Norwich Medical School, University of East Anglia, Norwich, UK.
James Paget University Hospital, Gorleston, UK.
Am J Rhinol Allergy. 2023 Nov;37(6):705-729. doi: 10.1177/19458924231190568. Epub 2023 Jul 25.
Chronic rhinosinusitis (CRS) is a heterogeneous condition characterized by differing inflammatory endotypes. The identification of suitable biomarkers could enable personalized approaches to treatment selection.
This study aimed to identify and summarize clinical studies of biomarkers in adults with CRS in order to inform future research into CRS endotypes.
We conducted systematic searches of MEDLINE and Web of Science from inception to January 30, 2022 and included all clinical studies of adult CRS patients and healthy controls measuring biomarkers using enzyme-linked immunosorbent assays or Luminex immunoassays. Outcomes included the name and tissue type of identified biomarkers and expression patterns within CRS phenotypes. Study quality was assessed using the National Institutes of Health quality assessment tool for observational cohort and cross-sectional studies. A narrative synthesis was performed.
We identified 78 relevant studies involving up to 9394 patients, predominantly with CRS with nasal polyposis. Studies identified 80 biomarkers from nasal tissue, 25 from nasal secretions, 14 from nasal lavage fluid, 24 from serum, and one from urine. The majority of biomarkers found to distinguish CRS phenotypes were identified in nasal tissue, especially in nasal polyps. Serum biomarkers were more commonly found to differentiate CRS from controls. The most frequently measured biomarker was IL-5, followed by IL-13 and IL-4. Serum IgE, IL-17, pentraxin-3 and nasal phospho-janus kinase 2, IL-5, IL-6, IL-17A, granulocyte-colony stimulating factor, and interferon gamma were identified as correlated with disease severity.
We have identified numerous potential biomarkers to differentiate a range of CRS phenotypes. Future studies should focus on the prognostic role of nasal tissue biomarkers or expand on the more limited studies of nasal secretions and nasal lavage fluid.We registered this study in PROSPERO (CRD42022302787).
慢性鼻-鼻窦炎(CRS)是一种异质性疾病,其特征为不同的炎症表型。鉴定合适的生物标志物可以实现针对治疗选择的个体化方法。
本研究旨在对成人 CRS 患者的生物标志物临床研究进行鉴定和总结,以便为未来的 CRS 表型研究提供信息。
我们对 MEDLINE 和 Web of Science 从建库至 2022 年 1 月 30 日进行了系统检索,纳入了所有使用酶联免疫吸附测定法或 Luminex 免疫测定法测量生物标志物的成人 CRS 患者和健康对照的临床研究。研究结果包括鉴定出的生物标志物的名称和组织类型,以及 CRS 表型中的表达模式。使用美国国立卫生研究院观察性队列和横断面研究质量评估工具对研究质量进行评估。采用叙述性综述进行分析。
我们共确定了 78 项相关研究,共纳入了多达 9394 例患者,其中主要为伴有鼻息肉的 CRS 患者。研究从鼻组织中鉴定出 80 种生物标志物,从鼻分泌物中鉴定出 25 种,从鼻灌洗液中鉴定出 14 种,从血清中鉴定出 24 种,从尿液中鉴定出 1 种。发现可区分 CRS 表型的大多数生物标志物均来自鼻组织,尤其是鼻息肉。血清生物标志物更常用于区分 CRS 与对照。测量最多的生物标志物是 IL-5,其次是 IL-13 和 IL-4。血清 IgE、IL-17、五聚素 3 和磷酸化 Janus 激酶 2、IL-5、IL-6、IL-17A、粒细胞集落刺激因子和干扰素 γ 被鉴定为与疾病严重程度相关。
我们已经鉴定出许多潜在的生物标志物来区分多种 CRS 表型。未来的研究应侧重于鼻组织生物标志物的预后作用,或扩展对鼻分泌物和鼻灌洗液研究较少的研究。我们在 PROSPERO(CRD42022302787)中对本研究进行了注册。