those with asthma, however, a significant difference in the extent of %LAA was not found between never- smokers and ex- smokers of asthmatics. Regarding the severity of, all asthmatics showed low attenuation areas < 5 mm in diameter of the lungs (type 1). In contrast, diffuse low attenuation areas without intervening normal lung (type 3) were observed in many patients with PE, and circumscribed low attenuation areas < 5 mm in I diameter with intervening normal lung (type 2) were in some. In addition to different severity of LAA between asthmatics and patients with PE, the ratio of expiratory LAA to inspiratory LAA was significantly different between asthmatics and patients with PE. Furthermore, a significant difference in the ratio of expiratory LAA to inspiratory LAA was observed between s and exsmokers of asthmatics : the ratio was significantly higher in s than in s of asthmatics. The results obtained here suggest that cigarette smoking induces more irreversible changes of the lungs compared with neversmoking. The higher ratio of expiratory LAA to inspiratory LAA of the lungs was closely correlated with %RV and %DLco, but not with %FVC. %FEV1.0 and FEV1.0%. References 1. Ashida K, Mitsunobu F, Mifune T, et al. : Clinical effects of spa therapy on patients with asthma accompanied by tous changes. J Jpn Assoc Phys Med Balneol Climatol 63 : 113-119, 2000. 2. Ashida K, Mitsunobu F, Mifune T, et al. : Effect of spa therapy on low attenuation area (LAA) of the lungs on high-resolution computed tomography (HRCT) and function in patients with asthma. J Jpn Assoc Phys Med Balneol Climatol64 : 203-209,2001. 3. Ashida, K, Mitsunobu F, Hosaki Y, et al. : Decrease in low attenuation area (LAA) of the lungs on high resolution computed tomography (HRCT) by long-term spa therapy in patients with asthma. J Jpn Assoc Phys Med Balneol Climatol 66 : 115122, 2003. 4. Paganin F, Trussard V, Setterre, P. et al. : Chest radiography and high resolution computed tomography of the lung in asthma. Am

Low attenation area in asthma and 40 Rev Respir Dis 147 : 405-410, 1993. 5. Angus RM, Davies ML, Cowman MD, al. : Computed tomographic scanning of the lungs in patients with allergic broncho aspergillosis and in asthmatic patients with a positive skin test to Aspergillus fumigatus. Thorax 49 : 586-589, 1994. 6. Park JW, Hong YK, Kim CW, et al. : High-resolution computed tomography in patients with : correlation with clinical features, functions and bronchial hyperresponsiveness. J Invest Allergol Clin Immunol 7 : 186-192, 1997. 7. Gevenois PA, Maertelaer V, DeVuyst P, et al. : Comparison of computed density and macroscopic morphometry in. Am J Respir Crit Care Med 154 : 187-192, 1997. 8. Gevenois PA, DeVuyst P, demaertelaer V, et al. : Comparison of computed density and microscopic morphometry in. Am J Respir Crit Care Med 154 : 187-192, 1996. 9. Newman KB, Lynch DA, Newman LS, et al. : Quantitative computed tomography detects air trapping due to asthma. Chest 106 : 105-109, 1994. 10. Miniati M, Filippi E, Falaschi F, et al. : Radiologic evaluation of in pa- tients with chronic obstructive disease : chest radiology versus high resolution computed tomography. Am J Respir Dis 151 : 1359-1367, 1995. 11. Ciba Guest Symposium Report : Terrniology, definitions, and classification of chronic and related conditions. Thorax 14 : 286-299, 1959. 12. Bergin C, Muller NL, Nichols DM, et al. : The diagnosis of. A computed tomographic - pathologic correlation. Am Rev Respir Dis 133 : 541-546, 1986. 13. Hruban RH, Meziane MA, Zehouni EA, et al. : High resolution computed tomography of inflax-fixed lungs. Pathologic-radiologic correlation of centrilobular. Am Rev Respir Dis 136 : 935-940, 1987. 14. Kuwano K, Matsuba K, Ikeda T, et al. the diagnosis of mild. Correlation of computed tomography and pathology scores. Am Rev Respir Dis 141 : 169-178, 1990. 15. Morgan MD : Detection and quantification of by computed tomography : a window of opportunity. Thorax 47 : 1001-1004, 1992. 16. Sakai F, Gamsu G, Im JG, et al. : Pulmonary function abnormalities in patients with CT-determined. J Comput Assist Tomog 11 : 963-968, 1987.