[基于多维特征的无监督聚类分析揭示了慢性鼻窦炎伴鼻息肉患者不同表型的临床特征和相关因素】。]

J Y Huang, Y G Luo, H Lyu, D Liu, Y F Wang, P Q Liu, L Tan, R Xiang, W Zhang, Y Xu
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引用次数: 0

摘要

目的利用常规临床参数,通过无监督聚类分析,发现慢性鼻炎伴鼻息肉(CRSwNP)患者不同聚类的临床特征。研究方法前瞻性地收集了2021年至2023年在武汉大学人民医院接受鼻内镜手术的155例CRSwNP患者的临床资料,其中男性112例,女性43例,年龄7至87岁。利用各种临床参数进行无监督聚类分析,包括年龄、性别、吸烟和饮酒史、局部嗜酸性粒细胞(EOS)和中性粒细胞(NEU)计数、合并过敏性鼻炎(AR)、合并哮喘、复发状况、血清特异性 IgE、总 IgE、细胞因子水平、通过外周血 EOS 计数和百分比、Lund-Mackay CT 评分、上颌窦和筛窦 CT 评分比值(E/M 比值)、视觉模拟量表(VAS)评分、Lund-Kennedy 内窥镜评分以及其他常见临床指标来阐明各组群的临床特征。统计分析使用 GraphPad Prism 9.5 软件进行。结果层次聚类分析确定了四个主要聚类(聚类 A1-A4),显示出不同的特征,如轻度鼻息肉伴有较高的外周血细胞因子水平、鼻息肉伴有过敏和哮喘、鼻息肉亚型以中性粒细胞为主且复发率高、鼻息肉伴有高嗜酸性粒细胞水平。进一步的子集聚类发现,两个轻度息肉群(群 B1-B2)具有细胞因子高表达和合并 AR 的特点;两个重度息肉群(群 B3-B4)症状严重,Lund-Mackay CT 评分高,Lund-Kennedy 内镜评分高。B3组和B4组之间的差异包括症状复杂程度、嗜酸性粒细胞浸润程度以及合并哮喘的可能性。对嗜酸性粒细胞鼻息肉的进一步聚类分析显示,该聚类的特点是高度嗜中性粒细胞浸润和鼻息肉反复发作。多指标相关性的综合分析表明了鼻息肉常见临床参数之间的关系,为深入了解 CRSwNP 的发病机制提供了宝贵的信息。结论本研究的聚类分析根据临床特征和疾病结局将 CRSwNP 患者分为不同的群组,为更精确的临床治疗策略提供了新的视角。
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[Unsupervised clustering analysis based on multidimensional features reveals distinct clinical characteristics and associated factors of different phenotypes in patients with chronic rhinosinusitis with nasal polyp].

Objective: To utilize routinely available clinical parameters to uncover the clinical features of different clusters in patients with chronic rhinosinusitis with nasal polyp (CRSwNP) through unsupervised clustering analysis. Methods: The clinical data from 155 CRSwNP patients undergoing nasal endoscopic surgery at Renmin Hospital of Wuhan University from 2021 to 2023 were prospectively collected, including 112 males and 43 females, aged from 7 to 87 years. Unsupervised clustering analysis was conducted using various clinical parameters, including age, gender, smoking and drinking history, local eosinophil (EOS) and neutrophil (NEU) counts, comorbid allergic rhinitis (AR), comorbid asthma, recurrence status, serum-specific IgE, total IgE, cytokine levels, peripheral blood EOS count and percentage, Lund-Mackay CT score, the ratio of CT scores for the maxillary sinus and ethmoid sinus (E/M ratio), visual analogue scale (VAS) score, Lund-Kennedy endoscopic score, and other common clinical indicators to elucidate the clinical characteristics of each cluster. Statistical analysis was conducted using GraphPad Prism 9.5 software. Results: Hierarchical clustering analysis identified four main clusters (Cluster A1-A4), showcasing distinct characteristics such as mild nasal polyps with higher peripheral blood cytokines levels, nasal polyps accompanied by allergies and asthma, a subtype of nasal polyps with high recurrence rates dominated by neutrophils, and nasal polyps with high eosinophil levels. Further subset clustering revealed two clusters of mild polyps (Cluster B1-B2) featuring high cytokine expression and comorbid AR; and two clusters of severe polyps (Cluster B3-B4) presented with severe symptoms, high Lund-Mackay CT score, and high Lund-Kennedy endoscopic score. Variations between Cluster B3 and B4 included symptom complexity, the degree of eosinophil infiltration, and the probability of comorbid asthma. Further clustering analysis for eosinophilic nasal polyps revealed a cluster characterized by highly neutrophilic infiltration and recurrent nasal polyps. The comprehensive analysis of multi-index correlations demonstrated valuable insights into the relationships between common clinical parameters of nasal polyps, providing valuable information for a deeper understanding of the pathogenesis of CRSwNP. Conclusion: The clustering analysis in this study categorizes CRSwNP patients into different clusters based on clinical features and disease outcomes, providing a new perspective for more precise clinical treatment strategies.

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