Meng Yifan, Yan Bing, Wang Yang, Wu Di, Zhang Luo, Wang Chengshuo
Department of Otolaryngology Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, 100730, China.
Beijing Key Laboratory of Nasal Diseases, Beijing Institute of Otolaryngology, Beijing, 100005, China.
World Allergy Organ J. 2020 Jun 17;13(7):100134. doi: 10.1016/j.waojou.2020.100134. eCollection 2020 Jul.
The diagnosis and treatment of nonallergic rhinitis with eosinophilia syndrome (NARES) remain controversial. The aim of this study was to evaluate whether Cystatin SN together with symptoms can be used to diagnose NARES and to measure the efficiency of medical treatment.
Seventy-five patients with chronic rhinitis (CR) and 18 control subjects were enrolled. Their clinical characteristics were reviewed and laboratory parameters were evaluated. The concentration of Cystatin SN in nasal secretions was determined using the enzyme-linked immunosorbent assay. The histological assessment of Cystatin SN in the nasal mucosa was conducted by hematoxylin and eosin staining. The logistic regression and receiver operating characteristic curves were used to assess the predictive value of parameters for NARES.
Nasal obstruction, sneezing, loss of smell, and total visual analogue scale (VAS) score were significantly different among the patients with CR. In particular, olfaction score was higher in patients with NARES than in those without NARES (AR, LAR, or IR). Similarly, the Cystatin SN level was significantly different between the control subjects and patients with CR. After treatment for 2 weeks, the Cystatin SN level and VAS score were significantly decreased in the NARES group. The accuracy of Cystatin SN together with local sIgE and loss of smell to diagnose NARES was up to 0.987 (sensitivity, 100%; specificity, 93.1%).
Cystatin SN with local sIgE and loss of smell may serve as one of the reliable and alternative biomarkers for the diagnosis of NARES and be used to evaluate disease severity and NARES treatment efficacy.
嗜酸性粒细胞增多综合征性非变应性鼻炎(NARES)的诊断和治疗仍存在争议。本研究的目的是评估胱抑素SN与症状联合使用是否可用于诊断NARES,并衡量药物治疗的效果。
纳入75例慢性鼻炎(CR)患者和18例对照受试者。回顾他们的临床特征并评估实验室参数。采用酶联免疫吸附测定法测定鼻分泌物中胱抑素SN的浓度。通过苏木精和伊红染色对鼻黏膜中的胱抑素SN进行组织学评估。采用逻辑回归和受试者工作特征曲线评估各参数对NARES的预测价值。
CR患者的鼻塞、打喷嚏、嗅觉减退及视觉模拟量表(VAS)总分存在显著差异。特别是,NARES患者的嗅觉评分高于非NARES患者(变应性鼻炎、局部变应性鼻炎或特发性鼻炎)。同样,对照受试者与CR患者之间的胱抑素SN水平也存在显著差异。治疗2周后,NARES组的胱抑素SN水平和VAS评分显著降低。胱抑素SN联合局部sIgE及嗅觉减退诊断NARES的准确率高达0.987(敏感性为100%;特异性为93.1%)。
胱抑素SN联合局部sIgE及嗅觉减退可作为诊断NARES的可靠替代生物标志物之一,用于评估疾病严重程度和NARES治疗效果。