Department of Otolaryngology-Head and Neck Surgery, Vanderbilt University Medical Center, Nashville, TN.
Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Int Forum Allergy Rhinol. 2019 Mar;9(3):255-264. doi: 10.1002/alr.22249. Epub 2018 Nov 28.
Olfactory dysfunction is a common symptom of chronic rhinosinusitis (CRS). We previously identified several cytokines potentially linked to smell loss, potentially supporting an inflammatory etiology for CRS-associated olfactory dysfunction. In the current study we sought to validate patterns of olfactory dysfunction in CRS using hierarchical cluster analysis, machine learning algorithms, and multivariate regression.
CRS patients undergoing functional endoscopic sinus surgery were administered the Smell Identification Test (SIT) preoperatively. Mucus was collected from the middle meatus using an absorbent polyurethane sponge and 17 inflammatory mediators were assessed using a multiplexed flow-cytometric bead assay. Hierarchical cluster analysis was performed to characterize inflammatory patterns and their association with SIT scores. The random forest approach was used to identify cytokines predictive of olfactory function.
One hundred ten patients were enrolled in the study. Hierarchical cluster analysis identified 5 distinct CRS clusters with statistically significant differences in SIT scores observed between individual clusters (p < 0.001). A majority of anosmic patients were found in a single cluster, which was additionally characterized by nasal polyposis (100%) and a high incidence of allergic fungal rhinosinusitis (50%) and aspirin-exacerbated respiratory disease (AERD) (33%). A random forest approach identified a strong association between olfaction and the cytokines interleukin (IL)-5 and IL-13. Multivariate modeling identified AERD, computed tomography (CT) score, and IL-2 as the variables most predictive of olfactory function.
Olfactory dysfunction is associated with specific CRS endotypes characterized by severe nasal polyposis, tissue eosinophilia, and AERD. Mucus IL-2 levels, CT score, and AERD were independently associated with smell loss.
嗅觉功能障碍是慢性鼻-鼻窦炎(CRS)的常见症状。我们之前确定了几种可能与嗅觉丧失相关的细胞因子,这些细胞因子可能支持 CRS 相关嗅觉功能障碍的炎症病因。在当前的研究中,我们试图使用层次聚类分析、机器学习算法和多元回归来验证 CRS 中嗅觉功能障碍的模式。
接受功能性内窥镜鼻窦手术的 CRS 患者在术前接受嗅觉识别测试(SIT)。使用吸收性聚氨酯海绵从中鼻道采集粘液,并使用多重流式细胞术珠测定法评估 17 种炎症介质。进行层次聚类分析以表征炎症模式及其与 SIT 评分的关联。使用随机森林方法识别预测嗅觉功能的细胞因子。
本研究共纳入 110 例患者。层次聚类分析确定了 5 个不同的 CRS 聚类,个体聚类之间 SIT 评分存在统计学差异(p < 0.001)。大多数嗅觉丧失患者集中在一个聚类中,该聚类还具有鼻息肉(100%)、变应性真菌性鼻-鼻窦炎(50%)和阿司匹林加重的呼吸道疾病(AERD)(33%)的高发病率。随机森林方法确定嗅觉与细胞因子白细胞介素(IL)-5 和 IL-13 之间存在很强的关联。多元建模确定 AERD、计算机断层扫描(CT)评分和 IL-2 是预测嗅觉功能的最具预测性的变量。
嗅觉功能障碍与严重的鼻息肉、组织嗜酸性粒细胞增多和 AERD 等特定 CRS 表型有关。粘液 IL-2 水平、CT 评分和 AERD 与嗅觉丧失独立相关。