4.7 Article

Prognostic and pharmacologic value of cystatin SN for chronic rhinosinusitis with nasal polyps

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 148, 期 2, 页码 450-460

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2021.01.036

关键词

Chronic rhinosinusitis with nasal polyps; CRSwNP; cystatin SN; cytokines; endotype; management

资金

  1. National Natural Science Foundation of China [81900917, 81630023, 81870698, 82025010]
  2. Beijing Natural Science Foundation [7194247]
  3. Beijing Municipal Administration of Hospitals incubating Program [PX2019007]
  4. CAMS Innovation Fund for Medical Sciences [2019I2M5022]
  5. Program for Changjiang Scholars and Innovative Research Team [IRT13082]
  6. National Key R&D Program of China [2018YFC0116800, 2016YFC20160905200]
  7. Research of Capital Health Security and Cultivation [Z18110700160000]
  8. Beijing Municipal Administration of Hospitals' Mission Plan [SML20150203]
  9. Beijing Municipal Administration of Hospitals' Innovation Program of Clinical Techniques [XMLX201816]
  10. Priming Scientific Research Foundation for the Senior Researcher in Beijing TongRen Hospital, Capital MedicalUniversity [2017YJJGGL005]
  11. Beijing Municipal Administration of Hospitals' Youth Programme [QML20150202]

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This study found that cystatin SN levels in nasal secretions are strongly associated with the uncontrolled status of CRSwNP patients, with higher concentrations indicating a lower risk of uncontrolled status. Enhanced medical treatment for patients with high cystatin SN levels can delay the onset of uncontrolled status.
Background: Integrated care pathways improve the management of patients with chronic rhinosinusitis with nasal polyps (CRSwNP). The application of integrated care pathways requires development of endotype-based biomarkers to stratifypatients. The value of cytokines and markers induced by cytokines for the management of CRSwNP is largely unknown. Objectives: Our aim was to determine the prognostic and pharmacologic value of type 2, non-type 2 cytokines, and markers associated with type 2 inflammation, including CCL26, periostin, and cystatin SN, in nasal secretions for CRSwNP. Methods: This retrospective study assigned 151 patients with CRSwNP to the discovery and validation phases. Concentrations of cytokines, CCL26, periostin, and cystatin SN in nasal secretions were determined by using Luminex and ELISA. Predictive significance was assessed with receiver operating characteristic curves. Survival analysis was performed by using Kaplan-Meier curves and Cox regression models. Results: Cystatin SN was an independent predictor of the uncontrolled status of CRSwNP over a 2-year follow-up after adjustment for other risk factors (hazard ratio = 1.168 and 1.132 in the discovery and validation phases, respectively; both P < .001). Patients with high cystatin SN concentrations presented with a faster onset and higher rate of uncontrolled status than did those with low levels (P < .001). Enhanced medical treatment for patients with high cystatin SN levels postponed the uncontrolled status in the discovery (P = .016) and validation (P = .002) phases but did not completely abolish it by the end of the follow-up. Conclusion: Cystatin SN levels in nasal secretions hold strong prognostic value and can facilitate medical instructions for managing CRSwNP.

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