Bullone Michela, Beauchamp Guy, Godbout Mireille, Martin James G, Lavoie Jean-Pierre
Department of Clinical Sciences, Faculty of Veterinary Medicine, Université de Montréal, St-Hyacinthe, Quebec, Canada.
Meakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, Quebec, Canada.
PLoS One. 2015 Sep 8;10(9):e0136284. doi: 10.1371/journal.pone.0136284. eCollection 2015.
Endobronchial ultrasonography (EBUS) revealed differences in the thickness of the layer representing subepithelial tissues (L2) between human asthmatics and controls, but whether this measurement correlates with airway smooth muscle (ASM) remodeling in asthma is unknown. In this study, we sought to determine the ability of EBUS to predict histological ASM remodeling in normal and equine asthmatic airways. We studied 109 isolated bronchi from the lungs of 13 horses. They underwent EBUS examination using a 30 MHz radial probe before being processed for histology. ASM remodeling parameters were evaluated in EBUS images (L2 thickness, L2 area, L2 area/internal perimeter [Pi] and L2 area/Pi2) and histological cuts (ASM area/Pi2), and compared. EBUS was then performed ex vivo on the lungs of 4 horses with heaves, an asthma-like condition of horses, and 7 controls to determine whether central bronchial remodeling could be detected with this technique. An optimized approach was developed based on data variability within airways, subjects, and groups, and then validated in 7 horses (3 controls, 4 with heaves) that underwent EBUS in vivo. L2 area was significantly associated to ASM area in isolated lungs (p<0.0001), in the absence of significant bias related to the airway size. Bronchial size significantly affected EBUS ASM-related parameters, except for L2 area/Pi2. L2 area/Pi2 was increased in the airways of asthmatic horses compared to controls, both ex vivo and in vivo (p<0.05). Bronchial histology confirmed our findings (AASM/Pi2 was increased in asthmatic horses compared to controls, p<0.05). In both horses with heaves and controls, L2 was composed of ASM for the outer 75% of its thickness and by ECM for the remaining inner 25%. In conclusion, EBUS reliably allows assessment of asthma-associated ASM remodeling of central airways in a non-invasive way.
支气管内超声检查(EBUS)显示,人类哮喘患者与对照组之间代表上皮下组织的层(L2)厚度存在差异,但该测量值是否与哮喘中的气道平滑肌(ASM)重塑相关尚不清楚。在本研究中,我们试图确定EBUS预测正常和马哮喘气道中组织学ASM重塑的能力。我们研究了来自13匹马肺部的109条离体支气管。在进行组织学处理之前,使用30 MHz径向探头对它们进行了EBUS检查。在EBUS图像(L2厚度、L2面积、L2面积/内周长[Pi]和L2面积/Pi2)和组织切片(ASM面积/Pi2)中评估ASM重塑参数,并进行比较。然后对4匹患有气喘(一种马的哮喘样疾病)的马和7匹对照马的肺进行离体EBUS检查,以确定该技术是否能检测到中央支气管重塑。基于气道、受试者和组内的数据变异性开发了一种优化方法,然后在7匹接受体内EBUS检查的马(3匹对照马、4匹患有气喘的马)中进行了验证。在离体肺中,L2面积与ASM面积显著相关(p<0.0001),且与气道大小无关,无显著偏差。支气管大小显著影响EBUS与ASM相关的参数,但L2面积/Pi2除外。与对照组相比,哮喘马气道中的L2面积/Pi2在离体和体内均增加(p<0.05)。支气管组织学证实了我们的发现(与对照组相比,哮喘马的AASM/Pi2增加,p<0.05)。在患有气喘的马和对照马中,L2厚度的外75%由ASM组成,其余内25%由细胞外基质组成。总之,EBUS能够以非侵入性方式可靠地评估中央气道与哮喘相关的ASM重塑。